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Neurology. Genetics|January 26, 2022
FDX2 and ISCU Gene Variations Lead to Rhabdomyolysis With Distinct Severity and Iron RegulationSebastian Montealegre, Elise Lebigot, Hugo Debruge, et al.Neurology. Genetics|May 24, 2019
Muscular dystrophy with arrhythmia caused by loss-of-function mutations in BVESWillem De Ridder, Isabelle Nelson, Bob Asselbergh, et al.Neurology. Genetics|May 24, 2019
Antisense oligonucleotides: A primerDaniel R Scoles, Eric V Minikel, Stefan M PulstNeurology. Genetics|June 14, 2019
Brain-derived neurotrophic factor, epigenetics in stroke skeletal muscle, and exercise trainingAlice S Ryan, Huichun Xu, Frederick M Ivey, et al.Neurology. Genetics|June 14, 2019
Novel pathogenic VPS13A gene mutations in Japanese patients with chorea-acanthocytosisYoshiaki Nishida, Masayuki Nakamura, Yuka Urata, et al.Neurology. Genetics|June 14, 2019
Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progressionAnna Vihola, Johanna Palmio, Olof Danielsson, et al.Neurology. Genetics|April 24, 2023
Clinical Features and Classification of Neuronal Intranuclear Inclusion DiseaseHongfei Tai, An Wang, Yumei Zhang, et al.Neurology. Genetics|April 24, 2023
Erratum: Expanding the Allelic Heterogeneity of ANO10-Associated Autosomal Recessive Cerebellar AtaxiaNeurology. Genetics|April 24, 2023
Transcriptome and Genome Analysis Uncovers a DMD Structural Variant: A Case ReportChiara Folland, Vijay Ganesh, Ben Weisburd, et al.Neurology. Genetics|April 24, 2023
New-Onset Refractory Status Epilepticus Due to a Novel MT-TF Variant: Time for Acute Genetic Testing Before Treatment?Elisabetta Indelicato, Johannes Pfeilstetter, Michael Zech, et al.Pageof 86