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European Journal of Pediatrics
|
December 1, 1988
Cardiomyopathy associated with carnitine loss in kidneys and small intestine
R Rodrigues Pereira, H R Scholte, I E Luyt-Houwen, et al.
Pediatrics
|
September 2, 2000
Functional hyperactivity of hepatic glutamate dehydrogenase as a cause of the hyperinsulinism/hyperammonemia syndrome: effect of treatment
J G Huijmans, M Duran, J B de Klerk, et al.
Journal of Translational Medicine
|
October 13, 2010
Patients with chronic fatigue syndrome performed worse than controls in a controlled repeated exercise study despite a normal oxidative phosphorylation capacity
Ruud C W Vermeulen, Ruud M Kurk, Frans C Visser, et al.
European Journal of Pediatrics
|
December 1, 1984
Glutaric aciduria type II: treatment with riboflavine, carnitine and insulin
P D Mooy, H Przyrembel, M A Giesberts, et al.
Revue Neurologique
|
January 1, 1989
[Mitochondrial myopathy. Encephalopathy with lactic acidosis and cerebral infarction]
A Destée, J J Martin, J P Muller, et al.
European Journal of Pediatrics
|
March 1, 1993
Problems with the biochemical diagnosis in mitochondrial (encephalo-)myopathies
J M Trijbels, H R Scholte, W Ruitenbeek, et al.
Molecular and Cellular Biochemistry
|
October 6, 1997
Rapid isolation of muscle and heart mitochondria, the lability of oxidative phosphorylation and attempts to stabilize the process in vitro by taurine, carnitine and other compounds
H R Scholte, Y Yu, J D Ross, et al.
The Journal of Pediatrics
|
May 1, 1996
Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemia
P D Maaswinkel-Mooij, C Van den Bogert, H R Scholte, et al.
European Journal of Pediatrics
|
August 1, 1984
Systemic carnitine deficiency: benefit of oral carnitine supplements vs. persisting biochemical abnormalities
M Duran, J B de Klerk, S K Wadman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 1, 1986
Myopathy with abnormal mitochondria, transient low electron transport capacity in the respiratory chain, and absence of energy transduction at sites 1 and 2 in vitro
U Trockel, H R Scholte, K V Toyka, et al.
Page
of 9
Search research articles
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Showing results (31-40 of 83) with videos related to
Sort By:
Page
of 9
European Journal of Pediatrics
|
December 1, 1988
Cardiomyopathy associated with carnitine loss in kidneys and small intestine
R Rodrigues Pereira, H R Scholte, I E Luyt-Houwen, et al.
Pediatrics
|
September 2, 2000
Functional hyperactivity of hepatic glutamate dehydrogenase as a cause of the hyperinsulinism/hyperammonemia syndrome: effect of treatment
J G Huijmans, M Duran, J B de Klerk, et al.
Journal of Translational Medicine
|
October 13, 2010
Patients with chronic fatigue syndrome performed worse than controls in a controlled repeated exercise study despite a normal oxidative phosphorylation capacity
Ruud C W Vermeulen, Ruud M Kurk, Frans C Visser, et al.
European Journal of Pediatrics
|
December 1, 1984
Glutaric aciduria type II: treatment with riboflavine, carnitine and insulin
P D Mooy, H Przyrembel, M A Giesberts, et al.
Revue Neurologique
|
January 1, 1989
[Mitochondrial myopathy. Encephalopathy with lactic acidosis and cerebral infarction]
A Destée, J J Martin, J P Muller, et al.
European Journal of Pediatrics
|
March 1, 1993
Problems with the biochemical diagnosis in mitochondrial (encephalo-)myopathies
J M Trijbels, H R Scholte, W Ruitenbeek, et al.
Molecular and Cellular Biochemistry
|
October 6, 1997
Rapid isolation of muscle and heart mitochondria, the lability of oxidative phosphorylation and attempts to stabilize the process in vitro by taurine, carnitine and other compounds
H R Scholte, Y Yu, J D Ross, et al.
The Journal of Pediatrics
|
May 1, 1996
Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemia
P D Maaswinkel-Mooij, C Van den Bogert, H R Scholte, et al.
European Journal of Pediatrics
|
August 1, 1984
Systemic carnitine deficiency: benefit of oral carnitine supplements vs. persisting biochemical abnormalities
M Duran, J B de Klerk, S K Wadman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 1, 1986
Myopathy with abnormal mitochondria, transient low electron transport capacity in the respiratory chain, and absence of energy transduction at sites 1 and 2 in vitro
U Trockel, H R Scholte, K V Toyka, et al.
Page
of 9