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Annals of Clinical and Translational Neurology|April 25, 2020
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiencyDario Ronchi, Edoardo Monfrini, Sara Bonato, et al.Human Mutation|May 12, 2009
A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological functionChiara Vantaggiato, Francesca Redaelli, Sestina Falcone, et al.Scientific Reports|April 14, 2022
Clinical and genetic features of a cohort of patients with MFN2-related neuropathyElena Abati, Arianna Manini, Daniele Velardo, et al.Journal of Neurology|February 26, 2009
Candidate gene analysis of selectin cluster in patients with multiple sclerosisChiara Fenoglio, Diego Scalabrini, Laura Piccio, et al.Journal of the Neurological Sciences|November 13, 2008
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunctionStefania Corti, Chiara Donadoni, Dario Ronchi, et al.Journal of Neurology|December 17, 2013
Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesisAndrea Citterio, Alessia Arnoldi, Elena Panzeri, et al.Cancer Research|April 6, 2007
Effect of human skin-derived stem cells on vessel architecture, tumor growth, and tumor invasion in brain tumor animal modelsFederica Pisati, Marzia Belicchi, Francesco Acerbi, et al.Science Translational Medicine|December 21, 2012
Genetic correction of human induced pluripotent stem cells from patients with spinal muscular atrophyStefania Corti, Monica Nizzardo, Chiara Simone, et al.Pediatric Neurology|March 1, 2006
Agenesis of the corpus callosum: clinical and genetic study in 63 young patientsMaria Francesca Bedeschi, Maria Clara Bonaglia, Rita Grasso, et al.Journal of Cellular and Molecular Medicine|July 26, 2022
MicroRNAs as serum biomarkers in Becker muscular dystrophyDelia Gagliardi, Mafalda Rizzuti, Roberta Brusa, et al.Pageof 34