| Adherence to Quality of Care Indicators and Location of Sickle Cell Care Within Indiana. | Meier ER, Janson IA, Hampton K, Bloom E, Duncan N, Roberson C, Rampersad A | J Community Health | 2020 |
| Keys to Recruiting and Retaining Seriously Ill African Americans With Sickle Cell Disease in Longitudinal Studies: Respectful Engagement and Persistence. | Suarez ML, Schlaeger JM, Angulo V, Shuey DA, Carrasco J, Roach KL, Ezenwa MO, Yao Y, Wang ZJ, Molokie RE, Wilkie DJ | Am J Hosp Palliat Care | 2020 |
| Acute Care Utilization at End of Life in Sickle Cell Disease: Highlighting the Need for a Palliative Approach. | Johnston EE, Adesina OO, Alvarez E, Amato H, Paulukonis S, Nichols A, Chamberlain LJ, Bhatia S | J Palliat Med | 2020 |
| GDF11 contributes to hepatic hepcidin (HAMP) inhibition through SMURF1-mediated BMP-SMAD signalling suppression. | Fang Z, Zhu Z, Zhang H, Peng Y, Liu J, Lu H, Li J, Liang L, Xia S, Wang Q, Fu B, Wu K, Zhang L, Ginzburg Y, Liu J, Chen H | Br. J. Haematol. | 2020 |
| Retinal Thickness and Microvascular Changes in Children With Sickle Cell Disease Evaluated by Optical Coherence Tomography (OCT) and OCT Angiography. | Ong SS, Linz MO, Li X, Liu TYA, Han IC, Scott AW | Am. J. Ophthalmol. | 2020 |
| Perioperative care of children with sickle cell disease: A systematic review and clinical recommendations. | Schyrr F, Dolci M, Nydegger M, Canellini G, Andreu-Ullrich H, Joseph JM, Diezi M, Cachat F, Rizzi M, Renella R | Am. J. Hematol. | 2020 |
| Neuropathic pain in individuals with sickle cell disease. | Sharma D, Brandow AM | Neurosci. Lett. | 2020 |
| Delta beta thalassemia. | Bain BJ | Am. J. Hematol. | 2020 |
| Evidence for interactions between inflammatory markers and renin-angiotensin system molecules in the occurrence of albuminuria in children with sickle cell anemia. | Belisário AR, Vieira ÉLM, de Almeida JA, Mendes FG, Miranda AS, Rezende PV, Viana MB, Simões E Silva AC | Cytokine | 2020 |
| Multicenter Evaluation of HemoTypeSC as a Point-of-Care Sickle Cell Disease Rapid Diagnostic Test for Newborns and Adults Across India. | Mukherjee MB, Colah RB, Mehta PR, Shinde N, Jain D, Desai S, Dave K, Italia Y, Raicha B, Serrao E | Am. J. Clin. Pathol. | 2020 |
| Recent advances in screening and diagnosis of hemoglobinopathy. | Ghosh K, Ghosh K, Agrawal R, Nadkarni AH | Expert Rev Hematol | 2020 |
| Quantification of whole-brain oxygenation extraction fraction and cerebral metabolic rate of oxygen consumption in adults with sickle cell anemia using individual T -based oxygenation calibrations. | Li W, Xu X, Liu P, Strouse JJ, Casella JF, Lu H, van Zijl PCM, Qin Q | Magn Reson Med | 2020 |
| Sickle Cell Intrahepatic Cholestasis with Acute Liver Failure and Acute Kidney Injury: Favourable Outcome with Exchange Transfusion. | Maji P, Malik R, Lodha R, Bagga A | Indian J Pediatr | 2020 |
| Platelet Extracellular Vesicles Drive Inflammasome-IL-1β-Dependent Lung Injury in Sickle Cell Disease. | Vats R, Brzoska T, Bennewitz MF, Jimenez MA, Pradhan-Sundd T, Tutuncuoglu E, Jonassaint J, Gutierrez E, Watkins SC, Shiva S, Scott MJ, Morelli AE, Neal MD, Kato GJ, Gladwin MT, Sundd P | Am. J. Respir. Crit. Care Med. | 2020 |
| Shedding New Light on Platelet Extracellular Vesicles in Sickle Cell Disease. | Middleton EA, Ware LB, Rondina MT | Am. J. Respir. Crit. Care Med. | 2020 |
| Retinal oximetry and fractal analysis of capillary maps in sickle cell disease patients and matched healthy volunteers. | Birkhoff WAJ, van Manen L, Dijkstra J, De Kam ML, van Meurs JC, Cohen AF | Graefes Arch. Clin. Exp. Ophthalmol. | 2020 |
| A QST-based Pain Phenotype in Adults With Sickle Cell Disease: Sensitivity and Specificity of Quality Descriptors. | Dyal BW, Ezenwa MO, Yoon SL, Fillingim RB, Yao Y, Schlaeger JM, Suarez ML, Wang ZJ, Molokie RE, Wilkie DJ | Pain Pract | 2020 |
| Curating the gnomAD database: Report of novel variants in the globin-coding genes and bioinformatics analysis. | Scheps KG, Hasenahuer MA, Parisi G, Targovnik HM, Fornasari MS | Hum. Mutat. | 2020 |
| Dengue in hospitalized children with sickle cell disease: A retrospective cohort study in the French departments of America. | Elenga N, Celicourt D, Muanza B, Elana G, Hocquelet S, Tarer V, Maillard F, Sibille G, Divialle Doumdo L, Petras M, Tressières B, Etienne-Julan M | J Infect Public Health | 2020 |
| Induction of Translational Readthrough across the Thalassemia-Causing Premature Stop Codon in β-Globin-Encoding mRNA. | Kar D, Sellamuthu K, Kumar SD, Eswarappa SM | Biochemistry | 2020 |
| Universal screening for social determinants of health in pediatric sickle cell disease: A quality-improvement initiative. | Power-Hays A, Li S, Mensah A, Sobota A | Pediatr Blood Cancer | 2020 |
| Erythrocyte Indices as Differential Diagnostic Biomarkers of Iron Deficiency Anemia and Thalassemia. | Düzenli Kar Y, Özdemir ZC, Emir B, Bör Ö | J. Pediatr. Hematol. Oncol. | 2020 |
| Evaluation of Efficacy, Safety, and Satisfaction Taking Deferasirox Twice Daily Versus Once Daily in Patients With Transfusion-Dependent Thalassemia. | Karimi M, Haghpanah S, Bahoush G, Ansari S, Azarkeivan A, Shahsavani A, Bazrafshan A, Jangjou A | J. Pediatr. Hematol. Oncol. | 2020 |
| LOVD-DASH: A comprehensive LOVD database coupled with diagnosis and an at-risk assessment system for hemoglobinopathies. | Zhang L, Zhang Q, Tang Y, Cong P, Ye Y, Chen S, Zhang X, Chen Y, Zhu B, Cai W, Chen S, Cai R, Guo X, Zhang C, Zhou Y, Zou J, Liu Y, Chen B, Yan S, Chen Y, Zhou Y, Ding H, Li X, Chen D, Zhong J, Shang X, Liu X, Qi M, Xu X | Hum. Mutat. | 2019 |
| Dual-energy X-ray absorptiometry pitfalls in Thalassemia Major. | Pellegrino F, Zatelli MC, Bondanelli M, Carnevale A, Cittanti C, Fortini M, Gamberini MR, Giganti M, Ambrosio MR | Endocrine | 2019 |
| Surface plasmon resonance based analysis of the binding of LYAR protein to the rs368698783 (G>A) polymorphic Aγ-globin gene sequences mutated in β-thalassemia. | Gemmo C, Breveglieri G, Marzaro G, Lampronti I, Cosenza LC, Gasparello J, Zuccato C, Fabbri E, Borgatti M, Chilin A, Finotti A, Gambari R | Anal Bioanal Chem | 2019 |
| Genotype-phenotype association analysis identifies the role of α globin genes in modulating disease severity of β thalassaemia intermedia in Sri Lanka. | Perera S, Allen A, Silva I, Hapugoda M, Wickramarathne MN, Wijesiriwardena I, Allen S, Rees D, Efremov DG, Fisher CA, Weatherall DJ, Premawardhena A | Sci Rep | 2019 |
| Gene therapy of hematological disorders: current challenges. | Al-Saif AM | Gene Ther. | 2019 |
| Transfusing children with hemoglobinopathies. | Allali S, Taylor M, Albinni S, Amiranoff D, de Montalembert M | Transfus Clin Biol | 2019 |
| Capillary electrophoresis and mutational images of hemoglobin sendagi [Β42 (CD1) PHE → VAL; HBB: C.127T→G]. | Recasens V, Ropero P, Lacalle L, Rodríguez-Vigil C, Montañés A, González FA, Pinzón S, Paúl P, Yus F, Rubio R, Díez R, Gómez A, Bustamante E | Clin. Biochem. | 2019 |
| Quadrupole-Time-of-Flight Mass Spectrometric Identification of Hemoglobin Subunits α, β, γ and δ in Unknown Peaks of High Performance Liquid Chromatography of Hemoglobin in β-Thalassemias. | Abdullah UYH, Ibrahim HM, Mahmud NB, Salleh MZ, Kek TL, Noorizhab MNFB, Jassim HM, Othman I, Zainal Abidin SA, Zilfalil BA, Wilairat P, Fucharoen S | Hemoglobin | 2019 |
| Sickling-preventive effects of rutin is associated with modulation of deoxygenated haemoglobin, 2,3-bisphosphoglycerate mutase, redox status and alteration of functional chemistry in sickle erythrocytes. | Muhammad A, Waziri AD, Forcados GE, Sanusi B, Sani H, Malami I, Abubakar IB, Oluwatoyin HY, Adinoyi OA, Mohammed HA | Heliyon | 2019 |
| T-cell deplete versus T-cell replete haploidentical hematopoietic stem cell transplantation for sickle cell disease: where are we? | Patel DA, Akinsete AM, Connelly JA, Kassim AA | Expert Rev Hematol | 2019 |
| Erythrocyte cAMP in Determining Frequency of Acute Pain Episodes in Sickle Cell Disease Patients from Odisha State, India. | Jit BP, Mohanty PK, Pradhan A, Purohit P, Das K, Patel S, Meher S, Sinha S, Mohanty JR, Behera RK, Das P | Hemoglobin | 2019 |
| Modelling the relationships between haemoglobin oxygen affinity and the oxygen cascade in humans. | Shepherd JRA, Dominelli PB, Roy TK, Secomb TW, Hoyer JD, Oliveira JL, Joyner MJ | J. Physiol. (Lond.) | 2019 |
| Multifocal electroretinogram findings in sickle cell maculopathy. | Beral L, Romana M, Lemonne N, Garnier Y, Billaud M, Acomat M, Zorobabel C, Etienne-Julan M, David T, Connes P | Eye (Lond) | 2019 |
| Severe oxidative stress in sickle cell disease patients with uncomplicated Plasmodium falciparum malaria in Kampala, Uganda. | Atiku SM, Louise N, Kasozi DM | BMC Infect. Dis. | 2019 |
| The experience of adults with sickle cell disease and their HLA-matched adult sibling donors after allogeneic hematopoietic stem cell transplantation. | Gallo AM, Patil CL, Knafl KA, Angst DA, Rondelli D, Saraf SL | J Adv Nurs | 2019 |
| The Inflammatory Response to Surgery in Sickle Cell Disease Patients Undergoing Cholecystectomy. | Adisa AO, Adedeji TA, Bolarinwa RA, Owojuyigbe TO, Jeje OA, Glasbey J, Akinola NO | JSLS | 2019 |
| Relationship of Pain Quality Descriptors and Quantitative Sensory Testing: Sickle Cell Disease. | Dyal BW, Ezenwa MO, Yoon SL, Fillingim RB, Yao Y, Schlaeger JM, Suarez ML, Wang ZJ, Molokie RE, Wilkie DJ | Nurs Res | 2019 |
| Use of 18F-Fluciclovine to Diagnose Recurrent Prostate Carcinoma in a Patient With Beta-Thalassemia. | Schmitt CR, Schmitt CT, Hinds PR, Sawyer KJ | Clin Nucl Med | 2019 |
| CRISPR/Cas9 Ribonucleoprotein-mediated Precise Gene Editing by Tube Electroporation. | Ma L, Jang L, Chen J, Song J, Yang D, Zhang J, Chen YE, Xu J | J Vis Exp | 2019 |
| MS-275 Chemical Analogues Promote Hemoglobin Production and Erythroid Differentiation of K562 Cells. | Voskou S, Phylactides M, Afantitis A, Melagraki G, Tsoumanis A, Koutentis PA, Mitsidi T, Mirallai SI, Kleanthous M | Hemoglobin | 2019 |
| Red blood cell alloimmunizations in beta-thalassemia patients in Casablanca/Morocco: Prevalence and risk factors. | El Kababi S, Benajiba M, El Khalfi B, Hachim J, Soukri A | Transfus Clin Biol | 2019 |
| In Vivo Outcome of Homology-Directed Repair at the HBB Gene in HSC Using Alternative Donor Template Delivery Methods. | Pattabhi S, Lotti SN, Berger MP, Singh S, Lux CT, Jacoby K, Lee C, Negre O, Scharenberg AM, Rawlings DJ | Mol Ther Nucleic Acids | 2019 |
| Erythrocyte and plasma oxidative stress appears to be compensated in patients with sickle cell disease during a period of relative health, despite the presence of known oxidative agents. | Detterich JA, Liu H, Suriany S, Kato RM, Chalacheva P, Tedla B, Shah PM, Khoo MC, Wood JC, Coates TD, Milne GL, Oh JY, Patel RP, Forman HJ | Free Radic. Biol. Med. | 2019 |
| Sickle cell disease complications: Prevalence and resource utilization. | Shah N, Bhor M, Xie L, Paulose J, Yuce H | PLoS ONE | 2019 |
