Ó. García-Campos

Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening program

C. Pérez-Cerdá, B. Merinero, M. Ugarte, 2019, European Journal of Human Genetics.

Novel mutation in STXBP1 gene in a patient with non-lesional Ohtahara syndrome.

J. Serratosa, B. G. Giráldez, R. Guerrero‐López, 2016, Neurologia.

Acute Striatal Necrosis in Hemiplegic Migraine With de Novo CACNA1A Mutation

B. Cormand, A. Macaya, M. García-Silva, 2011, Headache.

Acute Striatal Necrosis in Hemiplegic Migraine With de Novo CACNA 1 A Mutationhead

B. Cormand, A. Macaya, M. García-Silva, 2011 .

Uniparental disomy as a cause of spinal muscular atrophy and progressive myoclonic epilepsy: Phenotypic homogeneity due to the homozygous c.125C>T mutation in ASAH1

J. Serratosa, R. Guerrero‐López, J. Pardal-Fernández, 2015, Neuromuscular Disorders.

Molecular characterization of congenital myasthenic syndromes in Spain

J. Senderek, D. Beeson, T. Evangelista, 2017, Neuromuscular Disorders.

Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening program

C. Pérez-Cerdá, B. Merinero, M. Ugarte, 2019, European Journal of Human Genetics.

COVID-19 in children with neuromuscular disorders

C. Ortez, D. Gómez-Andrés, S. Pascual-Pascual, 2021, Journal of Neurology.