Manuel Gago-Castro

Santiago De Compostela, GA, Spain

Last Updated: 09/26/2026

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Found 31 publications

De novo heterozygous mutation in the MBD5 gene associated with bilateral band heterotopia and polymicrogyria

De novo heterozygous mutation in the MBD5 gene associated with bilateral band heterotopia and polymicrogyria

Journal: Revista de neurologia

Published: December 11, 2019

Treatment of choline kinase beta deficiency with citicoline

Treatment of choline kinase beta deficiency with citicoline

Journal: Revista de neurologia

Published: June 21, 2018

Severe neurological abnormalities in a young boy with impaired thyroid hormone sensitivity due to a novel mutation in the MCT8 gene.

Severe neurological abnormalities in a young boy with impaired thyroid hormone sensitivity due to a novel mutation in the MCT8 gene.

Journal: Hormones (Athens, Greece)

Published: March 06, 2017

Copy number variation analysis of patients with intellectual disability from North-West Spain.

Copy number variation analysis of patients with intellectual disability from North-West Spain.

Journal: Gene

Published: February 10, 2017

Retrospective analysis of the effect of a vagus nerve stimulator implanted in paediatric patients with refractory epilepsy

Retrospective analysis of the effect of a vagus nerve stimulator implanted in paediatric patients with refractory epilepsy

Journal: Revista de neurologia

Published: June 28, 2016

Corrigendum to "Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene" [Brain Dev. 38 (2016) 167-172].

Corrigendum to "Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene" [Brain Dev. 38 (2016) 167-172].

Journal: Brain & development

Published: May 04, 2016

Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes

Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes

Journal: Revista de neurologia

Published: September 10, 2015

Deletion of the RPS6KA3 gene in a female with a classical phenotype of Coffin-Lowry syndrome including stimulus-induced drop attacks

Deletion of the RPS6KA3 gene in a female with a classical phenotype of Coffin-Lowry syndrome including stimulus-induced drop attacks

Journal: Revista de neurologia

Published: July 10, 2015

Articular manifestations in patients with Lyme disease.

Articular manifestations in patients with Lyme disease.

Journal: Reumatologia clinica

Published: June 25, 2015

Lyme disease in paediatrics

Lyme disease in paediatrics

Journal: Anales de pediatria (Barcelona, Spain : 2003)

Published: February 11, 2015

Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene.

Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene.

Journal: Brain & development

Published: February 10, 2015

Dravet syndrome and mitochondrial disease, are they comorbid pathologies?

Dravet syndrome and mitochondrial disease, are they comorbid pathologies?

Journal: Revista de neurologia

Published: January 28, 2015

Showing 1-12 of 31

Last Updated: 09/26/2026