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Articles published in Haematologica

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Single Articles


    September 2023
  1. 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


  2. 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


  3. 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.
    PubMed    


    August 2023
  4. 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.
    PubMed    


  5. 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
  6. BACIGALUPO A
    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


  7. 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
  8. 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


  9. 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
  10. 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


  11. 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


  12. 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


  13. 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


  14. 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.
    PubMed    


  15. 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


  16. 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
  17. 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


  18. 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


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


  20. 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.
    PubMed    


    March 2023
  21. 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


  22. 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


  23. 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


  24. 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.
    PubMed    


  25. 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.
    PubMed    


  26. 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


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


  28. 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
  29. 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


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


  31. 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.
    PubMed    


    November 2022
  32. 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


  33. 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


  34. 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


  35. 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
  36. 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


  37. 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.
    PubMed    


  38. 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
  39. BALDUINI CL
    Images from the Haematologica Atlas of Hematologic Cytology: schistocytes in thrombotic microangiopathies.
    Haematologica. 2022;107:2008.
    PubMed    


  40. 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


  41. 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
  42. INVERNIZZI R
    Images from the Haematologica Atlas of Hematologic Cytology: congenital dyserythropoietic anemia type II.
    Haematologica. 2022;107:1736.
    PubMed    


  43. 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.
    PubMed    


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


  45. 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.
    PubMed    


  46. 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


  47. 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
  48. 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


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


  50. 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.
    PubMed    


  51. 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.
    PubMed    


  52. 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


  53. 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


  54. 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
  55. 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


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


  57. 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.
    PubMed    


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


  59. 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
  60. 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
  61. 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


  62. 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


  63. 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


  64. 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.
    PubMed    


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


  66. 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


  67. 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


  68. 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
  69. 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.
    PubMed    


  70. 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
  71. 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.
    PubMed    


    November 2021
  72. 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.
    Haematologica. 2021;106:3014-3016.
    PubMed    


    October 2021
  73. BROUSSE V, Holvoet L, Pescarmona R, Viel S, et al
    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?
    Haematologica. 2021;106:2746-2748.
    PubMed    


  74. VANDORPE DH, Shmukler BE, Ilboudo Y, Bhasin S, et al
    A Grammastola spatulata mechanotoxin-4 (GsMTx4)-sensitive cation channel mediates increased cation permeability in human hereditary spherocytosis of multiple genetic etiologies.
    Haematologica. 2021;106:2759-2762.
    PubMed    


  75. EL HOSS S, Cochet S, Godard A, Yan H, et al
    Fetal hemoglobin rescues ineffective erythropoiesis in sickle cell disease.
    Haematologica. 2021;106:2707-2719.
    PubMed     Abstract available


    September 2021
  76. MUSALLAM KM, Vitrano A, Meloni A, Pollina SA, et al
    Survival and causes of death in 2,033 patients with non-transfusion-dependent beta-thalassemia
    Haematologica. 2021;106:2489-2492.
    PubMed    


  77. MIWATA S, Narita A, Okuno Y, Suzuki K, et al
    Clinical diagnostic value of telomere length measurement in inherited bone marrow failure syndromes.
    Haematologica. 2021;106:2511-2515.
    PubMed    


  78. LIZARRALDE-IRAGORRI MA, Lefevre SD, Cochet S, El Hoss S, et al
    Oxidative stress activates red cell adhesion to laminin in sickle cell disease.
    Haematologica. 2021;106:2478-2488.
    PubMed     Abstract available


  79. VENUGOPAL J, Wang J, Mawri J, Guo C, et al
    Interleukin-1 receptor inhibition reduces stroke size in a murine model of sickle cell disease.
    Haematologica. 2021;106:2469-2477.
    PubMed     Abstract available


  80. KOUNTOURIS P, Michailidou K, Christou S, Hadjigavriel M, et al
    Effect of HBB genotype on survival in a cohort of transfusion-dependent thalassemia patients in Cyprus.
    Haematologica. 2021;106:2458-2468.
    PubMed     Abstract available


    August 2021
  81. COLIN E, Courtois G, Brouzes C, Pulman J, et al
    Biallelic mutations in the SARS2 gene presenting as congenital sideroblastic anemia.
    Haematologica. 2021 Aug 19. doi: 10.3324/haematol.2021.279138.
    PubMed     Abstract available


  82. BOATENG LA, Schonewille H, Ligthart PC, Javadi A, et al
    One third of alloantibodies in patients with sickle cell disease transfused with African blood are missed by the standard red blood cell test panel.
    Haematologica. 2021;106:2274-2276.
    PubMed    


    July 2021
  83. WANG C, McGraw KL, McLemore AF, Komrokji R, et al
    Dual pyroptotic biomarkers predict erythroid response in lower risk non-del(5q) myelodysplastic syndromes treated with lenalidomide and recombinant erythropoietin.
    Haematologica. 2021 Jul 29. doi: 10.3324/haematol.2021.278855.
    PubMed     Abstract available


  84. BEHRENS YL, Gohring G, Bawadi R, Coktu S, et al
    A novel classification of hematologic conditions in patients with Fanconi anemia.
    Haematologica. 2021 Jul 1. doi: 10.3324/haematol.2021.279332.
    PubMed     Abstract available


  85. LINDER GE, Chou ST
    Red cell transfusion and alloimmunization in sickle cell disease.
    Haematologica. 2021;106:1805-1815.
    PubMed     Abstract available


