Occurence of thrombotic thrombocytopenic purpura in a systemic lupus erythematosus patient with antiphospholipid antibodies in association with a decreased activity of von Willebrand factor-cleaving protease [1]

Lupus

Volumn 11, Issue 7, 2002, Pages 463-464

  Matsuda, J ^a   Sanaka, T ^a   Gohchi, K ^a   Matsui, K ^a   Uchida, S ^a   Matsumoto, M ^a   Fujimura, Y ^a  

^a TEIKYO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

PHOSPHOLIPID ANTIBODY; VON WILLEBRAND FACTOR; ADAM PROTEIN; ADAMTS13 PROTEIN, HUMAN; METALLOPROTEINASE;

ADULT; ANTIPHOSPHOLIPID SYNDROME; CASE REPORT; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; DIARRHEA; FEMALE; HUMAN; HUMAN TISSUE; LETTER; PRIORITY JOURNAL; SYSTEMIC LUPUS ERYTHEMATOSUS; THROMBOTIC THROMBOCYTOPENIC PURPURA; BLOOD; IMMUNOLOGY; METABOLISM;

ADAM PROTEINS; ADULT; ANTIBODIES, ANTIPHOSPHOLIPID; FEMALE; HUMANS; LUPUS ERYTHEMATOSUS, SYSTEMIC; METALLOENDOPEPTIDASES; PURPURA, THROMBOTIC THROMBOCYTOPENIC;

EID: 0036024145     PISSN: 09612033     EISSN: None     Source Type: Journal    
DOI: 10.1191/0961203302lu230xx     Document Type: Letter

References (5)

1. Acquired deficiency of von Willebrand factor-cleaving protease in a patient with thrombotic thrombocytopenic purpura
2. Antibodies to von willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura
3. Catastrophic antiphospholipid syndrome-clinical and laboratory features of 50 patients
4. Upshaw-Schulman syndrome revisted: A concept of congenital thrombotic thrombocytopenic purpura
5. Multiple thromboses in major arteries in a patient with antiphospholipid syndrome associated with excess of a large multimer of von Willebrand factor