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Anemia

Free Subscription Articles published in Am J Hematol Retrieve available abstracts of 261 articles: HTML format

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May 2024
1. NJOKU F, Pugh N, Brambilla D, Kroner B, et al
   Mortality in adults with sickle cell disease: Results from the sickle cell disease implementation consortium (SCDIC) registry.
   Am J Hematol. 2024;99:900-909.
   PubMed     Abstract available
   
   
   
2. GRIFFIN M, Kelly R, Brindel I, Maafa L, et al
   Real-world experience of pegcetacoplan in paroxysmal nocturnal hemoglobinuria.
   Am J Hematol. 2024;99:816-823.
   PubMed     Abstract available
   
   
   April 2024
3. JACKSON TA, Buscetta AJ, Ramirez HC, Bonham VL Jr, et al
   Leg ulcers are indicators of systemic dysfunction in individuals with sickle cell disease.
   Am J Hematol. 2024;99:767-769.
   PubMed     Abstract available
   
   
   
4. FATTIZZO B, Roth A, Broome CM, Khan U, et al
   COVID-19 vaccine safety and immunogenicity in patients with cold agglutinin disease receiving concomitant sutimlimab.
   Am J Hematol. 2024;99:789-791.
   PubMed     Abstract available
   
   
   
5. EAPEN M, Kou J, Andreansky M, Bhatia M, et al
   Long-term outcomes after unrelated donor transplantation for severe sickle cell disease on the BMT CTN 0601 trial.
   Am J Hematol. 2024;99:785-788.
   PubMed    
   
   
   
6. ITO S, Pandya A, Hauser RG, Krishnamurti L, et al
   Decreasing alloimmunization-specific mortality in sickle cell disease in the United States: Cost-effectiveness of a shared transfusion resource.
   Am J Hematol. 2024;99:570-576.
   PubMed     Abstract available
   
   
   
7. ALLALI S, Galacteros F, Oevermann L, Cannas G, et al
   Hydroxyurea is associated with later onset of acute splenic sequestration crisis in sickle cell disease: Lessons from the European Sickle Cell Disease Cohort-Hydroxyurea (ESCORT-HU) study.
   Am J Hematol. 2024;99:555-561.
   PubMed     Abstract available
   
   
   March 2024
8. GIARDINO S, Eikema DJ, Piepenbroek B, Algeri M, et al
   HLA-haploidentical stem cell transplantation in children with inherited bone marrow failure syndromes: A retrospective analysis on behalf of EBMT severe aplastic Anemia and pediatric diseases working parties.
   Am J Hematol. 2024 Mar 18. doi: 10.1002/ajh.27293.
   PubMed     Abstract available
   
   
   
9. SHORT V, Allen R, Earley CJ, Bahrain H, et al
   A randomized double-blind pilot study to evaluate the efficacy, safety, and tolerability of intravenous iron versus oral iron for the treatment of restless legs syndrome in patients with iron deficiency anemia.
   Am J Hematol. 2024 Mar 13. doi: 10.1002/ajh.27290.
   PubMed     Abstract available
   
   
   
10. SICA M, Notaro R
    The inhibition of several components of terminal complement pathway results in C3 binding to PNH red blood cells.
    Am J Hematol. 2024;99:505-507.
    PubMed     Abstract available
    
    
    
11. MUSALLAM KM, Barella S, Origa R, Ferrero GB, et al
    'Phenoconversion' in adult patients with beta-thalassemia.
    Am J Hematol. 2024;99:490-493.
    PubMed     Abstract available
    
    
    
12. JACOBS JW, Booth GS, Woo JS, Adkins BD, et al
    How the United States syphilis epidemic may portend a resurgence of an unusual hematologic condition: The connection between syphilis and paroxysmal cold hemoglobinuria.
    Am J Hematol. 2024;99:484-485.
    PubMed     Abstract available
    
    
    
