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Revista De Neurologia
|
November 30, 2013
[Juvenile Alpers disease]
Laura Pérez-Gay, Carmen Gómez-Lado, Jesús Eirís-Puñal, et al.
Gaceta Sanitaria
|
March 2, 2015
[Epidemiology of Lyme disease in a healthcare area in north-west Spain]
María Esther Vázquez-López, Robustiano Pego-Reigosa, Carolina Díez-Morrondo, et al.
Journal of Child Neurology
|
June 7, 2011
The influence of valproic acid and carbamazepine treatment on serum biotin and zinc levels and on biotinidase activity
Manuel Castro-Gago, Laura Pérez-Gay, Carmen Gómez-Lado, et al.
Pediatric Neurology
|
March 1, 2006
Epidemiology of pediatric mitochondrial respiratory chain disorders in northwest Spain
Manuel Castro-Gago, Manuel O Blanco-Barca, Yolanda Campos-González, et al.
Revista De Neurologia
|
October 24, 2013
[Microdeletion 2q23.1 and syndromic findings]
Laura Pérez-Gay, Carmen Gómez-Lado, Jesús Eirís-Puñal, et al.
Brain & Development
|
May 4, 2016
Corrigendum to "Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene" [Brain Dev. 38 (2016) 167-172]
Manuel Castro-Gago, David Dacruz-Alvarez, Elena Pintos-Martínez, et al.
American Journal of Medical Genetics. Part A
|
August 19, 2015
Interstitial microdeletions including the chromosome band 4q13.2 and the UBA6 gene as possible causes of intellectual disability and behavior disorder
Ines Quintela, Francisco Barros, Montse Fernandez-Prieto, et al.
Journal of Child Neurology
|
March 29, 2005
Neurogenic arthrogryposis multiplex congenita and velopharyngeal incompetence associated with chromosome 22q11.2 deletion
Manuel Castro-Gago, José Mariá Iglesias-Meleiro, Manuel Oscar Blanco-Barca, et al.
Brain & Development
|
May 27, 2015
Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene
Manuel Castro-Gago, David Dacruz-Alvarez, Elena Pintos-Martínez, et al.
Journal of Child Neurology
|
February 24, 2011
Primary adenosine monophosphate (AMP) deaminase deficiency in a hypotonic infant
Manuel Castro-Gago, Carmen Gómez-Lado, Laura Pérez-Gay, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 50) with videos related to
Sort By:
Page
of 5
Revista De Neurologia
|
November 30, 2013
[Juvenile Alpers disease]
Laura Pérez-Gay, Carmen Gómez-Lado, Jesús Eirís-Puñal, et al.
Gaceta Sanitaria
|
March 2, 2015
[Epidemiology of Lyme disease in a healthcare area in north-west Spain]
María Esther Vázquez-López, Robustiano Pego-Reigosa, Carolina Díez-Morrondo, et al.
Journal of Child Neurology
|
June 7, 2011
The influence of valproic acid and carbamazepine treatment on serum biotin and zinc levels and on biotinidase activity
Manuel Castro-Gago, Laura Pérez-Gay, Carmen Gómez-Lado, et al.
Pediatric Neurology
|
March 1, 2006
Epidemiology of pediatric mitochondrial respiratory chain disorders in northwest Spain
Manuel Castro-Gago, Manuel O Blanco-Barca, Yolanda Campos-González, et al.
Revista De Neurologia
|
October 24, 2013
[Microdeletion 2q23.1 and syndromic findings]
Laura Pérez-Gay, Carmen Gómez-Lado, Jesús Eirís-Puñal, et al.
Brain & Development
|
May 4, 2016
Corrigendum to "Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene" [Brain Dev. 38 (2016) 167-172]
Manuel Castro-Gago, David Dacruz-Alvarez, Elena Pintos-Martínez, et al.
American Journal of Medical Genetics. Part A
|
August 19, 2015
Interstitial microdeletions including the chromosome band 4q13.2 and the UBA6 gene as possible causes of intellectual disability and behavior disorder
Ines Quintela, Francisco Barros, Montse Fernandez-Prieto, et al.
Journal of Child Neurology
|
March 29, 2005
Neurogenic arthrogryposis multiplex congenita and velopharyngeal incompetence associated with chromosome 22q11.2 deletion
Manuel Castro-Gago, José Mariá Iglesias-Meleiro, Manuel Oscar Blanco-Barca, et al.
Brain & Development
|
May 27, 2015
Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene
Manuel Castro-Gago, David Dacruz-Alvarez, Elena Pintos-Martínez, et al.
Journal of Child Neurology
|
February 24, 2011
Primary adenosine monophosphate (AMP) deaminase deficiency in a hypotonic infant
Manuel Castro-Gago, Carmen Gómez-Lado, Laura Pérez-Gay, et al.
Page
of 5