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Neurologia (Barcelona, Spain)|March 17, 2007
[Hepatomioneuropathy secondary to mitochondrial DNA depletion]M O Blanco-Barca, C Gómez-Lado, Y Campos-González, et al.Revista De Neurologia|October 9, 2003
[Duplication of the PLP gene and the classical form of Pelizaeus-Merzbacher disease]M O Blanco-Barca, J Eirís-Puñal, C Soler-Regal, et al.Revista De Neurologia|December 29, 2000
[Benign congenital myopathy associated with a partial deficiency of complexes I and III of the mitochondrial respiratory chain]]M Castro-Gago, J Eirís, E Pintos, et al.Pediatric Neurology|April 28, 2006
Myostatin expression in muscular dystrophies and mitochondrial encephalomyopathiesManuel Castro-Gago, Manuel O Blanco-Barca, Jesús Eiris-Puñal, et al.Revista De Neurologia|February 14, 2004
[Hypomelanosis of Ito. A possibly under-diagnosed heterogeneous neurocutaneous syndrome]C Gómez-Lado, J Eirís-Puñal, O Blanco-Barca, et al.Revista De Neurologia|May 18, 2005
[Benign idiopathic external hydrocephalus (benign subdural collection) in 39 children: its natural history and relation to familial macrocephaly]M Castro-Gago, C Pérez-Gómez, M I Novo-Rodríguez, et al.Pediatric Neurology|March 1, 2006
Epidemiology of pediatric mitochondrial respiratory chain disorders in northwest SpainManuel Castro-Gago, Manuel O Blanco-Barca, Yolanda Campos-González, et al.Revista De Neurologia|July 16, 2003
[Mixed hypotonia, neurological regression and atrophy of the cerebellum: manifestations that suggest infantile neuroaxonal dystrophy]M O Blanco-Barca, J Eiris-Puñal, J Peña-Guitian, et al.Revista De Neurologia|June 18, 2004
[Smith-Magenis syndrome: a report of two new cases and an approximation to their characteristic behavioural phenotype]O Blanco-Barca, M Gallego-Blanco, C Ruiz-Ponte, et al.Anales De Pediatria (Barcelona, Spain : 2003)|February 11, 2005
[Aicardi-Goutières syndrome: report of two new cases]M O Blanco-Barca, M C Curros Novo, A Alvarez Moreno, et al.Pageof 2