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Articles published in Haematologica

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Single Articles

    June 2024
  1. MATTE A, Federti E, Recchiuti A, Hamza M, et al
    Epeleuton, a novel synthetic omega-3 fatty acid, reduces hypoxia/ reperfusion stress in a mouse model of sickle cell disease.
    Haematologica. 2024;109:1918-1932.
    PubMed     Abstract available

    May 2024
  2. QUDEIMAT A, Suryaprakash S, Madden R, Srinivasan A, et al
    Reduced toxicity conditioning for hematopoietic stem cell transplantation in children with Diamond-Blackfan anemia.
    Haematologica. 2024 May 30. doi: 10.3324/haematol.2024.285147.
    PubMed     Abstract available

  3. KOO J, Howell JC, Hornung L, Sabulski A, et al
    Infrequent fractures and resilient bone mineral density: bone health in patients with Fanconi anemia.
    Haematologica. 2024 May 30. doi: 10.3324/haematol.2024.285612.
    PubMed     Abstract available

  4. ZAHR RS, Rashkin SR, Ruiz MA, Elsherif L, et al
    Soluble urokinase plasminogen activator receptor is associated with kidney disease and its progression in sickle cell anemia.
    Haematologica. 2024 May 2. doi: 10.3324/haematol.2023.284920.
    PubMed     Abstract available

  5. PECKER LH, Federspiel J
    Sickle cell disease, pregnancy, and COVID-19 in France: plus ca change.
    Haematologica. 2024;109:1328-1330.

  6. KAMINSKI TW, Katoch O, Li Z, Hanway CB, et al
    Impaired hemoglobin clearance by sinusoidal endothelium promotes vaso-occlusion and liver injury in sickle cell disease.
    Haematologica. 2024;109:1535-1550.
    PubMed     Abstract available

  7. JOSEPH L, De Luna G, Bernit E, Cougoul P, et al
    A study of 28 pregnant women with sickle cell disease and COVID-19: elevated maternal and fetal morbidity rates.
    Haematologica. 2024;109:1562-1565.

    April 2024
  8. CONNOR MP, Prathapa N, Frey NV, Gill SI, et al
    Hypomethylating agents are associated with high rates of hematologic toxicity in patients with secondary myeloid neoplasms developing after acquired aplastic anemia.
    Haematologica. 2024 Apr 18. doi: 10.3324/haematol.2024.285275.
    PubMed     Abstract available

    Beyond adenosine triphosphate: unveiling the pleiotropic effects of pyruvate kinase activation in sickle cell anemia.
    Haematologica. 2024 Apr 18. doi: 10.3324/haematol.2024.285390.
    PubMed     Abstract available

  10. OLIVIER E, Zhang S, Yan Z, Bouhassira EE, et al
    Stem cell factor and erythropoietin-independent production of cultured reticulocytes.
    Haematologica. 2024 Apr 11. doi: 10.3324/haematol.2023.284427.
    PubMed     Abstract available

  11. DENIS M, Swartzrock L, Willner H, Bubb QR, et al
    Hematopoiesis post anti-CD117 monoclonal antibody treatment in wild-type and Fanconi anemia settings.
    Haematologica. 2024 Apr 4. doi: 10.3324/haematol.2023.284275.
    PubMed     Abstract available

  12. BOSE P, Masarova L, Pemmaraju N, Bledsoe SD, et al
    Sotatercept for anemia of myelofibrosis: a phase II investigator-initiated study.
    Haematologica. 2024 Apr 4. doi: 10.3324/haematol.2023.284078.

  13. DUBEY RK, Vats R, Brzoska T, Kaminski TW, et al
    Subcutaneous injection of IHP-102 prevents lung vaso-occlusion in sickle cell disease mice.
    Haematologica. 2024;109:1259-1263.

    March 2024
  14. ZHANG Q, Lin P, Mao A, Liu Y, et al
    An unusual case of thalassemia intermedia with inheritable complex repeats detected by single-molecule optical mapping.
    Haematologica. 2024;109:1000-1006.

  15. AL-SAMKARI H, Grace RF, Glenthoj A, Andres O, et al
    Bone mineral density in adult patients with pyruvate kinase deficiency on long-term mitapivat treatment.
    Haematologica. 2024;109:963-967.

