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Future Cardiology|September 17, 2021
Living with hypertrophic cardiomyopathy: a patient's perspectiveWendy Borsari, Lindsay Davis, Eric Meiers, et al.
BMC Medical Genetics|March 31, 2012
Functional effects of the TMEM43 Ser358Leu mutation in the pathogenesis of arrhythmogenic right ventricular cardiomyopathyRevathi Rajkumar, John C Sembrat, Barbara McDonough, et al.
European Journal of Human Genetics : EJHG|July 7, 2024
Genetic therapies for cardiomyopathy: survey of attitudes of the patient community for the CureHeart projectElizabeth Ormondroyd, Christopher Grace, Wendy Borsari, et al.
Stroke|December 10, 2008
Genomewide linkage in a large Caucasian family maps a new locus for intracranial aneurysms to chromosome 13qTeresa Santiago-Sim, Steven R Depalma, Kevin L Ju, et al.
Circulation|June 26, 2002
Assessment of diastolic function with Doppler tissue imaging to predict genotype in preclinical hypertrophic cardiomyopathyCarolyn Y Ho, Nancy K Sweitzer, Barbara McDonough, et al.
The New England Journal of Medicine|April 12, 2008
Shared genetic causes of cardiac hypertrophy in children and adultsHiroyuki Morita, Heidi L Rehm, Andres Menesses, et al.
Annals of Neurology|April 29, 2014
UBQLN2 mutation causing heterogeneous X-linked dominant neurodegenerationAkl C Fahed, Barbara McDonough, Cynthia M Gouvion, et al.
Circulation|May 3, 2006
Novel locus for an inherited cardiomyopathy maps to chromosome 7Lei Song, Steven R DePalma, Maria Kharlap, et al.
Circulation. Cardiovascular Genetics|September 6, 2012
Subtle abnormalities in contractile function are an early manifestation of sarcomere mutations in dilated cardiomyopathyNeal K Lakdawala, Jens J Thune, Steven D Colan, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 7, 2017
Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicingKaoru Ito, Parth N Patel, Joshua M Gorham, et al.
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