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Clinical Genetics|June 28, 2019
FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype-phenotype correlationsFlavie Ader, Pascal De Groote, Patricia Réant, et al.
International Journal of Cardiology|July 10, 2021
A novel risk model for predicting potentially life-threatening arrhythmias in non-ischemic dilated cardiomyopathy (DCM-SVA risk)Elham Kayvanpour, Arjan Sammani, Farbod Sedaghat-Hamedani, et al.
Genome Biology|September 15, 2017
Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathyMatthias Heinig, Michiel E Adriaens, Sebastian Schafer, et al.
Plos One|March 16, 2017
Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathyUlrike Esslinger, Sophie Garnier, Agathe Korniat, et al.
Plos One|February 15, 2020
Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathyUlrike Esslinger, Sophie Garnier, Agathe Korniat, et al.
Circulation. Genomic and Precision Medicine|March 16, 2018
Genetic Reduction in Left Ventricular Protein Kinase C-α and Adverse Ventricular Remodeling in Human SubjectsRay Hu, Michael P Morley, Jeffrey Brandimarto, et al.
Journal of the American College of Cardiology|November 17, 2018
Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) MutationsFernando Domínguez, Sofía Cuenca, Zofia Bilińska, et al.
Plos Genetics|October 27, 2010
Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathyKlaus Stark, Ulrike B Esslinger, Wibke Reinhard, et al.
European Heart Journal|April 5, 2011
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathyEric Villard, Claire Perret, Françoise Gary, et al.
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