  16. RISITANO AM, Frieri C
    Understanding pharmacological complement inhibition in paroxysmal nocturnal hemoglobinuria.
    Haematologica. 2024;109:704-708.

  17. KULASEKARARAJ AG, Lehtinen AE, Forsyth C, Gandhi S, et al
    Phase II trials of zilucoplan in paroxysmal nocturnal hemoglobinuria.
    Haematologica. 2024;109:929-935.

    February 2024
  18. LU Y, Zhu Q, Wang Y, Luo M, et al
    Enhancement of PRMT6 binding to a novel germline GATA1 mutation associated with congenital anemia.
    Haematologica. 2024 Feb 22. doi: 10.3324/haematol.2023.284183.
    PubMed     Abstract available

  19. XU ZL, Xu LP, Zhang YC, Zhou YH, et al
    The outcome and predictive model of allogeneic hematopoietic stem cell transplantation among elderly patients with severe aplastic anemia from the Chinese Blood and Marrow Transplant Registry Group.
    Haematologica. 2024 Feb 1. doi: 10.3324/haematol.2023.284581.
    PubMed     Abstract available

  20. LIU Y, Zhuang Y, Chen J, Zhong Z, et al
    Quantitative evaluation of the clinical severity of hemoglobin H disease in a cohort of 591 patients using a scoring system based on regression analysis.
    Haematologica. 2024;109:632-638.

    January 2024
  21. FOUDA RT, Cherukury HM, Kiven SB, Garcia NR, et al
    Colchicine reduces inflammation in a humanized transgenic murine model of sickle cell disease.
    Haematologica. 2024;109:308-311.

  22. THILAKARATHNE S, Jayaweera UP, Premawardhena A
    Unresolved laboratory issues of the heterozygous state of beta-thalassemia: a literature review.
    Haematologica. 2024;109:23-32.
    PubMed     Abstract available

    December 2023
  23. RAJPUT RV, Shah V, Shalhoub RN, West-Mitchell K, et al
    Granulocyte transfusions in severe aplastic anemia.
    Haematologica. 2023 Dec 7. doi: 10.3324/haematol.2023.283826.
    PubMed     Abstract available

  24. D'ALESSANDRO A, Nouraie SM, Zhang Y, Cendali F, et al
    Metabolic signatures of cardiorenal dysfunction in plasma from sickle cell patients as a function of therapeutic transfusion and hydroxyurea treatment.
    Haematologica. 2023;108:3418-3432.
    PubMed     Abstract available

  25. COLOMBATTI R, Casale M
    Early splenectomy in sickle cell disease: another piece of the puzzle.
    Haematologica. 2023;108:3197-3198.

  26. YAMASHITA D, Muramatsu H, Narita A, Wakamatsu M, et al
    Hematological abnormalities in Jacobsen syndrome: cytopenia of varying severities and morphological abnormalities in peripheral blood and bone marrow.
    Haematologica. 2023;108:3438-3443.

    November 2023
  27. ESPERTI S, Nader E, Stier A, Boisson C, et al
    Increased retention of functional mitochondria in mature sickle red blood cells is associated with increased sickling tendency, hemolysis and oxidative stress.
    Haematologica. 2023;108:3086-3094.
    PubMed     Abstract available

  28. TEFFERI A, Pardanani A, Gangat N
    Momelotinib (JAK1/JAK2/ACVR1 inhibitor): mechanism of action, clinical trial reports, and therapeutic prospects beyond myelofibrosis.
    Haematologica. 2023;108:2919-2932.
    PubMed     Abstract available

    October 2023
  29. GUERRA A, Parhiz H, Rivella S
    Novel potential therapeutics to modify iron metabolism and red cell synthesis in diseases associated with defective erythropoiesis.
    Haematologica. 2023;108:2582-2593.
    PubMed     Abstract available

  30. KALLEDA N, Flace A, Altermatt P, Ingoglia G, et al
    Ferroportin inhibitor vamifeport ameliorates ineffective erythropoiesis in a mouse model of beta-thalassemia with blood transfusions.
    Haematologica. 2023;108:2703-2714.
    PubMed     Abstract available

  31. VERSTOVSEK S, Foltz L, Gupta V, Hasserjian R, et al
    Safety and efficacy of zinpentraxin alfa as monotherapy or in combination with ruxolitinib in myelofibrosis: stage I of a phase II trial.
    Haematologica. 2023;108:2730-2742.
    PubMed     Abstract available

