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Human Genetics
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April 4, 2000
Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome
B Parfait, D Chretien, A Rötig, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Expression of respiratory chain deficiencies in human cultured cells
T Bourgeron, D Chretien, P Amati, et al.
European Journal of Pediatrics
|
February 1, 1994
Valproate-induced hepatic failure in a case of cytochrome c oxidase deficiency
B Chabrol, J Mancini, D Chretien, et al.
Biochimica Et Biophysica Acta
|
August 22, 1997
Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in human
P Rustin, T Bourgeron, B Parfait, et al.
Human Genetics
|
December 24, 1997
No mitochondrial cytochrome oxidase (COX) gene mutations in 18 cases of COX deficiency
B Parfait, A Percheron, D Chretien, et al.
Brain & Development
|
November 1, 1992
Deficiency in complex II of the respiratory chain, presenting as a leukodystrophy in two sisters with Leigh syndrome
M Burgeois, F Goutieres, D Chretien, et al.
European Journal of Pediatrics
|
April 1, 1996
Clinical presentations and laboratory investigations in respiratory chain deficiency
A Munnich, A Rötig, D Chretien, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 1, 1994
Reference charts for respiratory chain activities in human tissues
D Chretien, P Rustin, T Bourgeron, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 15, 1995
An improved spectrophotometric assay of pyruvate dehydrogenase in lactate dehydrogenase contaminated mitochondrial preparations from human skeletal muscle
D Chretien, M Pourrier, T Bourgeron, et al.
Biochemical Medicine and Metabolic Biology
|
August 1, 1993
Investigation of respiratory chain activity in human heart
P Rustin, D Chretien, T Bourgeron, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 49) with videos related to
Sort By:
Page
of 5
Human Genetics
|
April 4, 2000
Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome
B Parfait, D Chretien, A Rötig, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Expression of respiratory chain deficiencies in human cultured cells
T Bourgeron, D Chretien, P Amati, et al.
European Journal of Pediatrics
|
February 1, 1994
Valproate-induced hepatic failure in a case of cytochrome c oxidase deficiency
B Chabrol, J Mancini, D Chretien, et al.
Biochimica Et Biophysica Acta
|
August 22, 1997
Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in human
P Rustin, T Bourgeron, B Parfait, et al.
Human Genetics
|
December 24, 1997
No mitochondrial cytochrome oxidase (COX) gene mutations in 18 cases of COX deficiency
B Parfait, A Percheron, D Chretien, et al.
Brain & Development
|
November 1, 1992
Deficiency in complex II of the respiratory chain, presenting as a leukodystrophy in two sisters with Leigh syndrome
M Burgeois, F Goutieres, D Chretien, et al.
European Journal of Pediatrics
|
April 1, 1996
Clinical presentations and laboratory investigations in respiratory chain deficiency
A Munnich, A Rötig, D Chretien, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 1, 1994
Reference charts for respiratory chain activities in human tissues
D Chretien, P Rustin, T Bourgeron, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 15, 1995
An improved spectrophotometric assay of pyruvate dehydrogenase in lactate dehydrogenase contaminated mitochondrial preparations from human skeletal muscle
D Chretien, M Pourrier, T Bourgeron, et al.
Biochemical Medicine and Metabolic Biology
|
August 1, 1993
Investigation of respiratory chain activity in human heart
P Rustin, D Chretien, T Bourgeron, et al.
Page
of 5