A cohort study of the nature of paroxysmal nocturnal hemoglobinuria clones and PIG-A mutations in patients with aplastic anemia
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Reference38 articles.
1. Paroxysmal Nocturnal Haemoglobinuria in Thailand with Special Reference to an Association with Aplastic Anaemia
2. Stem cells in paroxysmal nocturnal haemoglobinuria and aplastic anaemia: increasing evidence for overlap of haemopoietic defect
3. The problem of clonality in aplastic anemia: Dr Dameshek's riddle, restated [see comments]
4. Hematopoietic cell destruction by immune mechanisms in acquired aplastic anemia
5. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria
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1. Swiss Survey on current practices and opinions on clinical constellations triggering the search for PNH clones;Frontiers in Medicine;2023-07-26
2. Clonal Evolution of Aplastic Anemia: A Brief Literature Review and a Case Report;Clinical oncohematology;2022
3. Time and residual hematopoiesis are crucial for PNH clones escape in hepatitis-associated aplastic anemia;Annals of Hematology;2021-07-16
4. The incidence and prevalence of patients with paroxysmal nocturnal haemoglobinuria and aplastic anaemia PNH syndrome: A retrospective analysis of the UK’s population‐based haematological malignancy research network 2004‐2018;European Journal of Haematology;2021-06-09
5. Clinical and prognostic significance of small paroxysmal nocturnal hemoglobinuria clones in myelodysplastic syndrome and aplastic anemia;Leukemia;2021-03-04
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