Showing results (1181-1190 of 1,478) with videos related to

Sort By:
Pageof 148
Journal of Medical Genetics|April 11, 2013
Troponin activator augments muscle force in nemaline myopathy patients with nebulin mutationsJosine Marieke de Winter, Danielle Buck, Carlos Hidalgo, et al.
Advanced Genetics (Hoboken, N.J.)|March 13, 2023
Mendelian Disorders in an Interstitial Cystitis/Bladder Pain Syndrome CohortElicia Estrella, Shira Rockowitz, Marielle Thorne, et al.
Annals of Neurology|July 6, 2004
Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutationsPankaj B Agrawal, Corinne D Strickland, Charles Midgett, et al.
Journal of Vascular and Interventional Radiology : JVIR|March 26, 2013
Changes of cine cerebrospinal fluid dynamics in patients with multiple sclerosis treated with percutaneous transluminal angioplasty: a case-control studyRobert Zivadinov, Christopher Magnano, Roberto Galeotti, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 22, 2016
Rich-Club Organization in Effective Connectivity among Cortical NeuronsSunny Nigam, Masanori Shimono, Shinya Ito, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 28, 2011
Spinal cord Toll-like receptor 4 mediates inflammatory and neuropathic hypersensitivity in male but not female miceRobert E Sorge, Michael L LaCroix-Fralish, Alexander H Tuttle, et al.
Frontiers in Digital Health|June 1, 2026
A maturity model framework for federated networks of trusted research environmentsJasper H C Luong, Jillian Beggs, Jason Ferris, et al.
Neurology. Genetics|July 15, 2025
Retrospective Cohort Analysis of Clinical, Molecular, and Histopathologic Characteristics of 275 Patients With Nemaline MyopathyClara Hildebrandt, Casie A Genetti, Tanya Logvinenko, et al.
The British Journal of Psychiatry : the Journal of Mental Science|March 7, 2022
Variations in COVID-19 vaccination uptake among people in receipt of psychotropic drugs: cross-sectional analysis of a national population-based prospective cohortSiobhán Murphy, Dermot O'Reilly, Rhiannon K Owen, et al.
European Journal of Medical Genetics|November 2, 2013
Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities - support for the role of K(ATP) channels in this conditionCatherine A Brownstein, Meghan C Towne, Lovelace J Luquette, et al.
Pageof 148