Complement Factor H Mutation in Familial Thrombotic Thrombocytopenic Purpura with ADAMTS13 Deficiency and Renal Involvement-Reference-Cited by-同舟云学术

Complement Factor H Mutation in Familial Thrombotic Thrombocytopenic Purpura with ADAMTS13 Deficiency and Renal Involvement

Published:2005-03-30 Issue:5 Volume:16 Page:1177-1183
ISSN:1046-6673
Container-title:Journal of the American Society of Nephrology
language:en
Short-container-title:JASN

Author:

Noris Marina,Bucchioni Sara,Galbusera Miriam,Donadelli Roberta,Bresin Elena,Castelletti Federica,Caprioli Jessica,Brioschi Simona,Scheiflinger Friedrich,Remuzzi Giuseppe

Publisher

American Society of Nephrology (ASN)

Subject

Nephrology,General Medicine

Reference40 articles.

1. Thrombotic Microangiopathies

2. Deficient Activity of von Willebrand Factor–Cleaving Protease in Chronic Relapsing Thrombotic Thrombocytopenic Purpura

3. von Willebrand Factor–Cleaving Protease in Thrombotic Thrombocytopenic Purpura and the Hemolytic–Uremic Syndrome

4. Antibodies to von Willebrand Factor–Cleaving Protease in Acute Thrombotic Thrombocytopenic Purpura

5. Structure of von Willebrand Factor-cleaving Protease (ADAMTS13), a Metalloprotease Involved in Thrombotic Thrombocytopenic Purpura

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