13. CORBACIOGLU S, Frangoul H, Locatelli F, Hobbs W, et al
    Defining curative endpoints for transfusion-dependent beta-thalassemia in the era of gene therapy and gene editing.
    Am J Hematol. 2024;99:422-429.
    PubMed     Abstract available
    
    
    
14. LOCATELLI F, Corbacioglu S, Hobbs W, Frangoul H, et al
    Defining curative endpoints for sickle cell disease in the era of gene therapy and gene editing.
    Am J Hematol. 2024;99:430-438.
    PubMed     Abstract available
    
    
    February 2024
15. POWER-HAYS A, Tomlinson GA, Tshilolo L, Santos B, et al
    Reducing transfusion utilization for children with sickle cell anemia in sub-Saharan Africa with hydroxyurea: Analysis from the phase I/II REACH trial.
    Am J Hematol. 2024 Feb 8. doi: 10.1002/ajh.27244.
    PubMed     Abstract available
    
    
    
16. ABDULLAHI SU, Sunusi S, Aminu H, Umar R, et al
    Transcranial doppler velocity in iron-deficient Nigerian children with sickle cell anemia.
    Am J Hematol. 2024 Feb 7. doi: 10.1002/ajh.27230.
    PubMed     Abstract available
    
    
    
17. TEFFERI A, Pardanani A, Gangat N
    Momelotinib expands the therapeutic armamentarium for myelofibrosis: Impact on hierarchy of treatment choices.
    Am J Hematol. 2024;99:300-308.
    PubMed     Abstract available
    
    
    
18. SOUISSI M, Daliphard S, Picard V, Lebigot E, et al
    Elevated MCHC reveals a Southeast Asian Ovalocytosis.
    Am J Hematol. 2024;99:331-332.
    PubMed    
    
    
    
19. CHEN M, Hankins JS, Zhang M, Ataga KI, et al
    Comparative pharmacovigilance assessment of adverse events associated with the use of hydroxyurea, L-glutamine, voxelotor, and crizanlizumab in sickle cell disease.
    Am J Hematol. 2024;99:E37-E41.
    PubMed     Abstract available
    
    
    
20. AFZALI-HASHEMI L, Dovern E, Baas KPA, Schrantee A, et al
    Cerebral hemodynamics and oxygenation in adult patients with sickle cell disease after stem cell transplantation.
    Am J Hematol. 2024;99:163-171.
    PubMed     Abstract available
    
    
    
21. GARBOWSKI MW, Ugidos M, Risueno A, Shetty JK, et al
    Luspatercept stimulates erythropoiesis, increases iron utilization, and redistributes body iron in transfusion-dependent thalassemia.
    Am J Hematol. 2024;99:182-192.
    PubMed     Abstract available
    
    
    January 2024
22. SHAGIDOV D, Guttmann-Raviv N, Cunat S, Frech L, et al
    A newly identified ferritin L-subunit variant results in increased proteasomal subunit degradation, impaired complex assembly, and severe hypoferritinemia.
    Am J Hematol. 2024;99:12-20.
    PubMed     Abstract available
    
    
    
23. SEIDL E, Wilson D, Odame I, Kirby-Allen M, et al
    Lung function decline in children with sickle cell disease treated with hydroxyurea.
    Am J Hematol. 2024;99:E19-E21.
    PubMed    
    
    
    December 2023
24. PINTO VM, Romano N, Balocco M, Carrara P, et al
    Reduction of extramedullary erythropoiesis and amelioration of anemia in a beta-thalassemia patient treated with thalidomide.
    Am J Hematol. 2023 Dec 26. doi: 10.1002/ajh.27189.
    PubMed     Abstract available
    
    
    
25. SOULIE A, Kamdem A, Neumann F, Hau I, et al
    Clinical events in a long-term prospective neonatal cohort of children with sickle cell disease: Evidence for a high disease burden without systematic preventive intensification with hydroxyurea.
    Am J Hematol. 2023;98:E395-E398.
    PubMed    
    
    
    
