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Revista De Neurologia|September 19, 2006
[Pyruvate dehydrogenase deficit associated to the C515T mutation in exon 6 of the E1alpha gene]O Blanco-Barca, C Gomez-Lado, E Rodrigo-Saez, et al.Revista De Neurologia|October 29, 2003
[Phenotypic variability of deletion 22q11.2. An analysis of 16 observations with special emphasis on the neurological manifestations]J Eirís-Puñal, J M Iglesias-Meleiro, M O Blanco-Barca, et al.Revista De Neurologia|June 17, 2003
[Multiple symmetric lipomatosis associated to polyneuropathology, atrophy of the cerebellum and mitochondrial cytopathy]M Castro-Gago, A Alonso, E Pintos-Martínez, et al.Revista De Neurologia|October 19, 2004
[Mitochondrial encephalomyopathies and West's syndrome: a frequently underdiagnosed association]O Blanco-Barca, E Pintos-Martínez, A Alonso-Martín, et al.Neurologia|March 30, 2026
Delphy study on epidemiology, clinical management, disease burden, and treatment in paediatric patients with Duchenne muscular dystrophy in SpainI Pitarch-Castellano, C I Ortez-González, A Nascimento-Osorio, et al.Pageof 2