| Contrast-enhanced ultrasound detects changes in microvascular blood flow in adults with sickle cell disease. | Lindner JR, Belcik T, Widlansky M, Harmann LM, Karafin MS, Wandersee NJ, Puligandla M, Neuberg D, Linden J, Field JJ | PLoS ONE | 2019 |
| Immune recovery after in vivo T-cell depletion myeloablative conditioning hematopoietic stem cell transplantation in severe beta-thalassemia children. | Qin F, Shi L, Li Q, Zhang Z, Liu L, Li J, Yang G, Lai YR | Eur. J. Haematol. | 2019 |
| Nrf2 controls iron homeostasis in haemochromatosis and thalassaemia via Bmp6 and hepcidin. | Lim PJ, Duarte TL, Arezes J, Garcia-Santos D, Hamdi A, Pasricha SR, Armitage AE, Mehta H, Wideman S, Santos AG, Santos-Gonçalves A, Morovat A, Hughes JR, Soilleux E, Wang CY, Bayer AL, Klenerman P, Willberg CB, Hartley RC, Murphy MP, Babitt JL, Ponka P, Porto G, Drakesmith H | Nat Metab | 2019 |
| Subperiosteal Orbital Hematoma: Imaging Findings of a Rare Complication of Sickle Cell Disease: Subperiosteal orbital hematoma is a rare entity mainly seen in pediatric patients with sickle cell disease and occurs secondary to local vascular disturbances following facial bone infarction. | Van de Voorde N, Parizel PM, Dekeyzer S | J Belg Soc Radiol | 2019 |
| Computational Analysis of Protein Structure Changes as a Result of Nondeletion Insertion Mutations in Human -Globin Gene Suggests Possible Cause of -Thalassemia. | Qadah T, Jamal MS | Biomed Res Int | 2019 |
| Doppler echocardiographic assessment of pulmonary artery pressure in children with sickle cell anaemia. | Lamina MO, Animasahun BA, Akinwumi IN, Njokanma OF | Cardiovasc Diagn Ther | 2019 |
| Interventions for treating neuropathic pain in people with sickle cell disease. | Asnani MR, Francis DK, Brandow AM, Hammond Gabbadon CE, Ali A | Cochrane Database Syst Rev | 2019 |
| The Impact of Perinatal Cobalt Chloride Exposure on Extramedullary Erythropoiesis, Tissue Iron Levels, and Transferrin Receptor Expression in Mice. | Gluhcheva Y, Pavlova E, Petrova E, Tinkov AA, Ajsuvakova OP, Skalnaya MG, Vladov I, Skalny AV | Biol Trace Elem Res | 2019 |
| Iranian patients with hemoglobin H disease: genotype-phenotype correlation. | Paridar M, Azizi E, Keikhaei B, Takhviji V, Baluchi I, Khosravi A | Mol. Biol. Rep. | 2019 |
| Development and characterization of cellular biosensors for HTS of erythroid differentiation inducers targeting the transcriptional activity of γ-globin and β-globin gene promoters. | Breveglieri G, Salvatori F, Finotti A, Cosenza LC, Zuccato C, Bianchi N, Breda L, Rivella S, Bresciani A, Bisbocci M, Borgatti M, Gambari R | Anal Bioanal Chem | 2019 |
| Impact of ET-1 and sex in glomerular hyperfiltration in humanized sickle cell mice. | Kasztan M, Pollock DM | Clin. Sci. | 2019 |
| β-Thalassemia in Iran: Things Everyone Needs to Know About This Disease. | Hadipour Dehshal M, Tabrizi Namini M, Hantoushzadeh R, Yousefi Darestani S | Hemoglobin | 2019 |
| Molecular prevalence of thalassemia and hemoglobinopathies among the Lao Loum Group in the Lao People's Democratic Republic. | Phanmany S, Chanprasert S, Munkongdee T, Svasti S, Leecharoenkiat K | Int J Lab Hematol | 2019 |
| Left ventricular non-compaction in patients with β-thalassemia: structural remodeling or cardiomyopathy? | Lazaros G, Vogiatzi G, Lazarou E, Vlachopoulos C, Tousoulis D | Intern Emerg Med | 2019 |
| Exon sequencing of the alpha-2-globin gene for the differential diagnosis of central cyanosis in newborns: a case report. | Shin C, Hong M, Kim M, Lee JH | BMC Pediatr | 2019 |
| Coinheritance of Hb City of Hope (: c.208G>A) and β-Thalassemia: Compromising the Molecular Diagnosis of the Codons 71/72 (+A) (: c.216_217insA) Mutation by Reverse Dot-Blot Hybridization. | Zhou JY, Jiang F, Li J, Chen GL, Li DZ | Hemoglobin | 2019 |
| Higher executive abilities following a blood transfusion in children and young adults with sickle cell disease. | Hood AM, King AA, Fields ME, Ford AL, Guilliams KP, Hulbert ML, Lee JM, White DA | Pediatr Blood Cancer | 2019 |
| Hereditary methemoglobinemia caused by Hb M-Hyde Park (Hb M-Akita) (HBB:c.277C > T; p.His93Tyr). | Schnedl WJ, Queissner R, Schenk M, Enko D, Mangge H | Wien. Klin. Wochenschr. | 2019 |
| Evaluation of maxillary sinus volume and surface area in children with β-thalassaemia using cone beam computed tomography. | Koparal M, Yalcın ED, Aksoy O, Ozcan-Kucuk A | Int. J. Pediatr. Otorhinolaryngol. | 2019 |
| Circadian period 2: a missing beneficial factor in sickle cell disease by lowering pulmonary inflammation, iron overload, and mortality. | Adebiyi MG, Zhao Z, Ye Y, Manalo J, Hong Y, Lee CC, Xian W, McKeon F, Culp-Hill R, D' Alessandro A, Kellems RE, Yoo SH, Han L, Xia Y | FASEB J. | 2019 |
| Klebsiella pneumoniae Multiple Liver Abscesses and Bacteremia in a Transfusion-dependent β Thalassemia Major Patient. | Rathnayake D, Somasuriyan K, Kumarasamy Thadsanamoorthy S, Maheshvaran U, Francis V | J. Pediatr. Hematol. Oncol. | 2019 |
| Anemia predicts lower white matter volume and cognitive performance in sickle and non-sickle cell anemia syndrome. | Choi S, O'Neil SH, Joshi AA, Li J, Bush AM, Coates TD, Leahy RM, Wood JC | Am. J. Hematol. | 2019 |
| Curative Therapies for Sickle Cell Disease. | Khemani K, Katoch D, Krishnamurti L | Ochsner J | 2019 |
| Increasing Educational Attainment in Adolescents with Sickle Cell Disease. | Harris KM, Dadekian JN, Abel RA, Jones B, Housten A, Ddamulira B, Chadwick-Mansker K, King AA | Soc Work Public Health | 2019 |
| Personalizing transfusion in sickle cell disease: where is the canary in the mine? | Fields ME | Transfusion | 2019 |
| Compliance with Deferoxamine Therapy and Thyroid Dysfunction of Patients with β-Thalassemia Major in Syria. | Yassouf MY, Alquobaili F, Kabalan Y, Mukhalalaty Y | Hemoglobin | 2019 |
| Investigation of RFLP Haplotypes β-Globin Gene Cluster in Beta-Thalassemia Patients in Central Iran. | Sajadpour Z, Amini-Farsani Z, Motovali-Bashi M, Yadollahi M, Yadollahi F | Int J Hematol Oncol Stem Cell Res | 2019 |
| Effective method of evaluating myocardial iron concentration in pediatric patients with thalassemia major. | Khaled A, Ezzat DA, Salem HA, Seif HM, Rabee H | J Blood Med | 2019 |
| Myeloid neoplasms in the setting of sickle cell disease: an intrinsic association with the underlying condition rather than a coincidence; report of 4 cases and review of the literature. | Li Y, Maule J, Neff JL, McCall CM, Rapisardo S, Lagoo AS, Yang LH, Crawford RD, Zhao Y, Wang E | Mod. Pathol. | 2019 |
| Air Drep-A Retrospective Study Evaluating the Influence of Weather Conditions and Viral Epidemics on Vaso-Occlusive Crises in Patients with Sickle Cell Disease Living in French Guiana. | Parriault MC, Cropet C, Fahrasmane A, Rogier S, Parisot M, Nacher M, Elenga N | Int J Environ Res Public Health | 2019 |
| Implementation of an Emergency Department Screening and Care Management Referral Process for Patients With Sickle Cell Disease. | Rushton S, Murray D, Talley C, Boyd S, Eason K, Earls M, Tanabe P | Prof Case Manag | 2019 |
| Providers' Perspectives on Treating Patients With Thalassemia. | Radke T, Paulukonis S, Hulihan MM, Feuchtbaum L | J. Pediatr. Hematol. Oncol. | 2019 |
| Treatment of post-transfusion hyperhaemolysis syndrome in Sickle Cell Disease with the anti-IL6R humanised monoclonal antibody Tocilizumab. | Sivapalaratnam S, Linpower L, Sirigireddy B, Agapidou A, Jain S, Win N, Tsitsikas DA | Br. J. Haematol. | 2019 |
| Therapeutically relevant engraftment of a CRISPR-Cas9-edited HSC-enriched population with HbF reactivation in nonhuman primates. | Humbert O, Radtke S, Samuelson C, Carrillo RR, Perez AM, Reddy SS, Lux C, Pattabhi S, Schefter LE, Negre O, Lee CM, Bao G, Adair JE, Peterson CW, Rawlings DJ, Scharenberg AM, Kiem HP | Sci Transl Med | 2019 |
| Paraoxonases (PON) 1, 2, and 3 Polymorphisms and PON-1 Activities in Patients with Sickle Cell Disease. | Reichert CO, de Macedo CG, Levy D, Sini BC, Monteiro AM, Gidlund M, Maselli LMF, Gualandro SFM, Bydlowski SP | Antioxidants (Basel) | 2019 |
| Management of Sickle Cell Disease Pain among Adolescent and Pediatric Patients. | Abdo S, Nuseir KQ, Altarifi AA, Barqawi M, Ayoub NM, Mukkatash TL | Brain Sci | 2019 |
| New and emerging treatments for vaso-occlusive pain in sickle cell disease. | Dampier C | Expert Rev Hematol | 2019 |
| Alloimmunization in Thalassemia Patients. | Joob B, Wiwanitkit V | Int J Prev Med | 2019 |
| Hydroxyurea: Pattern of Use, Patient Adherence, and Safety Profile in Patients with Sickle Cell Disease in Oman. | Jose J, Elsadek RA, Jimmy B, George P | Oman Med J | 2019 |
| Does Obstructive Sleep Apnea Increase Cognitive Deficits in Pediatric Sickle Cell Disease? | Bills SE, Katz T, McNeil J, Schatz J | J Int Neuropsychol Soc | 2019 |
| Improving the Care of Individuals With Sickle Cell Disease in the Emergency Department Using a Quality Improvement Framework: The Emergency Department Sickle Cell Assessment of Needs and Strengths (ED-SCANS). | Brennan-Cook J, Bonnabeau E, Harris-Bloom H, Tanabe P | Adv Emerg Nurs J | 2019 |
| Alpha Globin Gene Mutation: A Major Determinant of Hydroxyurea Response in Transfusion-Dependent HbE-β-Thalassaemia. | Biswas S, Ray R, Roy K, Bandyopadhyay A, Ghosh K, Bhattacharyya M | Acta Haematol. | 2019 |
| Combined genetic disruption of K-Cl cotransporters and Gardos channel KCNN4 rescues erythrocyte dehydration in the SAD mouse model of sickle cell disease. | Shmukler BE, Rivera A, Bhargava P, Nishimura K, Hsu A, Kim EH, Trudel M, Rust MB, Hubner CA, Brugnara C, Alper SL | Blood Cells Mol. Dis. | 2019 |
| Conjugate prodrug AN-233 induces fetal hemoglobin expression in sickle erythroid progenitors and β-YAC transgenic mice. | Oseghale AR, Zhu X, Li B, Peterson KR, Nudelman A, Rephaeli A, Xu H, Pace BS | Blood Cells Mol. Dis. | 2019 |
| Analgesic management of uncomplicated acute sickle-cell pain crisis in pediatrics: a systematic review and meta-analysis. | Saramba MI, Shakya S, Zhao D | J Pediatr (Rio J) | 2019 |
| Genetic comparison of sickle cell anaemia cohorts from Brazil and the United States reveals high levels of divergence. | Cruz PRS, Ananina G, Gil-da-Silva-Lopes VL, Simioni M, Menaa F, Bezerra MAC, Domingos IF, Araújo AS, Pellegrino R, Hakonarson H, Costa FF, de Melo MB | Sci Rep | 2019 |
| Zinc for Infection Prevention in Sickle Cell Anemia (ZIPS): study protocol for a randomized placebo-controlled trial in Ugandan children with sickle cell anemia. | Datta D, Namazzi R, Conroy AL, Cusick SE, Hume HA, Tagoola A, Ware RE, Opoka RO, John CC | Trials | 2019 |
| Survival and specific outcome of sickle cell disease patients after renal transplantation. | Gérardin C, Moktefi A, Couchoud C, Duquesne A, Ouali N, Gataut P, Karras A, Anglicheau D, Lefaucheur C, Figueres L, Albano L, Lionet A, Novion M, Ziliotis MJ, Louis M, Del Bello A, Matignon M, Dahan K, Habibi A, Galacteros F, Bartolucci P, Grimbert P, Audard V | Br. J. Haematol. | 2019 |
| Spontaneous Epidural Hemorrhage in Sickle Cell Disease, Are They All the Same? A Case Report and Comprehensive Review of the Literature. | Saha B, Saha A | Case Rep Hematol | 2019 |
