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Journal of Molecular and Cellular Cardiology Plus|June 30, 2025
Ultrastructure analysis of mitochondria, lipid droplet and sarcoplasmic reticulum apposition in human heart failureNadina R Latchman, Tyler L Stevens, Kenneth C Bedi, et al.
The Journal of Biological Chemistry|July 25, 2008
S100A1 and calmodulin compete for the same binding site on ryanodine receptorNathan T Wright, Benjamin L Prosser, Kristen M Varney, et al.
American Journal of Physiology. Cell Physiology|August 7, 2009
Augmentation of Cav1 channel current and action potential duration after uptake of S100A1 in sympathetic ganglion neuronsErick O Hernández-Ochoa, Benjamin L Prosser, Nathan T Wright, et al.
Biorxiv : the Preprint Server for Biology|February 20, 2025
Ultrastructure analysis of mitochondria, lipid droplet and sarcoplasmic reticulum apposition in human heart failureNadina R Latchman, Tyler L Stevens, Kenneth C Bedi, et al.
Neurology. Genetics|January 7, 2025
A Longitudinal Exploration of <i>CACNA1A</i>-Related Hemiplegic Migraine in Children Using Electronic Medical RecordsDonna Schaare, Laina Lusk, Alexis Karlin, et al.
Journal of Child Neurology|May 14, 2025
A Simple Intervention Improves Access to Telemedicine for Spanish-Speaking Families in an Outpatient Pediatric Epilepsy ClinicPamela Pojomovsky McDonnell, Yessenia Ortiz, Nicholas S Abend, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2016
Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsyKatherine L Helbig, Kelly D Farwell Hagman, Deepali N Shinde, et al.
Developmental Medicine and Child Neurology|April 11, 2026
Reliability and stability of cerebral palsy classification scales for individuals with STXBP1- and SYNGAP1-related disordersSamuel R Pierce, Julie M Orlando, Kristin G Cunningham, et al.
Epilepsy Research|March 26, 2013
Genetics of febrile seizure subtypes and syndromes: a twin studyJazmin Eckhaus, Kate M Lawrence, Ingo Helbig, et al.
Human Mutation|April 23, 2022
Computational analysis of neurodevelopmental phenotypes: Harmonization empowers clinical discoveryDavid Lewis-Smith, Shridhar Parthasarathy, Julie Xian, et al.
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