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Articles published in Ann Hematol

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Single Articles


    August 2022
  1. BEYAR-KATZ O, Perry C, On YB, Amit O, et al
    Thrombopoietin receptor agonist for treating bone marrow aplasia following anti-CD19 CAR-T cells-single-center experience.
    Ann Hematol. 2022;101:1769-1776.
    PubMed     Abstract available


  2. ZHOU F, Zhang F, Zhang L, Wu Q, et al
    A multicentre trial of intensive immunosuppressive therapy combined with umbilical cord blood for the treatment of severe aplastic anaemia.
    Ann Hematol. 2022;101:1785-1794.
    PubMed     Abstract available


  3. PIRIYAKHUNTORN P, Tantiworawit A, Kasitanon N, Louthrenoo W, et al
    Prevalence and characteristics of inflammatory rheumatic diseases in patients with thalassemia.
    Ann Hematol. 2022;101:1667-1675.
    PubMed     Abstract available


  4. JAFRI F, Seong G, Jang T, Cimpeanu E, et al
    L-glutamine for sickle cell disease: more than reducing redox.
    Ann Hematol. 2022;101:1645-1654.
    PubMed     Abstract available


  5. LOBITZ S, Frommel C, Brose A, Blankenstein O, et al
    Simultaneous newborn screening for sickle cell disease, biotinidase deficiency, and hereditary tyrosinemia type 1 with an optimized tandem mass spectrometry protocol.
    Ann Hematol. 2022;101:1859-1860.
    PubMed    


    July 2022
  6. AL-KURAISHY HM, Al-Gareeb AI, Kaushik A, Kujawska M, et al
    Hemolytic anemia in COVID-19.
    Ann Hematol. 2022 Jul 8. pii: 10.1007/s00277-022-04907.
    PubMed     Abstract available


  7. HAN B, Kim HJ, Yhim HY, Oh D, et al
    Sequential eradication of Helicobacter pylori as a treatment for immune thrombocytopenia in patients with moderate thrombocytopenia: a multicenter prospective randomized phase 3 study.
    Ann Hematol. 2022;101:1435-1445.
    PubMed     Abstract available


  8. JUNG EH, Park JH, Hwan Kim K, Kim JS, et al
    Characteristics of Sweet syndrome in patients with or without malignancy.
    Ann Hematol. 2022;101:1499-1508.
    PubMed     Abstract available


  9. ROPERO P, Gonzalez Fernandez FA, Nieto JM, Recasens V, et al
    Does size matter? Two new deletions in the HBB gene cause beta(0)-thalassemia.
    Ann Hematol. 2022;101:1465-1471.
    PubMed     Abstract available


  10. WU X, Cheng L, Liu X, Sun Y, et al
    Clinical characteristics and outcomes of 100 adult patients with pure red cell aplasia.
    Ann Hematol. 2022;101:1493-1498.
    PubMed     Abstract available


  11. PATSOURAKOS D, Aggeli C, Gatzoulis KA, Delicou S, et al
    Left atrial deformation indices in beta-thalassemia major patients.
    Ann Hematol. 2022;101:1473-1483.
    PubMed     Abstract available


  12. ADAM AS, Cotton F, Cantinieaux B, Benyaich S, et al
    Screening for hereditary spherocytosis in daily practice: what is the best algorithm using erythrocyte and reticulocyte parameters?
    Ann Hematol. 2022;101:1485-1491.
    PubMed     Abstract available


  13. COSTANTINI S, Meloni A, Spasiano A, Cinque P, et al
    The unexpected impact of cabozantinib on red blood cells consumption in patients with transfusion-dependent thalassemia.
    Ann Hematol. 2022;101:1621-1623.
    PubMed    


    June 2022
  14. MA X, Zuo Y, Xu Z, Zhang Y, et al
    Comparable clinical outcomes of haploidentical hematopoietic stem cell transplantation in patients with hepatitis-associated aplastic anemia and non-hepatitis-associated aplastic anemia.
    Ann Hematol. 2022 Jun 23. pii: 10.1007/s00277-022-04885.
    PubMed     Abstract available