26. HATEM A, Esperti S, Murciano N, Qiao M, et al
    Adverse effects of delta-9-tetrahydrocannabinol on sickle red blood cells.
    Am J Hematol. 2023;98:E383-E386.
    PubMed     Abstract available
    
    
    
27. BARAKAT A, Jasuja R, Tomlinson L, Wenzel Z, et al
    Effects of 2,3-DPG knockout on SCD phenotype in Townes SCD model mice.
    Am J Hematol. 2023;98:1838-1846.
    PubMed     Abstract available
    
    
    November 2023
28. KHO S, Siregar NC, Qotrunnada L, Fricot A, et al
    Retention of uninfected red blood cells causing congestive splenomegaly is the major mechanism of anemia in malaria.
    Am J Hematol. 2023 Nov 27. doi: 10.1002/ajh.27152.
    PubMed     Abstract available
    
    
    
29. HONG HG, Gouveia MH, Ogwang MD, Kerchan P, et al
    Sickle cell allele HBB-rs334(T) is associated with decreased risk of childhood Burkitt lymphoma in East Africa.
    Am J Hematol. 2023 Nov 27. doi: 10.1002/ajh.27149.
    PubMed     Abstract available
    
    
    
30. KUTER DJ, Piatek C, Roth A, Siddiqui A, et al
    Fostamatinib for warm antibody autoimmune hemolytic anemia: Phase 3, randomized, double-blind, placebo-controlled, global study (FORWARD).
    Am J Hematol. 2023 Nov 6. doi: 10.1002/ajh.27144.
    PubMed     Abstract available
    
    
    
31. PINCEZ T, Lettre G
    Re-assessing the effect of fetal hemoglobin on stroke in the Cooperative Study of Sickle Cell Disease.
    Am J Hematol. 2023;98:E309-E311.
    PubMed    
    
    
    
32. THOMAS B, Visanica S, Poussing S, Gerard D, et al
    Is this really thalassemia?
    Am J Hematol. 2023;98:1814-1815.
    PubMed    
    
    
    
33. 
    Withdrawal: "Primary prevention of sickle cell disease using preimplantation genetic testing and in vitro fertilization is cost-effective." Christina N. Cordeiro Mitchell, Apoorva Pradhan, Bhuchitra Singh, Rakhi P. Naik, Valerie L. Baker, Sophie M. La
    Am J Hematol. 2023;98:1819.
    PubMed     Abstract available
    
    
    
34. DI MAURO M, El Hoss S, Nardo-Marino A, Stuart-Smith S, et al
    Males with sickle cell disease have higher risks of cerebrovascular disease, increased inflammation, and a reduced response to hydroxyurea.
    Am J Hematol. 2023;98:E341-E344.
    PubMed     Abstract available
    
    
    October 2023
35. CASIMIR M, Colard M, Dussiot M, Roussel C, et al
    Erythropoietin downregulates red blood cell clearance, increasing transfusion efficacy in severely anemic recipients.
    Am J Hematol. 2023 Oct 4. doi: 10.1002/ajh.27117.
    PubMed     Abstract available
    
    
    
36. ARCHER NM, Gnangnon B, Mikdar M, Ciuculescu MF, et al
    F-erythrocytes promote Plasmodium falciparum proliferation in sickle cell disease.
    Am J Hematol. 2023;98:1598-1605.
    PubMed     Abstract available
    
    
    
37. STEINBERG MH, Gladwin MT
    "Severity" in adult sickle cell disease.
    Am J Hematol. 2023;98:1508-1511.
    PubMed    
    
    
    
38. WALSH PS, Brousseau DC, Coleman KD
    Return visits after emergency department treatment for sickle cell pain crises.
    Am J Hematol. 2023;98:E266-E268.
    PubMed    
    
    
    September 2023
39. VAN DIJK MJ, van Oirschot BA, Harrison AN, Recktenwald SM, et al
    A novel missense variant in ATP11C is associated with reduced red blood cell phosphatidylserine flippase activity and mild hereditary hemolytic anemia.
    Am J Hematol. 2023 Sep 6. doi: 10.1002/ajh.27088.
    PubMed     Abstract available
    
