MANUEL
CASTRO GAGO
Investigador no período 1993-2023
![Foto de Joaquín](/img/nophoto.png)
Joaquín
Arenas Barbero
Publicacións nas que colabora con Joaquín Arenas Barbero (16)
2016
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Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene
Brain and Development, Vol. 38, Núm. 1, pp. 167-172
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Erratum: Corrigendum to “Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene” (Brain and Development (2016) 38(1) (167–172) (S0387760415001023) (10.1016/j.braindev.2015.05.008))
Brain and Development
2014
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Exome sequencing identifies a CHKB mutation in Spanish patient with Megaconial Congenital Muscular Dystrophy and mtDNA depletion
European Journal of Paediatric Neurology, Vol. 18, Núm. 6, pp. 796-800
2009
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Respiratory chain complex I deficiency in an infant with Ohtahara syndrome
Brain and Development, Vol. 31, Núm. 4, pp. 322-325
2008
2006
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Epidemiology of pediatric mitochondrial respiratory chain disorders in northwest Spain
Pediatric Neurology, Vol. 34, Núm. 3, pp. 204-211
2004
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Mitochondrial encephalomyopathies and West's syndrome: A frequently underdiagnosed association
Revista de Neurologia, Vol. 39, Núm. 7, pp. 618-623
2003
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Lipomatosis simétrica múltiple asociada a polineuropatía, atrofia de cerebelo y citopatía mitocondrial
Revista de Neurologia, Vol. 36, Núm. 11, pp. 1026-1029
2001
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Congenital hydranencephalic-hydrocephalic syndrome with proliferative vasculopathy: A possible relation with mitochondrial dysfunction
Journal of Child Neurology, Vol. 16, Núm. 11, pp. 858-862
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Mitochondrial myopathy, cardiomyopathy and psychiatric illness in a Spanish family harbouring the mtDNA 3303C>T mutation
Journal of Inherited Metabolic Disease, Vol. 24, Núm. 6, pp. 685-687
2000
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Benign congenital myopathy associated with a partial deficiency of complexes I and III of the mitochondrial respiratory chain
Revista de neurologia, Vol. 31, Núm. 9, pp. 838-841
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Mitochondrial encephalomyopathies
Revista de Neurologia
1999
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Congenital hydranencephalic-hydrocephalic syndrome associated with mitochondrial dysfunction
Journal of Child Neurology, Vol. 14, Núm. 2, pp. 131-135
1998
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Clinical heterogeneity associated with mitochondrial DNA depletion in muscle
Neuromuscular Disorders, Vol. 8, Núm. 8, pp. 568-573
1996
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Leber's congenital amaurosis associated with mitochondrial dysfunction
Journal of Child Neurology, Vol. 11, Núm. 2, pp. 108-111
1993
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FORMA INFANTIL PRECOZ DE CITOPATIA MITOCONDRIAL POR DEFICIT DE LOS COMPLEJOS I Y IV DE LA CADENA RESPIRATORIA
Revista Espanola de Pediatria, Vol. 49, Núm. 290, pp. 163-167