  15. HWANG YY, Chan TSY, Chan FHY, Lau CWP, et al
    Eltrombopag as frontline treatment of aplastic anaemia in routine practice: implications on cost and efficacy.
    Ann Hematol. 2022;101:1163-1172.
    PubMed     Abstract available


  16. ZHOU X, Jiang P, Gao L, Yang J, et al
    Immune reconstitution and survival of patients with parvovirus B19 related pure red cell aplasia after haplo-PBSCT.
    Ann Hematol. 2022;101:1333-1342.
    PubMed     Abstract available


  17. ESCRIBANO SERRAT S, Del Campo Balguerias G, Martinez Nieto J, Medina Salazar F, et al
    Pincered red cells in hereditary spherocytosis.
    Ann Hematol. 2022;101:1393-1394.
    PubMed    


    May 2022
  18. PIRES DA SILVA BGP, Fonseca NP, Catto LFB, Pereira GC, et al
    The spectrum of paroxysmal nocturnal hemoglobinuria clinical presentation in a Brazilian single referral center.
    Ann Hematol. 2022;101:999-1007.
    PubMed     Abstract available


  19. POPLAWSKA M, Dutta D, Jayaram M, Chong NS, et al
    Genes modulating intestinal permeability and microbial community are dysregulated in sickle cell disease.
    Ann Hematol. 2022;101:1009-1013.
    PubMed     Abstract available


    April 2022
  20. KAYNAR LA, Gokcen S, Can F, Yegin ZA, et al
    Comparison of daily oral iron replacement therapy with every other day treatment in female reproductive age patients with iron-deficiency anemia.
    Ann Hematol. 2022 Apr 23. pii: 10.1007/s00277-022-04835.
    PubMed     Abstract available


  21. WERNER R, Lohr B, Lodemann P, Chemnitz JM, et al
    Autoimmune basal ganglia encephalitis with hemolytic anemia.
    Ann Hematol. 2022 Apr 21. pii: 10.1007/s00277-022-04848.
    PubMed    


  22. PROCHASKA MT, Huisingh-Scheetz M, Meltzer D
    Sex differences in fatigue and symptoms of anemia in relation to hemoglobin level in hospitalized patients.
    Ann Hematol. 2022 Apr 11. pii: 10.1007/s00277-022-04830.
    PubMed    


  23. LI S, Guo P, Mi L, Chai X, et al
    A novel SPTB mutation causes hereditary spherocytosis via loss-of-function of beta-spectrin.
    Ann Hematol. 2022;101:731-738.
    PubMed     Abstract available


    March 2022
  24. BAHATI YL, Delanghe J, Balaluka GB, Philippe J, et al
    Exploration of the relationship between anemia and iron and zinc deficiencies in children under 5 years of age living in the malaria endemic area of South Kivu/Democratic Republic of Congo.
    Ann Hematol. 2022 Mar 23. pii: 10.1007/s00277-022-04816.
    PubMed     Abstract available


  25. TOLU SS, Crouch A, Choi J, Gao Q, et al
    Hydroxyurea and fetal hemoglobin effect on leg ulcers in patients with sickle cell disease.
    Ann Hematol. 2022;101:541-548.
    PubMed     Abstract available


  26. LUFTINGER R, Zubarovskaya N, Galimard JE, Cseh A, et al
    Busulfan-fludarabine- or treosulfan-fludarabine-based myeloablative conditioning for children with thalassemia major.
    Ann Hematol. 2022;101:655-665.
    PubMed     Abstract available


  27. BAYRAKTAROGLU S, Karadas N, Onen S, Karapinar DY, et al
    Modern management of iron overload in thalassemia major patients guided by MRI techniques: real-world data from a long-term cohort study.
    Ann Hematol. 2022;101:521-529.
    PubMed     Abstract available


  28. SOULIERES D, Mercier-Ross J, Fradette C, Rozova A, et al
    The pharmacokinetic and safety profile of single-dose deferiprone in subjects with sickle cell disease.
    Ann Hematol. 2022;101:533-539.
    PubMed     Abstract available


