Flowcytometric detection of PNH defect in Indian patients with aplastic anemia and myelodysplastic syndromes [2]

American Journal of Hematology

Volumn 65, Issue 3, 2000, Pages 264-265

  Varma, Neelam ^a   Garewal, Gurjeevan ^a   Varma, Subhash ^a   Vohra, Harpreet ^a  

^a POSTGRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH   (India)

Author keywords

[No Author keywords available]

Indexed keywords

HEMOSIDERIN;

APLASTIC ANEMIA; CLINICAL FEATURE; DISEASE ASSOCIATION; FLOW CYTOMETRY; FOLLOW UP; HUMAN; INDIAN; LETTER; MAJOR CLINICAL STUDY; MYELODYSPLASTIC SYNDROME; PAROXYSMAL NOCTURNAL HEMOGLOBINURIA; PRIORITY JOURNAL; REFRACTORY ANEMIA;

ANEMIA, APLASTIC; FLOW CYTOMETRY; HEMOGLOBINURIA, PAROXYSMAL; HUMAN; INDIA; MYELODYSPLASTIC SYNDROMES;

EID: 0033784272     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8652(200011)65:3<264::AID-AJH17>3.0.CO;2-L     Document Type: Letter

References (4)

1. Paroxysmal nocturnal hemoglobinuria: An acquired genetic disease
2. Paroxysmal nocturnal haemoglobinuria clones in patients with myelodysplastic syndromes
3. Deficiency of glycosylphosphatidyl inositol-anchored proteins in patients with aplastic anaemia does not affect response to immunosuppressive therapy
4. Late haematological complications in severe aplastic anaemia