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Neil E Bowles

Showing results (51-60 of 65) with videos related to

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International Journal of Cardiology|December 14, 2020
A burden of sarcomere gene variants in fetal-onset patients with left ventricular noncompactionKeiichi Hirono, Yukiko Hata, Sayaka Watanabe Ozawa, et al.
Molecular Genetics and Metabolism|October 22, 2003
Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosisBhagyalaxmi Mohapatra, Shinawe Jimenez, Jiuann Huey Lin, et al.
Molecular Genetics and Metabolism|January 24, 2006
Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneityYanlin Xing, Fukiko Ichida, Taro Matsuoka, et al.
American Journal of Medical Genetics. Part A|August 19, 2015
Exome analysis of a family with Wolff-Parkinson-White syndrome identifies a novel disease locusNeil E Bowles, Chuanchau J Jou, Cammon B Arrington, et al.
Journal of the American College of Cardiology|August 7, 2010
Viral endomyocardial infection is an independent predictor and potentially treatable risk factor for graft loss and coronary vasculopathy in pediatric cardiac transplant recipientsMousumi Moulik, John P Breinholt, William J Dreyer, et al.
Circulation Research|August 19, 2006
Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathyZhao Yang, Neil E Bowles, Steven E Scherer, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|August 21, 2018
Clinical and Echocardiographic Impact of Tafazzin Variants on Dilated Cardiomyopathy Phenotype in Left Ventricular Non-Compaction Patients in Early InfancyKeiichi Hirono, Yukiko Hata, Makoto Nakazawa, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic herniaCammon B Arrington, Steven B Bleyl, Nori Matsunami, et al.
Journal of the American College of Cardiology|December 10, 2003
Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compactionMatteo Vatta, Bhagyalaxmi Mohapatra, Shinawe Jimenez, et al.
Circulation|September 8, 2005
Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in childrenZhao Yang, Colin J McMahon, Liana R Smith, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
International Journal of Cardiology|December 14, 2020
A burden of sarcomere gene variants in fetal-onset patients with left ventricular noncompactionKeiichi Hirono, Yukiko Hata, Sayaka Watanabe Ozawa, et al.
Molecular Genetics and Metabolism|October 22, 2003
Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosisBhagyalaxmi Mohapatra, Shinawe Jimenez, Jiuann Huey Lin, et al.
Molecular Genetics and Metabolism|January 24, 2006
Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneityYanlin Xing, Fukiko Ichida, Taro Matsuoka, et al.
American Journal of Medical Genetics. Part A|August 19, 2015
Exome analysis of a family with Wolff-Parkinson-White syndrome identifies a novel disease locusNeil E Bowles, Chuanchau J Jou, Cammon B Arrington, et al.
Journal of the American College of Cardiology|August 7, 2010
Viral endomyocardial infection is an independent predictor and potentially treatable risk factor for graft loss and coronary vasculopathy in pediatric cardiac transplant recipientsMousumi Moulik, John P Breinholt, William J Dreyer, et al.
Circulation Research|August 19, 2006
Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathyZhao Yang, Neil E Bowles, Steven E Scherer, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|August 21, 2018
Clinical and Echocardiographic Impact of Tafazzin Variants on Dilated Cardiomyopathy Phenotype in Left Ventricular Non-Compaction Patients in Early InfancyKeiichi Hirono, Yukiko Hata, Makoto Nakazawa, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic herniaCammon B Arrington, Steven B Bleyl, Nori Matsunami, et al.
Journal of the American College of Cardiology|December 10, 2003
Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compactionMatteo Vatta, Bhagyalaxmi Mohapatra, Shinawe Jimenez, et al.
Circulation|September 8, 2005
Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in childrenZhao Yang, Colin J McMahon, Liana R Smith, et al.
Pageof 7