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Hard-To-Treat Idiopathic Refractory Autoimmune Haemolytic Anaemia with Reticulocytopenia

European journal of case reports in internal medicine, 2020-12, Vol.7 (12), p.002112-002112

2020

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Posttransfusion hyperhemolysis is arrested by targeting macrophage activation with novel use of Tocilizumab

Transfusion (Philadelphia, Pa.), 2020-01, Vol.60 (1), p.30-35

2020

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Successful treatment with plasma exchange in life‐threatening hyperhemolytic syndrome unrelated to sickle cell disease

Transfusion (Philadelphia, Pa.), 2023-05, Vol.63 (5), p.1100-1106

2023

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Hyporegenerative anemia in anti‐M‐associated hemolytic disease of the fetus

Transfusion (Philadelphia, Pa.), 2021-06, Vol.61 (6), p.1908-1915

2021

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Pure red cell aplasia after major or bidirectional ABO incompatible hematopoietic stem cell transplantation: to treat or not to treat, that is the question

Bone marrow transplantation (Basingstoke), 2021-04, Vol.56 (4), p.769-778

2021

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Hemolytic disease and reticulocytopenia of the newborn attributable to maternal immunoglobulin G anti‐M reacting optimally at cold temperatures

Transfusion (Philadelphia, Pa.), 2021-03, Vol.61 (3), p.974-978

2021

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Erythroblastic synartesis associated with lymphoproliferative disorder: There can be more than meets the eye

Clinical immunology (Orlando, Fla.), 2022-03, Vol.236, p.108951-108951, Article 108951

2022

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Hyperhemolysis in a patient with sickle cell disease and recent SARS‐CoV‐2 infection, with complex auto‐ and alloantibody work‐up, successfully treated with tocilizumab

Transfusion (Philadelphia, Pa.), 2022-07, Vol.62 (7), p.1446-1451

2022

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Congenital anaemia associated with loss-of-function variants in DNA polymerase epsilon 1

Journal of medical genetics, 2024-03, Vol.61 (3), p.239-243

2024

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Clinical and immune features of human parvovirus B19 infection in allogeneic stem cell transplantation recipients: A retrospective monocentric study

Transplant infectious disease, 2023-10, Vol.25 (5), p.e14118-e14118

2023

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325 Aplastic crisis induced by human parvovirus B19 as an initial presentation of hereditary spherocytosis in a child – a case report

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 2), p.A137-A137

2021

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Eltrombopag restores erythropoiesis in refractory adult acquired pure red cell aplasia

International journal of hematology, 2021-07, Vol.114 (1), p.124-128

2021

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An update on the pathogenesis and diagnosis of Diamond-Blackfan anemia [version 1; peer review: 2 approved]

F1000 research, 2018, Vol.7, p.1350

2018

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Neutrophilic Erythrophagocytosis and Reticulocytopenia: A Rare Manifestation of Cold Autoimmune Hemolytic Anemia

Turkish journal of haematology, 2022-01, Vol.39 (3), p.211-212

2022

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Role of Absolute Reticulocyte Count in the Assessment of Renal Function and Erythropoietin Response in Adults with Sickle Cell Anemia Seen at the Lagos University Teaching Hospital

American journal of clinical pathology, 2018-09, Vol.150 (suppl_1), p.S114-S115

2018

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Successful Treatment of Antibody-mediated Pure Red Cell Aplasia Induced by Continuous Erythropoietin Receptor Activator with Prednisolone

Internal Medicine, 2022/07/15, Vol.61(14), pp.2209-2213

2022

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Effective treatment of refractory monoclonal gammopathy‐associated pure red cell aplasia with isatuximab, pomalidomide and dexamethasone

EJHaem, 2024-08, Vol.5 (4), p.838-841

2024

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How we evaluate red blood cell compatibility and transfusion support for patients with sickle cell disease undergoing hematopoietic progenitor cell transplantation

Transfusion (Philadelphia, Pa.), 2018-11, Vol.58 (11), p.2483-2489

2018

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Dynamics of G6PD activity in patients receiving weekly primaquine for therapy of Plasmodium vivax malaria