| Clinical meaning of PROMIS pain domains for children with sickle cell disease. | Singh A, Panepinto JA | Blood Adv | 2019 |
| Red Blood Cell Alloimmunization in Transfused Patients With Sickle Cell Disease in Sub-Saharan Africa; a Systematic Review and Meta-Analysis. | Boateng LA, Ngoma AM, Bates I, Schonewille H | Transfus Med Rev | 2019 |
| Long-term sequential deferiprone and deferasirox therapy in transfusion-dependent thalassaemia patients: a prospective clinical trial. | Vitrano A, Ruffo GB, Pepe A, D'Ascola DG, Caruso V, Filosa A, Masera N, Pitrolo L, Rigano P, Cuccia L, Giangreco A, Di Maggio R, Maggio A | Br. J. Haematol. | 2019 |
| Sickle cell trait, estimated glomerular filtration rate, and risk of adverse outcomes in chronic kidney disease. | Sood R, Surapaneni A, Luo S, Appel LJ, Winkler C, Grams ME, Naik RP | Am. J. Hematol. | 2019 |
| A Novel Pathogenic β-Thalassemia Mutation Identified at Codon 8 (: c.27delG) in a Bangladeshi Family Acquired . | Hasan KN, Sufian A, Mazumder AK, Khaleque MA, Rahman M, Akhteruzzaman S | Hemoglobin | 2019 |
| Foveal avascular zone morphology and parafoveal capillary perfusion in sickle cell retinopathy. | Lynch G, Scott AW, Linz MO, Han I, Andrade Romo JS, Linderman RE, Carroll J, Rosen RB, Chui TY | Br J Ophthalmol | 2019 |
| Sickle Cell Education: A Survey of Antenatal Healthcare Givers. | Aboagye S, Torto M, Asah-Opoku K, Nuamah MA, Oppong SA, Samba A | Am. J. Trop. Med. Hyg. | 2019 |
| Ultrasound-guided recruitment maneuvers in pediatric acute chest syndrome due to sickle cell disease. | Bobillo-Perez S, Rodriguez-Fanjul J, Girona-Alarcon M, Cambra FJ, Jordan I, Balaguer M | Med Intensiva | 2019 |
| Germline mosaicism in an α-thalassemia family: Incidental identification by prenatal ultrasound. | Xu LL, Liu YN, Zhen L, Li DZ | Prenat. Diagn. | 2019 |
| National trends in hydroxyurea and opioid prescribing for sickle cell disease by office-based physicians in the United States, 1997-2017. | Su ZT, Segal JB, Lanzkron S, Ogunsile FJ | Pharmacoepidemiol Drug Saf | 2019 |
| Comparison of serology and molecular detection of common red cell antigens in multitransfused thalassemia major and sickle cell disease patients. | Shah A, Patel P, Patel K, Patel B, Jariwala K, Sharma P, Mishra K, Ghosh K | Transfus. Apher. Sci. | 2019 |
| Chronic pain persists in adults with sickle cell disease despite regular red cell transfusions. | Karafin MS, Mullins DE, Johnson ST, Nischik D, Feng M, Simpson P, Field JJ | Transfus. Apher. Sci. | 2019 |
| Challenges of blood transfusions in β-thalassemia. | Shah FT, Sayani F, Trompeter S, Drasar E, Piga A | Blood Rev. | 2019 |
| Splenectomy is not associated with a higher tricuspid regurgitant jet velocity in people with sickle cell anemia. | Sinha AA, Adusumilli T, Cohen HW, Nouraie M, Little J, Manwani D | Pediatr Blood Cancer | 2019 |
| Combined and differential effects of alpha-thalassemia and HbF-quantitative trait loci in Senegalese hydroxyurea-free children with sickle cell anemia. | Gueye Tall F, Martin C, Ndour EHM, Renoux C, Ly ID, Connes P, Gueye PM, Diallo RN, Diagne I, Diop PA, Cissé A, Lopez Sall P, Joly P | Pediatr Blood Cancer | 2019 |
| Gene therapy of hemoglobinopathies: progress and future challenges. | Ikawa Y, Miccio A, Magrin E, Kwiatkowski JL, Rivella S, Cavazzana M | Hum. Mol. Genet. | 2019 |
| Quality of life in patients with β-thalassemia: A prospective study of transfusion-dependent and non-transfusion-dependent patients in Greece, Italy, Lebanon, and Thailand. | Cappellini MD, Kattamis A, Viprakasit V, Sutcharitchan P, Pariseau J, Laadem A, Jessent-Ciaravino V, Taher A | Am. J. Hematol. | 2019 |
| Prevention of Morbidity in Sickle Cell Disease (POMS2a)-overnight auto-adjusting continuous positive airway pressure compared with nocturnal oxygen therapy: a randomised crossover pilot study examining patient preference and safety in adults and children. | Howard J, Lee SA, Inusa B, Cheng MYE, Bavenjit C, Reading IC, Wakeford SA, Gavlak JC, Murphy PB, Hart N, Gupta A, Sahota S, Jacob E, Chorozoglou M, Ossai C, Gwam M, Kirkham FJ, Wade AM, Liossi C | Trials | 2019 |
| Impact of Depression in Sickle Cell Disease Hospitalization-Related Outcomes: An Analysis of the National Inpatient Sample (NIS). | Onyeaka HK, Queeneth U, Rashid W, Ahmad N, Rajan SK, Jaladi PR, Patel RS | Medicina (Kaunas) | 2019 |
| Characterizing complication risk from multisite, intermittent transfusions for the treatment of sickle cell disease. | Tang A, Branscomb J, Zhou M, Snyder A, Eckman J | Pediatr Blood Cancer | 2019 |
| Beta-thalassemia major complicated by intracranial hemorrhage and critical illness polyneuropathy. | Sanju S, Tullu MS, Karande S, Muranjan MN, Parekh P | J Postgrad Med | 2019 |
| The Role of Cognitive Behavioral Therapy in Opioid Use Reduction in Pediatric Sickle Cell Disease: Protocol for a Systematic Review. | Anderson AT, Tran N, Smith K, Kelley-Quon LI | JMIR Res Protoc | 2019 |
| Case Report: Kryptonite-A Rare Case of Left-Sided Bilothorax in a Sickle Cell Patient. | Reddy VD, Al-Khateeb A, Hussain M, Patel V, Kadri M, Patel R, Maruboyina SP, Miller RA, DePasquale JR | Case Rep Pulmonol | 2019 |
| QT Prolongation and Associated Ventricular Tachycardia due to Cardiac Iron Load in a Patient with Thalassemia Major. | Demirtas D, Demirtas AO, Sumbul HE, Koc AS | Case Rep Hematol | 2019 |
| Acacia Senegal (Gum Arabic) Supplementation Modulate Lipid Profile and Ameliorated Dyslipidemia among Sickle Cell Anemia Patients. | Kaddam L, Fadl-Elmula I, Eisawi OA, Abdelrazig HA, Saeed AM | J Lipids | 2019 |
| [The History of Beta Thalassaemia in Sardinia: The Contribution of the Italian Schools of Pediatrics]. | Martini M, Tornali C, Bragazzi NL, Paluan F, Vardeu MF | Acta Med Hist Adriat | 2019 |
| Towards New Frontiers of Direct Oral Anticoagulants: Sickle Cell Disease. | Boccatonda A, Santilli F | Acta Haematol. | 2019 |
| The genetics of human hematopoiesis and its disruption in disease. | Bao EL, Cheng AN, Sankaran VG | EMBO Mol Med | 2019 |
| Sickle cell trait and risk of cognitive impairment in African-Americans: The REGARDS cohort. | Cahill CR, Leach JM, McClure LA, Irvin MR, Zakai NA, Naik R, Unverzagt F, Wadley VG, Hyacinth HI, Manly J, Judd SE, Winkler C, Cushman M | EClinicalMedicine | 2019 |
| Sickle cell trait: A sigh of relief? | Wood JC | EClinicalMedicine | 2019 |
| A pilot test of the Adult Sickle Cell Quality of Life Measurement Information System (ASCQ-Me) and the Jenerette Self-Care Assessment (J-SAT) Tools in adults with sickle cell disease. | Bulgin D, Douglas C, Tanabe P | Pilot Feasibility Stud | 2019 |
| Splenic sequestration crisis as an index manifestation of heterozygous hemoglobinopathy in an adult. | Edo-Osagie E, Enofe I, Hakeem H, Rai M, Adomako E, Tismenetsky M, Janosky M | Oxf Med Case Reports | 2019 |
| Sickle cell disease in anaemic children in a Sierra Leonean district hospital: a case series. | Italia MB, Kirolos S | Oxf Med Case Reports | 2019 |
| Fetal hemoglobin does not inhibit growth. | Archer NM, Petersen N, Duraisingh MT | Blood Adv | 2019 |
| Sickle Cell Disease and Infections in High- and Low-Income Countries. | Cannas G, Merazga S, Virot E | Mediterr J Hematol Infect Dis | 2019 |
| Prevalence of TEM, SHV, and CTX-M Genes among ESBL-Producing and Isolated from Thalassemia Patients in Erbil, Iraq. | Pishtiwan AH, Khadija KM | Mediterr J Hematol Infect Dis | 2019 |
| Sickle Cell Disease and Pregnancy. | Jain D, Atmapoojya P, Colah R, Lodha P | Mediterr J Hematol Infect Dis | 2019 |
| Homozygous Deletion Alpha-Thalassemia and Hereditary Persistence of Fetal Hemoglobin, Two Genetic Factors Predictive the Reduction of Morbidity and Mortality During Pregnancy in Sickle Cell Patients. A Report from the Democratic Republic of Congo. | Mikobi TM, Lukusa PT, Muamba JM, Rhama T | Mediterr J Hematol Infect Dis | 2019 |
| Molecular Analysis of Non-Transfusion Dependent Thalassemia Associated with Hemoglobin E-β-Thalassemia Disease without α-Thalassemia. | Phanrahan P, Yamsri S, Teawtrakul N, Fucharoen G, Sanchaisuriya K, Fucharoen S | Mediterr J Hematol Infect Dis | 2019 |
| Economic Evaluation of Chelation Regimens for β-Thalassemia Major: a Systematic Review. | Li J, Lin Y, Li X, Zhang J | Mediterr J Hematol Infect Dis | 2019 |
| On artherogenic index of plasma in sickle cell anaemia patients. | Akinbami AA, Uche EI, Suleiman AM, Ogbenna AA, Olowoselu FO, Augustine B, Badiru MA, Bamiro RA, Kamson OR | Pan Afr Med J | 2019 |
| Frequency of Alpha Thalassaemia in homozygous Beta Thalassaemia paediatric patients and its clinical impact at a blood disease centre in Karachi, Pakistan. | Hassan J, Nadeem M, Ansari SH, Ahmed S, Parveen S, Shamsi T | J Pak Med Assoc | 2019 |
| Pediatric to Adult Transition in Sickle Cell Disease: Survey Results from Young Adult Patients. | Travis K, Wood A, Yeh P, Allahabadi S, Chien LC, Curtis S, Hammond A, Kohn J, Ogugbuaja C, Rees M, Shumway J, Sheehan V | Acta Haematol. | 2019 |
| Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia. | Yahouédéhou SCMA, da Guarda CC, Figueiredo CVB, Santiago RP, Carvalho SP, Fiuza LM, Ndidi US, Oliveira RM, Carvalho MOS, Nascimento VML, Rocha LC, Lyra IM, Adorno EV, Goncalves MS | PLoS ONE | 2019 |
| Differential effects of adenylyl cyclase-protein kinase A cascade on shear-induced changes of sickle cell deformability. | Ugurel E, Connes P, Yavas G, Eglenen B, Turkay M, Aksu AC, Renoux C, Joly P, Gauthier A, Hot A, Bertrand Y, Cannas G, Yalcin O | Clin. Hemorheol. Microcirc. | 2019 |
| First Description of Hb San Diego (: c.328G>A) in a Chinese Family with Congenital Erythrocytosis. | Xiong H, Chen S | Hemoglobin | 2019 |
| The Spectrum of α-Thalassemia Mutations in the Lak Population of Iran. | Moradi K, Aznab M, Tahmasebi S, Dastafkan Z, Omidniakan L, Ahmadi M, Alibakhshi R | Hemoglobin | 2019 |
| Gallstone Pancreatitis and Extramedullary ArticleTitlespinal Hematopoiesis in Hb E/beta Thalassemia. | Goldie L, Kinzang W, Thangjam G, Konsam V | J Assoc Physicians India | 2019 |
| Iron status and inherited haemoglobin disorders modify the effects of micronutrient powders on linear growth and morbidity among young Lao children in a double-blind randomised trial. | Hess SY, Wessells KR, Hinnouho GM, Barffour MA, Sanchaisuriya K, Arnold CD, Brown KH, Larson CP, Fucharoen S, Kounnavong S | Br. J. Nutr. | 2019 |
| Fe enrichment in mice for β-thalassaemia studies via Mössbauer spectroscopy of blood samples. | Charitou G, Tsertos C, Parpottas Y, Kleanthous M, Lederer CW, Phylactides M | Eur. Biophys. J. | 2019 |
| [Analysis of hematological phenotype and genotype of Hb Q-Thailand in Fujian area]. | Chen L, Chen M, Zhang M, Wang Y, Huang H, Li Y, Xu L | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2019 |
| Targeting sickle cell disease root-cause pathophysiology with small molecules. | Saunthararajah Y | Haematologica | 2019 |
