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Annals of Neurology
|
August 1, 1983
Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency
S DiMauro, J F Nicholson, A P Hays, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 1, 1977
The clinical and biochemical implications of pyruvate carboxylase deficiency
D C DeVivo, M W Haymond, M P Leckie, et al.
Biomedical & Environmental Mass Spectrometry
|
February 1, 1990
Stable isotope dilution analysis of 4-hydroxybutyric acid: an accurate method for quantification in physiological fluids and the prenatal diagnosis of 4-hydroxybutyric aciduria
K M Gibson, S Aramaki, L Sweetman, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Comparative biochemical studies in fibroblasts from patients with different forms of Leigh syndrome
M E Vazquez-Memije, S Shanske, F M Santorelli, 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.
Annals of Neurology
|
March 1, 1994
Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features
R Tawil, L J Ptacek, S G Pavlakis, et al.
Neuromuscular Disorders : NMD
|
January 1, 1992
Melas: an original case and clinical criteria for diagnosis
M Hirano, E Ricci, M R Koenigsberger, et al.
Neurology
|
June 1, 1980
Carnitine "deficiency": lack of response to carnitine therapy
J E Carroll, M H Brooke, D C DeVivo, et al.
Revue Neurologique
|
January 1, 1991
Clinical syndromes associated with ragged red fibers
L P Rowland, D M Blake, M Hirano, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 31, 1995
Abnormal calcium homeostasis and mitochondrial polarization in a human encephalomyopathy
A M Moudy, S D Handran, M P Goldberg, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 75) with videos related to
Sort By:
Page
of 8
Annals of Neurology
|
August 1, 1983
Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency
S DiMauro, J F Nicholson, A P Hays, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 1, 1977
The clinical and biochemical implications of pyruvate carboxylase deficiency
D C DeVivo, M W Haymond, M P Leckie, et al.
Biomedical & Environmental Mass Spectrometry
|
February 1, 1990
Stable isotope dilution analysis of 4-hydroxybutyric acid: an accurate method for quantification in physiological fluids and the prenatal diagnosis of 4-hydroxybutyric aciduria
K M Gibson, S Aramaki, L Sweetman, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Comparative biochemical studies in fibroblasts from patients with different forms of Leigh syndrome
M E Vazquez-Memije, S Shanske, F M Santorelli, 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.
Annals of Neurology
|
March 1, 1994
Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features
R Tawil, L J Ptacek, S G Pavlakis, et al.
Neuromuscular Disorders : NMD
|
January 1, 1992
Melas: an original case and clinical criteria for diagnosis
M Hirano, E Ricci, M R Koenigsberger, et al.
Neurology
|
June 1, 1980
Carnitine "deficiency": lack of response to carnitine therapy
J E Carroll, M H Brooke, D C DeVivo, et al.
Revue Neurologique
|
January 1, 1991
Clinical syndromes associated with ragged red fibers
L P Rowland, D M Blake, M Hirano, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 31, 1995
Abnormal calcium homeostasis and mitochondrial polarization in a human encephalomyopathy
A M Moudy, S D Handran, M P Goldberg, et al.
Page
of 8