    
    
40. PORTER JB, Scrimgeour A, Martinez A, James L, et al
    SLN124, a GalNAc conjugated 19-mer siRNA targeting tmprss6, reduces plasma iron and increases hepcidin levels of healthy volunteers.
    Am J Hematol. 2023;98:1425-1435.
    PubMed     Abstract available
    
    
    
41. LIU H, Xia L, Weng J, Zhang F, et al
    Efficacy and safety of the C5 inhibitor crovalimab in complement inhibitor-naive patients with PNH (COMMODORE 3): A multicenter, Phase 3, single-arm study.
    Am J Hematol. 2023;98:1407-1414.
    PubMed     Abstract available
    
    
    
42. ELALFY MS, Hamdy M, Adly A, Ebeid FSE, et al
    Efficacy and safety of early-start deferiprone in infants and young children with transfusion-dependent beta thalassemia: Evidence for iron shuttling to transferrin in a randomized, double-blind, placebo-controlled, clinical trial (START).
    Am J Hematol. 2023;98:1415-1424.
    PubMed     Abstract available
    
    
    
43. MUSALLAM KM, Lombard L, Kistler KD, Arregui M, et al
    Epidemiology of clinically significant forms of alpha- and beta-thalassemia: A global map of evidence and gaps.
    Am J Hematol. 2023;98:1436-1451.
    PubMed     Abstract available
    
    
    
44. VON SIEBENTHAL HK, Moretti D, Zimmermann MB, Stoffel NU, et al
    Effect of dietary factors and time of day on iron absorption from oral iron supplements in iron deficient women.
    Am J Hematol. 2023;98:1356-1363.
    PubMed     Abstract available
    
    
    
45. NYANGASA S, Solomon D, Njiro B, Faisal A, et al
    The rate and pattern of fetal hemoglobin decline adjusted to sickle cell status of newborns in Dar es Salaam, Tanzania: A prospective cohort study.
    Am J Hematol. 2023;98:E241-E243.
    PubMed     Abstract available
    
    
    
46. PIRAN S, Alhomsi N, Warkentin TE
    Recurrent severe thrombocytopenia in critical illness complicated by hemolysis.
    Am J Hematol. 2023;98:1490-1496.
    PubMed    
    
    
    August 2023
47. NAIR M, Choudhury SS, Rani A, Solomi C 5th, et al
    The complex relationship between iron status and anemia in pregnant and postpartum women in India: Analysis of two Indian study cohorts of uncomplicated pregnancies.
    Am J Hematol. 2023 Aug 31. doi: 10.1002/ajh.27059.
    PubMed     Abstract available
    
    
    
48. AGARWAL S, Stanek JR, Vesely SK, Creary SE, et al
    Pregnancy-related thromboembolism in women with sickle cell disease: An analysis of National Medicaid Data.
    Am J Hematol. 2023 Aug 8. doi: 10.1002/ajh.27045.
    PubMed     Abstract available
    
    
    
49. PATNAIK MM, Tefferi A
    Luspatercept use for lower risk myelodysplastic syndromes: Active but not enough.
    Am J Hematol. 2023;98:1171-1175.
    PubMed    
    
    
    
50. SACHDEV V, Limerick E, Nguyen ML, Li W, et al
    Cardiac effects 2 years after successful non-myeloablative human leukocyte antigen-matched related donor hematopoietic cell transplants in sickle cell disease.
    Am J Hematol. 2023;98:E219-E221.
    PubMed    
    
    
    
51. ROTH A, Barcellini W, D'Sa S, Miyakawa Y, et al
    Sustained inhibition of complement C1s with sutimlimab over 2 years in patients with cold agglutinin disease.
    Am J Hematol. 2023;98:1246-1253.
    PubMed     Abstract available
    
    
    
52. LANINO L, Restuccia F, Perego A, Ubezio M, et al
    Real-world efficacy and safety of luspatercept and predictive factors of response in patients with lower risk myelodysplastic syndromes with ring sideroblasts.
    Am J Hematol. 2023;98:E204-E208.
    PubMed    
    