| Epidemiology and risk factors of transfusion transmitted infections in thalassemia major: a multicenter study in Pakistan. | Yasmeen H, Hasnain S | Hematol Transfus Cell Ther | 2019 |
| Shine & Lal index as a predictor for early detection of β-thalassemia carriers in a limited resource area in Bandung, Indonesia. | Maskoen AM, Reniarti L, Sahiratmadja E, Sisca J, Effendi SH | BMC Med. Genet. | 2019 |
| Hb Alcorn County: A β-Globin Variant [β40(C6)Arg→Thr; : c.122G>C (p.Arg41Thr)] with Increased Oxygen Affinity. | Luu HS, McCavit TL, Park JY, Mitui M, Lopez DD, Timmons CF | Hemoglobin | 2019 |
| A Multidimensional Electronic Hydroxyurea Adherence Intervention for Children With Sickle Cell Disease: Single-Arm Before-After Study. | Creary S, Chisolm D, Stanek J, Hankins J, O'Brien SH | JMIR Mhealth Uhealth | 2019 |
| Real-world experience using hydroxyurea in children with sickle cell disease in Lilongwe, Malawi. | Mvalo T, Topazian HM, Kamthunzi P, Chen JS, Kambalame I, Mafunga P, Mumba N, Chiume M, Paseli K, Tegha G, Kumwenda W, Heimlich JB, Ellis G, Key N, Gopal S, Hoffman I, Ataga KI, Westmoreland KD | Pediatr Blood Cancer | 2019 |
| Antisickling Drugs Targeting βCys93 Reduce Iron Oxidation and Oxidative Changes in Sickle Cell Hemoglobin. | Kassa T, Wood F, Strader MB, Alayash AI | Front Physiol | 2019 |
| Receptor for Advanced Glycation End Products Antagonism Blunts Kidney Damage in Transgenic Townes Sickle Mice. | Charrin E, Faes C, Sotiaux A, Skinner S, Pialoux V, Joly P, Connes P, Martin C | Front Physiol | 2019 |
| Health related quality of life among children with transfusion dependent β-thalassaemia major and haemoglobin E β-thalassaemia in Sri Lanka: a case control study. | Mettananda S, Pathiraja H, Peiris R, Bandara D, de Silva U, Mettananda C, Premawardhena A | Health Qual Life Outcomes | 2019 |
| Unusual β-Globin Haplotype Distribution in Newborns from Bengo, Angola. | Borges E, Tchonhi C, Couto CSB, Gomes V, Amorim A, Prata MJ, Brito M | Hemoglobin | 2019 |
| Noninvasive prenatal detection of hemoglobin Bart hydrops fetalis via maternal plasma dispensed with parental haplotyping using the semiconductor sequencing platform. | Yang J, Peng CF, Qi Y, Rao XQ, Guo F, Hou Y, He W, Wu J, Chen YY, Zhao X, Wang YN, Peng H, Wang D, Du L, Luo MY, Huang QF, Liu HL, Yin A | Am. J. Obstet. Gynecol. | 2019 |
| Genomic variants in members of the Krüppel-like factor gene family are associated with disease severity and hydroxyurea treatment efficacy in β-hemoglobinopathies patients. | Stratopoulos A, Kolliopoulou A, Karamperis K, John A, Kydonopoulou K, Esftathiou G, Sgourou A, Kourakli A, Vlachaki E, Chalkia P, Theodoridou S, Papadakis MN, Gerou S, Symeonidis A, Katsila T, Ali BR, Papachatzopoulou A, Patrinos GP | Pharmacogenomics | 2019 |
| An approach to revising mHealth interventions for children and families: A case example in sickle cell disease. | Phillips S, Kanter J, Ruggiero KJ, Mueller M, Johnson MA, Kelechi TJ | Res Nurs Health | 2019 |
| An Hb-mediated circulating macrophage contributing to pulmonary vascular remodeling in sickle cell disease. | Redinus K, Baek JH, Yalamanoglu A, Shin HKH, Moldova R, Harral JW, Swindle D, Pak D, Ferguson SK, Nuss R, Hassell K, Nozik-Grayck E, Palmer AF, Fini MA, Karoor V, Stenmark KR, Buehler PW, Irwin DC | JCI Insight | 2019 |
| Insights into determinants of spleen injury in sickle cell anemia. | El Hoss S, Cochet S, Marin M, Lapouméroulie C, Dussiot M, Bouazza N, Elie C, de Montalembert M, Arnaud C, Guitton C, Pellegrino B, Odièvre MH, Moati F, Le Van Kim C, Aronovicz YC, El Nemer W, Brousse V | Blood Adv | 2019 |
| Sickle cell disease nephropathy: an update on risk factors and potential biomarkers in pediatric patients. | Belisário AR, da Silva AA, Silva CV, de Souza LM, Wakabayashi EA, Araújo SA, Simoes-E-Silva AC | Biomark Med | 2019 |
| Cardiac expression of HMOX1 and PGF in sickle cell mice and haem-treated wild type mice dominates organ expression profiles via Nrf2 (Nfe2l2). | Gbotosho OT, Ghosh S, Kapetanaki MG, Lin Y, Weidert F, Bullock GC, Ofori-Acquah SF, Kato GJ | Br. J. Haematol. | 2019 |
| Frequency of silent brain lesions and aspirin protection evaluation over 3 years follow-up in beta thalassemia patients. | Karimi M, Haghpanah S, Pishdad P, Zahedi Z, Parand S, Safaei S | Ann. Hematol. | 2019 |
| TTP-like syndrome associated with hemoglobin SC disease treated successfully with plasma and red cell exchange. | Kodali S, Ramachandran P, Richard IN, Wang JC | Leuk Res Rep | 2019 |
| Immunostick Test for Detecting ζ-Globin Chains and Screening of the Southeast Asian α-Thalassemia 1 Deletion. | Pata S, Pongpaiboon M, Laopajon W, Munkongdee T, Paiboonsukwong K, Pornpresert S, Fucharoen S, Kasinrerk W | Biol Proced Online | 2019 |
| An Uncommon Variant Hemoglobin: Hb Ty Gard Detected from Gujarat, India. | Wahengbam AKGS, Kumari K, Singh RK, Rao VR, Saraswathy KN, Dharajiya K, Das R, Murry B | Indian J Hematol Blood Transfus | 2019 |
| Clinico-Hematological Presentation of Rare Hemoglobin Variant (HB-O Indonesia) in 3 Families. | Kumar R, Patel P, Gwal A, Bharti PK, Colah R, Rajasubramaniam S | Indian J Hematol Blood Transfus | 2019 |
| Hemoglobin Titusville [α2 Codon 94 G>A]: A Rare Alpha Globin Chain Variant Causing Low Oxygen Saturation. | Das Gupta A, Hariharan P, Daruwalla M, Sidhwa K, Pawar R, Nadkarni A | Indian J Hematol Blood Transfus | 2019 |
| Polyneuropathy Associated with Severe Iron Overload and Oxidative Stress in β-Thalassemia Patients. | El-Tagui MH, Salama KM, El-Sabbagh MH, Youness ER, Ragaey M, Abdel-Salam A | Indian J Hematol Blood Transfus | 2019 |
| Spectrum of Hemoglobinopathies: A New Revelation in a Tertiary Care Hospital of Odisha. | Ray GK, Jena RK | Indian J Hematol Blood Transfus | 2019 |
| Hb Gibbon [β124(H2)Pro→Thr (: c.373C>A, p.P125T)], an Asymptomatic Novel Hemoglobin Variant Detected by Newborn Screening. | Wolf A, Rohr JM, Amador C, Starr LJ, Hoyer JD, Ford JB | Hemoglobin | 2019 |
| Metabolic impact of red blood cell exchange with rejuvenated red blood cells in sickle cell patients. | Gehrke S, Shah N, Gamboni F, Kamyszek R, Srinivasan AJ, Gray A, Landrigan M, Welsby I, D'Alessandro A | Transfusion | 2019 |
| Genetic variation influencing hemoglobin levels and risk for anemia across populations. | Barrera-Reyes PK, Tejero ME | Ann. N. Y. Acad. Sci. | 2019 |
| Sickle cell disease: a review for the internist. | Pinto VM, Balocco M, Quintino S, Forni GL | Intern Emerg Med | 2019 |
| Association of sickle cell trait with measures of cognitive function and dementia in African Americans. | Chen N, Caruso C, Alonso A, Derebail VK, Kshirsagar AV, Sharrett AR, Key NS, Gottesman RF, Grove ML, Bressler J, Boerwinkle E, Windham BG, Mosley TH, Hyacinth HI | eNeurologicalSci | 2019 |
| Candidemia complicating biliary atresia in an infant with hemoglobinopathy. | Kyriakidis I, Palabougiouki M, Vasileiou E, Tragiannidis A, Stamou M, Moudiou T, Vyzantiadis T, Gombakis N, Hatzistilianou M | Turk Pediatri Ars | 2019 |
| Association Between Periodic Limb Movements in Sleep and Cerebrovascular Changes in Children With Sickle Cell Disease. | Lin J, Morrone K, Manwani D, Chernin R, Silver EJ, Shifteh K, Sin S, Arens R, Graw-Panzer K | J Clin Sleep Med | 2019 |
| Shared Care for Adults with Sickle Cell Disease: An Analysis of Care from Eight Health Systems. | Mainous AG, Rooks B, Tanner RJ, Carek PJ, Black V, Coates TD | J Clin Med | 2019 |
| Anemia Severity in β-Thalassemia Correlates with Elevated Levels of microRNA-125b in Activated Phagocytic Monocytes. | Kuno S, Penglong T, Srinoun K | Hemoglobin | 2019 |
| Kidney ultrasound findings according to kidney function in sickle cell anemia. | Patel R, Kang S, Valeshabad AK, Shah BN, Han J, Gowhari M, Molokie RE, Xie K, Lash JP, Gordeuk VR, Saraf SL | Am. J. Hematol. | 2019 |
| Fat Embolism Syndrome in a Child with Sickle Cell Disease. | Maroni A, Dauger S, Chomton M | J. Pediatr. | 2019 |
| Resolution of Acute Priapism in Two Children With Sickle Cell Disease Who Received Nitrous Oxide. | Greenwald MH, Gutman CK, Morris CR | Acad Emerg Med | 2019 |
| [False positive Kleihauer test and hereditary persistence of fetal hemoglobin]. | Picard L, Delabaere A, Serre Sapin AF, Giansily Blaizot M, Gallot D | Gynecol Obstet Fertil Senol | 2019 |
| Prevalence of endocrine disorders and their associated factors in transfusion-dependent thalassemia patients: a historical cohort study in Southern Iran. | Bordbar M, Bozorgi H, Saki F, Haghpanah S, Karimi M, Bazrafshan A, Zekavat OR | J. Endocrinol. Invest. | 2019 |
| Hydroxyurea Use for Sickle Cell Disease Among Medicaid-Enrolled Children. | Brousseau DC, Richardson T, Hall M, Ellison AM, Shah SS, Raphael JL, Bundy DG, Arnold S | Pediatrics | 2019 |
| Sickle cell disease: a new era. | Simpson S | Lancet Haematol | 2019 |
| Knowledge, beliefs and practices regarding sickle cell eye disease of patients at the sickle cell unit, Jamaica. | Mowatt L, Ajanaku A, Knight-Madden J | Pan Afr Med J | 2019 |
| Sex differences in physical activity among Ghanaian patients with sickle cell disease. | Nyante GG, Oppong C, Bonney E | Pan Afr Med J | 2019 |
| An Electronic Teaching Module for Improving Knowledge of Self-Management of Vaso-Occlusive Pain Crises in Patients With Sickle Cell Disease: Pilot Questionnaire Study. | Tam T, Baer MR, Hsu LL, Law JY | JMIR Mhealth Uhealth | 2019 |
| Detection of a Large Novel α-Thalassemia Deletion in an Autochthonous Belgian Family. | Heireman L, Luyckx A, Schynkel K, Dheedene A, Delaunoy M, Adam AS, Gulbis B, Dierick J | Hemoglobin | 2019 |
| Invasive Yersiniosis in a Pediatric Patient With β-Thalassemia Major: Acute Decompensation After Rapid Blood Transfusion. | Hsu G, Jones A, Thornton B | Pediatr Emerg Care | 2019 |
| Longitudinal Trend in Emergency Department Reliance for Pain Among Sickle Cell Disease Patients in Wisconsin. | Singh A, Yan K, Brandow AM, Panepinto JA | J. Pediatr. Hematol. Oncol. | 2019 |
| A case of bone marrow necrosis and fat embolism in a sickle-cell disease patient. | Debus J, Dumont B, Le Breton C, Emery M, Peynaud-Debayle E, Affo L | Ann. Biol. Clin. (Paris) | 2019 |
| Global gene expression reveals an increase of HMGB1 and APEX1 proteins and their involvement in oxidative stress, apoptosis and inflammation pathways among beta-thalassaemia intermedia and major phenotypes. | Maia de Oliveira da Silva JP, Brugnerotto AF, S Romanello K, K L Teixeira K, Lanaro C, S Duarte A, G L Costa G, da Silva Araújo A, C Bezerra MA, de Farias Domingos I, Pereira Martins DA, Malavazi I, F Costa F, da Cunha AF | Br. J. Haematol. | 2019 |
| Urinary dysfunction in transgenic sickle cell mice: model of idiopathic overactive bladder syndrome. | Karakus S, Anele UA, Silva FH, Musicki B, Burnett AL | Am. J. Physiol. Renal Physiol. | 2019 |
| A Medication Adherence App for Children With Sickle Cell Disease: Qualitative Study. | Curtis K, Lebedev A, Aguirre E, Lobitz S | JMIR Mhealth Uhealth | 2019 |