  29. LI S, Chen K, Huang C, Zhang N, et al
    First report of successful treatment for hemoglobin Bristol-Alesha by hemopoietic stem cell transplantation.
    Ann Hematol. 2022;101:617-619.
    PubMed     Abstract available


  30. ROSETTI M, De la Salle B, Farneti G, Clementoni A, et al
    The added value of digital morphological analysis in the evaluation of peripheral blood films: the report of an UKNEQAS external quality assessment sample.
    Ann Hematol. 2022;101:729-730.
    PubMed    


  31. FARFAN-QUIROGA G, Hermosilla-Fernandez MDM, Feliu-Sanchez J, Najera-Irazu MJ, et al
    A new case of Bicetre hemoglobin in an adult male: clinical observations over a period of four years.
    Ann Hematol. 2022;101:701-702.
    PubMed    


    February 2022
  32. VIROT E, Thuret I, Jardel S, Herbrecht R, et al
    Pregnancy outcome in women with transfused beta-thalassemia in France.
    Ann Hematol. 2022;101:289-296.
    PubMed     Abstract available


  33. MARTINS SR, Toledo SLO, da Silva AJ, Mendes FS, et al
    Endothelial dysfunction biomarkers in sickle cell disease: is there a role for ADMA and PAI-1?
    Ann Hematol. 2022;101:273-280.
    PubMed     Abstract available


  34. DINGLI D, Matos JE, Lehrhaupt K, Krishnan S, et al
    The burden of illness in patients with paroxysmal nocturnal hemoglobinuria receiving treatment with the C5-inhibitors eculizumab or ravulizumab: results from a US patient survey.
    Ann Hematol. 2022;101:251-263.
    PubMed     Abstract available


  35. HOSOKAWA K, Nakao S
    Assay sensitivity of flow cytometric PNH analysis: response to Brando and Gatti.
    Ann Hematol. 2022;101:461-464.
    PubMed    


  36. BRANDO B, Gatti A
    Re: Hosokawa K et al. Assay sensitivity of flow cytometric PNH analysis.
    Ann Hematol. 2022;101:459-460.
    PubMed    


  37. DAS S, Karmakar K, Mukherjee R, Panda S, et al
    Acute stroke in young adult secondary to moyamoya angiopathy unveiling HbE-beta thalassemia.
    Ann Hematol. 2022;101:449-451.
    PubMed    


    January 2022
  38. SUN YX, Feng Q, Wang SW, Li X, et al
    HLA-G-ILT2 interaction contributes to suppression of bone marrow B cell proliferation in acquired aplastic anemia.
    Ann Hematol. 2022 Jan 18. pii: 10.1007/s00277-022-04757.
    PubMed     Abstract available


  39. GHANEM P, Marrone K, Shanbhag S, Brahmer JR, et al
    Current challenges of hematologic complications due to immune checkpoint blockade: a comprehensive review.
    Ann Hematol. 2022;101:1-10.
    PubMed     Abstract available


  40. YILDIRIM N, Unal S, Yalcinkaya A, Karahan F, et al
    Evaluation of the relationship between intravascular hemolysis and clinical manifestations in sickle cell disease: decreased hemopexin during vaso-occlusive crises and increased inflammation in acute chest syndrome.
    Ann Hematol. 2022;101:35-41.
    PubMed     Abstract available


  41. SOKOL J, Guman T, Chudej J, Hlebaskova M, et al
    Ixazomib, lenalidomide, and dexamethasone combination in "real-world" clinical practice in patients with relapsed/refractory multiple myeloma.
    Ann Hematol. 2022;101:81-89.
    PubMed     Abstract available


  42. ABULHAMAIL A, AlShebli A, Merdad L, Wali S, et al
    Prevalence of and risk factors for obstructive sleep apnea in children with sickle cell: a multicentric cross sectional study.
    Ann Hematol. 2022;101:43-57.
    PubMed     Abstract available


  43. TARTAGLIONE I, Manara R, di Concilio R, Quarta A, et al
    Non-transfusion-dependent thalassemia in Italy: less blues, no role of reds.
    Ann Hematol. 2022;101:241-242.
    PubMed    


