Showing results (221-230 of 855) with videos related to

Sort By:
Pageof 86
Neurology. Genetics|September 3, 2021
Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish CohortAyşe Candayan, Arman Çakar, Gulshan Yunisova, et al.
Neurology. Genetics|July 20, 2016
APOE polymorphisms influence longitudinal lipid trends preceding intracerebral hemorrhageChia-Ling Phuah, Miriam R Raffeld, Alison M Ayres, et al.
Neurology. Genetics|July 20, 2016
Progressive myoclonus epilepsy associated with SACS gene mutationsFábio A Nascimento, Laura Canafoglia, Danah Aljaafari, et al.
Neurology. Genetics|June 18, 2020
Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophyMajida Charif, Arnaud Chevrollier, Naïg Gueguen, et al.
Neurology. Genetics|August 19, 2016
Pathogenic mtDNA mutations causing mitochondrial myopathy: The need for muscle biopsySteven A Hardy, Emma L Blakely, Andrew I Purvis, et al.
Neurology. Genetics|September 5, 2025
Vascular NOTCH3 Deposition Load: Association With NOTCH3 Genotype and CADASIL Disease SeverityYu-Wen Cheng, Chih-Hao Chen, Chi-Chao Chao, et al.
Neurology. Genetics|May 12, 2021
Expanding the Spectrum of Movement Disorders Associated With C9orf72 Hexanucleotide ExpansionsCarlos Estevez-Fraga, Francesca Magrinelli, Davina Hensman Moss, et al.
Neurology. Genetics|May 14, 2021
Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor SubtypesIsabel Alfradique-Dunham, Rami Al-Ouran, Rainer von Coelln, et al.
Neurology. Genetics|August 4, 2021
Mutation in ZDHHC15 Leads to Hypotonic Cerebral Palsy, Autism, Epilepsy, and Intellectual DisabilitySara A Lewis, Somayeh Bakhtiari, Jennifer Heim, et al.
Neurology. Genetics|November 23, 2016
De novo FGF12 mutation in 2 patients with neonatal-onset epilepsyIlaria Guella, Linda Huh, Marna B McKenzie, et al.
Pageof 86