| 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 |
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| 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 |
