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Developmental Medicine and Child Neurology|May 23, 2019
Cognitive impairment in children with CACNA1A mutationsVeronique Humbertclaude, Florence Riant, Benjamin Krams, et al.Epilepsia|August 3, 2005
Antiglial cell autoantibodies and childhood epilepsy: a case reportAgathe Roubertie, Hassan Boukhaddaoui, Victor Sieso, et al.Retina (Philadelphia, Pa.)|December 14, 2020
A ROD-CONE DYSTROPHY IS SYSTEMATICALLY ASSOCIATED TO THE RTN4IP1 RECESSIVE OPTIC ATROPHYIsabelle Meunier, Béatrice Bocquet, Majida Charif, et al.Journal of Inherited Metabolic Disease|June 29, 2023
Natural history of GM1 gangliosidosis-Retrospective cohort study of 61 French patients from 1998 to 2019Domitille Laur, Samia Pichard, Soumeya Bekri, et al.Annals of Clinical and Translational Neurology|March 13, 2020
FGF14-related episodic ataxia: delineating the phenotype of Episodic Ataxia type 9Julie Piarroux, Florence Riant, Véronique Humbertclaude, et al.European Journal of Medical Genetics|July 7, 2012
Focal polymicrogyria are associated with submicroscopic chromosomal rearrangements detected by CGH microarray analysisChloe Quelin, Yoann Saillour, Karine Poirier, et al.Frontiers in Neurology|January 29, 2026
French virtual multidisciplinary team meeting for pediatric movement disorders (PMD-vMDT): a three-year surveyMarie-Céline François-Heude, Bérénice Lecardonnel, Matthildi Papathanasiou, et al.Epilepsia|September 27, 2003
FOunder effect in patients with Unverricht-Lundborg disease on reunion islandBruno Moulard, Françoise Darcel, Didier Mignard, et al.Molecular Genetics and Metabolism Reports|March 5, 2026
Incidental maternal glutaric aciduria type I detection through newborn screening: A case reportPierre-Edouard Grillet, Cecilia Marelli, Etienne Mondésert, et al.Molecular Genetics and Metabolism|January 7, 2023
Deep brain stimulation effect in genetic dyskinetic cerebral palsy: The case of ADCY5- related diseaseLaura Cif, Diane Demailly, Claire Gehin, et al.Pageof 14