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Manuel Castro-Gago

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Pediatric Neurology|November 1, 2006
Treatment of mitochondrial encephalomyopathies with a xanthine oxidase inhibitorManuel Castro-Gago, Manuel Oscar Blanco-Barca, María Inés Novo-Rodríguez, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 6, 2014
Exome sequencing identifies a CHKB mutation in Spanish patient with megaconial congenital muscular dystrophy and mtDNA depletionManuel Castro-Gago, David Dacruz-Alvarez, Elena Pintos-Martínez, et al.
Gene|May 17, 2017
Copy number variation analysis of patients with intellectual disability from North-West SpainInés Quintela, Jesús Eirís, Carmen Gómez-Lado, et al.
Hormones (Athens, Greece)|July 26, 2017
Severe neurological abnormalities in a young boy with impaired thyroid hormone sensitivity due to a novel mutation in the MCT8 geneTeresa Rego, Carmen Gomez Lado, Paloma Cabanas Rodríguez, et al.
Journal of Child Neurology|March 23, 2006
Evolution of serum lipids and lipoprotein (a) levels in epileptic children treated with carbamazepine, valproic acid, and phenobarbitalManuel Castro-Gago, María Inés Novo-Rodríguez, Manuel Oscar Blanco-Barca, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 12, 2013
Glutaric aciduria type I: outcome of patients with early- versus late-diagnosisMa Luz Couce, Olalla López-Suárez, Ma Dolores Bóveda, et al.
Orphanet Journal of Rare Diseases|April 29, 2014
Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disordersAna Fernández-Marmiesse, Marcos Morey, Merce Pineda, et al.
Plos One|April 29, 2011
Evolutionary analyses of entire genomes do not support the association of mtDNA mutations with Ras/MAPK pathway syndromesAlberto Gómez-Carballa, María Cerezo, Emilia Balboa, et al.
Nature Genetics|May 1, 2012
Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degenerationJijun Wan, Michael Yourshaw, Hafsa Mamsa, et al.
American Journal of Medical Genetics. Part A|January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Pediatric Neurology|November 1, 2006
Treatment of mitochondrial encephalomyopathies with a xanthine oxidase inhibitorManuel Castro-Gago, Manuel Oscar Blanco-Barca, María Inés Novo-Rodríguez, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 6, 2014
Exome sequencing identifies a CHKB mutation in Spanish patient with megaconial congenital muscular dystrophy and mtDNA depletionManuel Castro-Gago, David Dacruz-Alvarez, Elena Pintos-Martínez, et al.
Gene|May 17, 2017
Copy number variation analysis of patients with intellectual disability from North-West SpainInés Quintela, Jesús Eirís, Carmen Gómez-Lado, et al.
Hormones (Athens, Greece)|July 26, 2017
Severe neurological abnormalities in a young boy with impaired thyroid hormone sensitivity due to a novel mutation in the MCT8 geneTeresa Rego, Carmen Gomez Lado, Paloma Cabanas Rodríguez, et al.
Journal of Child Neurology|March 23, 2006
Evolution of serum lipids and lipoprotein (a) levels in epileptic children treated with carbamazepine, valproic acid, and phenobarbitalManuel Castro-Gago, María Inés Novo-Rodríguez, Manuel Oscar Blanco-Barca, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 12, 2013
Glutaric aciduria type I: outcome of patients with early- versus late-diagnosisMa Luz Couce, Olalla López-Suárez, Ma Dolores Bóveda, et al.
Orphanet Journal of Rare Diseases|April 29, 2014
Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disordersAna Fernández-Marmiesse, Marcos Morey, Merce Pineda, et al.
Plos One|April 29, 2011
Evolutionary analyses of entire genomes do not support the association of mtDNA mutations with Ras/MAPK pathway syndromesAlberto Gómez-Carballa, María Cerezo, Emilia Balboa, et al.
Nature Genetics|May 1, 2012
Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degenerationJijun Wan, Michael Yourshaw, Hafsa Mamsa, et al.
American Journal of Medical Genetics. Part A|January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
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