Search research articles
Contact Us
Filters
Showing results (11-20 of 38) with videos related to
Page
of 4
Sort By:
Neurology
|
November 1, 1991
Adult Reye's syndrome: a review with new evidence for a generalized defect in intramitochondrial enzyme processing
R N Van Coster, D C De Vivo, D Blake, et al.
Journal De Genetique Humaine
|
December 1, 1989
[Urgent needs in genetics: clinical diagnosis of acute amino acid disorders of delayed onset]
J M Saudubray, S Lyonnet, A Lombes, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 25, 2000
[Diagnostic approach to metabolic myopathies]
J M Cuisset, J C Cuvellier, C De Sèze, et al.
Journal of Medical Genetics
|
September 18, 2007
Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation
A Saada, A Shaag, S Arnon, et al.
Histochemistry and Cell Biology
|
January 1, 1995
Immunohistochemical analysis of muscle cytochrome c oxidase deficiency in children
S Possekel, A Lombes, H Ogier de Baulny, et al.
Metabolic Brain Disease
|
March 26, 2009
MPTP intoxication in mice: a useful model of Leigh syndrome to study mitochondrial diseases in childhood
E Lagrue, B Abert, L Nadal, et al.
Annals of the New York Academy of Sciences
|
January 1, 1988
Clinical and biochemical studies on cytochrome oxidase deficiencies
E A Schon, E Bonilla, A Lombes, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Mitochondrial encephalomyopathies
S DiMauro, M Zeviani, C T Moraes, et al.
Neurology
|
April 1, 1991
Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome
A Lombes, H Nakase, H J Tritschler, et al.
Journal of Medical Genetics
|
January 13, 2010
A novel FTL insertion causing neuroferritinopathy
S Batey, I Vuillaume, D Devos, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 38) with videos related to
Sort By:
Page
of 4
Neurology
|
November 1, 1991
Adult Reye's syndrome: a review with new evidence for a generalized defect in intramitochondrial enzyme processing
R N Van Coster, D C De Vivo, D Blake, et al.
Journal De Genetique Humaine
|
December 1, 1989
[Urgent needs in genetics: clinical diagnosis of acute amino acid disorders of delayed onset]
J M Saudubray, S Lyonnet, A Lombes, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 25, 2000
[Diagnostic approach to metabolic myopathies]
J M Cuisset, J C Cuvellier, C De Sèze, et al.
Journal of Medical Genetics
|
September 18, 2007
Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation
A Saada, A Shaag, S Arnon, et al.
Histochemistry and Cell Biology
|
January 1, 1995
Immunohistochemical analysis of muscle cytochrome c oxidase deficiency in children
S Possekel, A Lombes, H Ogier de Baulny, et al.
Metabolic Brain Disease
|
March 26, 2009
MPTP intoxication in mice: a useful model of Leigh syndrome to study mitochondrial diseases in childhood
E Lagrue, B Abert, L Nadal, et al.
Annals of the New York Academy of Sciences
|
January 1, 1988
Clinical and biochemical studies on cytochrome oxidase deficiencies
E A Schon, E Bonilla, A Lombes, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Mitochondrial encephalomyopathies
S DiMauro, M Zeviani, C T Moraes, et al.
Neurology
|
April 1, 1991
Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome
A Lombes, H Nakase, H J Tritschler, et al.
Journal of Medical Genetics
|
January 13, 2010
A novel FTL insertion causing neuroferritinopathy
S Batey, I Vuillaume, D Devos, et al.
Page
of 4