Acquired type 3-like von Willebrand syndrome preceded full-blown systemic lupus erythematosus

Blood Coagulation and Fibrinolysis

Volumn 13, Issue 4, 2002, Pages 361-365

  Niiya, M ^a   Niiya, Kenji ^a   Takazawa, Y ^a   Hayashi, Y ^a   Tanio, Y ^a   Kushiro, M ^a   Tanimizu, M ^a   Hasegawa, H ^a   Tanimoto, M ^a  

^a OKAYAMA UNIVERSITY MEDICAL SCHOOL   (Japan)

Author keywords

Acquired von Willebrand syndrome; Inhibitor; Prednisolone; Systemic lupus erythematosus; Vasopressin

Indexed keywords

BLOOD CLOTTING FACTOR 8; DNA ANTIBODY; DOUBLE STRANDED DNA; PREDNISOLONE; PROTEIN INHIBITOR; RISTOCETIN; THROMBOPLASTIN; VASOPRESSIN; VON WILLEBRAND FACTOR;

ADOLESCENT; ARTHRALGIA; ARTICLE; BLEEDING TENDENCY; BLEEDING TIME; CASE REPORT; DIAGNOSTIC TEST; DISEASE ASSOCIATION; DISEASE COURSE; DRUG INFUSION; EPISTAXIS; FAMILY HISTORY; FATIGUE; FEMALE; FEVER; GINGIVA BLEEDING; HUMAN; HYPOCOMPLEMENTEMIA; LABORATORY TEST; LEUKOPENIA; PARTIAL THROMBOPLASTIN TIME; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN ELECTROPHORESIS; STEROID THERAPY; SYSTEMIC LUPUS ERYTHEMATOSUS; THROMBOCYTE AGGLUTINATION; THROMBOCYTE COUNT; TREATMENT OUTCOME; VON WILLEBRAND DISEASE;

ADOLESCENT; DEAMINO ARGININE VASOPRESSIN; FEMALE; HEMORRHAGE; HUMANS; LUPUS ERYTHEMATOSUS, SYSTEMIC; PREDNISOLONE; VON WILLEBRAND DISEASE;

EID: 0036592482     PISSN: 09575235     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001721-200206000-00013     Document Type: Article

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