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Pediatric Neurology|August 10, 2005
Familial arachnoid cystsGema Arriola, Pedro de Castro, Alfonso VerdúBrain & Development|April 12, 2003
Dandy-Walker malformation in an infant with tetrasomy 9pMaría R Cazorla Calleja, Alfonso Verdú, Valentin FélixBrain & Development|September 22, 2009
Early infantile epileptic encephalopathy with unusual favourable outcomeMaría Rosario Cazorla, Alfonso Verdú, Carmen Montes, et al.Pediatric Neurology|April 18, 2007
Neuroimage findings in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiencyMaría R Cazorla, Alfonso Verdú, Celia Pérez-Cerdá, et al.Journal of Paediatrics and Child Health|February 24, 2007
Varicella encephalopathy in immunocompetent childrenAmparo Carreño, Jesús López-Herce, Alfonso Verdú, et al.Neuromuscular Disorders : NMD|January 24, 2009
Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patientAlberto Blázquez, Mari Carmen Gil-Borlado, María Morán, et al.Neuromuscular Disorders : NMD|January 13, 2015
Uniparental disomy as a cause of spinal muscular atrophy and progressive myoclonic epilepsy: phenotypic homogeneity due to the homozygous c.125C>T mutation in ASAH1Beatriz G Giráldez, Rosa Guerrero-López, Laura Ortega-Moreno, et al.Journal of Child Neurology|July 27, 2012
Late infantile neuronal ceroid lipofuscinosis: mutations in the CLN2 gene and clinical course in Spanish patientsMaría S Pérez-Poyato, Mercé Pineda Marfa, Isidre Ferrer Abizanda, et al.Epilepsia|January 29, 2013
Clinical, biochemical, and molecular studies in pyridoxine-dependent epilepsy. Antisense therapy as possible new therapeutic optionBelén Pérez, Luis González Gutiérrez-Solana, Alfonso Verdú, et al.Pageof 1