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R C Sengers

Showing results (51-60 of 144) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1981
Estimation of energy metabolism in human skeletal muscle homogenate as a diagnostic aidW Ruitenbeek, R C Sengers, J M Trijbels, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 31, 1986
[Malignant hyperthermia: case-finding of subjects at risk]W A Viering, R C Sengers, A M Stadhouders, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
The use of chorionic villi in prenatal diagnosis of mitochondriopathiesW Ruitenbeek, R C Sengers, J M Trijbels, et al.
European Journal of Pediatrics|February 24, 2001
Nuclear genes and oxidative phosphorylation disorders: a reviewJ A Smeitink, R C Sengers, F J Trijbels, et al.
The New England Journal of Medicine|February 14, 1974
Letter: Pyruvate decarboxylase deficiency in liverJ L Willems, L A Monnens, J M Trijbels, et al.
Molecular and Cellular Biochemistry|October 6, 1997
Defects in the mitochondrial energy metabolism outside the respiratory chain and the pyruvate dehydrogenase complexF J Trijbels, W Ruitenbeek, M Huizing, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Benign mitochondrial encephalomyopathy in a patient with complex I deficiencyJ M Trijbels, W Ruitenbeek, R C Sengers, et al.
Neuropadiatrie|November 1, 1975
Infantile Gaucher's disease: glucocerebrosidase deficiency in peripheral blood leukocytes and cultured fibroblastsR C Sengers, K J Lamers, J A Bakkeren, et al.
European Journal of Pediatrics|March 13, 1978
Chronic mild diarrhoea, stunted growth and neuromuscular abnormalitiesR C Sengers, A M Stadhouders, H H Jaspar, et al.
European Journal of Pediatrics|May 1, 1988
Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activityW Sperl, W Ruitenbeek, J M Trijbels, et al.
Pageof 15

Showing results (51-60 of 144) with videos related to

Sort By:
Pageof 15
Journal of Inherited Metabolic Disease|January 1, 1981
Estimation of energy metabolism in human skeletal muscle homogenate as a diagnostic aidW Ruitenbeek, R C Sengers, J M Trijbels, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 31, 1986
[Malignant hyperthermia: case-finding of subjects at risk]W A Viering, R C Sengers, A M Stadhouders, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
The use of chorionic villi in prenatal diagnosis of mitochondriopathiesW Ruitenbeek, R C Sengers, J M Trijbels, et al.
European Journal of Pediatrics|February 24, 2001
Nuclear genes and oxidative phosphorylation disorders: a reviewJ A Smeitink, R C Sengers, F J Trijbels, et al.
The New England Journal of Medicine|February 14, 1974
Letter: Pyruvate decarboxylase deficiency in liverJ L Willems, L A Monnens, J M Trijbels, et al.
Molecular and Cellular Biochemistry|October 6, 1997
Defects in the mitochondrial energy metabolism outside the respiratory chain and the pyruvate dehydrogenase complexF J Trijbels, W Ruitenbeek, M Huizing, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Benign mitochondrial encephalomyopathy in a patient with complex I deficiencyJ M Trijbels, W Ruitenbeek, R C Sengers, et al.
Neuropadiatrie|November 1, 1975
Infantile Gaucher's disease: glucocerebrosidase deficiency in peripheral blood leukocytes and cultured fibroblastsR C Sengers, K J Lamers, J A Bakkeren, et al.
European Journal of Pediatrics|March 13, 1978
Chronic mild diarrhoea, stunted growth and neuromuscular abnormalitiesR C Sengers, A M Stadhouders, H H Jaspar, et al.
European Journal of Pediatrics|May 1, 1988
Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activityW Sperl, W Ruitenbeek, J M Trijbels, et al.
Pageof 15