(Q33374478)

English

Normal levels of ADAMTS13 and factor H are present in the pharmaceutically licensed plasma for transfusion (Octaplas) and in the universally applicable plasma (Uniplas) in development

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scholarly article

1 reference

Europe PubMed Central

26 July 2017

Normal levels of ADAMTS13 and factor H are present in the pharmaceutically licensed plasma for transfusion (Octaplas) and in the universally applicable plasma (Uniplas) in development (English)

1 reference

Europe PubMed Central

26 July 2017

author name string

A Heger

1

1 reference

Europe PubMed Central

26 July 2017

C Kannicht

2

1 reference

Europe PubMed Central

26 July 2017

J Römisch

3

1 reference

Europe PubMed Central

26 July 2017

T-E Svae

4

1 reference

Europe PubMed Central

26 July 2017

publication date

1 April 2007

1 reference

Europe PubMed Central

26 July 2017

1 reference

Europe PubMed Central

26 July 2017

92

1 reference

Europe PubMed Central

26 July 2017

3

1 reference

Europe PubMed Central

26 July 2017

206-212

1 reference

Europe PubMed Central

26 July 2017

Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

A perspective on the measurement of ADAMTS13 in thrombotic thrombocytopaenic purpura

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

Therapeutic plasma exchange and plasma infusion in thrombotic microvascular syndromes

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

Plasma therapy in thrombotic thrombocytopenic purpura: review of the literature and the Bern experience in a subgroup of patients with severe acquired ADAMTS-13 deficiency

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

Effect of plasma exchange on plasma ADAMTS13 metalloprotease activity, inhibitor level, and clinical outcome in patients with idiopathic and nonidiopathic thrombotic thrombocytopenic purpura.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

Manufacture and composition of fresh frozen plasma and virus-inactivated therapeutic plasma preparations: correlation between composition and therapeutic efficacy

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

Solvent/detergent-treated plasma: composition, efficacy, and safety

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

Plasma exchange with solvent/detergent-treated plasma of resistant thrombotic thrombocytopenic purpura

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

The Canadian apheresis registry

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

VWF73, a region from D1596 to R1668 of von Willebrand factor, provides a minimal substrate for ADAMTS-13

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

FRETS-VWF73, a first fluorogenic substrate for ADAMTS13 assay

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

Characterization of factor VIII/von Willebrand factor concentrates using a modified method of von Willebrand factor multimer analysis

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

Von Willebrand factor--cleaving protease activity in congenital thrombotic thrombocytopenic purpura

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

Comparison of von Willebrand factor antigen, von Willebrand factor-cleaving protease and protein S in blood components used for treatment of thrombotic thrombocytopenic purpura

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

Measurement of ADAMTS13 activity and inhibitors

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

Analysis on the molecular species and concentration of circulating ADAMTS13 in Blood.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

A comparison of two methods for the discrimination of VWF:AG multimers

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

Different regulation of factor H and FHL-1/reconectin by inflammatory mediators and expression of the two proteins in rheumatoid arthritis (RA).

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2006.00884.X

21 January 2018

Identifiers

10.1111/J.1423-0410.2006.00884.X

1 reference

Europe PubMed Central

26 July 2017

1 reference

Europe PubMed Central

26 July 2017

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