| Hydroxycarbamide treatment in children with Sickle Cell Anaemia is associated with more intact white matter integrity: a quantitative MRI study. | Kapustin D, Leung J, Odame I, Williams S, Shroff M, Kassner A | Br. J. Haematol. | 2019 |
| International Comparison of Thalassemia Registries: Challenges and Opportunities. | Noori T, Ghazisaeedi M, Aliabad GM, Mehdipour Y, Mehraeen E, Conte R, Safdari R | Acta Inform Med | 2019 |
| The Relationship Between Psychological Distress and Religious Practices and Coping in Malaysian Parents of Children with Thalassemia. | Chong LT, Chong MC, Tang LY, Ramoo V, Chui PL, Hmwe NTT | J Pediatr Nurs | 2019 |
| [Study of - maximum systolic velocities and mean maximum velocities of skull base arteries recorded with transcranial Doppler in adult sickle cell patients without neurovascular complication]. | Desnos L, Allaert F, Etienne-Julan M, Blanchet-Deverly A | J Med Vasc | 2019 |
| Prevalence and factors associated with renal dysfunction among children with sickle cell disease attending the sickle cell disease clinic at a tertiary hospital in Northwestern Tanzania. | Kimaro FD, Jumanne S, Sindato EM, Kayange N, Chami N | PLoS ONE | 2019 |
| Oral aspects of sickle cell disease. | Grossman S, Bailey E, Makdissi J | Br Dent J | 2019 |
| Molecular characteristics of α-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics. | Charoenwijitkul T, Singha K, Fucharoen G, Sanchaisuriya K, Thepphitak P, Wintachai P, Karnpean R, Fucharoen S | Clin. Biochem. | 2019 |
| Detection of Hb H disease caused by a novel mutation and -- deletion using capillary electrophoresis. | Li Y, Liang L, Tian M, Qin T, Wu X | J. Clin. Lab. Anal. | 2019 |
| A Phase 3 Randomized Trial of Voxelotor in Sickle Cell Disease. | Vichinsky E, Hoppe CC, Ataga KI, Ware RE, Nduba V, El-Beshlawy A, Hassab H, Achebe MM, Alkindi S, Brown RC, Diuguid DL, Telfer P, Tsitsikas DA, Elghandour A, Gordeuk VR, Kanter J, Abboud MR, Lehrer-Graiwer J, Tonda M, Intondi A, Tong B, Howard J, | N. Engl. J. Med. | 2019 |
| Need for a universal thalassemia screening programme in India? A public health perspective. | Thiyagarajan A, Bhattacharya S, Sharma N, Srivastava A, Dhar DK | J Family Med Prim Care | 2019 |
| New Advances in Evaluation of Hearing in a Sample of Egyptian Children with β-Thalassemia Major. | Alzaree FA, Shehata MA, Atti MA, Elzaree GA, El-Kassas GM | Open Access Maced J Med Sci | 2019 |
| Cellular adaptation mediated through Nrf2-induced glutamate cysteine ligase up-regulation against oxidative stress caused by iron overload in β-thalassemia/HbE patients. | Somparn N, Prawan A, Senggunprai L, Kukongviriyapan U, Jetsrisuparb A, Lee MH, Kim DH, Kukongviriyapan V, Surh YJ | Free Radic. Res. | 2019 |
| Fertility in Patients with Thalassemia and Outcome of Pregnancies: A Turkish Experience | Akıncı B, Yaşar AŞ, Özdemir Karadaş N, Önder Siviş Z, Hekimci Özdemir H, Yılmaz Karapınar D, Balkan C, Kavaklı K, Aydınok Y | Turk J Haematol | 2019 |
| Transcranial Doppler and Magnetic Resonance in Tanzanian Children With Sickle Cell Disease. | Kija EN, Saunders DE, Munubhi E, Darekar A, Barker S, Cox TCS, Mango M, Soka D, Komba J, Nkya DA, Cox SE, Kirkham FJ, Newton CRJC | Stroke | 2019 |
| Current perspectives of sickle cell disease in Nigeria: changing the narratives. | Ojewunmi OO, Adeyemo TA, Ayinde OC, Iwalokun B, Adekile A | Expert Rev Hematol | 2019 |
| Considering the spleen in sickle cell disease. | El Hoss S, Brousse V | Expert Rev Hematol | 2019 |
| Metabolomic Investigation of β-Thalassemia in Chorionic Villi Samples. | Monni G, Murgia F, Corda V, Peddes C, Iuculano A, Tronci L, Balsamo A, Atzori L | J Clin Med | 2019 |
| Serum homocysteine and disease severity in sickle cell anemia patients in Lagos. | Uche E, Adelekan O, Akinbami A, Osunkalu V, Ismail K, Ogbenna AA, Badiru M, Dosunmu A, Oluwole E, Kamson O | J Blood Med | 2019 |
| Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India. | Dehury S, Meher S, Patel S, Das K, Jana A, Bhattacharya S, Sahoo S, Sarkar B, Mohanty PK | Hemoglobin | 2019 |
| A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia. | Klei TRL, Kheradmand Kia S, Veldthuis M, Dehbozorgian J, Karimi M, Geissler J, Sellink E, Thiel-Valkhof M, Burger P, van Alphen F, Meijer AB, van Bruggen R, van Zwieten R | Hemoglobin | 2019 |
| A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the Gene Misdiagnosed as β-Thalassemia Intermedia Due to a Gene Mutation. | Yang K, Ren Q, Wu Y, Zhou Y, Yin X | Hemoglobin | 2019 |
| Association of alpha hemoglobin-stabilizing protein (AHSP) gene mutation and disease severity among HbE-beta thalassemia patients. | Ray R, Kalantri SA, Bhattacharjee S, Biswas A, Shahab A, Biswas S, Bhattacharyya M | Ann. Hematol. | 2019 |
| Co-existing iron deficiency/overload in beta-thalassemia trait. | Yousafzai YM, Wahid QUA, Khan S, Mir A, Khan A, Raziq F | J Pak Med Assoc | 2019 |
| Antiplatelet agents for preventing vaso-occlusive events in people with sickle cell disease: a systematic review. | Martí-Carvajal A, Abd El Aziz MA, Martí-Amarista C, Solà I | Clin Adv Hematol Oncol | 2019 |
| The effect of the coinheritance of Glucose-6-phosphate dehydrogenase deficiency on the severity of sickle cell disease. | Fasola FA, Fowodu FO, Shokunbi WA, Kotila TR | Niger Postgrad Med J | 2019 |
| Oxysterol concentrations are associated with cholesterol concentrations and anemia in pediatric patients with sickle cell disease. | Yalcinkaya A, Samadi A, Lay I, Unal S, Sabuncuoglu S, Oztas Y | Scand. J. Clin. Lab. Invest. | 2019 |
| Quantifying the Levels of Knowledge, Attitude, and Practice Associated with Sickle Cell Disease and Premarital Genetic Counseling in 350 Saudi Adults. | Al-Qattan HM, Amlih DF, Sirajuddin FS, Alhuzaimi DI, Alageel MS, Bin Tuwaim RM, Al Qahtani FH | Adv Hematol | 2019 |
| Relationship of Omega-3 fatty acids DHA and EPA with the inflammatory biomarker hs-CRP in children with sickle cell anemia. | Setty BNY, Betal SG, Miller RE, Brown DS, Meier M, Cahill M, Lerner NB, Apollonsky N, Stuart MJ | Prostaglandins Leukot. Essent. Fatty Acids | 2019 |
| Electron paramagnetic resonance oximetry as a novel approach to monitor the effectiveness and quality of red blood cell transfusions. | Hou H, Baek JH, Zhang H, Wood F, Gao Y, Flood AB, Swartz HM, Buehler PW | Blood Transfus | 2019 |
| Laparoscopic Sleeve Gastrectomy in Sickle Cell Disease: a Case Series. | Han J, Gowhari M, Gordeuk VR, Saraf SL | Obes Surg | 2019 |
| Effect of whole body vibration training on bone mineral density and functional capacity in children with thalassemia. | Eid MA, Aly SM | Physiother Theory Pract | 2019 |
| Prevalence and Risk Factors for Cardiac and Liver Iron Overload in Adults with Thalassemia in Malaysia. | Ngim CF, Lee MY, Othman N, Lim SM, Ng CS, Ramadas A | Hemoglobin | 2019 |
| A Cell-free DNA Barcode-Enabled Single-Molecule Test for Noninvasive Prenatal Diagnosis of Monogenic Disorders: Application to β-Thalassemia. | Yang X, Zhou Q, Zhou W, Zhong M, Guo X, Wang X, Fan X, Yan S, Li L, Lai Y, Wang Y, Huang J, Ye Y, Zeng H, Chuan J, Du Y, Ma C, Li P, Song Z, Xu X | Adv Sci (Weinh) | 2019 |
| Early Kidney Damage Markers after Deferasirox Treatment in Patients with Thalassemia Major: A Case-Control Study. | Badeli H, Baghersalimi A, Eslami S, Saadat F, Rad AH, Basavand R, Papkiadeh SR, Darbandi B, Kooti W, Peluso I | Oxid Med Cell Longev | 2019 |
| Faster Sickling Kinetics and Sickle Cell Shape Evolution during Repeated Deoxygenation and Oxygenation Cycles. | Du E, Dao M | Exp Mech | 2019 |
| Editing the Sickle Cell Disease Mutation in Human Hematopoietic Stem Cells: Comparison of Endonucleases and Homologous Donor Templates. | Romero Z, Lomova A, Said S, Miggelbrink A, Kuo CY, Campo-Fernandez B, Hoban MD, Masiuk KE, Clark DN, Long J, Sanchez JM, Velez M, Miyahira E, Zhang R, Brown D, Wang X, Kurmangaliyev YZ, Hollis RP, Kohn DB | Mol. Ther. | 2019 |
| [Associations of parental thalassemia with preterm birth and low birth weight]. | Huang XC, Qiu XQ, Zeng XY, Liu S, Wei FL, Li YN, Liu T, Wu YN, Feng BY, Jiang QJ, Huang DP | Zhonghua Liu Xing Bing Xue Za Zhi | 2019 |
| A nationwide survey of hospital-based thalassemia patients and standards of care and a preliminary assessment of the national prevention program in Sri Lanka. | Premawardhana AP, Mudiyanse R, De Silva ST, Jiffry N, Nelumdeniya U, de Silva U, Lamabadusuriya SP, Pushpakumara K, Dissanayaka R, Jansz M, Rifaya I, Navarathne U, Thirukumaran V, Arambepola M, Dayanada Bandara W, Vaidyanatha U, Mendis D, Weerasekara K, De Silva N, Shantha Kumara DK, Amarasena SD, Hemantha KK, Refai MACM, Silva I, Hameed N, Rajiyah F, Mettananda S, Allen A, Weatherall DJ, Oliveri NF | PLoS ONE | 2019 |
| [Genotypic and Phenotypic Analysis of αβ-Thalassemia in Children]. | Ren ZM, Xiao WW, Liu SX, Liu YQ, Li B, Chen YS | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2019 |
| [Analysis of Genetic Screening in Couples of Reproductive Age for Thalassemia in Lingshui Li Autonomous County of Hainan Province]. | Tu ZH, Zhou Z, Wu WX, Wang XP, Zhou YZ, Huang CD, Ma N, Ruan HL, Zhao LQ, Wang J | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2019 |
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| Management of the aging beta-thalassemia transfusion-dependent population - The Italian experience. | Pinto VM, Poggi M, Russo R, Giusti A, Forni GL | Blood Rev. | 2019 |
| A sickle cell disease patient with dural venous sinus thrombosis: a case report and literature review. | Wang MK, Shergill R, Jefkins M, Cheung J | Hemoglobin | 2019 |
| Systematic Review: Pain and Emotional Functioning in Pediatric Sickle Cell Disease. | Reader SK, Rockman LM, Okonak KM, Ruppe NM, Keeler CN, Kazak AE | J Clin Psychol Med Settings | 2019 |
| A randomized controlled trial evaluating the effects of amlodipine on myocardial iron deposition in pediatric patients with thalassemia major. | Khaled A, Salem HA, Ezzat DA, Seif HM, Rabee H | Drug Des Devel Ther | 2019 |
| Effect of acute exercise on RBC deformability and RBC nitric oxide synthase signalling pathway in young sickle cell anaemia patients. | Grau M, Jerke M, Nader E, Schenk A, Renoux C, Collins B, Dietz T, Bizjak DA, Joly P, Bloch W, Connes P, Prokop A | Sci Rep | 2019 |
| Emerging disease-modifying therapies for sickle cell disease. | Carden MA, Little J | Haematologica | 2019 |
| The Spectrum of β-Thalassemia Mutations in Siirt Province, Southeastern Turkey. | Yılmaz S | Hemoglobin | 2019 |
| The Role of Patient-Physician Communication on the Use of Hydroxyurea in Adult Patients with Sickle Cell Disease. | Jabour SM, Beachy S, Coburn S, Lanzkron S, Eakin MN | J Racial Ethn Health Disparities | 2019 |
| Multifactorial Painful Leg Ulcers Due to Hyperhomocysteinemia, Plasminogen Activator Inhibitor-1 4G/5G Heterozygote Gene Mutation, and Beta Thalassemia Minor: A Case Report. | Çaytemel C, Topaloğlu Demir F, Büyükbabani N, Türkoğlu Z, Uzuner EG | Int J Low Extrem Wounds | 2019 |
| Free heme regulates placenta growth factor through NRF2-antioxidant response signaling. | Kapetanaki MG, Gbotosho OT, Sharma D, Weidert F, Ofori-Acquah SF, Kato GJ | Free Radic. Biol. Med. | 2019 |
