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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 deafness
S 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 survey
J 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 disorder
M Hirano, G Silvestri, D M Blake, et al.
Revue Neurologique
|
January 1, 1991
Mitochondrial encephalomyopathies: biochemical approach
S 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 genetics
A Lombes, J R Mendell, H Nakase, et al.
Pediatric Research
|
November 1, 1990
Cytochrome c oxidase deficiency
S 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 states
J P Bonnefont, N B Specola, A Vassault, et al.
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of 4
Search research articles
Search
Showing results (31-40 of 38) with videos related to
Sort By:
Page
of 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 deafness
S 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 survey
J 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 disorder
M Hirano, G Silvestri, D M Blake, et al.
Revue Neurologique
|
January 1, 1991
Mitochondrial encephalomyopathies: biochemical approach
S 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 genetics
A Lombes, J R Mendell, H Nakase, et al.
Pediatric Research
|
November 1, 1990
Cytochrome c oxidase deficiency
S 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 states
J P Bonnefont, N B Specola, A Vassault, et al.
Page
of 4