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Brain : a Journal of Neurology|September 24, 2013
RAD51 deficiency disrupts the corticospinal lateralization of motor controlCécile Gallea, Traian Popa, Cécile Hubsch, et al.European Journal of Human Genetics : EJHG|May 2, 2013
Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disordersCaroline Nava, Boris Keren, Cyril Mignot, et al.Journal of Medical Genetics|October 19, 2023
Loss-of-function variants in <i>ZEB1</i> cause dominant anomalies of the corpus callosum with favourable cognitive prognosisSolveig Heide, Emanuela Argilli, Stéphanie Valence, et al.Tremor and Other Hyperkinetic Movements (New York, N.Y.)|December 12, 2019
Association of Rare Genetic Variants in Opioid Receptors with Tourette SyndromeChristel Depienne, Sorana Ciura, Oriane Trouillard, et al.Brain : a Journal of Neurology|February 27, 2018
Mechanistic basis of an epistatic interaction reducing age at onset in hereditary spastic paraplegiaTimothy Newton, Rachel Allison, James R Edgar, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2022
Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18-Year StudyAngela Rosenbohm, Hendrik Pott, Mirja Thomsen, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2022
The mitochondrial seryl-tRNA synthetase SARS2 modifies onset in spastic paraplegia type 4Livia Parodi, Mathieu Barbier, Maxime Jacoupy, et al.Journal of Medical Genetics|October 25, 2023
Further characterisation of <i>ARX</i>-related disorders in females due to inherited or de novo variantsMathilde Gras, Solveig Heide, Boris Keren, et al.Tremor and Other Hyperkinetic Movements (New York, N.Y.)|July 17, 2023
Correction: Association of Rare Genetic Variants in Opioid Receptors with Tourette SyndromeChristel Depienne, Sorana Ciura, Oriane Trouillard, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 3, 2023
Intronic <i>FGF14</i> GAA repeat expansions are a common cause of ataxia syndromes with neuropathy and bilateral vestibulopathyDavid Pellerin, Carlo Wilke, Andreas Traschütz, et al.Pageof 18