| Diversity of RH and transfusion support in Brazilian sickle cell disease patients with unexplained Rh antibodies. | Dinardo CL, Kelly S, Dezan MR, Ribeiro IH, Castilho SL, Schimidt LC, Valgueiro MDC, Preiss LR, Custer B, Sabino EC, Westhoff CM, | Transfusion | 2019 |
| Male sickle cell patients, compensated transpubertal hypogonadism and normal final growth. | Martins PRJ, De Vito FB, Resende GAD, Kerbauy J, Pereira GA, Moraes-Souza H, Figueiredo MS, Verreschi IT | Clin. Endocrinol. (Oxf) | 2019 |
| Related and unrelated donor transplantation for β-thalassemia major: results of an international survey. | Li C, Mathews V, Kim S, George B, Hebert K, Jiang H, Li C, Zhu Y, Keesler DA, Boelens JJ, Dvorak CC, Agarwal R, Auletta JJ, Goyal RK, Hanna R, Kasow K, Shenoy S, Smith AR, Walters MC, Eapen M | Blood Adv | 2019 |
| CRISPR-Cas9 gene editing for patients with haemoglobinopathies. | The Lancet Haematology | Lancet Haematol | 2019 |
| Total Serum Magnesium Levels and Calcium-To-Magnesium Ratio in Sickle Cell Disease. | Antwi-Boasiako C, Kusi-Mensah YA, Hayfron-Benjamin C, Aryee R, Dankwah GB, Kwawukume LA, Darkwa EO | Medicina (Kaunas) | 2019 |
| Cases of malaria in travellers with sickle cell disease - Chemoprophylaxis is important for this risk group. | Bachmeyer C, Steichen O, Moreno-Sabater A, Magne D, Valin N, Mattioni S, Santin A, Lionnet F | Travel Med Infect Dis | 2019 |
| Identifying Clinical and Research Priorities in Sickle Cell Lung Disease. An Official American Thoracic Society Workshop Report. | Ruhl AP, Sadreameli SC, Allen JL, Bennett DP, Campbell AD, Coates TD, Diallo DA, Field JJ, Fiorino EK, Gladwin MT, Glassberg JA, Gordeuk VR, Graham LM, Greenough A, Howard J, Kato GJ, Knight-Madden J, Kopp BT, Koumbourlis AC, Lanzkron SM, Liem RI, Machado RF, Mehari A, Morris CR, Ogunlesi FO, Rosen CL, Smith-Whitley K, Tauber D, Terry N, Thein SL, Vichinsky E, Weir NA, Cohen RT, Klings ES | Ann Am Thorac Soc | 2019 |
| Enhancing the care of patients with sickle cell disease. | De D, Blackmore A, Taylor H | Nurs Stand | 2019 |
| Lentiviral and genome-editing strategies for the treatment of β-hemoglobinopathies. | Magrin E, Miccio A, Cavazzana M | Blood | 2019 |
| Prevalence and correlates of microalbuminuria in Yemeni children with sickle cell disease. | Al-Musawa FE, Al-Saqladi AM | Saudi J Kidney Dis Transpl | 2019 |
| Brief Screening Measures Identify Risk for Psychological Difficulties Among Children with Sickle Cell Disease. | Hood AM, Reife I, King AA, White DA | J Clin Psychol Med Settings | 2019 |
| Family planning practices in couples with children affected by β-thalassemia major and its relationship with their education: An epidemiological study. | Biswas B, Basu K, Naskar NN, Dasgupta A, Paul B, Basu R | J Educ Health Promot | 2019 |
| Barriers to the use of hydroxyurea in the management of sickle cell disease in Nigeria. | Adeyemo TA, Diaku-Akinwunmi IN, Ojewunmi OO, Bolarinwa AB, Adekile AD | Hemoglobin | 2019 |
| Current and emerging treatments for sickle cell disease. | Monus T, Howell CM | JAAPA | 2019 |
| Quantitative prediction of erythrocyte sickling for the development of advanced sickle cell therapies. | Lu L, Li Z, Li H, Li X, Vekilov PG, Karniadakis GE | Sci Adv | 2019 |
| The Effect of Antioxidants on the Properties of Red Blood Cells From Patients With Sickle Cell Anemia. | Al Balushi H, Hannemann A, Rees D, Brewin J, Gibson JS | Front Physiol | 2019 |
| Double Heterozygosity for Hb Durham-N.C. (: c.344T>C) [β114(G16)Leu→Pro] and the IVS-I-110 (: c.93-21G>A) Causing a Severe β-Thalassemia Phenotype. | Cannata M, Cassarà F, Vinciguerra M, Licari P, Passarello C, Leto F, Lo Pinto C, Pitrolo L, Ganci R, Maggio A, Giambona A | Hemoglobin | 2019 |
| Cellular Iron Metabolism and Regulation. | Gao G, Li J, Zhang Y, Chang YZ | Adv. Exp. Med. Biol. | 2019 |
| Antioxidant properties and membrane stabilization effects of methanol extract of leaves on normal and sickle erythrocytes. | Anosike CA, Igboegwu ON, Nwodo OFC | J Tradit Complement Med | 2019 |
| Differential Diagnosis of Iron-Deficiency Anemia from β-Thalassemia Trait Using an Intelligent Model in Comparison with Discriminant Indexes. | Kabootarizadeh L, Jamshidnezhad A, Koohmareh Z | Acta Inform Med | 2019 |
| Improving Care for Patients with Sickle Cell Disease: a Qualitative Study of Hospitalized Sickle Cell Patients. | Del Pino-Jones A, Bowden K, Misky G, Jones CD | J Gen Intern Med | 2019 |
| Sickle cell disease in Africa: an urgent need for longitudinal cohort studies. | Wonkam A, Makani J | Lancet Glob Health | 2019 |
| The epidemiology of sickle cell disease in children recruited in infancy in Kilifi, Kenya: a prospective cohort study. | Uyoga S, Macharia AW, Mochamah G, Ndila CM, Nyutu G, Makale J, Tendwa M, Nyatichi E, Ojal J, Otiende M, Shebe M, Awuondo KO, Mturi N, Peshu N, Tsofa B, Maitland K, Scott JAG, Williams TN | Lancet Glob Health | 2019 |
| Clinical and molecular characterization of novel deletions causing epsilon gamma delta beta thalassemia: Report of two cases. | Repnikova E, Roberts J, Mc Dermott S, Farooqi MS, Iqbal NT, Silvey M, Nolen J, Taboada E, Li W | Pathol. Res. Pract. | 2019 |
| The Role of Family Functioning in the Development of Executive Functions in Preschool Children with Sickle Cell Anemia. | Downes M, de Haan M, Telfer PT, Kirkham FJ | Dev Neuropsychol | 2019 |
| Coinheritance of Hb A-Melbourne (: c.130G>A) and Hb E (: c.79G>A) in Laos and Simultaneous High Resolution Melt Detection of Hb A-Melbourne and Hb A-Lampang (: c.142G>A) in a Single Tube. | Jomoui W, Panichchob P, Rujirachaivej P, Panyasai S, Tepakhan W | Hemoglobin | 2019 |
| Pulmonary Artery Pseudoaneurysm in a Child With β-Thalassemia Major. | Qureshi TN, Haider SR, Al Rawas A, Al Sukaiti R, Al Kindi H, Al Senaidi KS, Elshinawy M, Wali Y | J. Pediatr. Hematol. Oncol. | 2019 |
| Frequency of Interleukins IL1ß/IL18 and Inflammasome NLRP1/NLRP3 Polymorphisms in Sickle Cell Anemia Patients and their Association with Severity Score. | de Almeida E, Frantz SR, Cesar P, Tarragô AM, de Amorim Xabregas L, Garcia NP, Costa AG, de Paula EV, Malheiro A | Curr. Mol. Med. | 2019 |
| Substance P modulates electroacupuncture analgesia in humanized mice with sickle cell disease. | Wang Y, Lei J, Jha RK, Kiven S, Gupta K | J Pain Res | 2019 |
| [Effect of genetic modifiers on the clinical severity of β-thalassemia]. | Zhang QQ, Shang X, Lin WY, Xu XM | Yi Chuan | 2019 |
| Posterior Reversible Encephalopathy Syndrome in adult sickle-cell patients: Case series and literature review. | Vargas A, Testai FD | J Clin Neurosci | 2019 |
| Ticagrelor versus placebo for the reduction of vaso-occlusive crises in pediatric sickle cell disease: Rationale and design of a randomized, double-blind, parallel-group, multicenter phase 3 study (HESTIA3). | Heeney MM, Abboud MR, Amilon C, Andersson M, Githanga J, Inusa B, Kanter J, Leonsson-Zachrisson M, Michelson AD, Berggren AR, | Contemp Clin Trials | 2019 |
| High erythropoietin may be associated with vascular complications in patients with secondary erythrocytosis caused by high oxygen affinity variant hemoglobin Coimbra. | Santos BC, Jorge SE, de Albuquerque DM, Gilli SCO, Sonati MF, Fertrin KY, Costa FF | Blood Cells Mol. Dis. | 2019 |
| Validation of a composite vascular high-risk profile for adult patients with sickle cell disease. | Nouraie M, Little JA, Hildesheim M, Gibbs JSR, Morris CR, Machado RF, Kato GJ, Gordeuk VR, Gladwin MT | Am. J. Hematol. | 2019 |
| Corrigendum to | Masilamani V, Al Salhi MS, Devanesan S, AlGahtani FH, Abu-Salah KM, Ahamad I, Agastian P | Photodiagnosis Photodyn Ther | 2019 |
| Association of plasma homocysteine level with vaso-occlusive crisis in sickle cell anemia patients of Odisha, India. | Meher S, Patel S, Das K, Dehury S, Jit BP, Maske MM, Das P, Dash BP, Mohanty PK | Ann. Hematol. | 2019 |
| Haemoglobinopathies from the cardiac point of view. | Romano MMD | Hematol Transfus Cell Ther | 2019 |
| SIMENS-LIS4SC, a Laboratory Information System for Biological Tests of Sickle Cell Screening and Healthcare. | Diallo AH, Camara G, Lamy JB, Lo M, Diagne I, Makalou D, Diop M, Doupa D | Stud Health Technol Inform | 2019 |
| Hb Guangxi [β65(E9)Lys→Glu (>AG); : c.196A>G]: A Novel β-Globin Variant. | Xu M, Chen WD, Wang YJ, Zhou Y, Li J, Xu AP, Ji L | Hemoglobin | 2019 |
| Cholelithiasis in patients with paediatric sickle cell anaemia in a Saudi hospital. | Alhawsawi ZM, Alshenqeti AM, Alqarafi AM, Alhussayen LK, Turkistani WA | J Taibah Univ Med Sci | 2019 |
| The autophagy-activating kinase ULK1 mediates clearance of free α-globin in β-thalassemia. | Lechauve C, Keith J, Khandros E, Fowler S, Mayberry K, Freiwan A, Thom CS, Delbini P, Romero EB, Zhang J, Motta I, Tillman H, Cappellini MD, Kundu M, Weiss MJ | Sci Transl Med | 2019 |
| The challenges of handling deferasirox in sickle cell disease patients older than 40 years. | Ribeiro LB, Soares EA, Costa FF, Gilli SCO, Olalla Saad ST, Benites BD | Hematology | 2019 |
| HLA-haploidentical hematopoietic stem cell transplantation in pediatric patients with hemoglobinopathies: current practice and new approaches. | Oevermann L, Schulte JH, Hundsdörfer P, Hakimeh D, Kogel F, Lang P, Corbacioglu S, Eggert A, Sodani P | Bone Marrow Transplant. | 2019 |
| Sickle Cell Trait, European Ancestry, and Longitudinal Tracking of HbA Among African Americans: The Jackson Heart Study. | Echouffo-Tcheugui JB, Mwasongwe SE, Sims M, Dagogo-Jack S, Golden SH, Correa A, Musani SK | Diabetes Care | 2019 |
| Correlates of successful transition in young adults with sickle cell disease. | Darbari I, Jacobs E, Gordon O, Weiss D, Winship K, Casella JF, Strouse JJ, Takemoto CM | Pediatr Blood Cancer | 2019 |
| Thirty-year risk of ischemic stroke in individuals with sickle cell trait and modification by chronic kidney disease: The atherosclerosis risk in communities (ARIC) study. | Caughey MC, Derebail VK, Key NS, Reiner AP, Gottesman RF, Kshirsagar AV, Heiss G | Am. J. Hematol. | 2019 |
| Hemoglobin S and C affect biomechanical membrane properties of -infected erythrocytes. | Fröhlich B, Jäger J, Lansche C, Sanchez CP, Cyrklaff M, Buchholz B, Soubeiga ST, Simpore J, Ito H, Schwarz US, Lanzer M, Tanaka M | Commun Biol | 2019 |
| Effect of Health Education Programme on the Knowledge of and Attitude about Sickle Cell Anaemia among Male Secondary School Students in the Jazan Region of Saudi Arabia: Health Policy Implications. | Kotb MM, Almalki MJ, Hassan Y, Al Sharif A, Khan M, Sheikh K | Biomed Res Int | 2019 |
| Asymptomatic actinomycosis in a girl with thalassemia major. | Yu U, Wang X | IDCases | 2019 |
| Effects of Individualized Treadmill Endurance Training on Oxidative Stress in Skeletal Muscles of Transgenic Sickle Mice. | Gouraud E, Charrin E, Dubé JJ, Ofori-Acquah SF, Martin C, Skinner S, Chatel B, Boreau A, Messonnier LA, Connes P, Pialoux V, Hautier C, Faes C | Oxid Med Cell Longev | 2019 |
