(Q28188198)

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Is ADAMTS-13 deficiency specific for thrombotic thrombocytopenic purpura? No

scientific article (publication date: April 2003)

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Is ADAMTS-13 deficiency specific for thrombotic thrombocytopenic purpura? No (English)

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G Remuzzi

1

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language of work or name

English

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publication date

April 2003

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published in

Journal of Thrombosis and Haemostasis

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volume

1

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issue

4

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page(s)

632-4

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cites work

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

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Crossref

reference URL

https://api.crossref.org/works/10.1046/J.1538-7836.2003.00170.X

retrieved

20 April 2017

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

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reference URL

https://api.crossref.org/works/10.1046/J.1538-7836.2003.00170.X

retrieved

20 April 2017

Aetiology and pathogenesis of thrombotic thrombocytopenic purpura and haemolytic uraemic syndrome: the role of von Willebrand factor-cleaving protease

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Crossref

reference URL

https://api.crossref.org/works/10.1046/J.1538-7836.2003.00170.X

retrieved

20 April 2017

Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura

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Crossref

reference URL

https://api.crossref.org/works/10.1046/J.1538-7836.2003.00170.X

retrieved

20 April 2017

von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1538-7836.2003.00170.X

retrieved

21 January 2018

Moschcowitz, multimers, and metalloprotease.

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Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1538-7836.2003.00170.X

retrieved

21 January 2018

Specific von Willebrand factor-cleaving protease in thrombotic microangiopathies: a study of 111 cases

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1538-7836.2003.00170.X

retrieved

21 January 2018

Factor V Leiden: a genetic risk factor for thrombotic microangiopathy in patients with normal von Willebrand factor-cleaving protease activity.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1538-7836.2003.00170.X

retrieved

21 January 2018

von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1538-7836.2003.00170.X

retrieved

21 January 2018

Plasma therapy in von Willebrand factor protease deficiency

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1538-7836.2003.00170.X

retrieved

21 January 2018

Decreased von Willebrand factor protease activity associated with thrombocytopenic disorders

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1538-7836.2003.00170.X

retrieved

21 January 2018

Changes in health and disease of the metalloprotease that cleaves von Willebrand factor.

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1538-7836.2003.00170.X

retrieved

21 January 2018

Combined kidney and liver transplantation for familial haemolytic uraemic syndrome

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1538-7836.2003.00170.X

retrieved

21 January 2018

Haemolytic-uraemic syndrome: basic science

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1538-7836.2003.00170.X

retrieved

21 January 2018

Identifiers

DOI

10.1046/J.1538-7836.2003.00170.X

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PubMed publication ID

12871391

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ResearchGate publication ID

10653997

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(Q28188198)

Is ADAMTS-13 deficiency specific for thrombotic thrombocytopenic purpura? No

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