Genetic defects leading to hereditary thrombotic thrombocytopenic purpura-Reference-Cited by-同舟云学术

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Genetic defects leading to hereditary thrombotic thrombocytopenic purpura

Published:2004-01 Issue:1 Volume:41 Page:34-40
ISSN:0037-1963
Container-title:Seminars in Hematology
language:en
Short-container-title:Seminars in Hematology

Author:

Kokame Koichi,Miyata Toshiyuki

Publisher

Elsevier BV

Subject

Hematology

Reference42 articles.

1. Hyaline thombrosis of the terminal arterioles and capillaries; a hitherto undescribed disease;Moschcowitz;Proc NY Pathol Soc,1924

2. Upshaw-Schulman syndrome revisited;Kinoshita;Int J Hematol,2001

3. Structure and function of von Willebrand factor;Fujimura,1994

4. Von Willebrand factor;Furlan;Ann Hematol,1996

5. von Willebrand factor;Ruggeri;J Clin Invest,1997

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1. Congenital thrombotic thrombocytopenic purpura in children;Russian journal of hematology and transfusiology;2023-12-28

2. Pathological Background and Clinical Procedures in Oral Surgery Haemostasis Disorders: A Narrative Review;Applied Sciences;2023-02-05

3. Thirty five novel nsSNPs may effect on ADAMTS13 protein leading to Thrombotic thrombocytopenic purpura (TTP) using bioinformatics approach;2019-09-05

4. Unique case of autoantibody mediated inactivation of ADAMTS13 in an Indian TTP patient;Blood Cells, Molecules, and Diseases;2019-07

5. Child-onset thrombotic thrombocytopenic purpura caused by p.R498C and p.G259PfsX133 mutations in ADAMTS13;European Journal of Haematology;2018-06-25

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