Paroxysmal nocturnal hemoglobinuria is not a cause of anemia in patients with myelofibrosis
Author:
Publisher
Informa UK Limited
Subject
Cancer Research,Oncology,Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/10428194.2013.876628
Reference10 articles.
1. Diagnosis and management of paroxysmal nocturnal hemoglobinuria
2. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria
3. Relationship between the membrane inhibitor of reactive lysis and the erythrocyte phenotypes of paroxysmal nocturnal hemoglobinuria.
4. Management of Paroxysmal Nocturnal Hemoglobinuria in the Era of Complement Inhibitory Therapy
5. Detection of paroxysmal nocturnal hemoglobinuria clones in patients with myelodysplastic syndromes and related bone marrow diseases, with emphasis on diagnostic pitfalls and caveats
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1. Management of paroxysmal nocturnal hemoglobinuria in CALR mutated post‐essential thrombocythemia myelofibrosis: A case report;eJHaem;2024-04
2. Пароксизмальная ночная гемоглобинурия и первичный миелофиброз — крайне редкое сочетание клональных заболеваний системы крови: обзор литературы и описание двух собственных клинических наблюдений из практики;Clinical Oncohematology;2024-04-01
3. Paroxysmal Nocturnal Hemoglobinuria in the Context of a Myeloproliferative Neoplasm: A Case Report and Review of the Literature;Frontiers in Oncology;2021-11-11
4. Abnormally Short Erythrocyte LifeSpan in Three Patients with Primary Myelofibrosis Despite Successful Control of Splenomegaly;The American Journal of the Medical Sciences;2021-02
5. Expansion of paroxysmal nocturnal hemoglobinuria clones in MPLW515L mutation harboring primary myelofibrosis;Annals of Hematology;2020-05-23
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