    September 2023
  32. DEZERN AE, Zahurak M, Jones RJ, Brodsky RA, et al
    Uniform conditioning regardless of donor in bone marrow transplantation for severe aplastic anemia.
    Haematologica. 2023 Sep 7. doi: 10.3324/haematol.2023.284022.
    PubMed     Abstract available

  33. BROUSSE V, Bernaudin F, Melaine A, Goguillot M, et al
    Severity and burden of sickle cell disease in France: a nationwide real-world study.
    Haematologica. 2023;108:2476-2486.
    PubMed     Abstract available

  34. MATTE A, Kosinski PA, Federti E, Dang L, et al
    Mitapivat, a pyruvate kinase activator, improves transfusion burden and reduces iron overload in beta-thalassemic mice.
    Haematologica. 2023;108:2535-2541.

    August 2023
  35. GRIFFIN M, Eikema DJ, Verheggen I, Kulagin A, et al
    SARS-CoV-2 vaccination in 361 non-transplanted patients with aplastic anemia and/or paroxysmal nocturnal hemoglobinuria.
    Haematologica. 2023 Aug 16. doi: 10.3324/haematol.2023.283863.

  36. CIUDAD M, Ouandji S, Lamarthee B, Cladiere C, et al
    Regulatory T-cell dysfunctions are associated with increase in tumor necrosis factor alpha in autoimmune hemolytic anemia and participate in Th17 polarization.
    Haematologica. 2023 Aug 3. doi: 10.3324/haematol.2023.282859.
    PubMed     Abstract available

    July 2023
    Long term survivors in severe aplastic anemia: standard mortality rates now comparable to controls?
    Haematologica. 2023 Jul 13. doi: 10.3324/haematol.2023.283523.
    PubMed     Abstract available

  38. ALKOBTAWI M, Sbeih M, Souaid K, Ngo QT, et al
    Contribution of fetal microchimeric cells to maternal wound healing in sickle cell ulcers.
    Haematologica. 2023;108:1920-1933.
    PubMed     Abstract available

    June 2023
  39. DROR Y
    Correcting the aberrant Fanconi anemia transcriptional program by gene therapy.
    Haematologica. 2023 Jun 8. doi: 10.3324/haematol.2023.283031.
    PubMed     Abstract available

  40. NAKAMURA R, Patel BA, Kim S, Wong FL, et al
    Conditional survival and standardized mortality ratios of patients with severe aplastic anemia surviving at least one year after hematopoietic cell transplantation or immunosuppressive therapy.
    Haematologica. 2023 Jun 1. doi: 10.3324/haematol.2023.282781.
    PubMed     Abstract available

    May 2023
  41. MECHRAOUI A, Ithier G, Pages J, Haouari Z, et al
    Early splenectomy in a large cohort of children with sickle cell anemia: risks and consequences.
    Haematologica. 2023 May 25. doi: 10.3324/haematol.2022.282556.
    PubMed     Abstract available

  42. LIU Y, Schmiderer L, Hjort M, Lang S, et al
    Engineered human Diamond-Blackfan anemia disease model confirms therapeutic effects of clinically applicable lentiviral vector at single-cell resolution.
    Haematologica. 2023 May 18. doi: 10.3324/haematol.2022.282068.
    PubMed     Abstract available

  43. PAGLIUCA S, Kulasekararaj AG, Eikema DJ, Piepenbroek B, et al
    Current use of androgens in bone marrow failure disorders: a report from the Severe Aplastic Anemia Working Party of the European Society of Blood and Marrow Transplantation.
    Haematologica. 2023 May 18. doi: 10.3324/haematol.2023.282935.
    PubMed     Abstract available

  44. FEDERTI E, Vinchi F, Iatcenko I, Ghigo A, et al
    Duality of Nrf2 in iron-overload cardiomyopathy.
    Haematologica. 2023;108:1335-1348.
    PubMed     Abstract available

  45. ATAGA KI, Zhou Q, Saraf SL, Hankins JS, et al
    Sex differences in progression of kidney disease in sickle cell disease.
    Haematologica. 2023;108:1436-1441.

