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Journal of Neuroscience Methods
|
May 30, 1998
Cytochrome c oxidase assay in minute amounts of human skeletal muscle using single wavelength spectrophotometers
O Miró, F Cardellach, A Barrientos, 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.
Biochimica Et Biophysica Acta
|
July 10, 1997
Sequence and structure of the human OXA1L gene and its upstream elements
A Rötig, B Parfait, L Heidet, 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.
The Journal of Clinical Investigation
|
February 17, 2000
RXRalpha overexpression in cardiomyocytes causes dilated cardiomyopathy but fails to rescue myocardial hypoplasia in RXRalpha-null fetuses
V Subbarayan, M Mark, N Messadeq, 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
|
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.
Acta Chirurgica Belgica
|
July 1, 1975
[Preliminary results of immuno-surgical treatment of primary melanoma (author's transl)]
R Vanwicjk, P Rustin, S Malek-Mansour, 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.
Page
of 16
Search research articles
Search
Showing results (41-50 of 157) with videos related to
Sort By:
Page
of 16
Journal of Neuroscience Methods
|
May 30, 1998
Cytochrome c oxidase assay in minute amounts of human skeletal muscle using single wavelength spectrophotometers
O Miró, F Cardellach, A Barrientos, 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.
Biochimica Et Biophysica Acta
|
July 10, 1997
Sequence and structure of the human OXA1L gene and its upstream elements
A Rötig, B Parfait, L Heidet, 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.
The Journal of Clinical Investigation
|
February 17, 2000
RXRalpha overexpression in cardiomyocytes causes dilated cardiomyopathy but fails to rescue myocardial hypoplasia in RXRalpha-null fetuses
V Subbarayan, M Mark, N Messadeq, 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
|
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.
Acta Chirurgica Belgica
|
July 1, 1975
[Preliminary results of immuno-surgical treatment of primary melanoma (author's transl)]
R Vanwicjk, P Rustin, S Malek-Mansour, 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.
Page
of 16