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A Lombes

Showing results (31-40 of 38) with videos related to

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Journal of Medical Genetics|August 1, 1995
Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafnessS Manouvrier, A Rötig, G Hannebique, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Clinical approach to inherited metabolic diseases in the neonatal period: a 20-year surveyJ M Saudubray, H Ogier, J P Bonnefont, et al.
Ceskoslovenska Pediatrie|January 1, 1990
[Clinical approach to hereditary metabolic disorders in neonates. Review of 20 years' experience]J M Saudubray, H Ogier, J P Bonnefont, et al.
Neurology|April 1, 1994
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorderM Hirano, G Silvestri, D M Blake, et al.
Revue Neurologique|January 1, 1991
Mitochondrial encephalomyopathies: biochemical approachS Dimauro, C T Moraes, S Shanske, et al.
Annals of Neurology|July 1, 1989
Myoclonic epilepsy and ragged-red fibers with cytochrome oxidase deficiency: neuropathology, biochemistry, and molecular geneticsA Lombes, J R Mendell, H Nakase, et al.
Pediatric Research|November 1, 1990
Cytochrome c oxidase deficiencyS DiMauro, A Lombes, H Nakase, et al.
European Journal of Pediatrics|December 1, 1990
The fasting test in paediatrics: application to the diagnosis of pathological hypo- and hyperketotic statesJ P Bonnefont, N B Specola, A Vassault, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Journal of Medical Genetics|August 1, 1995
Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafnessS Manouvrier, A Rötig, G Hannebique, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Clinical approach to inherited metabolic diseases in the neonatal period: a 20-year surveyJ M Saudubray, H Ogier, J P Bonnefont, et al.
Ceskoslovenska Pediatrie|January 1, 1990
[Clinical approach to hereditary metabolic disorders in neonates. Review of 20 years' experience]J M Saudubray, H Ogier, J P Bonnefont, et al.
Neurology|April 1, 1994
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorderM Hirano, G Silvestri, D M Blake, et al.
Revue Neurologique|January 1, 1991
Mitochondrial encephalomyopathies: biochemical approachS Dimauro, C T Moraes, S Shanske, et al.
Annals of Neurology|July 1, 1989
Myoclonic epilepsy and ragged-red fibers with cytochrome oxidase deficiency: neuropathology, biochemistry, and molecular geneticsA Lombes, J R Mendell, H Nakase, et al.
Pediatric Research|November 1, 1990
Cytochrome c oxidase deficiencyS DiMauro, A Lombes, H Nakase, et al.
European Journal of Pediatrics|December 1, 1990
The fasting test in paediatrics: application to the diagnosis of pathological hypo- and hyperketotic statesJ P Bonnefont, N B Specola, A Vassault, et al.
Pageof 4