  46. WANG L, Liu S, Luo J, Mo Q, et al
    Targeting a thrombopoietin-independent strategy in the discovery of a novel inducer of megakaryocytopoiesis, DMAG, for the treatment of thrombocytopenia.
    Haematologica. 2023;108:1394-1411.
    PubMed     Abstract available

  47. KULASEKARARAJ A, Brodsky R, Kulagin A, Jang JH, et al
    Biosimilars in rare diseases: a focus on paroxysmal nocturnal hemoglobinuria.
    Haematologica. 2023;108:1232-1243.
    PubMed     Abstract available

    April 2023
  48. ROSATO BE, Marra R, Del Giudice F, Nostroso A, et al
    One gene, two opposite phenotypes: a case report of hereditary anemia due to a loss-offunction variant in the EPAS1 gene.
    Haematologica. 2023 Apr 27. doi: 10.3324/haematol.2022.282457.
    PubMed     Abstract available

  49. LASAGA M, Rio P, Vilas-Zornoza A, Planell N, et al
    Gene therapy restores the transcriptional program of hematopoietic stem cells in Fanconi anemia.
    Haematologica. 2023 Apr 6. doi: 10.3324/haematol.2022.282418.
    PubMed     Abstract available

  50. NARDO-MARINO A, Brousse V
    Splenectomy in sickle cell disease: do benefits outweigh risks?
    Haematologica. 2023;108:954-955.

  51. PINTO VM, Gianesin B, Piel FB, Longo F, et al
    Morbidity and mortality of sickle cell disease patients is unaffected by splenectomy: evidence from three decades of follow-up in a high-income setting.
    Haematologica. 2023;108:1158-1162.

    March 2023
  52. DEVILLIER R, Eikema DJ, Dufour C, Aljurf M, et al
    Graft-versus-host disease and relapse/rejection-free survival after allogeneic transplantation for idiopathic severe aplastic anemia: a comprehensive analysis from the SAAWP of the EBMT.
    Haematologica. 2023 Mar 23. doi: 10.3324/haematol.2022.281876.
    PubMed     Abstract available

  53. KOO J, Grom-Mansencal I, Howell JC, Rios JM, et al
    Gonadal function in pediatric Fanconi anemia patients treated with hematopoietic stem cell transplant.
    Haematologica. 2023 Mar 9. doi: 10.3324/haematol.2022.282094.
    PubMed     Abstract available

  54. GALINDO-NAVARRO P, Delgado-Garcia A, Rodriguez-Gil MA, Puerta-Puerta JM, et al
    Venetoclax for treating refractory autoimmune hemolytic anemia in chronic lymphocytic leukemia: report of two cases in Spain.
    Haematologica. 2023 Mar 2. doi: 10.3324/haematol.2022.281850.
    PubMed     Abstract available

  55. JASH A, Howie HL, Hay AM, Luckey CJ, et al
    Identification of multiple genetic loci associated with red blood cell alloimmunization in mice.
    Haematologica. 2023;108:905-908.

  56. FALGUIERE C, Allali S, Khazem B, Kamdem A, et al
    Delayed hemolytic transfusion reaction in children with sickle cell disease: first 5-year retrospective study in mainland France.
    Haematologica. 2023;108:889-894.

  57. PINCEZ T, Lo KS, D'Orengiani APHD, Garrett ME, et al
    Variation and impact of polygenic hematologic traits in monogenic sickle cell disease.
    Haematologica. 2023;108:870-881.
    PubMed     Abstract available

  58. CONRAN N
    Pain mechanisms in sickle cell disease. Are we closer to a breakthrough?
    Haematologica. 2023;108:663-664.

  59. KHASABOVA IA, Gable J, Johns M, Khasabov SG, et al
    Inhibition of DAGLbeta as a therapeutic target for pain in sickle cell disease.
    Haematologica. 2023;108:859-869.
    PubMed     Abstract available

    February 2023
  60. SAKURAI M, Kogure Y, Mizuno K, Matsuki E, et al
    Long-term reduction in the incidence of aplastic anemia and immune thrombocytopenia during the COVID-19 pandemic.
    Haematologica. 2023 Feb 16. doi: 10.3324/haematol.2022.282351.
    PubMed     Abstract available

  61. HE Y, Guo X, Wang ZJ
    Therapeutic potential of beta-lactam ceftriaxone for chronic pain in sickle cell disease.
    Haematologica. 2023;108:633-637.

