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Articles published in Haematologica

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    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.

    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.

  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
    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.

  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.

  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.

    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.

  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.

  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.

  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.

  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.

    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.

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

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

  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.

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

  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.

  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

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

  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.

  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.

  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

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

  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.

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

  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.

    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.

  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.

  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.

    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.

    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.

  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.

  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.

  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.

  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.

    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.

  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.

    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

  100. NANOU A, Toumpeki C, Fanis P, Bianchi N, et al
    Sex-specific transcriptional profiles identified in beta-thalassemia patients.
    Haematologica. 2021;106:1207-1211.

    March 2021
  101. AL-SAMKARI H, Kessler CM, Auerbach M
    Recognition of thrombotic risk of thrombocytosis in iron deficiency
    Haematologica. 2021;106:661-663.

  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.
    Haematologica. 2021;106:918-922.

  103. BOUSSAID I, Le Goff S, Floquet C, Gautier EF, et al
    Integrated analyses of translatome and proteome identify the rules of translation selectivity in RPS14-deficient cells.
    Haematologica. 2021;106:746-758.
    PubMed     Abstract available

  104. JIMENEZ K, Leitner F, Leitner A, Scharbert G, et al
    Iron deficiency-induced thrombocytosis increases thrombotic tendency in rats.
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