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Hypertrophic remodelling in cardiac regulatory myosin light chain (MYL2) founder mutation carriers.
Claes, Godelieve R F; van Tienen, Florence H J; Lindsey, Patrick; Krapels, Ingrid P C; Helderman-van den Enden, Apollonia T J M; Hoos, Marije B; Barrois, Yvette E G; Janssen, Johanna W H; Paulussen, Aimée D C; Sels, Jan-Willem E M; Kuijpers, Simone H H; van Tintelen, J Peter; van den Berg, Maarten P; Heesen, Wilfred F; Garcia-Pavia, Pablo; Perrot, Andreas; Christiaans, Imke; Salemink, Simone; Marcelis, Carlo L M; Smeets, Hubert J M; Brunner, Han G; Volders, Paul G A; van den Wijngaard, Arthur.
Afiliação
  • Claes GR; Department of Clinical Genetics, Unit Clinical Genomics, Maastricht University Medical Centre, P.O. Box 5800, 6229 GR Maastricht, The Netherlands School for Cardiovascular Diseases, Maastricht University Medical Centre, Maastricht, The Netherlands lieve.claes@mumc.nl.
  • van Tienen FH; Department of Clinical Genetics, Unit Clinical Genomics, Maastricht University Medical Centre, P.O. Box 5800, 6229 GR Maastricht, The Netherlands School for Cardiovascular Diseases, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Lindsey P; Department of Clinical Genetics, Unit Clinical Genomics, Maastricht University Medical Centre, P.O. Box 5800, 6229 GR Maastricht, The Netherlands School for Cardiovascular Diseases, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Krapels IP; Department of Clinical Genetics, Unit Clinical Genomics, Maastricht University Medical Centre, P.O. Box 5800, 6229 GR Maastricht, The Netherlands School for Cardiovascular Diseases, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Helderman-van den Enden AT; Department of Clinical Genetics, Unit Clinical Genomics, Maastricht University Medical Centre, P.O. Box 5800, 6229 GR Maastricht, The Netherlands School for Cardiovascular Diseases, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Hoos MB; Department of Clinical Genetics, Unit Clinical Genomics, Maastricht University Medical Centre, P.O. Box 5800, 6229 GR Maastricht, The Netherlands School for Cardiovascular Diseases, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Barrois YE; Department of Clinical Genetics, Unit Clinical Genomics, Maastricht University Medical Centre, P.O. Box 5800, 6229 GR Maastricht, The Netherlands School for Cardiovascular Diseases, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Janssen JW; Department of Clinical Genetics, Unit Clinical Genomics, Maastricht University Medical Centre, P.O. Box 5800, 6229 GR Maastricht, The Netherlands.
  • Paulussen AD; Department of Clinical Genetics, Unit Clinical Genomics, Maastricht University Medical Centre, P.O. Box 5800, 6229 GR Maastricht, The Netherlands School for Cardiovascular Diseases, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Sels JW; Department of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University Medical Centre, Maastricht, The Netherlands Department of Intensive Care, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Kuijpers SH; Department of Cardiology, Máxima Medical Centre, Eindhoven, The Netherlands.
  • van Tintelen JP; Department of Clinical Genetics, Academic Medical Centre, Amsterdam, The Netherlands.
  • van den Berg MP; Department of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
  • Heesen WF; Department of Cardiology, VieCuri Medical Centre, Venlo, The Netherlands.
  • Garcia-Pavia P; Heart Failure and Inherited Cardiac Diseases Unit, Department of Cardiology, Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain.
  • Perrot A; Charité-Universitätsmedizin Berlin, Experimental & Clinical Research Centre, A Joint Cooperation Between the Charité Medical Faculty and the Max-Delbrück Centre for Molecular Medicine, Berlin, Germany.
  • Christiaans I; Department of Clinical Genetics, Academic Medical Centre, Amsterdam, The Netherlands.
  • Salemink S; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Marcelis CL; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Smeets HJ; Department of Clinical Genetics, Unit Clinical Genomics, Maastricht University Medical Centre, P.O. Box 5800, 6229 GR Maastricht, The Netherlands.
  • Brunner HG; Department of Clinical Genetics, Unit Clinical Genomics, Maastricht University Medical Centre, P.O. Box 5800, 6229 GR Maastricht, The Netherlands Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Volders PG; Department of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • van den Wijngaard A; Department of Clinical Genetics, Unit Clinical Genomics, Maastricht University Medical Centre, P.O. Box 5800, 6229 GR Maastricht, The Netherlands School for Cardiovascular Diseases, Maastricht University Medical Centre, Maastricht, The Netherlands.
Eur Heart J ; 37(23): 1815-22, 2016 06 14.
Article em En | MEDLINE | ID: mdl-26497160

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipertrofia Ventricular Esquerda / Efeito Fundador / Cadeias Leves de Miosina / Miosinas Cardíacas / Mutação Tipo de estudo: Risk_factors_studies / Screening_studies Limite: Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Eur Heart J Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipertrofia Ventricular Esquerda / Efeito Fundador / Cadeias Leves de Miosina / Miosinas Cardíacas / Mutação Tipo de estudo: Risk_factors_studies / Screening_studies Limite: Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Eur Heart J Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda