ADAMTS-13 in the Diagnosis and Management of Thrombotic Microangiopathies. - Wikidata - awgldk - TriplyDB

ADAMTS-13 in the Diagnosis and Management of Thrombotic Microangiopathies.

ADAMTS-13 in the Diagnosis and Management of Thrombotic Microangiopathies.

http://www.wikidata.org/entity/Q33418645

about

Deficiency in mouse hyaluronidase 2: a new mechanism of chronic thrombotic microangiopathy.Association of acquired thrombotic thrombocytopaenic purpura in a patient with pernicious anaemia.

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P2860

ADAMTS-13 in the Diagnosis and Management of Thrombotic Microangiopathies.

http://www.wikidata.org/entity/Q33418645

description

2014 nî lūn-bûn

@nan

2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

ADAMTS-13 in the Diagnosis and Management of Thrombotic Microangiopathies.

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ADAMTS-13 in the Diagnosis and Management of Thrombotic Microangiopathies.

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type

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ADAMTS-13 in the Diagnosis and Management of Thrombotic Microangiopathies.

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ADAMTS-13 in the Diagnosis and Management of Thrombotic Microangiopathies.

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ADAMTS-13 in the Diagnosis and Management of Thrombotic Microangiopathies.

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ADAMTS-13 in the Diagnosis and Management of Thrombotic Microangiopathies.

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Rambam Maimonides Medical Journal

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ADAMTS-13 in the Diagnosis and Management of Thrombotic Microangiopathies.

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Galit Sarig

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P2860

Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family

ADAMTS-13 metalloprotease interacts with the endothelial cell-derived ultra-large von Willebrand factor

Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity

Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura

The molecular biology of thrombotic microangiopathy

Hemolytic uremic syndrome-associated Shiga toxins promote endothelial-cell secretion and impair ADAMTS13 cleavage of unusually large von Willebrand factor multimers

Successful management of pregnancy in women with a history of thrombotic thrombocytopaenic purpura

N-acetylcysteine reduces the size and activity of von Willebrand factor in human plasma and mice

Antibody inhibitors to von Willebrand factor metalloproteinase and increased binding of von Willebrand factor to platelets in ticlopidine-associated thrombotic thrombocytopenic purpura.

Management of thrombotic thrombocytopenic purpura.

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e0026

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scholarly article

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10.5041/RMMJ.10160

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