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Association between genetic variants in the HIF1A-VEGF pathway and left ventricular regional myocardial deformation in patients with hypertrophic cardiomyopathy.
Pieles, Guido E; Alkon, Jaime; Manlhiot, Cedric; Fan, Chun-Po Steve; Kinnear, Caroline; Benson, Leland N; Mital, Seema; Friedberg, Mark K.
Afiliação
  • Pieles GE; Department of Pediatrics, Labatt Family Heart Centre, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada. guido.pieles@bristol.ac.uk.
  • Alkon J; NIHR Cardiovascular Biomedical Research Centre, Bristol Heart Institute, Bristol, UK. guido.pieles@bristol.ac.uk.
  • Manlhiot C; Department of Pediatrics, Labatt Family Heart Centre, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Fan CS; Department of Pediatrics, Labatt Family Heart Centre, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Kinnear C; Department of Pediatrics, Labatt Family Heart Centre, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Benson LN; Department of Pediatrics, Labatt Family Heart Centre, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Mital S; Department of Pediatrics, Labatt Family Heart Centre, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Friedberg MK; Department of Pediatrics, Labatt Family Heart Centre, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Pediatr Res ; 89(3): 628-635, 2021 02.
Article em En | MEDLINE | ID: mdl-32375165
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Cardiomiopatia Hipertrófica / Disfunção Ventricular Esquerda / Polimorfismo de Nucleotídeo Único / Fator A de Crescimento do Endotélio Vascular / Subunidade alfa do Fator 1 Induzível por Hipóxia / Ventrículos do Coração Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Cardiomiopatia Hipertrófica / Disfunção Ventricular Esquerda / Polimorfismo de Nucleotídeo Único / Fator A de Crescimento do Endotélio Vascular / Subunidade alfa do Fator 1 Induzível por Hipóxia / Ventrículos do Coração Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article