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Stem Cell Research & Therapy|November 4, 2025
Apremilast improves cardiomyocyte cohesion and arrhythmia in different models for arrhythmogenic cardiomyopathyKonstanze Stangner, Orsela Dervishi, Janina Kuhnert, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|December 9, 2024
Eccentric hypertrophy impairs outcome after TAVRR Thalmann, V Obermeier, Dominik S Westphal, et al.
American Journal of Medical Genetics. Part A|November 25, 2022
Genetic and phenotypic spectrum in the NONO-associated syndromic disorderFranziska Roessler, Anita E Beck, Ball Susie, et al.
Genome Medicine|April 13, 2021
Functional interpretation of ATAD3A variants in neuro-mitochondrial phenotypesZheng Yie Yap, Yo Han Park, Saskia B Wortmann, et al.
Annals of Internal Medicine|December 23, 2024
Impaired Wnt/Planar Cell Polarity Signaling in Yellow Nail SyndromeAlina Kurolap, Chofit Chai Gadot, Orly Eshach Adiv, et al.
European Journal of Human Genetics : EJHG|April 2, 2024
De novo variants in GABRA4 are associated with a neurological phenotype including developmental delay, behavioral abnormalities and epilepsySamin A Sajan, Ralph Gradisch, Florian D Vogel, et al.
Clinical Genetics|February 23, 2021
De novo variants in neurodevelopmental disorders-experiences from a tertiary care centerTheresa Brunet, Robert Jech, Melanie Brugger, et al.
European Heart Journal|July 2, 2025
Long QT syndrome in children and adolescents: risk factors and outcomes in a large German cohortLea Lippert, Tobias Burkard, Franziska Markel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 26, 2019
Defining clinical subgroups and genotype-phenotype correlations in NBAS-associated disease across 110 patientsChristian Staufner, Bianca Peters, Matias Wagner, et al.
Nature Cardiovascular Research|August 28, 2024
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathyNadine Spielmann, Gregor Miller, Tudor I Oprea, et al.
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