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E Pintos-Martínez

Showing results (1-10 of 16) with videos related to

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Journal of Neurosurgical Sciences|March 29, 2000
Intradural cervical chordoma. Case reportM Gelabert-González, E Pintos-Martínez, A Caparrini-Escondrillas, et al.
Neurocirugia (Asturias, Spain)|January 17, 2003
[Cemento-ossifying fibroma of the skull]M Gelabert-González, J Fernández-Villa, E Pintos-Martínez, et al.
Revista De Neurologia|June 1, 2002
[Muscular dystrophy due to a deficit of gamma-sarcoglycan. A report of three patients with the Delta-521t mutation]J Eirís-Puñal, E Pintos-Martínez, A Lasa, et al.
Revista De Neurologia|June 8, 2001
[Early onset adhalinopathy (LGMD2D) mimicking congenital muscular dystrophy]M Castro-Gago, M I Novo-Rodríguez, E Pintos-Martínez, et al.
Revista De Neurologia|September 21, 2000
[Mitochondrial encephalopathies]M Castro-Gago, M I Novo-Rodríguez, E Pintos-Martínez, et al.
Gastroenterologia Y Hepatologia|June 20, 2001
[Epidermoid cyst: a rare cause of cystic liver disease]J Fernández-Castroagudín, M Bustamante Montalvo, M Delgado Blanco, et al.
Revista De Neurologia|March 8, 2007
[Pontocerebellar hypoplasia type 1: a case report]C Gómez-Lado, G Landín-Iglesias, E Pintos-Martínez, et al.
Revista De Neurologia|October 21, 1999
[Severe form of juvenile type II glycogenosis in a compound-heterozygous boy (Tyr-292--> Cys/Arg-854-->Stop)]M Castro-Gago, J Eirís-Puñal, A Rodríguez-Núñez, et al.
Journal of Child Neurology|March 1, 1996
Leber's congenital amaurosis associated with mitochondrial dysfunctionM Castro-Gago, E Pintos-Martínez, A Beiras-Iglesias, et al.
Revista De Neurologia|October 17, 1998
[Western type cerebro-muscular dystrophy and congenital merosin deficiency muscular dystrophy: two terms for the same disorder]M Castro-Gago, M I Novo-Rodríguez, E Pintos-Martínez, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Journal of Neurosurgical Sciences|March 29, 2000
Intradural cervical chordoma. Case reportM Gelabert-González, E Pintos-Martínez, A Caparrini-Escondrillas, et al.
Neurocirugia (Asturias, Spain)|January 17, 2003
[Cemento-ossifying fibroma of the skull]M Gelabert-González, J Fernández-Villa, E Pintos-Martínez, et al.
Revista De Neurologia|June 1, 2002
[Muscular dystrophy due to a deficit of gamma-sarcoglycan. A report of three patients with the Delta-521t mutation]J Eirís-Puñal, E Pintos-Martínez, A Lasa, et al.
Revista De Neurologia|June 8, 2001
[Early onset adhalinopathy (LGMD2D) mimicking congenital muscular dystrophy]M Castro-Gago, M I Novo-Rodríguez, E Pintos-Martínez, et al.
Revista De Neurologia|September 21, 2000
[Mitochondrial encephalopathies]M Castro-Gago, M I Novo-Rodríguez, E Pintos-Martínez, et al.
Gastroenterologia Y Hepatologia|June 20, 2001
[Epidermoid cyst: a rare cause of cystic liver disease]J Fernández-Castroagudín, M Bustamante Montalvo, M Delgado Blanco, et al.
Revista De Neurologia|March 8, 2007
[Pontocerebellar hypoplasia type 1: a case report]C Gómez-Lado, G Landín-Iglesias, E Pintos-Martínez, et al.
Revista De Neurologia|October 21, 1999
[Severe form of juvenile type II glycogenosis in a compound-heterozygous boy (Tyr-292--> Cys/Arg-854-->Stop)]M Castro-Gago, J Eirís-Puñal, A Rodríguez-Núñez, et al.
Journal of Child Neurology|March 1, 1996
Leber's congenital amaurosis associated with mitochondrial dysfunctionM Castro-Gago, E Pintos-Martínez, A Beiras-Iglesias, et al.
Revista De Neurologia|October 17, 1998
[Western type cerebro-muscular dystrophy and congenital merosin deficiency muscular dystrophy: two terms for the same disorder]M Castro-Gago, M I Novo-Rodríguez, E Pintos-Martínez, et al.
Pageof 2