  62. RAI P, Okhomina VI, Kang G, Akil N, et al
    The effects of cardio-selective beta blockade on diastolic dysfunction in children with sickle cell disease.
    Haematologica. 2023;108:594-598.

    November 2022
  63. LIU YL, Shibuya A, Glader B, Wilkes MC, et al
    Animal models of Diamond-Blackfan anemia: updates and challenges.
    Haematologica. 2022 Nov 17. doi: 10.3324/haematol.2022.282042.
    PubMed     Abstract available

  64. AFZALI-HASHEMI L, Vaclavu L, Wood JC, Biemond BJ, et al
    Assessment of functional shunting in patients with sickle cell disease.
    Haematologica. 2022;107:2708-2719.
    PubMed     Abstract available

  65. LI X, Chatla S, Wilson AF, Wu L, et al
    Persistent DNA damage and oncogenic stress-induced Trem1 promotes leukemia in mice.
    Haematologica. 2022;107:2576-2588.
    PubMed     Abstract available

  66. ROSSATO P, Federti E, Matte A, Glantschnig H, et al
    Evidence of protective effects of recombinant ADAMTS13 in a humanized model of sickle cell disease.
    Haematologica. 2022;107:2650-2660.
    PubMed     Abstract available

    October 2022
  67. HERNANDEZ G, Romero-Cortadellas L, Ferrer-Cortes X, Venturi V, et al
    Mutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III.
    Haematologica. 2022 Oct 6. doi: 10.3324/haematol.2022.281277.
    PubMed     Abstract available

  68. GANGAT N, Bleeker J, Lynch D, Olteanu H, et al
    Daratumumab for treatment-refractory acquired idiopathic pure red cell aplasia.
    Haematologica. 2022;107:2523-2526.

  69. GALADANCI NA, Johnson W, Carson A, Hellemann G, et al
    Factors associated with left ventricular hypertrophy in children with sickle cell disease: results from the DISPLACE study.
    Haematologica. 2022;107:2466-2473.
    PubMed     Abstract available

    September 2022
    Images from the Haematologica Atlas of Hematologic Cytology: schistocytes in thrombotic microangiopathies.
    Haematologica. 2022;107:2008.

  71. KHWAJA J, D'Sa S, Minnema MC, Kersten MJ, et al
    IgM monoclonal gammopathies of clinical significance: diagnosis and management.
    Haematologica. 2022;107:2037-2050.
    PubMed     Abstract available

  72. GILAD O, Dgany O, Noy-Lotan S, Krasnov T, et al
    Syndromes predisposing to leukemia are a major cause of inherited cytopenias in children.
    Haematologica. 2022;107:2081-2095.
    PubMed     Abstract available

    August 2022
    Images from the Haematologica Atlas of Hematologic Cytology: congenital dyserythropoietic anemia type II.
    Haematologica. 2022;107:1736.

  74. BENCHEIKH L, Nguyen KA, Chadebech P, Kiger L, et al
    Preclinical evaluation of the preservation of red blood cell concentrates by hypoxic storage technology for transfusion in sickle cell disease.
    Haematologica. 2022;107:1944-1949.

  75. LEMAIRE B, Abramowski SW
    Alloimmunization against Fy3 is a serious threat in the era of cell therapy.
    Haematologica. 2022;107:1986-1987.

  76. KNAUS A, Vergez F, Garcia C, Engels H, et al
    Occurrence of a paroxysmal nocturnal hemoglobinuria clone in an essential thrombocythemia: a link between PIGV and MPL.
    Haematologica. 2022;107:1989-1993.

  77. LOPINTO J, Gendreau S, Berti E, Bartolucci P, et al
    Effects of corticosteroids in patients with sickle cell disease and acute complications: a systematic review and meta-analysis.
    Haematologica. 2022;107:1914-1921.
    PubMed     Abstract available

  78. GUTIERREZ-RODRIGUES F, Beerman I, Groarke EM, Patel BA, et al
    Utility of plasma cell-free DNA for de novo detection and quantification of clonal hematopoiesis.
    Haematologica. 2022;107:1815-1826.
    PubMed     Abstract available

    July 2022
  79. DE SOUZA LV, Hoffmann A, Fischer C, Petzer V, et al
    Comparative analysis of oral and intravenous iron therapy in rat models of inflammatory anemia and iron deficiency.
    Haematologica. 2022 Jul 7. doi: 10.3324/haematol.2022.281149.
    PubMed     Abstract available

    Images from the Haematologica Atlas of Hematologic Cytology: parvovirus-induced pure red cell aplasia.
    Haematologica. 2022;107:1493.

