Zobrazeno 1 - 3 of 3 pro vyhledávání: '"Şükrü Candan"'
1
Titin truncating mutations: A rare cause of dilated cardiomyopathy in the young
Autor: Helen Bornaun, Leanne E. Felkin, Diane Fatkin, Christine E. Seidman, Şükrü Candan, Christopher S. Hayward, Craig C. Benson, Peter S. Macdonald, Angharad M. Roberts, Anne Keogh, Lien Lam, Wendy K. Chung, Daniel S. Herman, Amy E. Roberts, Leslie B. Smoot, Jonathan G. Seidman, Roddy Walsh, Stuart A. Cook, Paul J.R. Barton, James S. Ware
Publikováno v: Progress in Pediatric Cardiology. 40:41-45
Truncating mutations in the TTN gene are the most common genetic cause of dilated cardiomyopathy in adults but their role in young patients is unknown. We studied 82 young dilated cardiomyopathy subjects and found that the prevalence of truncating TT
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a92acfce681cd9c38da3488636fc673
https://doi.org/10.1016/j.ppedcard.2016.01.003
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2
PEDIATRIC CARDIOMYOPATHY MUTATIONS IN A HIGHLY CONSANGUINEOUS POPULATION
Autor: Christine E. Seidman, Şükrü Candan, Steven R. DePalma, Akl C. Fahed, Jonathan G. Seidman, Kazum Öztarhan, Hatip Aydin, Helen Bornaun, Betül Erer, Ahmet Ekmekçi, Barbara McDonough, Alireza Haghighi
Publikováno v: Journal of the American College of Cardiology. 67:1399
Pediatric-onset cardiomyopathy is more common in inbred and highly consanguineous populations that are enriched for familial and recessive disease. The genetic causes of pediatric cardiomyopathy remain poorly understood. Nearly one quarter of marriag
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0066da0259c924691d8be1c288f3f720
https://doi.org/10.1016/s0735-1097(16)31400-0
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Plný text Recenzováno Digitální knihovna AV ČR
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