PLoS neglected tropical diseases, 2021-09, Vol.15 (9), p.e0009690-e0009690

2021

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Effect of high-dose or split-dose artesunate on parasite clearance in artemisinin-resistant falciparum malaria

Clinical infectious diseases, 2013-03, Vol.56 (5), p.e48-e58

2013

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Pure red cell aplasia, a disease of a great diversity

Journal of Applied Hematology, 2020, Vol.11 (1), p.1

2020

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Use of IV immunoglobulin to treat steroid resistant, immune checkpoint inhibitor‐induced pure red cell aplasia: A case report

EJHaem, 2024-08, Vol.5 (4), p.825-828

2024

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361 Hyperhemolysis in a Case of Sickle Cell Anemia

American journal of clinical pathology, 2018-01, Vol.149 (suppl_1), p.S157-S157

2018

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An Unusual Case of Hyperhemolysis Syndrome and Delayed Hemolytic Transfusion Reaction due to Anti-Jk(a) and Anti-P1 Antibodies

Case reports in medicine, 2023-12, Vol.2023, p.5290115-5

2023

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Tacrolimus-Associated Pure Red Cell Aplasia in a Patient With Renal Transplant

Experimental and clinical transplantation, 2022-12, Vol.20 (12), p.1131-1133

2022

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Hard-To-Treat Idiopathic Refractory Autoimmune Haemolytic Anaemia with Reticulocytopenia

Posttransfusion hyperhemolysis is arrested by targeting macrophage activation with novel use of Tocilizumab

Successful treatment with plasma exchange in life‐threatening hyperhemolytic syndrome unrelated to sickle cell disease

Hyporegenerative anemia in anti‐M‐associated hemolytic disease of the fetus

Pure red cell aplasia after major or bidirectional ABO incompatible hematopoietic stem cell transplantation: to treat or not to treat, that is the question

Hemolytic disease and reticulocytopenia of the newborn attributable to maternal immunoglobulin G anti‐M reacting optimally at cold temperatures

Erythroblastic synartesis associated with lymphoproliferative disorder: There can be more than meets the eye

Hyperhemolysis in a patient with sickle cell disease and recent SARS‐CoV‐2 infection, with complex auto‐ and alloantibody work‐up, successfully treated with tocilizumab

Congenital anaemia associated with loss-of-function variants in DNA polymerase epsilon 1

Clinical and immune features of human parvovirus B19 infection in allogeneic stem cell transplantation recipients: A retrospective monocentric study

325 Aplastic crisis induced by human parvovirus B19 as an initial presentation of hereditary spherocytosis in a child – a case report

Eltrombopag restores erythropoiesis in refractory adult acquired pure red cell aplasia

An update on the pathogenesis and diagnosis of Diamond-Blackfan anemia [version 1; peer review: 2 approved]

Neutrophilic Erythrophagocytosis and Reticulocytopenia: A Rare Manifestation of Cold Autoimmune Hemolytic Anemia

Role of Absolute Reticulocyte Count in the Assessment of Renal Function and Erythropoietin Response in Adults with Sickle Cell Anemia Seen at the Lagos University Teaching Hospital

Successful Treatment of Antibody-mediated Pure Red Cell Aplasia Induced by Continuous Erythropoietin Receptor Activator with Prednisolone

Effective treatment of refractory monoclonal gammopathy‐associated pure red cell aplasia with isatuximab, pomalidomide and dexamethasone

How we evaluate red blood cell compatibility and transfusion support for patients with sickle cell disease undergoing hematopoietic progenitor cell transplantation

Dynamics of G6PD activity in patients receiving weekly primaquine for therapy of Plasmodium vivax malaria

Effect of high-dose or split-dose artesunate on parasite clearance in artemisinin-resistant falciparum malaria

Pure red cell aplasia, a disease of a great diversity

Use of IV immunoglobulin to treat steroid resistant, immune checkpoint inhibitor‐induced pure red cell aplasia: A case report

361 Hyperhemolysis in a Case of Sickle Cell Anemia

An Unusual Case of Hyperhemolysis Syndrome and Delayed Hemolytic Transfusion Reaction due to Anti-Jk(a) and Anti-P1 Antibodies

Tacrolimus-Associated Pure Red Cell Aplasia in a Patient With Renal Transplant

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