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Metabolites|December 27, 2024
The Role of Beta-Hydroxybutyrate in Mitigating the Inflammatory and Metabolic Consequences of Uric AcidNicole P Remund, John G Larsen, Marley J Shin, et al.JCO Precision Oncology|January 23, 2018
DNA Methylation-Based Classifier for Accurate Molecular Diagnosis of Bone SarcomasS Peter Wu, Benjamin T Cooper, Fang Bu, et al.Human Mutation|June 29, 2010
Recessive mutations in RYR1 are a common cause of congenital fiber type disproportionNigel F Clarke, Leigh B Waddell, Sandra T Cooper, et al.ESC Heart Failure|February 19, 2026
Impact of cannabidiol on myocardial recovery in patients with acute myocarditis: primary results of the ARCHER studyDennis M McNamara, Leslie T Cooper, Matthias G Friedrich, et al.Neurology|October 28, 2025
Expert Consensus on Genetic Diagnostic Approaches for Patients With Limb-Girdle Muscular DystrophyVolker Straub, Amanda R Clause, Sandra Donkervoort, et al.Journal of Neuropathology and Experimental Neurology|March 18, 2011
Dysferlin, annexin A1, and mitsugumin 53 are upregulated in muscular dystrophy and localize to longitudinal tubules of the T-system with stretchLeigh B Waddell, Frances A Lemckert, Xi F Zheng, et al.International Journal of Cardiology|July 9, 2023
Cardiac fludeoxyglucose-18 positron emission tomography in genotype-positive arrhythmogenic cardiomyopathyRaquel Neves, Andrew S Tseng, Ramin Garmany, et al.Frontiers in Cardiovascular Medicine|February 6, 2023
Sex and age differences in sST2 in cardiovascular diseaseDanielle J Beetler, Katelyn A Bruno, Damian N Di Florio, et al.Nanoscale Advances|July 13, 2026
Isolation of extracellular vesicles from minimal volume ascites fluid using strong anion exchange beadsTyler T Cooper, Lorena Veliz, Farzaneh Afzali, et al.Neurology|September 4, 2016
Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndromeGina L O'Grady, Corien Verschuuren, Michaela Yuen, et al.Pageof 84