  44. MUSALLAM KM, Cappellini MD, Daar S, Taher AT, et al
    Morbidity-free survival and hemoglobin level in non-transfusion-dependent beta-thalassemia: a 10-year cohort study.
    Ann Hematol. 2022;101:203-204.
    PubMed    


  45. ACQUAVIVA G, Nonne G, Murtas A, Longu F, et al
    Cytomegalovirus reactivation in patients under immunosuppressive treatment for autoimmune haemolytic anaemia.
    Ann Hematol. 2022;101:227-228.
    PubMed    


  46. DEBUREAUX PE, Ruggiu M, Mathis S, Mirouse A, et al
    Aggressive lymphoma, hemophagocytic lymphohistiocytosis, and G6PD crisis: a lytic cocktail.
    Ann Hematol. 2022;101:219-221.
    PubMed    


    December 2021
  47. EL-KHAZRAGY N, Matbouly S, Hanna DH, Mahran NA, et al
    Circulating miRNAs and tissue iron overload in transfusion-dependent beta-thalassemia major: novel predictors and follow-up guide.
    Ann Hematol. 2021;100:2909-2917.
    PubMed     Abstract available


  48. KARIMI M, Zarei T, Bahmanimehr A, Aramesh A, et al
    Long-term safety and efficacy of hydroxyurea in patients with non-transfusion-dependent beta-thalassemia: a comprehensive single-center experience.
    Ann Hematol. 2021;100:2901-2907.
    PubMed     Abstract available


    November 2021
  49. VIVES-CORRONS JL, Krishnevskaya E, Hernandez-Rodriguez I, Payan-Pernia S, et al
    Red cell ektacytometry in two patients with chronic hemolytic anemia and three new alpha-spectrin variants.
    Ann Hematol. 2021 Nov 29. pii: 10.1007/s00277-021-04723.
    PubMed     Abstract available


  50. JIANG Z, Jiang X, Chen M
    Severe aplastic anemia in a patient with erythropoietic protoporphyria successfully treated by avatrombopag.
    Ann Hematol. 2021 Nov 26. pii: 10.1007/s00277-021-04726.
    PubMed    


  51. MATSUYAMA Y, Hosoi H, Horitani R, Kawamoto S, et al
    Management of warm autoimmune hemolytic anemia related to band 3-positive colon carcinoma.
    Ann Hematol. 2021 Nov 5. pii: 10.1007/s00277-021-04714.
    PubMed    


  52. DUCA L, Nava I, Tavazzi D, Marcon A, et al
    Epidemiological shift of glucose-6-phosphate dehydrogenase mutations in northern Italy in the last 15 years.
    Ann Hematol. 2021;100:2683-2688.
    PubMed     Abstract available


  53. KULAGIN AD, Ptushkin VV, Lukina EA, Davydkin IL, et al
    Randomized multicenter noninferiority phase III clinical trial of the first biosimilar of eculizumab.
    Ann Hematol. 2021;100:2689-2698.
    PubMed     Abstract available


  54. TEAWTRAKUL N, Chansai S, Yamsri S, Ungarreevittaya P, et al
    JAK2V617F mutation in patients with beta-thalassemia disease: prevalence and clinical characteristics.
    Ann Hematol. 2021;100:2863-2865.
    PubMed    


    October 2021
  55. EL FAKIH R, Alfraih F, Alhayli S, Ahmed SO, et al
    Frontline-matched sibling donor transplant of aplastic anemia patients using primed versus steady-state bone marrow grafts.
    Ann Hematol. 2021 Oct 31. pii: 10.1007/s00277-021-04708.
    PubMed     Abstract available


  56. BIASSI TP, Guerra-Shinohara EM, Moretti PNS, de Freitas Dutra V, et al
    miRNA profile and disease severity in patients with sickle cell anemia.
    Ann Hematol. 2021 Oct 22. pii: 10.1007/s00277-021-04665.
    PubMed     Abstract available


