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Human Mutation|October 15, 2008
Analysis of the DYSF mutational spectrum in a large cohort of patientsMartin Krahn, Christophe Béroud, Véronique Labelle, et al.
American Journal of Respiratory and Critical Care Medicine|May 23, 2023
Cardiorespiratory Monitoring Data to Predict Respiratory Outcomes in Extremely Preterm InfantsNamasivayam Ambalavanan, Debra E Weese-Mayer, Anna Maria Hibbs, et al.
JACC. Clinical Electrophysiology|November 24, 2018
Early Repolarization Pattern Inheritance in the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry (CASPER)Navraj Malhi, Petsy P So, Christopher C Cheung, et al.
European Journal of Human Genetics : EJHG|December 16, 2018
A National French consensus on gene lists for the diagnosis of myopathies using next-generation sequencingMartin Krahn, Valérie Biancalana, Mathieu Cerino, et al.
JACC. Clinical Electrophysiology|December 21, 2024
International Multicenter Cohort Study on Beta-Blocker-Free Treatment Strategies for Catecholaminergic Polymorphic Ventricular Tachycardia PatientsRaquel Neves, Sahej Bains, J Martijn Bos, et al.
Neurology. Genetics|December 22, 2017
Clinical heterogeneity and phenotype/genotype findings in 5 families with GYG1 deficiencyRabah Ben Yaou, Aurélie Hubert, Isabelle Nelson, et al.
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