  86. KAUR K, Huang Y, Raman SV, Kraut E, et al
    Myocardial injury and coronary microvascular disease in sickle cell disease.
    Haematologica. 2021;106:2018-2021.
    PubMed    


  87. GILMARTIN AG, Groy A, Gore ER, Atkins C, et al
    In vitro and in vivo induction of fetal hemoglobin with a reversible and selective DNMT1 inhibitor.
    Haematologica. 2021;106:1979-1987.
    PubMed     Abstract available


    June 2021
  88. BREWIN JN, Rooks H, Gardner K, Senior H, et al
    Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC).
    Haematologica. 2021;106:1770-1773.
    PubMed     Abstract available


  89. LAVINYA AA, Razali RA, Razak MA, Mohamed R, et al
    Homozygous Southeast Asian Ovalocytosis in five live-born neonates.
    Haematologica. 2021;106:1758-1761.
    PubMed     Abstract available


  90. MIKKELSEN SU, Safavi S, Dimopoulos K, O'Rourke CJ, et al
    Structural aberrations are associated with poor survival in patients with clonal cytopenia of undetermined significance.
    Haematologica. 2021;106:1762-1766.
    PubMed     Abstract available


  91. SRISUWANANUKORN A, Han J, Raslan R, Gowhari M, et al
    Antimicrobial resistance is a risk factor for mortality in adults with sickle cell disease.
    Haematologica. 2021;106:1745-1748.
    PubMed     Abstract available


  92. SINGER ST, Fischer R, Allen I, Lal A, et al
    Pituitary iron and factors predictive of fertility status in transfusion dependent thalassemia.
    Haematologica. 2021;106:1740-1744.
    PubMed     Abstract available


  93. ALLALI S, Taylor M, Brice J, Montalembert M, et al
    Chronic organ injuries in children with sickle cell disease.
    Haematologica. 2021;106:1535-1544.
    PubMed     Abstract available


    May 2021
  94. PELLEGRIN S, Severn CE, Toye AM
    Towards manufactured red blood cells for the treatment of inherited anemia.
    Haematologica. 2021 May 27. doi: 10.3324/haematol.2020.268847.
    PubMed     Abstract available


  95. MESSONNIER LA, Riccetti M, Chatel B, Galacteros F, et al
    How to implement endurance exercise training in sickle cell disease.
    Haematologica. 2021;106:1476-1479.
    PubMed    


    April 2021
  96. ZAIMOKU Y, Patel BA, Shalhoub R, Groarke EM, et al
    Predicting response of severe aplastic anemia to immunosuppression combined with eltrombopag.
    Haematologica. 2021 Apr 29. doi: 10.3324/haematol.2021.278413.
    PubMed     Abstract available


  97. BROUSSE V, Pondarre C, Kossorotoff M, Arnaud C, et al
    Brain injury pathophysiology study by a multimodal approach in children with sickle cell anemia with no intra or extra cranial arteriopathy.
    Haematologica. 2021 Apr 22. doi: 10.3324/haematol.2020.278226.
    PubMed     Abstract available


  98. CORRE T, Ponte B, Pivin E, Pruijm M, et al
    Heritability and association with distinct genetic loci of erythropoietin levels in the general population.
    Haematologica. 2021 Apr 8. doi: 10.3324/haematol.2021.278389.
    PubMed     Abstract available


  99. CORRE T, Ponte B, Pivin E, Pruijm M, et al
    Heritability and association with distinct genetic loci of erythropoietin levels in the general population.
    Haematologica. 2021 Apr 8. doi: 10.3324/haematol.2021.278389.
    PubMed     Abstract available


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    Sex-specific transcriptional profiles identified in beta-thalassemia patients.
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    March 2021
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    Recognition of thrombotic risk of thrombocytosis in iron deficiency
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  102. BAROZZI S, Di Buduo CA, Marconi C, Bozzi V, et al
    Pathogenetic and clinical study of a patient with thrombocytopenia due to the p.E527K gain-of-function variant of SRC.
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    Integrated analyses of translatome and proteome identify the rules of translation selectivity in RPS14-deficient cells.
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    Iron deficiency-induced thrombocytosis increases thrombotic tendency in rats.
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    February 2021
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    Hemoglobin switching in mice carrying the Klf1(Nan) variant.
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    January 2021
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    Successful gene therapy of Diamond-Blackfan anemia in a mouse model and human CD34+ cord blood hematopoietic stem cells using a clinically applicable lentiviral vector.
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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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    Characterization of breakthrough hemolysis events observed in the phase 3 randomized studies of ravulizumab versus eculizumab in adults with paroxysmal nocturnal hemoglobinuria.
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    December 2020
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    Hypoxia-inducible erythropoietin expression: details matter.
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    November 2020
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    Rapid decline in estimated glomerular filtration rate in sickle cell anemia: results of a multicenter pooled analysis.
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    100-year-old Haematologica images: bothriocephalus and pernicious anemia.
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    PubMed    


  114. MENAPACE LA, Thein SL
    COVID-19 and sickle cell disease.
    Haematologica. 2020;105:2501-2504.
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    October 2020
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    Pyridoxamine: another vitamin for sickle cell disease?
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    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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  118. 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.
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    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.
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  120. GIRELLI D, Busti F
    Replacing the suppressed hormone: toward a better treatment for iron overload in beta-thalassemia major?
    Haematologica. 2020;105:1752-1754.
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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.
    Haematologica. 2020;105:2691-2693.
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    March 2020
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    Staying hydrated is important also for erythroblasts.
    Haematologica. 2020;105:528-529.
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