  57. PEREIRA-MARTINS DA, Coelho-Silva JL, Domingos IF, Weinhauser I, et al
    The ratio of ATP11C/PLSCR1 mRNA transcripts has clinical significance in sickle cell anemia.
    Ann Hematol. 2021 Oct 14. pii: 10.1007/s00277-021-04696.
    PubMed     Abstract available


  58. SHOKRGOZAR N, Karimi M, Golmoghaddam H, Rezaei N, et al
    Expression of the immune checkpoint receptors CTLA-4, LAG-3, and TIM-3 in beta-thalassemia major patients: correlation with alloantibody production and regulatory T cells (Tregs) phenotype.
    Ann Hematol. 2021;100:2463-2469.
    PubMed     Abstract available


  59. ABDULHAI F, Jaffa MA, Elias J, Zakka P, et al
    Digital thermography and vascular involvement in beta-thalassemia intermedia.
    Ann Hematol. 2021;100:2471-2477.
    PubMed     Abstract available


    September 2021
  60. HIRAMOTO N, Yamazaki H, Nakamura Y, Uchida N, et al
    Total body irradiation-containing conditioning regimens without antithymocyte globulin in adults with aplastic anemia undergoing umbilical cord blood transplantation.
    Ann Hematol. 2021 Sep 21. pii: 10.1007/s00277-021-04664.
    PubMed     Abstract available


  61. THONG EWS, Tan SS, Sethi SK, Chee YL, et al
    Falsely elevated serum vitamin B12 levels in a case of pernicious anemia.
    Ann Hematol. 2021 Sep 10. pii: 10.1007/s00277-021-04612.
    PubMed    


  62. WOUTERS HJCM, Conrads-Frank A, Koinig KA, Smith A, et al
    The anemia-independent impact of myelodysplastic syndromes on health-related quality of life.
    Ann Hematol. 2021 Sep 2. pii: 10.1007/s00277-021-04654.
    PubMed     Abstract available


  63. JANG T, Mo G, Stewart C, Khoury L, et al
    Obesity and diabetes mellitus in patients with sickle cell disease.
    Ann Hematol. 2021;100:2203-2205.
    PubMed     Abstract available


  64. BOGA C, Asma S, Leblebisatan G, Sen N, et al
    Comparison of the clinical course of COVID-19 infection in sickle cell disease patients with healthcare professionals.
    Ann Hematol. 2021;100:2195-2202.
    PubMed     Abstract available


    August 2021
  65. CHENOU F, Hounkpe BW, Domingos IF, Tonasse WV, et al
    Effect of hydroxyurea therapy on intravascular hemolysis and endothelial dysfunction markers in sickle cell anemia patients.
    Ann Hematol. 2021 Aug 28. pii: 10.1007/s00277-021-04636.
    PubMed     Abstract available


  66. YAMADA S, Kajikawa S, Nakagawa N, Kondo Y, et al
    Coombs' test positive autoimmune hemolytic anemia accompanied by myelodysplastic syndrome that became Coombs' test negative after azacitidine administration.
    Ann Hematol. 2021 Aug 27. pii: 10.1007/s00277-021-04652.
    PubMed    


  67. ATIPIMONPAT A, Siwaponanan P, Khuhapinant A, Svasti S, et al
    Extracellular vesicles from thalassemia patients carry iron-containing ferritin and hemichrome that promote cardiac cell proliferation.
    Ann Hematol. 2021;100:1929-1946.
    PubMed     Abstract available


  68. TRANEKAER S, Hansen DL, Biemond BJ, Sorensen AL, et al
    Priapism in patients with hemolytic disorders: a nationwide retrospective cohort study.
    Ann Hematol. 2021;100:1947-1951.
    PubMed     Abstract available


  69. SINGHA K, Fucharoen G, Fucharoen S
    delta-Hemoglobinopathies in Thailand: screening, molecular basis, genotype-phenotype interaction, and implication for prevention and control of thalassemia.
    Ann Hematol. 2021;100:1953-1963.
    PubMed     Abstract available


  70. HOSOKAWA K, Ishiyama K, Ikemoto T, Sugimori C, et al
    The clinical significance of PNH-phenotype cells accounting for < 0.01% of total granulocytes detected by the Clinical and Laboratory Standards Institute methods in patients with bone marrow failure.
    Ann Hematol. 2021;100:1975-1982.
    PubMed     Abstract available


