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Brain Research. Molecular Brain Research|December 8, 2004
Human blood genomics: distinct profiles for gender, age and neurofibromatosis type 1Yang Tang, Aigang Lu, Ruiqiong Ran, et al.Journal of Neuromuscular Diseases|February 20, 2025
A Parent Project Muscular Dystrophy-sponsored International Workshop Report on Endocrine and Bone Issues in Patients with Duchenne Muscular Dystrophy: An Ever-changing LandscapeLeanne M Ward, David R Weber, Sze Choong Wong, et al.Neurology|February 1, 2023
DMD Genotypes and Motor Function in Duchenne Muscular Dystrophy: A Multi-institution Meta-analysis With Implications for Clinical TrialsFrancesco Muntoni, James Signorovitch, Gautam Sajeev, et al.Plos One|May 20, 2025
Frontal cortex hyperactivation and gamma desynchrony in Fragile X syndrome: Correlates of auditory hypersensitivityErnest V Pedapati, Lauren E Ethridge, Yanchen Liu, et al.Biorxiv : the Preprint Server for Biology|June 25, 2024
Frontal Cortex Hyperactivation and Gamma Desynchrony in Fragile X Syndrome: Correlates of Auditory HypersensitivityErnest V Pedapati, Lauren E Ethridge, Yanchen Liu, et al.Lancet (London, England)|March 13, 2022
Repeated intravenous cardiosphere-derived cell therapy in late-stage Duchenne muscular dystrophy (HOPE-2): a multicentre, randomised, double-blind, placebo-controlled, phase 2 trialCraig M McDonald, Eduardo Marbán, Suzanne Hendrix, et al.European Journal of Neurology|October 25, 2022
The spectrum of functional tic-like behaviours: Data from an international registryDavide Martino, Tammy Hedderly, Tara Murphy, et al.European Journal of Neurology|January 1, 2023
European Society for the Study of Tourette Syndrome 2022 criteria for clinical diagnosis of functional tic-like behaviours: International consensus from experts in tic disordersTamara Pringsheim, Christos Ganos, Christelle Nilles, et al.Neurology. Genetics|February 25, 2025
The Spastic Paraplegia-Centers of Excellence Research Network (SP-CERN): Clinical Trial Readiness for Hereditary Spastic ParaplegiaLuca Schierbaum, Vicente Quiroz, Kathryn Yang, et al.Human Mutation|June 12, 2008
Molecular and clinical genetics of mitochondrial diseases due to POLG mutationsLee-Jun C Wong, Robert K Naviaux, Nicola Brunetti-Pierri, et al.Pageof 21