    
    
53. GROS M, Pondarre C, Arnaud C, Kamdem A, et al
    Lung function after matched-related donor allogeneic hematopoietic stem cell transplantation in children with sickle cell disease.
    Am J Hematol. 2023;98:E212-E215.
    PubMed    
    
    
    
54. LIU A, Kremyanskaya M, Mehrazin R, Si Q, et al
    Erythropoietin-secreting metanephric adenoma presenting as erythrocytosis.
    Am J Hematol. 2023 Aug 1. doi: 10.1002/ajh.27047.
    PubMed    
    
    
    July 2023
55. ZHANG L, Zhao J, Li R, Pan H, et al
    Low risk of relapse in aplastic anemia patients after SARS-CoV-2 omicron infection: A prospective NICHE cohort.
    Am J Hematol. 2023 Jul 14. doi: 10.1002/ajh.27028.
    PubMed    
    
    
    
56. MCGLOTHLIN J, Abeykoon J, Al-Hattab E, Ashrani AA, et al
    Bortezomib and daratumumab in refractory autoimmune hemolytic anemia.
    Am J Hematol. 2023 Jul 7. doi: 10.1002/ajh.27025.
    PubMed    
    
    
    
57. POWERS JM, Auerbach M
    When taking iron, a glass of orange juice a day keeps anemia away.
    Am J Hematol. 2023 Jul 4. doi: 10.1002/ajh.27017.
    PubMed    
    
    
    
58. RIBEIL JA, Pollock G, Frangoul H, Steinberg MH, et al
    An integrated therapeutic approach to sickle cell disease management beyond infancy.
    Am J Hematol. 2023;98:1087-1096.
    PubMed     Abstract available
    
    
    
59. ALLALI S, Elie J, Mayrand L, de Montalembert M, et al
    Sputum IL-6 level as a potential predictor of acute chest syndrome during vaso-occlusive crisis in children with sickle cell disease: Exploratory prospective prognostic accuracy study.
    Am J Hematol. 2023;98:E175-E178.
    PubMed    
    
    
    
60. D'ALESSANDRO A, Nouraie SM, Zhang Y, Cendali F, et al
    In vivo evaluation of the effect of sickle cell hemoglobin S, C and therapeutic transfusion on erythrocyte metabolism and cardiorenal dysfunction.
    Am J Hematol. 2023;98:1017-1028.
    PubMed     Abstract available
    
    
    June 2023
61. URIO F, Nkya S, Mgaya J, Rooks H, et al
    Gender effect on production and enrichment of F cell numbers in sickle cell disease patients in Tanzania.
    Am J Hematol. 2023;98:E139-E141.
    PubMed    
    
    
    
62. PINTO VM, Russo R, Quintino S, Rosato BE, et al
    Coinheritance of PIEZO1 variants and multi-locus red blood cell defects account for the symptomatic phenotype in beta-thalassemia carriers.
    Am J Hematol. 2023;98:E130-E133.
    PubMed     Abstract available
    
    
    
63. BORDONI V, Casale M, Pinto VM, Carsetti R, et al
    Inflammatory and senescence-associated mediators affect the persistence of humoral response to COVID-19 mRNA vaccination in transfusion-dependent beta-thalassemic patients.
    Am J Hematol. 2023;98:E145-E147.
    PubMed    
    
    
    
64. CHEN PH, Gorshein E, Tormey C, Siddon AJ, et al
    "Double-hit" ineffective erythropoiesis-concurrent beta-thalassemia with alpha-gene triplication and myelodysplastic syndrome with SF3B1 mutation.
    Am J Hematol. 2023;98:984-988.
    PubMed    
    
    
    May 2023
65. PEFFAULT DE LATOUR R, Risitano AM
    Complement inhibition in medicine: Hematology and beyond; complement inhibition in hematology: PNH and beyond.
    Am J Hematol. 2023;98 Suppl 4:S3-S4.
    PubMed    
    
