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M Castro Gago

Showing results (151-160 of 157) with videos related to

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Revista De Neurologia|December 11, 2019
[De novo heterozygous mutation in the MBD5 gene associated with bilateral band heterotopia and polymicrogyria]M Castro-Gago, C Gómez-Lado, F Barros-Angueira, et al.
Journal of Inherited Metabolic Disease|January 5, 2002
Mitochondrial myopathy, cardiomyopathy and psychiatric illness in a Spanish family harbouring the mtDNA 3303C > T mutationY Campos, A García, J Eiris, et al.
Revista De Neurologia|October 19, 2004
[Mitochondrial encephalomyopathies and West's syndrome: a frequently underdiagnosed association]O Blanco-Barca, E Pintos-Martínez, A Alonso-Martín, et al.
Revista De Neurologia|January 19, 2000
[Early mitochondrial encephalomyopathy due to complex IV deficiency consistent with Alpers-Huttenlocher syndrome: report of two cases]M Castro-Gago, V González-Conde, M J Fernández-Seara, et al.
Neuromuscular Disorders : NMD|March 27, 1999
Clinical heterogeneity associated with mitochondrial DNA depletion in muscleY Campos, M A Martín, T García-Silva, et al.
Journal of Child Neurology|December 6, 2001
Congenital hydranencephalic-hydrocephalic syndrome with proliferative vasculopathy: a possible relation with mitochondrial dysfunctionM Castro-Gago, E Pintos-Martínez, J Forteza-Vila, et al.
Revista De Neurologia|April 2, 1999
[Rett's syndrome in the Spanish population]M Pineda, A Aracil, A Vernet, et al.
Pageof 16

Showing results (151-160 of 157) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 157 results.
Revista De Neurologia|December 11, 2019
[De novo heterozygous mutation in the MBD5 gene associated with bilateral band heterotopia and polymicrogyria]M Castro-Gago, C Gómez-Lado, F Barros-Angueira, et al.
Journal of Inherited Metabolic Disease|January 5, 2002
Mitochondrial myopathy, cardiomyopathy and psychiatric illness in a Spanish family harbouring the mtDNA 3303C > T mutationY Campos, A García, J Eiris, et al.
Revista De Neurologia|October 19, 2004
[Mitochondrial encephalomyopathies and West's syndrome: a frequently underdiagnosed association]O Blanco-Barca, E Pintos-Martínez, A Alonso-Martín, et al.
Revista De Neurologia|January 19, 2000
[Early mitochondrial encephalomyopathy due to complex IV deficiency consistent with Alpers-Huttenlocher syndrome: report of two cases]M Castro-Gago, V González-Conde, M J Fernández-Seara, et al.
Neuromuscular Disorders : NMD|March 27, 1999
Clinical heterogeneity associated with mitochondrial DNA depletion in muscleY Campos, M A Martín, T García-Silva, et al.
Journal of Child Neurology|December 6, 2001
Congenital hydranencephalic-hydrocephalic syndrome with proliferative vasculopathy: a possible relation with mitochondrial dysfunctionM Castro-Gago, E Pintos-Martínez, J Forteza-Vila, et al.
Revista De Neurologia|April 2, 1999
[Rett's syndrome in the Spanish population]M Pineda, A Aracil, A Vernet, et al.
Pageof 16