  81. DERCHI G, Musallam KM, Pinto VM, Graziadei G, et al
    Tricuspid-valve regurgitant jet velocity as a risk factor for death in beta-thalassemia.
    Haematologica. 2022;107:1714-1718.

  82. ROTH A, Barcellini W, D'Sa S, Miyakawa Y, et al
    Complement C1s inhibition with sutimlimab results in durable response in cold agglutinin disease: CARDINAL study 1-year interim follow-up results.
    Haematologica. 2022;107:1698-1702.

  83. ALLARD P, Alhaj N, Lobitz S, Cario H, et al
    Genetic modifiers of fetal hemoglobin affect the course of sickle cell disease in patients treated with hydroxyurea.
    Haematologica. 2022;107:1577-1588.
    PubMed     Abstract available

  84. VERSTOVSEK S, Mesa R, Talpaz M, Kiladjian JJ, et al
    Retrospective analysis of pacritinib in patients with myelofibrosis and severe thrombocytopenia.
    Haematologica. 2022;107:1599-1607.
    PubMed     Abstract available

  85. ABUGA KM, Muriuki JM, Uyoga SM, Mwai K, et al
    Hepcidin regulation in Kenyan children with severe malaria and non-typhoidal Salmonella bacteremia.
    Haematologica. 2022;107:1589-1598.
    PubMed     Abstract available

    June 2022
  86. DONG P, Chen L, Wu H, Huo J, et al
    Impaired immunosuppressive role of myeloid-derived suppressor cells in acquired aplastic anemia.
    Haematologica. 2022 Jun 23. doi: 10.3324/haematol.2021.280292.
    PubMed     Abstract available

    Introduction to a review series on the treatment of thrombocytopenic disorders: something old, something new.
    Haematologica. 2022;107:1239-1242.

  88. NISHIMURA JI, Ando K, Masuko M, Noji H, et al
    Tesidolumab (LFG316) for treatment of C5-variant patients with paroxysmal nocturnal hemoglobinuria.
    Haematologica. 2022;107:1483-1488.

    Does the world need germline editing for beta-thalassemia?
    Haematologica. 2022;107:1235-1236.

  90. GEISNESS AC, Azul M, Williams D, Szafraniec H, et al
    Ionophore-mediated swelling of erythrocytes as a therapeutic mechanism in sickle cell disease.
    Haematologica. 2022;107:1438-1447.
    PubMed     Abstract available

    May 2022
  91. XU ZL, Xu LP, Wu DP, Wang SQ, et al
    Comparable long-term outcomes between upfront haploidentical and identical sibling donor transplant in aplastic anemia: a national registry-based study.
    Haematologica. 2022 May 26. doi: 10.3324/haematol.2022.280758.
    PubMed     Abstract available

    April 2022
  92. ROSATO BE, Alper SL, Tomaiuolo G, Russo R, et al
    Hereditary anemia caused by multilocus inheritance of PIEZO1, SLC4A1 and ABCB6 mutations: a diagnostic and therapeutic challenge.
    Haematologica. 2022 Apr 21. doi: 10.3324/haematol.2022.280799.
    PubMed     Abstract available

  93. ALTINTAS B, Giri N, McReynolds LJ, Best A, et al
    Genotype-phenotype and outcome associations in patients with Fanconi anemia: The National Cancer Institute cohort.
    Haematologica. 2022 Apr 14. doi: 10.3324/haematol.2021.279981.
    PubMed     Abstract available

  94. BREGOLAT NF, Ruetten M, Da Silva MC, Aboouf MA, et al
    Iron- and erythropoietin-resistant anemia in a spontaneous breast cancer mouse model.
    Haematologica. 2022 Apr 7. doi: 10.3324/haematol.2022.280732.
    PubMed     Abstract available

  95. BENNINGHOVEN-FREY KM, Neuhaus N, Lahtinen AK, Krallmann C, et al
    Early testicular maturation is sensitive to depletion of spermatogonial pool in sickle cell disease.
    Haematologica. 2022;107:975-979.