    
    
66. KULASEKARARAJ AG, Lazana I
    Paroxysmal nocturnal hemoglobinuria: Where are we going.
    Am J Hematol. 2023;98 Suppl 4:S33-S43.
    PubMed     Abstract available
    
    
    
67. DUVAL A, Fremeaux-Bacchi V
    Complement biology for hematologists.
    Am J Hematol. 2023;98 Suppl 4:S5-S19.
    PubMed     Abstract available
    
    
    
68. LEON J, LeStang MB, Sberro-Soussan R, Servais A, et al
    Complement-driven hemolytic uremic syndrome.
    Am J Hematol. 2023;98 Suppl 4:S44-S56.
    PubMed     Abstract available
    
    
    
69. PANSE J
    Paroxysmal nocturnal hemoglobinuria: Where we stand.
    Am J Hematol. 2023;98 Suppl 4:S20-S32.
    PubMed     Abstract available
    
    
    
70. DIAMANTOPOULOS PT, Solomou E, Symeonidis A, Pappa V, et al
    The prognostic significance of macrocytosis in patients with myelodysplastic neoplasms.
    Am J Hematol. 2023;98:E119-E122.
    PubMed    
    
    
    
71. POURDIEU C, El Hoss S, Le Roux E, Pages J, et al
    Relevance of Howell-Jolly body counts for measuring spleen function in sickle cell disease.
    Am J Hematol. 2023;98:E110-E112.
    PubMed    
    
    
    
72. GAARTMAN AE, van Tuijn CFJ, Nur E, Vogt L, et al
    The association between renal function decline and disease severity in sickle cell disease.
    Am J Hematol. 2023;98:E95-E97.
    PubMed    
    
    
    April 2023
73. TEFFERI A, Vannucchi AM
    JAK2 inhibitor treatment of anemia in myelofibrosis.
    Am J Hematol. 2023 Apr 21. doi: 10.1002/ajh.26934.
    PubMed    
    
    
    
74. AGGARWAL N, Manley AL, Shalhoub R, Durrani J, et al
    Alemtuzumab in relapsed immune severe aplastic anemia: Long-term results of a phase II study.
    Am J Hematol. 2023 Apr 6. doi: 10.1002/ajh.26924.
    PubMed     Abstract available
    
    
    
75. ONI MO, Archer NM
    Intranasal fentanyl works-Why are we not using it more to treat acute pain in sickle cell disease?
    Am J Hematol. 2023;98:564-565.
    PubMed    
    
    
    
76. REES CA, Brousseau DC, Ahmad FA, Bennett J, et al
    Intranasal fentanyl and discharge from the emergency department among children with sickle cell disease and vaso-occlusive pain: A multicenter pediatric emergency medicine perspective.
    Am J Hematol. 2023;98:620-627.
    PubMed     Abstract available
    
    
    
77. REDJOUL R, Beckerich F, de Luna G, Leclerc M, et al
    ABO blood barrier to engraftment after allogeneic stem cell transplantation in sickle cell disease: A case-story with two successive HLA-matched sibling donors.
    Am J Hematol. 2023;98:692-696.
    PubMed    
    
    
    March 2023
78. RISINGER M, Kim PS, Rodriguez RX, Narvaez Rivas M, et al
    Hemolytic anemia and macrothrombocytopenia: a lipid problem?
    Am J Hematol. 2023 Mar 28. doi: 10.1002/ajh.26916.
    PubMed    
    
    
    
79. RAI P, Okhomina VI, Kang G, Martinez HR, et al
    Longitudinal effect of disease-modifying therapy on left ventricular diastolic function in children with sickle cell anemia.
    Am J Hematol. 2023 Mar 8. doi: 10.1002/ajh.26911.
    PubMed     Abstract available
    
    
    
80. LANSER L, Plaikner M, Schroll A, Burkert FR, et al
    Tissue iron distribution in patients with anemia of inflammation: results of a pilot study.
    Am J Hematol. 2023 Mar 7. doi: 10.1002/ajh.26909.
    PubMed     Abstract available
    