| Treatment of dental and orthodontic complications in thalassaemia. | Mulimani P, Abas AB, Karanth L, Colombatti R, Kulkarni P | Cochrane Database Syst Rev | 2019 |
| A case of compound heterozygous hemoglobin Köln/hemoglobin E in an Indian family. | Mittal N, Garg A, Kashyap R, Agarwal S | Pediatr Hematol Oncol | 2019 |
| The Experience and Health-Related Quality of Life after Haploidentical Stem Cell Transplantation for Adults with Sickle Cell Disease. | Hastings B, Patil C, Gallo AM | West J Nurs Res | 2019 |
| Occurrence of acute myeloid leukemia in hydroxyurea-treated sickle cell disease patient. | Regan S, Yang X, Finnberg NK, El-Deiry WS, Pu JJ | Cancer Biol. Ther. | 2019 |
| Approximately 40 000 children with sickle cell anemia require screening with TCD and treating with hydroxyurea for stroke prevention in three states in northern Nigeria. | Galadanci AA, Galadanci NA, Jibir BW, Abdullahi SU, Idris N, Gambo S, Ali Abubakar SA, Kabo NA, Bello-Manga H, Haliru L, Bashir I, Aliyu MH, Galadanci JA, DeBaun MR | Am. J. Hematol. | 2019 |
| Evaluation of the Effect of Support-Training System of Peer Group on Promotion of Self-Care in β-Thalassemia Major Patients in Southern Iran. | Safaei S, Abedi H, Parand S, Karimi M | Hemoglobin | 2019 |
| Thalassemia and Moyamoya syndrome: unfurling an intriguing association. | Das S, Dubey S, Acharya M, Chatterjee S, Lahiri D, Das G, Ray BK, Kraemer M | J. Neurol. | 2019 |
| Dysfunction of the auditory system in sickle cell anaemia: a systematic review with meta-analysis. | Rissatto-Lago MR, Fernandes LDC, Alves AAG, de Oliveira ACG, de Andrade CLO, Salles C, Ladeia AMT | Trop. Med. Int. Health | 2019 |
| Red blood cells microparticles are associated with hemolysis markers and may contribute to clinical events among sickle cell disease patients. | Olatunya OS, Lanaro C, Longhini AL, Penteado CFF, Fertrin KY, Adekile A, Saad STO, Costa FF | Ann. Hematol. | 2019 |
| Allogenic hematopoietic stem cell transplantation in sickle cell disease. | Galal A, Asslan M | Curr. Opin. Hematol. | 2019 |
| Quality of life in pre-adolescent children with sickle cell disease in Brazil. | Oliveira CDL, Kelly S, de Almeida-Neto C, Carneiro-Proietti AB, Camargos Piassi FC, Salomon T, Flor-Park MV, Maximo C, Rodrigues DW, Mota RA, Teixeira CM, Loureiro P, Sabino EC, Custer B, | Pediatr Hematol Oncol | 2019 |
| Ischemic stroke in children and young adults with sickle cell disease in the post-STOP era. | Kwiatkowski JL, Voeks JH, Kanter J, Fullerton HJ, Debenham E, Brown L, Adams RJ, | Am. J. Hematol. | 2019 |
| Transfusion practices in the care of pregnant women with sickle cell disease in Ouagadougou. | Zamané H, Sanou F, Kiemtoré S, Kain DP, Sawadogo AK, Bonané-Thiéba B | Int J Gynaecol Obstet | 2019 |
| Effect of different iron chelation regimens on bone mass in transfusion-dependent thalassemia patients. | Bordbar M, Haghpanah S, Zekavat OR, Saki F, Bazrafshan A, Bozorgi H | Expert Rev Hematol | 2019 |
| Nitric oxide loading reduces sickle red cell adhesion and vaso-occlusion in vivo. | McMahon TJ, Shan S, Riccio DA, Batchvarova M, Zhu H, Telen MJ, Zennadi R | Blood Adv | 2019 |
| Hematopoietic stem cell transplantation and cellular therapy in sickle cell disease: where are we now? | Tanhehco YC, Bhatia M | Curr. Opin. Hematol. | 2019 |
| Mechanisms of alloimmunization in sickle cell disease. | Hudson KE, Fasano RM, Karafin MS, Hendrickson JE, Francis RO | Curr. Opin. Hematol. | 2019 |
| Single-Incision Pediatric Endosurgery Cholecystectomy Performed by Residents in Children with Sickle Cell Disease. | Raboe E, Owiwi Y, Al Nofeai Z, Ghallab A, Zainelabdeen AS, Alsaggaf AA, Zidan M, Fayez M, Atta A, Alofi T, Sindi OA, Almanea A, Alharbi IA, Madani H, Seet M, Sait A, Fallatah R | J Laparoendosc Adv Surg Tech A | 2019 |
| Noninvasive optical assessment of resting-state cerebral blood flow in children with sickle cell disease. | Lee SY, Cowdrick KR, Sanders B, Sathialingam E, McCracken CE, Lam WA, Joiner CH, Buckley EM | Neurophotonics | 2019 |
| Genetic modulators of fetal hemoglobin expression and ischemic stroke occurrence in African descendant children with sickle cell anemia. | Nicolau M, Vargas S, Silva M, Coelho A, Ferreira E, Mendonça J, Vieira L, Kjöllerström P, Maia R, Silva R, Dias A, Ferreira T, Morais A, Soares IM, Lavinha J, Faustino P | Ann. Hematol. | 2019 |
| A Novel Frameshift Mutation at Codon 2 (-T) (: c.9delT) and First Report of Three New β-Globin Mutations From Azerbaijan. | Bayramov B, Aliyeva G, Asadov C, Mammadova T, Karimova N, Eynullazadeh K, Gafarova S, Akbarov S, Farhadova S, Safarzadeh Z, Abbasov M | Hemoglobin | 2019 |
| Reticulocyte Hemoglobin Equivalent (Ret-He) Combined with Red Blood Cell Distribution Width Has a Differentially Diagnostic Value for Thalassemias. | Lian Y, Shi J, Nie N, Huang Z, Shao Y, Zhang J, Huang J, Li X, Ge M, Jin P, Wang M, Zheng Y | Hemoglobin | 2019 |
| Vascular Instability and Neurological Morbidity in Sickle Cell Disease: An Integrative Framework. | Stotesbury H, Kawadler JM, Hales PW, Saunders DE, Clark CA, Kirkham FJ | Front Neurol | 2019 |
| Genetic diversity of CD14, CD28, CTLA-4 and ICOS gene promoter polymorphism in African and American sickle cell disease. | Seamans BN, Pellechio SL, Capria AL, Agyingi SE, Morenikeji OB, Ojurongbe O, Thomas BN | Hum. Immunol. | 2019 |
| Association of frequency of hereditary hemochromatosis (HFE) gene mutations (H63D and C282Y) with iron overload in beta-thalassemia major patients in Pakistan. | Sharif Y, Irshad S, Tariq A, Rasheed S, Tariq MH | Saudi Med J | 2019 |
| Iron overload and malignancies in patients with haemoglobinopathies: A single center experience. | Rigoli L, Petrungaro A, Di Bella C, Caruso R | Transfus. Apher. Sci. | 2019 |
| The effect of quercetin on iron overload and inflammation in β-thalassemia major patients: A double-blind randomized clinical trial. | Sajadi Hezaveh Z, Azarkeivan A, Janani L, Hosseini S, Shidfar F | Complement Ther Med | 2019 |
| Pharmacokinetics and pharmacodynamics of single dose of inhaled nebulized sodium nitrite in healthy and hemoglobin E/β-thalassemia subjects. | Sirirat K, Sriwantana T, Kaewchuchuen J, Paiboonsukwong K, Fucharoen S, Ritthidej G, Parakaw T, Srihirun S, Vivithanaporn P, Sritara P, Sibmooh N | Nitric Oxide | 2019 |
| [Cephalometric evaluation of patients with β-thalassemia major living in Azerbaijan]. | Shadlinskaya RV, Gasymova ZV, Gasymov OF | Stomatologiia (Mosk) | 2019 |
| Hemoglobin-based Oxygen Carriers: Current State-of-the-art and Novel Molecules. | Sen Gupta A | Shock | 2019 |
| Hemoglobin-based Oxygen Carriers (HBOC)-What the Next Generation Holds: When Red Blood Cells are not an Option. | Hill-Pryor C, Pusateri AE, Weiskopf RB | Shock | 2019 |
| Rifaximin for sickle cell disease. | Lim SH, Dutta D, Moore J | Am. J. Hematol. | 2019 |
| Hemoglobin alters vitamin carrier uptake and vitamin D metabolism in proximal tubule cells: implications for sickle cell disease. | Gliozzi ML, Rbaibi Y, Long KR, Vitturi DA, Weisz OA | Am. J. Physiol., Cell Physiol. | 2019 |
| Antenatal screening for haemoglobinopathies: current status, barriers and ethics. | Chakravorty S, Dick MC | Br. J. Haematol. | 2019 |
| Evaluation of hydroxyurea genotoxicity in patients with sickle cell disease. | Oliveira EAM, Boy KA, Santos APP, Machado CDS, Velloso-Rodrigues C, Gerheim PSAS, Mendonça LM | Einstein (Sao Paulo) | 2019 |
| Profile of crizanlizumab and its potential in the prevention of pain crises in sickle cell disease: evidence to date. | Riley TR, Riley TT | J Blood Med | 2019 |
| Decoding the role of SOD2 in sickle cell disease. | Dosunmu-Ogunbi AM, Wood KC, Novelli EM, Straub AC | Blood Adv | 2019 |
| [Serum level of soluble transferrin receptor in children with hemoglobin H disease]. | Ren ZM, Huang LL, Huang BX, Li CG, Chen YS | Zhongguo Dang Dai Er Ke Za Zhi | 2019 |
| Prevalence and genetic analysis of thalassemia in neonates in Wuhan area: a national megacity in central China. | Cai W, Xiong Q, Tong J, Dai X, Zhou B, Shen S, Hu X | J. Matern. Fetal. Neonatal. Med. | 2019 |
| Updated mechanisms underlying sickle cell disease-associated pain. | Du S, Lin C, Tao YX | Neurosci. Lett. | 2019 |
| Systematic Review of l-glutamine for Prevention of Vaso-occlusive Pain Crisis in Patients with Sickle Cell Disease. | Cieri-Hutcherson NE, Hutcherson TC, Conway-Habes EE, Burns BN, White NA | Pharmacotherapy | 2019 |
| Animal Models of Normal and Disturbed Iron and Copper Metabolism. | Wang X, Garrick MD, Collins JF | J. Nutr. | 2019 |
| Iron stores in pregnant women with sickle cell disease: a protocol for a systematic review and meta-analysis. | Aroke D, Momo Kadia B, Njim T | BMJ Open | 2019 |
| Magnesium for treating sickle cell disease. | Than NN, Soe HHK, Palaniappan SK, Abas AB, De Franceschi L | Cochrane Database Syst Rev | 2019 |
| Treatment Status of Patients with B-Thalassemia Major in Northern Iran: Thalassemia Registry System. | Kosaryan M, Karami H, Darvishi-Khezri H, Akbarzadeh R, Aliasgharian A, Bromand K | Iran. J. Public Health | 2019 |
| Megestrol Acetate Induced Paradoxical Embolism in a Sickle Cell Disease Patient. | Dominguez L, Tatar F, Malakooti SK, Kulchinsky RP | Cureus | 2019 |
| Mini review: leg ulcers - a secondary complication of sickle cell disease. | AlDallal SM | Int J Gen Med | 2019 |
| Clinical Transformation in Care for Patients With Sickle Cell Disease at an Urban Academic Medical Center. | Rizk S, Axelrod D, Riddick-Burden G, Congdon-Martin E, McKenzie S, Haines C, Ward L, McAna J, Crawford AG | Am J Med Qual | 2019 |
| CRISPR/Cas9 gene correction of HbH-CS thalassemia-induced pluripotent stem cells. | Yingjun X, Yuhuan X, Yuchang C, Dongzhi L, Ding W, Bing S, Yi Y, Dian L, Yanting X, Zeyu X, Nengqing L, Diyu C, Xiaofang S | Ann. Hematol. | 2019 |
| Investigation of JAK2V617F Mutation Prevalence in Patients with Beta Thalassemia Major. | Tahannejad Asadi Z, Yarahmadi R, Saki N, Jalali MT, Amin Asnafi A, Tangestani R | Lab Med | 2019 |
| Stem cell transplantation in sickle-cell disease. | Sheth S | Lancet Haematol | 2019 |
| Echocardiographic Screening of Cardiovascular Status in Pediatric Sickle Cell Disease. | Allen KY, Jones S, Jackson T, DeCost G, Stephens P, Hanna BD, Cohen MS, Smith-Whitley K, Mercer-Rosa L, Natarajan SS | Pediatr Cardiol | 2019 |
| Construction and Analysis of a Long Non-Coding RNA (lncRNA)-Associated ceRNA Network in β-Thalassemia and Hereditary Persistence of Fetal Hemoglobin. | Jia W, Jia S, Chen P, He Y | Med. Sci. Monit. | 2019 |
| Hepatobiliary Complications in Children with Sickle Cell Disease: A Retrospective Review of Medical Records from 616 Patients. | Allali S, de Montalembert M, Brousse V, Heilbronner C, Taylor M, Brice J, Manzali E, Garcelon N, Lacaille F | J Clin Med | 2019 |
| Selenium Status and Hemolysis in Sickle Cell Disease Patients. | Delesderrier E, Cople-Rodrigues CS, Omena J, Kneip Fleury M, Barbosa Brito F, Costa Bacelo A, Correa Koury J, Citelli M | Nutrients | 2019 |
