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Frontiers in Neurology|September 24, 2021
Sodium Levels Predict Disability at Discharge in Guillain-Barré Syndrome: A Retrospective Cohort StudyDelia Gagliardi, Irene Faravelli, Manuel Alfredo Podestà, et al.BMC Neurology|August 28, 2020
Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENGDavide Villa, Claudia Cinnante, Gloria Valcamonica, et al.Journal of Neuroscience Research|August 17, 2018
Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1Michela Ripolone, Valeria Lucchini, Dario Ronchi, et al.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.American Journal of Human Genetics|June 23, 2015
RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial EncephalomyopathyAurelio Reyes, Laura Melchionda, Alessia Nasca, et al.Parkinsonism & Related Disorders|March 10, 2019
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathyEdoardo Monfrini, Letizia Straniero, Sara Bonato, et al.Pharmacological Research|February 7, 2012
Nitric oxide donor and non steroidal anti inflammatory drugs as a therapy for muscular dystrophies: evidence from a safety study with pilot efficacy measures in adult dystrophic patientsMaria Grazia D'Angelo, Sandra Gandossini, Filippo Martinelli Boneschi, et al.Brain : a Journal of Neurology|September 14, 2013
Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15Chiara Vantaggiato, Claudia Crimella, Giovanni Airoldi, et al.Journal of Autoimmunity|September 30, 2021
Consumption of complement in a 26-year-old woman with severe thrombotic thrombocytopenia after ChAdOx1 nCov-19 vaccinationMassimo Cugno, Paolo Macor, Mara Giordano, et al.Human Molecular Genetics|October 11, 2019
Loss of the nucleoporin Aladin in central nervous system and fibroblasts of Allgrove SyndromeGiacomo Bitetto, Dario Ronchi, Sara Bonato, et al.Pageof 3