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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 28, 2015
Two new cases of serine deficiency disorders treated with l-serineA Brassier, V Valayannopoulos, N Bahi-Buisson, et al.Revue Neurologique|May 2, 2020
Guidance for the care of neuromuscular patients during the COVID-19 pandemic outbreak from the French Rare Health Care for Neuromuscular Diseases NetworkG Solé, E Salort-Campana, Y Pereon, et al.Neuromuscular Disorders : NMD|May 23, 2001
X-linked myopathy with excessive autophagy: a clinicopathological study of five new familiesB Chabrol, D Figarella-Branger, M Coquet, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 25, 2011
[Association of type 1 diabetes mellitus and epilepsy in children. A cohort of 10 cases]E Caietta, C Halbert, A Lépine, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 17, 2021
Clinical characteristics of COVID-19 infection in polyhandicapped persons in FranceM-C Rousseau, M Hully, M Milh, et al.Journal Francais D'Ophtalmologie|April 12, 2008
[Primary exotropia: importance of cerebral MRI]C Baeteman, D Denis, C Loudot, et al.Neuropediatrics|March 17, 2006
Molar tooth sign and superior vermian dysplasia: a radiological, clinical, and genetic studyS Romano, N Boddaert, I Desguerre, et al.Clinical Genetics|April 8, 2017
Comprehensive molecular screening strategy of OCLN in band-like calcification with simplified gyration and polymicrogyriaE M Jenkinson, J H Livingston, M C O'Driscoll, et al.Human Genetics|June 1, 1997
Biochemical and genetic studies of four patients with pyruvate dehydrogenase E1 alpha deficiencyC Marsac, C Benelli, I Desguerre, et al.American Journal of Medical Genetics. Part A|June 15, 2007
Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndromeA Cano, C Rouzier, S Monnot, et al.Pageof 19