Acquired deficiency of von Willebrand factor-cleaving protease in a patient suffering from acute systemic lupus erythematosus [2]

Rheumatology

Volumn 40, Issue 8, 2001, Pages 940-942

  Gungor T ^a   Furlan, M ^b   Lammle B ^b   Kuhn, F ^a   Seger, R A ^a  

^a UNIVERSITY CHILDREN S HOSPITAL   (Switzerland)

^b UNIVERSITY OF BERN   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

AZATHIOPRINE; BETA2 GLYCOPROTEIN 1; DNA ANTIBODY; DOUBLE STRANDED DNA; HEMOGLOBIN; IMMUNOGLOBULIN; IMMUNOGLOBULIN A; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M; IMMUNOSUPPRESSIVE AGENT; LACTATE DEHYDROGENASE; LUPUS ANTICOAGULANT; METHYLPREDNISOLONE; PHOSPHOLIPID ANTIBODY; PREDNISONE; PROTEINASE; VON WILLEBRAND FACTOR;

ACUTE DISEASE; ANEMIA; ANTIBODY DETECTION; BONE MARROW EXAMINATION; CASE REPORT; ENZYME ACTIVITY; ENZYME DEFICIENCY; ERYTHROCYTE CONCENTRATE; ERYTHROPOIESIS; FATIGUE; FEMALE; HUMAN; LETTER; MEGAKARYOPOIESIS; NEUROLOGIC DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; PETECHIA; PHYSICAL EXAMINATION; PRIORITY JOURNAL; RASH; SCHOOL CHILD; SYSTEMIC LUPUS ERYTHEMATOSUS; THROMBOCYTOPENIA; THROMBOTIC THROMBOCYTOPENIC PURPURA;

EID: 0034861756     PISSN: 14620324     EISSN: None     Source Type: Journal    
DOI: 10.1093/rheumatology/40.8.940     Document Type: Letter

References (10)

1. Review of thrombotic thrombocytopenic purpura in the setting of systemic lupus erythematosus
2. Thrombotic thrombocytopenic purpura and autoimmunity: A tale of shadows and suspects
3. The pathophysiology and management of thrombotic thrombocytopenic purpura
4. Thrombotic microangiopathies in the 1980s: Clinical features, response to treatment, and the impact of the human immunodeficiency virus epidemic
5. Von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome
6. Acquired deficiency of von Willebrand factor-cleaving protease in a patient with thrombotic thrombocytopenic purpura
7. Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura
8. Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura
9. Systemic lupus erythematosus and thrombotic microangiopathies
10. Thrombotic microangiopathy and the antiphospholipid antibody syndrome