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Volumn 23, Issue 1, 1995, Pages 81-87
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A pathogenetic link between aplastic anemia and paroxysmal nocturnal hemoglobinuria is suggested by a high frequency of aplastic anemia patients with a deficiency of phosphatidylinositol glycan anchored proteins
a
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Author keywords
Aplastic anemia; Paroxysmal nocturnal hemoglobinuria; Phosphaticlylinositol glycan anchor
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Indexed keywords
CYCLOSPORIN A;
GRANULOCYTE COLONY STIMULATING FACTOR;
INTERLEUKIN 3;
LYMPHOCYTE ANTIBODY;
METHYLPREDNISOLONE;
PHOSPHATIDYLINOSITOL GLYCAN;
UNCLASSIFIED DRUG;
ADULT;
AGED;
APLASTIC ANEMIA;
ARTICLE;
CONTROLLED STUDY;
FEMALE;
HUMAN;
INTRAVENOUS DRUG ADMINISTRATION;
MAJOR CLINICAL STUDY;
MALE;
ORAL DRUG ADMINISTRATION;
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA;
PRIORITY JOURNAL;
SUBCUTANEOUS DRUG ADMINISTRATION;
ADOLESCENT;
ADULT;
AGED;
ANEMIA, APLASTIC;
ANTIBODIES, MONOCLONAL;
ERYTHROCYTES;
FEMALE;
FLOW CYTOMETRY;
GLYCOSYLPHOSPHATIDYLINOSITOLS;
GRANULOCYTES;
HEMOGLOBINURIA, PAROXYSMAL;
HUMAN;
IMMUNOSUPPRESSION;
LYMPHOCYTES;
MALE;
MIDDLE AGE;
MONOCYTES;
SUPPORT, NON-U.S. GOV'T;
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EID: 0028897137
PISSN: 0301472X
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (140)
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References (0)
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