    February 2022
  96. AVENOSO D, Marsh JCW, Potter V, Pagliuca A, et al
    SARS-CoV-2 infection in aplastic anemia.
    Haematologica. 2022;107:541-543.

  97. ABDULMALIK O, Darwish NHE, Muralidharan-Chari V, Taleb MA, et al
    Sulfated non-anticoagulant heparin derivative modifies intracellular hemoglobin, inhibits cell sickling in vitro, and prolongs survival of sickle cell mice under hypoxia.
    Haematologica. 2022;107:532-540.
    PubMed     Abstract available

  98. PINCEZ T, Fernandes H, Leblanc T, Michel G, et al
    Long term follow-up of pediatric-onset Evans syndrome: broad immunopathological manifestations and high treatment burden.
    Haematologica. 2022;107:457-466.
    PubMed     Abstract available

  99. CASALE M, Forni GL, Cassinerio E, Pasquali D, et al
    Risk factors for endocrine complications in transfusion-dependent thalassemia patients on chelation therapy with deferasirox: a risk assessment study from a multi-center nation-wide cohort.
    Haematologica. 2022;107:467-477.
    PubMed     Abstract available

    January 2022
  100. BREWIN J, El Hoss S, Strouboulis J, Rees D, et al
    A novel index to evaluate ineffective erythropoiesis in hematological diseases offers insights into sickle cell disease.
    Haematologica. 2022;107:338-341.

  101. TZOUNAKAS VL, Anastasiadi AT, Stefanoni D, Cendali F, et al
    Beta thalassemia minor is a beneficial determinant of red blood cell storage lesion.
    Haematologica. 2022;107:112-125.
    PubMed     Abstract available

    December 2021
  102. ELABBADI A, Voiriot G, Tristan A, Gibelin A, et al
    Lower respiratory tract infection with Staphylococcus aureus in sickle-cell adult patients with severe acute chest syndrome - the STAPHACS Study.
    Haematologica. 2021;106:3236-3239.

    November 2021
  103. HOOGENBOOM WS, Fleysher R, Soby S, Mirhaji P, et al
    Individuals with sickle cell disease and sickle cell trait demonstrate no increase in mortality or critical illness from COVID-19 - a fifteen hospital observational study in the Bronx, New York.
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    October 2021
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    Low incidence of COVID-19 severe complications in a large cohort of children with sickle cell disease: a protective role for basal interferon-1 activation?
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    A Grammastola spatulata mechanotoxin-4 (GsMTx4)-sensitive cation channel mediates increased cation permeability in human hereditary spherocytosis of multiple genetic etiologies.
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    September 2021
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    Clinical diagnostic value of telomere length measurement in inherited bone marrow failure syndromes.
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    August 2021
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    July 2021
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    June 2021
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    May 2021
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    How to implement endurance exercise training in sickle cell disease.
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    April 2021
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    March 2021
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    February 2021
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    January 2021
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    Severe delayed hemolytic transfusion reaction due to anti-Fy3 in a patient with sickle cell disease undergoing red cell exchange prior to hematopoietic progenitor cell collection for gene therapy.
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    December 2020
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    November 2020
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    100-year-old Haematologica images: bothriocephalus and pernicious anemia.
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    COVID-19 and sickle cell disease.
    Haematologica. 2020;105:2501-2504.

    October 2020
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    Pyridoxamine: another vitamin for sickle cell disease?
    Haematologica. 2020;105:2348-2350.

    September 2020
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    Detectable mutations precede late myeloid neoplasia in aplastic anemia.
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    Real-time national survey of COVID-19 in hemoglobinopathy and rare inherited anemia patients.
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  149. MODEPALLI S, Hattangadi SM
    Novel use for selective inhibitors of nuclear export in beta-thalassemia: block of HSP70 export from the nucleus via exportin Xpo1 improves ineffective erythropoiesis.
    Haematologica. 2020;105:2188-2189.

    July 2020
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    Apparent recessive inheritance of sideroblastic anemia type 2 due to uniparental isodisomy at the SLC25A38 locus.
    Haematologica. 2020;105:2883-2886.

  151. GIRELLI D, Busti F
    Replacing the suppressed hormone: toward a better treatment for iron overload in beta-thalassemia major?
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    June 2020
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    COVID-19 in patients with sickle cell disease - a case series from a UK Tertiary Hospital.
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    March 2020
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    Staying hydrated is important also for erythroblasts.
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