Paroxysmal nocturnal hemoglobinuria presenting as aplastic anemia in a child
- 1 July 1964
- journal article
- research article
- Published by Elsevier in The American Journal of Medicine
- Vol. 37 (1) , 130-139
- https://doi.org/10.1016/0002-9343(64)90217-7
Abstract
No abstract availableKeywords
This publication has 53 references indexed in Scilit:
- Red-Cell Abnormalities and Haemolysis in Aplastic AnaemiaBritish Journal of Haematology, 1962
- Reticulocyte Destruction in Paroxysmal Nocturnal HaemoglobinuriaBritish Journal of Haematology, 1962
- Failure of In-Vivo Inhibition of Acetylcholinesterase to Affect Erythrocyte Life-Span: The Significance of the Enzyme Defect in Paroxysmal Nocturnal HaemoglobinuriaBritish Journal of Haematology, 1961
- A Possible Specific Chromosome Abnormality in Human Chronic Myeloid LeukæmiaNature, 1960
- The Fatty-Acid Composition of Red Cells in Paroxysmal Nocturnal HaemoglobinuriaBritish Journal of Haematology, 1959
- The Phospholipid Distribution in the Erythrocyte in Paroxysmal Nocturnal HaemoglobinuriaBritish Journal of Haematology, 1959
- POTASSIUM TRANSPORT IN THE ACETYLCHOLINESTERASE-DEFICIENT ERYTHROCYTES OF PAROXYSMAL NOCTURNAL HEMOGLOBINURIA (PNH)*Journal of Clinical Investigation, 1959
- PAROXYSMAL NOCTURNAL' HÆMOGLOBINURIAThe Lancet, 1957
- PAROXYSMAL NOCTURNAL HÆMOGLOBINURIA MARCHIAFAVA—MICHELI SYNDROMEThe Lancet, 1955
- Chronic hemolytic anemia with paroxysmal nocturnal hemoglobinuria (marchiafava-micheli syndrome): Report of a case with marked thrombocytopenia in a five-year-old childThe Journal of Pediatrics, 1943