    
    
81. COHEN AR
    Thalassemia enters a new age ... And more lies ahead.
    Am J Hematol. 2023;98:379-380.
    PubMed    
    
    
    
82. AL-SAMKARI H, Grace RF, Glenthoj A, Andres O, et al
    Early-onset reduced bone mineral density in patients with pyruvate kinase deficiency.
    Am J Hematol. 2023;98:E57-E60.
    PubMed    
    
    
    
83. ADESINA OO, Brunson A, Fisch SC, Yu B, et al
    Pregnancy outcomes in women with sickle cell disease in California.
    Am J Hematol. 2023;98:440-448.
    PubMed     Abstract available
    
    
    
84. FORNI GL, Gianesin B, Musallam KM, Longo F, et al
    Overall and complication-free survival in a large cohort of patients with beta-thalassemia major followed over 50 years.
    Am J Hematol. 2023;98:381-387.
    PubMed     Abstract available
    
    
    
85. RECCHIUTI A, Federti E, Matte A, Mazzi F, et al
    Impaired pro-resolving mechanisms promote abnormal NETosis, fueling autoimmunity in sickle cell disease.
    Am J Hematol. 2023;98:E45-E48.
    PubMed    
    
    
    February 2023
86. ALHOMOUD M, Soave R, Kluk MJ, Shore T, et al
    Acute Hemolytic Anemia After Hematopoietic Stem Cell Transplantation: An Unusual Invader.
    Am J Hematol. 2023 Feb 6. doi: 10.1002/ajh.26873.
    PubMed    
    
    
    
87. BAIN BJ, Myburgh J, Lund K, Chaidos A, et al
    G6PD deficiency in patients identified as female.
    Am J Hematol. 2023;98:359-360.
    PubMed    
    
    
    January 2023
88. GLASPY J, Gabrail NY, Locantore-Ford P, Lee T, et al
    Open-label, Phase 2 study of roxadustat for the treatment of anemia in patients receiving chemotherapy for non-myeloid malignancies.
    Am J Hematol. 2023 Jan 29. doi: 10.1002/ajh.26865.
    PubMed     Abstract available
    
    
    
89. KANG HA, Barner JC, Lawson KA, Rascati K, et al
    Impact of adherence to hydroxyurea on health outcomes among patients with sickle cell disease.
    Am J Hematol. 2023;98:90-101.
    PubMed     Abstract available
    
    
    
90. KANTER J, Thompson AA, Pierciey FJ Jr, Hsieh M, et al
    Lovo-cel gene therapy for sickle cell disease: Treatment process evolution and outcomes in the initial groups of the HGB-206 study.
    Am J Hematol. 2023;98:11-22.
    PubMed     Abstract available
    
    
    December 2022
91. ZHANG Y, Zhou H, Jiang Z, Wu D, et al
    Safety and efficacy of jaktinib in the treatment of Janus kinase inhibitor-naive patients with myelofibrosis: Results of a phase II trial.
    Am J Hematol. 2022;97:1510-1519.
    PubMed     Abstract available
    
    
    November 2022
92. SEBASTIANI P, Steinberg MH
    Fetal Hemoglobin per Erythrocyte (HbF/F-cell) After Gene Therapy for Sickle Cell Anemia.
    Am J Hematol. 2022 Nov 24. doi: 10.1002/ajh.26791.
    PubMed    
    
    
    
93. POTHAST CR, van Dijk K, Pool ES, Halkes CJM, et al
    SARS-CoV-2 mRNA vaccination of aplastic anemia patients is safe and effective.
    Am J Hematol. 2022 Nov 13. doi: 10.1002/ajh.26780.
    PubMed    
    
    
    
