Zobrazeno 1 - 4
of 4
pro vyhledávání: '"A. M. C. Vermeer"'
Autor:
S. N. van der Crabben, F. L. Komdeur, E. J. Nossent, R. H. Lekanne Deprez, E. A. Broekhuizen, C. van der Werf, A. M. C. Vermeer, H. W. M. Niessen, A. C. Houweling
Publikováno v:
Cardiogenetics, Vol 11, Iss 2, Pp 68-72 (2021)
Sudden death, especially at a young age, may be caused by an underlying genetic cause. Hereditary conditions with an increased risk of sudden death at a young age include cardiomyopathies, arrhythmia syndromes, and hereditary thoracic aortic aneurysm
Externí odkaz:
https://doaj.org/article/65b137ada75e494c89e69f1cd9d86902
Autor:
Yigal M Pinto, Joeri A Jansweijer, Karin Y van Spaendonck-Zwarts, Michael W T Tanck, J Peter van Tintelen, Imke Christiaans, J Martijn Bos, Arthur J Moss, Heikki Swan, Annika Rydberg, Jacob Tfelt-Hansen, Iacopo Olivotto, Philippe Charron, Juan R Gimeno, Maarten P van den Berg, Jasper J van der Smagt, Alexa M C Vermeer, Sylvia G Priori, Michael J Ackerman, Arthur AM Wilde
Publikováno v:
Open Heart, Vol 6, Iss 1 (2019)
Background Mutations in genes encoding ion channels or sarcomeric proteins are an important cause of hereditary cardiac disease. However, the severity of the resultant disease varies considerably even among those with an identical mutation. Such clin
Externí odkaz:
https://doaj.org/article/d80eef2a41b34518888d3b17f89ded1b
Autor:
R. H. Lekanne Deprez, E. A. Broekhuizen, C. van der Werf, F. L. Komdeur, S. N. van der Crabben, E. J. Nossent, A. M. C. Vermeer, Arjan C. Houweling, H. W. M. Niessen
Publikováno v:
van der Crabben, S N, Komdeur, F L, Nossent, E J, Deprez, R H L, Broekhuizen, E A, van der Werf, C, Vermeer, A M C, Niessen, H W M & Houweling, A C 2021, ' Genetic Diagnosis in Sudden Cardiac Death: The Crucial Role of Multidisciplinary Care ', Cardiogenetics, vol. 11, no. 2, pp. 68-72 . https://doi.org/10.3390/cardiogenetics11020008
Cardiogenetics, 11(2), 68-72
Cardiogenetics, Vol 11, Iss 8, Pp 68-72 (2021)
Cardiogenetics, 11(2), 68-72
Cardiogenetics, Vol 11, Iss 8, Pp 68-72 (2021)
Sudden death, especially at a young age, may be caused by an underlying genetic cause. Hereditary conditions with an increased risk of sudden death at a young age include cardiomyopathies, arrhythmia syndromes, and hereditary thoracic aortic aneurysm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c99032d8d8346a9598aa6381c0722df8
https://research.vumc.nl/en/publications/8c25cc73-d085-4308-a9b8-928836b4cd67
https://research.vumc.nl/en/publications/8c25cc73-d085-4308-a9b8-928836b4cd67
Autor:
Alexa M C, Vermeer, Klaartje, van Engelen, Alex V, Postma, Marieke J H, Baars, Imke, Christiaans, Simone, De Haij, Sabine, Klaassen, Barbara J M, Mulder, Bernard, Keavney
Publikováno v:
American journal of medical genetics. Part C, Seminars in medical genetics. (3)
Left ventricular noncompaction (LVNC) is a relatively common genetic cardiomyopathy, characterized by prominent trabeculations with deep intertrabecular recesses in mainly the left ventricle. Although LVNC often occurs in an isolated entity, it may a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a8b0bb1e9baf4175b20d15ca517df627
https://pubmed.ncbi.nlm.nih.gov/23794396
https://pubmed.ncbi.nlm.nih.gov/23794396