  71. OKAMOTO H, Uoshima N, Kamitsuji Y, Kawata E, et al
    Paroxysmal nocturnal hemoglobinuria complicated with essential thrombocythemia harboring concomitant PIGA, CALR, and ASXL1 mutations.
    Ann Hematol. 2021;100:2113-2115.
    PubMed    


  72. ROBIER C, Hoefler G, Aubell K, Hubmann E, et al
    Acquired elliptocytosis as presenting sign of a myelodysplastic syndrome associated with deletion of chromosome 20 and mutations in TET2, DNMT3A, and U2AF1.
    Ann Hematol. 2021;100:2111-2112.
    PubMed    


  73. JAMWAL M, Mallik N, Aravindan AV, Jain A, et al
    Hemolytic erythrocytosis: an amalgamated phenotype from coinherited Chuvash polycythemia and G6PD Kerala-Kalyan with acquired transient stomatocytosis.
    Ann Hematol. 2021;100:2107-2109.
    PubMed    


    July 2021
  74. NORASETTHADA L, Wongkhantee S, Chaipokam J, Charoenprasert K, et al
    Adult aplastic anemia in Thailand: incidence and treatment outcome from a prospective nationwide population-based study.
    Ann Hematol. 2021 Jul 16. pii: 10.1007/s00277-021-04566.
    PubMed     Abstract available


  75. YANG W, Zhao X, Peng G, Zhang L, et al
    Time and residual hematopoiesis are crucial for PNH clones escape in hepatitis-associated aplastic anemia.
    Ann Hematol. 2021 Jul 16. pii: 10.1007/s00277-021-04553.
    PubMed     Abstract available


  76. CAO J, Pei R, Zhang P, Liu X, et al
    Successful haploidentical transplantation using plasma exchange and post-transplantation cyclophosphamide for severe aplastic anemia patients with anti-human leukocyte antigen donor-specific antibodies.
    Ann Hematol. 2021 Jul 6. pii: 10.1007/s00277-021-04497.
    PubMed     Abstract available


  77. GOREN SAHIN D, Akay OM, Keklik M, Okan V, et al
    Clinical characteristics and therapeutic outcomes of paroxysmal nocturnal hemoglobinuria patients in Turkey: a multicenter experience.
    Ann Hematol. 2021;100:1667-1675.
    PubMed     Abstract available


  78. ELZAEEM DI, Sharkawi EAE, Zaki EM, Ghobrial AG, et al
    Comparative study of IgG binding to megakaryocytes in immune and myelodysplastic thrombocytopenic patients.
    Ann Hematol. 2021;100:1701-1709.
    PubMed     Abstract available


  79. NJUE L, Medri C, Keller P, Diepold M, et al
    The rare hemoglobin variant Hb Mizuho: report of a Swiss family and literature review.
    Ann Hematol. 2021;100:1677-1683.
    PubMed     Abstract available


  80. RICCHI P, Costantini S, Spasiano A, Cinque P, et al
    Hepatocellular carcinoma in patients with thalassemia in the post-DAA era: not a disappearing entity.
    Ann Hematol. 2021;100:1907-1910.
    PubMed    


  81. MUSALLAM KM, Cappellini MD, Taher AT
    Variations in hemoglobin level and morbidity burden in non-transfusion-dependent beta-thalassemia.
    Ann Hematol. 2021;100:1903-1905.
    PubMed    


  82. TRAN QUANG V, Tarfi S, Loustau V, Moutereau S, et al
    A belated diagnosis of G6PD deficiency in an 81-year-old woman.
    Ann Hematol. 2021;100:1901-1902.
    PubMed    


    June 2021
  83. BATISTA JVGF, Pereira-Martins DA, Falcao DA, Domingos IF, et al
    Association of KLOTHO polymorphisms with clinical complications of sickle cell anemia.
    Ann Hematol. 2021 Jun 14. pii: 10.1007/s00277-021-04532.
    PubMed     Abstract available


  84. KRECAK I, Cengic M, Skoric I, Nakic M, et al
    Concomitant autoimmune hemolytic anemia and pure red cell aplasia in a patient with chronic lymphocytic leukemia successfully treated with ibrutinib.
    Ann Hematol. 2021 Jun 10. pii: 10.1007/s00277-021-04570.
    PubMed    


  85. AL-TAWFIQ JA, Rabaan AA, AlEdreesi MH
    Frequency of bacteremia in patients with sickle cell disease: a longitudinal study.
    Ann Hematol. 2021;100:1411-1416.
    PubMed     Abstract available


  86. ARPACI A, Gul BU, Ozcan O, Ilhan G, et al
    Presentation of two new mutations in the 3'untranslated region of the beta-globin gene and evaluating the molecular spectrum of thalassemia mutations in the Mediterranean region of Turkey.
    Ann Hematol. 2021;100:1429-1438.
    PubMed     Abstract available


  87. BHURANI D, Kapoor J, Yadav N, Khushoo V, et al
    Experience with combination of hydroxyurea and low-dose thalidomide in transfusion-dependent beta thalassemia patients.
    Ann Hematol. 2021;100:1417-1427.
    PubMed     Abstract available


  88. MAROUF R, Adekile AD, El-Muzaini H, Abdulla R, et al
    Neutrophil gelatinase-associated lipocalin as a biomarker of nephropathy in sickle cell disease.
    Ann Hematol. 2021;100:1401-1409.
    PubMed     Abstract available


  89. TAMAI Y, Ito S, Hasegawa A
    Paroxysmal nocturnal haemoglobinuria associated with a novel phosphatidylinositol glycan class A (PIGA) mutation in a patient with Klinefelter syndrome.
    Ann Hematol. 2021;100:1625-1627.
    PubMed    


    May 2021
  90. HERBRETEAU L, Le Calloch R, Arnaud B, Cassou N, et al
    Eculizumab, a real-life successful treatment for refractory cold agglutinin-mediated auto-immune hemolytic anemia secondary to lymphoproliferative disorders.
    Ann Hematol. 2021 May 18. pii: 10.1007/s00277-021-04557.
    PubMed    


  91. QIN X, Zhu YP, Luo CJ, Zhou M, et al
    Optimizing conditioning regimen with low-dose irradiation or busulfan enables the outcome of transplantation from a 6-7/8 HLA-matched donor comparable to that from an 8/8 HLA-matched unrelated donor in severe aplastic anemia patients under 40 years.
    Ann Hematol. 2021 May 14. pii: 10.1007/s00277-021-04540.
    PubMed     Abstract available


  92. BALLAS SK
    Opioids are not a major cause of death of patients with sickle cell disease.
    Ann Hematol. 2021;100:1133-1138.
    PubMed     Abstract available


    April 2021
  93. MENDOZA E, Duque X, Moran S, Martinez-Andrade G, et al
    Hepcidin and other indicators of iron status, by alpha-1 acid glycoprotein levels, in a cohort of Mexican infants.
    Ann Hematol. 2021;100:879-890.
    PubMed     Abstract available


  94. RAMSAY Z, Gabbadon CH, Asnani M
    Numb chin syndrome in sickle cell disease: a case series of Jamaican patients.
    Ann Hematol. 2021;100:913-919.
    PubMed     Abstract available


  95. HATAIRAKTHAM S, Masaratana P, Hantaweepant C, Srisawat C, et al
    Curcuminoids supplementation ameliorates iron overload, oxidative stress, hypercoagulability, and inflammation in non-transfusion-dependent beta-thalassemia/Hb E patients.
    Ann Hematol. 2021;100:891-901.
    PubMed     Abstract available


    March 2021
  96. YOUSSEF JG, Zahiruddin F, Youssef G, Padmanabhan S, et al
    G6PD deficiency and severity of COVID19 pneumonia and acute respiratory distress syndrome: tip of the iceberg?
    Ann Hematol. 2021;100:667-673.
    PubMed     Abstract available


  97. SAEIDNIA M, Nowrouzi-Sohrabi P, Erfani M, Fazeli P, et al
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