94. GANGAT N, Begna KH, Al-Kali A, Hogan W, et al
    Predictors of anemia response to momelotinib therapy in myelofibrosis and impact on survival.
    Am J Hematol. 2022 Nov 8. doi: 10.1002/ajh.26778.
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97. MINNITI C, Brugnara C, Steinberg MH
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102. MKOMBACHEPA M, Khamis B, Rwegasira G, Urio F, et al
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104. LEWIS J, Greenway SC, Khan F, Singh G, et al
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105. MORIS W, Koek GH, van Deursen CTBM
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109. NARDO-MARINO A, Glenthoj A, Brewin JN, Petersen J, et al
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111. SZEPETOWSKI S, Berger C, Joly P, Baron-Joly S, et al
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112. NAGALAPURAM V, Kanter J
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145. OLUPOT-OLUPOT P, Connon R, Kiguli S, Opoka RO, et al
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147. ANGELI AM, Megna B, Mazepa M, Ivy ZK, et al
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149. PATNAIK MM, Santini V
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150. ANDOLFO I, Alper SL, Iolascon A
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151. TVEDT THA, Steien E, Ovrebo B, Haaverstad R, et al
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154. FEJTKOVA M, Sukova M, Hlozkova K, Skvarova Kramarzova K, et al
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155. RIBEIL JA
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158. GREEN SE, Singh ZN, Baer MR
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161. JOHNSON S, Gordeuk VR, Machado R, Gibbs JSR, et al
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167. LONGORIA JN, Pugh NL, Gordeuk V, Hsu LL, et al
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169. HEBBEL RP, Vercellotti GM
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194. FAN BE, Cao L, Gallardo CA, Lee SMS, et al
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196. WAHEED A, Kuter DJ
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197. MONTALBAN-BRAVO G, Kanagal-Shamanna R, Darbaniyan F, Siddiqui MT, et al
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198. KULASEKARARAJ AG, Brodsky RA, Hill A
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199. GURUNG K, Bain BJ
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200. KIRK SE, Scheurer ME, Bernhardt MB, Mahoney DH, et al
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201. PANAGIOTA V, Meggendorfer M, Kubasch AS, Gabdoulline R, et al
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203. RAMIREZ MJ, Pujol R, Trujillo-Quintero JP, Minguillon J, et al
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204. KIM SJ, Song J, Reading NS, Lautersztain J, et al
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206. BAIN BJ
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207. MAQUET J, Lafaurie M, Walter O, Sailler L, et al
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209. MINNITI CP, Knight-Madden J, Tonda M, Gray S, et al
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210. AL-ALI AK, Alsulaiman A, Alfarhan M, Safaya S, et al
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211. MCGRATH M, Quint EH, Weyand AC
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212. ARCHULETA J, van der Graaf M, Kaptein FHJ, Althaus L, et al
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214. LANZKRON S, Smith-Whitley K
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215. PATNAIK MM, Tefferi A
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216. DENTON CC, Shah P, Suriany S, Liu H, et al
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217. MUSALLAM KM, Rivella S, Taher AT
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219. ROMANA M, Reminy K, Moeckesch B, Charlot K, et al
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220. AUERBACH M, Henry D, DeLoughery TG
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221. KARKOSKA K, Quinn CT, Niss O, Pfeiffer A, et al
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226. GLADWIN MT, Kato GJ, Gordeuk VR
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227. RAB MAE, Kanne CK, Bos J, van Oirschot BA, et al
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228. ROSANWO TO, Kean LS, Archer NM
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231. COSTA E, Tibalinda P, Sterzi E, Leufkens HMG, et al
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235. DAVIS BH
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236. ANGELUCCI E
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237. HE Y, Jiang H, Li C, Zhu Y, et al
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240. HEBERT N, Rakotoson MG, Bodivit G, Audureau E, et al
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242. DE CASTRO C, Grossi F, Weitz IC, Maciejewski J, et al
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244. ONALO R, Cooper P, Cilliers A, Vorster BC, et al
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248. GALADANCI NA, Abdullahi SU, Ali Abubakar S, Wudil Jibir B, et al
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251. TISDALE JF, Pierciey FJ Jr, Bonner M, Thompson AA, et al
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