Thrombin generation abnormalities in Quebec platelet disorder.

Brunet, Justin G; Sharma, Tanmya; Tasneem, Subia; Liang, Minggao; Wilson, Michael D; Rivard, Georges E; Hayward, Catherine P M

Brunet, Justin G; Sharma, Tanmya; Tasneem, Subia; Liang, Minggao; Wilson, Michael D; Rivard, Georges E; Hayward, Catherine P M.

Afiliação

Brunet JG; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
Sharma T; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
Tasneem S; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
Liang M; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Wilson MD; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Rivard GE; Molecular Genetics, University of Toronto, Toronto, ON, Canada.
Hayward CPM; Heart & Stroke Richard Lewar Centre of Excellence in Cardiovascular Research, Toronto, ON, Canada.

Int J Lab Hematol ; 42(6): 801-809, 2020 Dec.

Article em En | MEDLINE | ID: mdl-32761872

Assuntos

Deficiência do Fator V/sangue; Proteínas de Membrana/sangue; Trombina/metabolismo; Adulto; Idoso; Deficiência do Fator V/genética; Feminino; Humanos; Masculino; Proteínas de Membrana/genética; Pessoa de Meia-Idade; Trombina/genética

Palavras-chave

coagulation; factor V; fibrinolysis; platelet function; procoagulant activity

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Trombina / Deficiência do Fator V / Proteínas de Membrana Tipo de estudo: Clinical_trials Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Lab Hematol Ano de publicação: 2020 Tipo de documento: Article

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