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Challenges in diagnosis of von Willebrand disease in the presence of combined mutations of different genes.
Nava, Tiago; Dubé, Evemie; Gauthier, Julie; Vézina, Catherine; Bonnefoy, Arnaud; Lillicrap, David; Rivard, Georges-Etienne.
Afiliação
  • Nava T; Centre d'hémostase pédiatrique et adulte du CHU Sainte-Justine, Montreal University, Montréal, Quebec, Canada.
  • Dubé E; Division of Pediatric Hematology-Oncology, University Hospital of Geneva, Geneva, Switzerland.
  • Gauthier J; Centre d'hémostase pédiatrique et adulte du CHU Sainte-Justine, Montreal University, Montréal, Quebec, Canada.
  • Vézina C; Centre d'hémostase pédiatrique et adulte du CHU Sainte-Justine, Montreal University, Montréal, Quebec, Canada.
  • Bonnefoy A; Montreal Children's Hospital, McGill University, Montréal, Quebec, Canada.
  • Lillicrap D; Centre d'hémostase pédiatrique et adulte du CHU Sainte-Justine, Montreal University, Montréal, Quebec, Canada.
  • Rivard GE; Department of Medicine, Department of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada.
Haemophilia ; 25(2): e113-e117, 2019 03.
Article em En | MEDLINE | ID: mdl-30690834
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças de von Willebrand / Mutação Tipo de estudo: Diagnostic_studies Limite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças de von Willebrand / Mutação Tipo de estudo: Diagnostic_studies Limite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article