Development of clinical paroxysmal nocturnal haemoglobinuria in children with aplastic anaemia
Author:
Affiliation:
1. Department of Paediatrics; Nagoya University Graduate School of Medicine; Nagoya Japan
Funder
Sanofi K.K.
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.14790/fullpdf
Reference15 articles.
1. Paroxysmal nocturnal hemoglobinuria in pediatric patients;Curran;Pediatric Blood & Cancer,2012
2. Paroxysmal nocturnal hemoglobinuria: natural history of disease subcategories;Latour;Blood,2008
3. N-RAS gene mutation in patients with aplastic anemia and aplastic anemia/paroxysmal nocturnal hemoglobinuria during evolution to clonal disease;Mortazavi;Blood,2000
4. Different roles of glycosylphosphatidylinositol in various hematopoietic cells as revealed by a mouse model of paroxysmal nocturnal hemoglobinuria;Murakami;Blood,1999
5. Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes;Muramatsu;Genetics in Medicine,2017
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3. Analysis of baseline characteristics, disease burden and long-term follow-up of 167 patients with Paroxysmal Nocturnal Hemoglobinuria at a single center in Brazil;Blood Cells, Molecules, and Diseases;2021-12
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