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M Castro Gago

Showing results (141-150 of 157) with videos related to

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Anales Espanoles De Pediatria|November 1, 1987
[Malformations of the central nervous system. Round table]M Castro-Gago, M D Lluch, J López Sastre, et al.
Revista De Neurologia|October 29, 2003
[Phenotypic variability of deletion 22q11.2. An analysis of 16 observations with special emphasis on the neurological manifestations]J Eirís-Puñal, J M Iglesias-Meleiro, M O Blanco-Barca, et al.
Revista De Neurologia|October 31, 2000
[Hereditary neuropathy with liability to pressure palsies (tomaculous neuropathy). Clinical, electrophysical and molecular study of two affected families]J Eirís-Punal, M Vidal-Lijó, F Barros-Angueira, et al.
Journal of Child Neurology|March 12, 1999
Congenital hydranencephalic-hydrocephalic syndrome associated with mitochondrial dysfunctionM Castro-Gago, A Alonso, E Pintos-Martínez, et al.
Anales Espanoles De Pediatria|July 1, 1996
[Juvenile nephronophthisis with tapetoretinal degeneration, skeletal changes and special phenotypic traits]M Castro-Gago, P Meseguer Yebra, M J Fernández-Seara, et al.
Anales Espanoles De Pediatria|October 1, 1988
[Polymyositis and dermatomyositis in childhood]A Rodríguez Núñez, J M Fernández Bustillo, E Rodríguez Pérez, et al.
Anales Espanoles De Pediatria|November 1, 1992
[Lafora disease in childhood]J Eiris Puñal, A Rodríguez Núñez, D Escribano Rey, et al.
Clinical Endocrinology|September 1, 1985
Glucocorticoid deficiency with achalasia of the cardia and lack of lacrimationM Pombo, J Devesa, A Taborda, et al.
Revista De Neurologia|June 17, 2003
[Multiple symmetric lipomatosis associated to polyneuropathology, atrophy of the cerebellum and mitochondrial cytopathy]M Castro-Gago, A Alonso, E Pintos-Martínez, et al.
Journal of Lipid Research|December 10, 1997
A two-base deletion in exon 6 of the 3-hydroxy-3-methylglutaryl coenzyme A lyase (HL) gene producing the skipping of exons 5 and 6 determines 3-hydroxy-3-methylglutaric aciduriaN Casals, J Pié, C H Casale, et al.
Pageof 16

Showing results (141-150 of 157) with videos related to

Sort By:
Pageof 16
Anales Espanoles De Pediatria|November 1, 1987
[Malformations of the central nervous system. Round table]M Castro-Gago, M D Lluch, J López Sastre, et al.
Revista De Neurologia|October 29, 2003
[Phenotypic variability of deletion 22q11.2. An analysis of 16 observations with special emphasis on the neurological manifestations]J Eirís-Puñal, J M Iglesias-Meleiro, M O Blanco-Barca, et al.
Revista De Neurologia|October 31, 2000
[Hereditary neuropathy with liability to pressure palsies (tomaculous neuropathy). Clinical, electrophysical and molecular study of two affected families]J Eirís-Punal, M Vidal-Lijó, F Barros-Angueira, et al.
Journal of Child Neurology|March 12, 1999
Congenital hydranencephalic-hydrocephalic syndrome associated with mitochondrial dysfunctionM Castro-Gago, A Alonso, E Pintos-Martínez, et al.
Anales Espanoles De Pediatria|July 1, 1996
[Juvenile nephronophthisis with tapetoretinal degeneration, skeletal changes and special phenotypic traits]M Castro-Gago, P Meseguer Yebra, M J Fernández-Seara, et al.
Anales Espanoles De Pediatria|October 1, 1988
[Polymyositis and dermatomyositis in childhood]A Rodríguez Núñez, J M Fernández Bustillo, E Rodríguez Pérez, et al.
Anales Espanoles De Pediatria|November 1, 1992
[Lafora disease in childhood]J Eiris Puñal, A Rodríguez Núñez, D Escribano Rey, et al.
Clinical Endocrinology|September 1, 1985
Glucocorticoid deficiency with achalasia of the cardia and lack of lacrimationM Pombo, J Devesa, A Taborda, et al.
Revista De Neurologia|June 17, 2003
[Multiple symmetric lipomatosis associated to polyneuropathology, atrophy of the cerebellum and mitochondrial cytopathy]M Castro-Gago, A Alonso, E Pintos-Martínez, et al.
Journal of Lipid Research|December 10, 1997
A two-base deletion in exon 6 of the 3-hydroxy-3-methylglutaryl coenzyme A lyase (HL) gene producing the skipping of exons 5 and 6 determines 3-hydroxy-3-methylglutaric aciduriaN Casals, J Pié, C H Casale, et al.
Pageof 16