| Clinical phenotypes and outcomes of precapillary pulmonary hypertension of sickle cell disease. | Savale L, Habibi A, Lionnet F, Maitre B, Cottin V, Jais X, Chaouat A, Artaud-Macari E, Canuet M, Prevot G, Chantalat-Auger C, Montani D, Sitbon O, Galacteros F, Simonneau G, Parent F, Bartolucci P, Humbert M | Eur. Respir. J. | 2019 |
| Antibiotics for treating acute chest syndrome in people with sickle cell disease. | Martí-Carvajal AJ, Conterno LO, Knight-Madden JM | Cochrane Database Syst Rev | 2019 |
| Newborn Screening With Sickle Cell Point of Care: A Valuable Resource in Low-Income Settings. | Ware RE, Odame I | Pediatrics | 2019 |
| Newborn Screening for Sickle Cell Disease Using Point-of-Care Testing in Low-Income Setting. | Alvarez OA, Hustace T, Voltaire M, Mantero A, Liberus U, Saint Fleur R | Pediatrics | 2019 |
| A Heterozygous Variant (: c.379delG, p.Val127Cysfs*32) Associated with a Mild β-Thalassemia Intermedia Phenotype in a Turkish Child. | Gürlek-Gökçebay D, Akpinar-Tekgunduz S, Erdem HB, Yarali N | Hemoglobin | 2019 |
| Splenectomy for people with thalassaemia major or intermedia. | Sharma A, Easow Mathew M, Puri L | Cochrane Database Syst Rev | 2019 |
| Spectral domain optical coherence tomography findings in Turkish sickle-cell disease and beta thalassemia major patients. | Ulusoy MO, Türk H, Kıvanç SA | J Curr Ophthalmol | 2019 |
| Role of some members of chemokine/cytokine network in the pathogenesis of thalassemia and sickle cell hemoglobinopathies: a mini review. | Mousavi Z, Yazdani Z, Moradabadi A, Hoseinpourkasgari F, Hassanshahi G | Exp Hematol Oncol | 2019 |
| Prevalence and Factors Associated with Human Parvovirus B19 Infection in Sickle Cell Patients Hospitalized in Tanzania. | Urio F, George H, Tluway F, Nyambo TB, Mmbando BP, Makani J | Mediterr J Hematol Infect Dis | 2019 |
| Dengue with Normal Platelet Count and no Hemoconcentration: Automated Hematogram in Cases with Underlying Thalassemia. | Joob B, Wiwanitkit V | Iran J Pathol | 2019 |
| Insulin secretion-sensitivity index-2 could be a novel marker in the identification of the role of pancreatic iron deposition on beta-cell function in thalassemia major. | Karadas N, Yurekli B, Bayraktaroglu S, Aydinok Y | Endocr. J. | 2019 |
| The effect of positive thinking training on the quality of life of parents of adolescent with thalassemia. | Sadeghloo A, Shamsaee P, Hesari E, Akhondzadeh G, Hojjati H | Int J Adolesc Med Health | 2019 |
| Serum Potassium, Sodium, and Chloride Levels in Sickle Cell Disease Patients and Healthy Controls: A Case-Control Study at Korle-Bu Teaching Hospital, Accra. | Antwi-Boasiako C, Kusi-Mensah YA, Hayfron-Benjamin C, Aryee R, Dankwah GB, Abla KL, Owusu Darkwa E, Botchway FA, Sampene-Donkor E | Biomark Insights | 2019 |
| Prevalence of hemoglobin abnormalities in an apparently healthy population in Benin. | Zohoun A, Baglo Agbodande T, Zohoun L, Anani L | Hematol Transfus Cell Ther | 2019 |
| Extensive multilineage analysis in patients with mixed chimerism after allogeneic transplantation for sickle cell disease: insight into hematopoiesis and engraftment thresholds for gene therapy. | Magnani A, Pondarré C, Bouazza N, Magalon J, Miccio A, Six E, Roudaut C, Arnaud C, Kamdem A, Touzot F, Gabrion A, Magrin E, Couzin C, Fusaro M, André I, Vernant JP, Gluckman E, Bernaudin F, Bories D, Cavazzana M | Haematologica | 2019 |
| Airway Inflammation and Lung Function in Sickle Cell Disease. | De A, Agrawal S, Morrone K, Zhang J, Bjorklund NL, Manwani D, Rastogi D | Pediatr Allergy Immunol Pulmonol | 2019 |
| Relating retinal blood flow and vessel morphology in sickle cell retinopathy. | Cano J, Farzad S, Khansari MM, Tan O, Huang D, Lim JI, Shahidi M | Eye (Lond) | 2019 |
| The monoclonal antibody against γ-globin chain; , accurately measured F cells in SEA-α thalassemia 1 trait. | Tangpan L, Jansai T, Kerdpoo S, Kiewkarnkha T, Limweeraprajak E, Tatu T | J Immunoassay Immunochem | 2019 |
| Review of Sickle Cell Disease and Spinal Pathology. | Rudy HL, Yang D, Nam AD, Cho W | Global Spine J | 2019 |
| Why, Who, When, and How? Rationale for Considering Allogeneic Stem Cell Transplantation in Children with Sickle Cell Disease. | Bernaudin F | J Clin Med | 2019 |
| Awareness of Ocular Manifestations, Complications, and Treatment of Sickle Cell Disease in the Eastern Province of Saudi Arabia: A Cross-Sectional Study. | Alshehri AM, Feroze KB, Amir MK | Middle East Afr J Ophthalmol | 2019 |
| Hemoglobin S and Glucose-6-Phosphate Dehydrogenase Deficiency Coinheritance in AS and SS Individuals in Malaria-Endemic Region: A Study in Calabar, Nigeria. | Okafor IM, Okoroiwu HU, Ekechi CA | J Glob Infect Dis | 2019 |
| Low levels of coagulation inhibitors: A high-risk thrombotic factor in thalassemic patients. | Mousavi Z, Soleymani S, Hassanshahi G, Nikbakht R, Mirzaee Khalilabadi R | Rev Clin Esp | 2019 |
| Randomized Pilot Study: A Mobile Technology-based Self-management Intervention for Sickle Cell Pain. | Ezenwa MO, Yao Y, Nguyen MT, Mandernach MW, Hunter CT, Yoon SL, Fedele D, Lucero RJ, Lyon D, Wilkie DJ | West J Nurs Res | 2019 |
| Knowledge and attitude toward genetic diseases and genetic tests among pre-marriage individuals: A cross-sectional study in northern Iran. | Hashemi-Soteh MB, Nejad AV, Ataei G, Tafazoli A, Ghasemi D, Siamy R | Int J Reprod Biomed (Yazd) | 2019 |
| Minihepcidins improve ineffective erythropoiesis and splenomegaly in a new mouse model of adult beta-thalassemia major. | Casu C, Chessa R, Liu A, Gupta R, Drakesmith H, Fleming R, Ginzburg YZ, MacDonald B, Rivella S | Haematologica | 2019 |
| Thalassemia and Hemoglobinopathies in an Ethnic Minority Group in Northern Vietnam. | Anh TM, Sanchaisuriya K, Kieu GN, Tien DN, Thu HBT, Sanchaisuriya P, Fucharoen S, Fucharoen G, Schelp FP | Hemoglobin | 2019 |
| Evaluation of Outcomes and Quality of Care in Children with Sickle Cell Disease Diagnosed by Newborn Screening: A Real-World Nation-Wide Study in France. | Brousse V, Arnaud C, Lesprit E, Quinet B, Odièvre MH, Etienne-Julan M, Guillaumat C, Elana G, Belloy M, Garnier N, Chamouine A, Dumesnil C, Montalembert M, Pondarre C, Bernaudin F, Couque N, Boutin E, Bardakjian J, Djennaoui F, Ithier G, Benkerrou M, Thuret I | J Clin Med | 2019 |
| Attrition from Care and Clinical Outcomes in a Cohort of Sickle Cell Disease Patients in a Tribal Area of Western India. | Dave K, Chinnakali P, Thekkur P, Desai S, Vora C, Desai G | Trop Med Infect Dis | 2019 |
| Allogeneic Hematopoietic Stem Cell Transplantation for Adults with Sickle Cell Disease. | Saraf SL, Rondelli D | J Clin Med | 2019 |
| The emerging challenge of sickle cell nephropathy. | Baptista RB, Almeida E | Nephrol. Dial. Transplant. | 2019 |
| Marital status and paternity in patients with Transfusion- Dependent Thalassemia (TDT) and Non Transfusion-Dependent Thalassemia (NTDT): an ICET - A survey in different countries. | De Sanctis V, Soliman AT, El-Hakim I, Christou S, Mariannis D, Karimi M, Ladis V, Kattamis A, Daar S, Yassin M, Canatan D, Galati MC, Raiola G, Campisi S, Kakkar S, Kaleva V, Saki F, Ellinides A, Pikis G, Christodoulides C, Abdulla M, Di Maio S, Theodoridis C, Elsedfy H, Kattamis C | Acta Biomed | 2019 |
| Responsive Parenting Behaviors and Cognitive Function in Children With Sickle Cell Disease. | Yarboi J, Prussien KV, Bemis H, Williams E, Watson KH, McNally C, Henry L, King AA, DeBaun MR, Compas BE | J Pediatr Psychol | 2019 |
| Peripheral nerve pathology in sickle cell disease mice. | Sadler KE, Lewis TR, Waltz TB, Besharse JC, Stucky CL | Pain Rep | 2019 |
| Detection of Extramedullary Hematopoietic Tissue in a Patient with Beta-Thalassemia Major on Tc99m-Sestamibi Parathyroid Scintigraphy. | Valotassiou V, Angelidis G, Alexiou S, Psimadas D, Tsougos I, Georgoulias P | Indian J Nucl Med | 2019 |
| Noninvasive prenatal screening test for compound heterozygous beta thalassemia using an amplification refractory mutation system real-time polymerase chain reaction technique. | Suwannakhon N, Pangeson T, Seeratanachot T, Mahingsa K, Pingyod A, Bumrungpakdee W, Sanguansermsri T | Hematol Rep | 2019 |
| Rare double heterozygosity for poly A(A〉 G) and CD17(A〉 T) of beta thalassemia intermedia in a Chinese family. | Xie J, Zhou Y, Xiao Q, Long R, Li L, Li L | Hematol Rep | 2019 |
| Concurrent juvenile myelomonocytic leukemia with thalassemia in a case with infection from Sabah, Malaysian Borneo. | Abdullah MA, Abdullah SM, Kumar SV, Hoque MZ | Hematol Rep | 2019 |
| First gene therapy for β-thalassemia approved. | Harrison C | Nat. Biotechnol. | 2019 |
| Development of a forward-oriented therapeutic lentiviral vector for hemoglobin disorders. | Uchida N, Hsieh MM, Raines L, Haro-Mora JJ, Demirci S, Bonifacino AC, Krouse AE, Metzger ME, Donahue RE, Tisdale JF | Nat Commun | 2019 |
| Reversal of a rheologic cardiomyopathy following hematopoietic stem cell transplantation for sickle cell disease. | Sachdev V, Hsieh M, Jeffries N, Noreuil A, Li W, Sidenko S, Hannoush H, Limerick E, Wilson D, Tisdale J, Fitzhugh C | Blood Adv | 2019 |
| Knowledge and Beliefs Regarding Thalassemia in an Urban Population. | Ebrahim S, Raza AZ, Hussain M, Khan A, Kumari L, Rasheed R, Mahmood S, Khatri MA, Bijoora M, Zaheer R, Sattar N, Sohail W, Zakir H, Jafry FH, Memon A, Anwer S, Fatima K | Cureus | 2019 |
| Gene Therapy For Beta-Thalassemia: Updated Perspectives. | Karponi G, Zogas N | Appl Clin Genet | 2019 |
| Thalassaemia. | Barnett R | Lancet | 2019 |
| The impact of Host vs. Graft mismatches on rejection of haploidentical bone marrow transplants in thalassemia patients using posttransplant cyclophosphamide. | Marwah P, Soni R, Ramprakash S, Raghuram CP, Trivedi D, Kumar Agarwal R, Dhanya R, Sedai A, Kumari A, Parmar L, Faulkner L | Bone Marrow Transplant. | 2019 |
| Cas9 interrogates genomic DNA with very high specificity and can be used for mammalian genome editing. | Acharya S, Mishra A, Paul D, Ansari AH, Azhar M, Kumar M, Rauthan R, Sharma N, Aich M, Sinha D, Sharma S, Jain S, Ray A, Jain S, Ramalingam S, Maiti S, Chakraborty D | Proc. Natl. Acad. Sci. U.S.A. | 2019 |
| Parental Attitudes Towards Prenatal Genetic Testing For Sickle Cell Disease. | Stevens EM, Patterson CA, Tchume-Johnson T, Antiel RM, Flake A, Smith-Whitley K, Barakat LP | J. Pediatr. Hematol. Oncol. | 2019 |
| The controversial role of red cell transfusions for sickle cell pain. | Karafin MS, Field JJ | Curr. Opin. Hematol. | 2019 |
| Noninvasive prenatal diagnosis of β-thalassemia by relative haplotype dosage without analyzing proband. | Li H, Du B, Jiang F, Guo Y, Wang Y, Zhang C, Zeng X, Xie Y, Ouyang S, Xian Y, Chen M, Liu W, Sun X | Mol Genet Genomic Med | 2019 |
| Morpho-functional evaluation of lung aeration as a marker of sickle-cell acute chest syndrome severity in the ICU: a prospective cohort study. | Garnier M, Hafiani EM, Arbelot C, Blayau C, Labbe V, Stankovic-Stojanovic K, Lionnet F, Bonnet F, Fulgencio JP, Fartoukh M, Quesnel C | Ann Intensive Care | 2019 |
