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J M Trijbels

Showing results (71-80 of 177) with videos related to

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Neurology|July 1, 1996
Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscleH A Bentlage, U Wendel, H Schägger, et al.
The International Journal of Biochemistry|January 1, 1979
Reconstitution of malate-aspartate and alpha-glycerophosphate shuttle activity in rat skeletal muscle mitochondriaH Bookelman, J M Trijbels, R C Sengers, et al.
European Journal of Pediatrics|November 1, 1988
Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approachJ M Trijbels, R C Sengers, W Ruitenbeek, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Mitochondrial myopathies: multiple enzyme defects in the respiratory chainW Ruitenbeek, J M Trijbels, J C Fischer, et al.
Nephron|January 1, 1987
The urinary excretion of total hydroxylysine and its glycosides in normal persons, and in patients suffering from Alport's syndrome--contribution of the peptide-bound fractionC H Schröder, L A Monnens, H M van Lith-Zanders, et al.
Biochemical Medicine|December 1, 1978
The effect of exogenous cytochrome c on pyruvate oxidation by rat skeletal muscle mitochondria isolated in sucrose or KCI mediumH Bookelman, J M Trijbels, R C Sengers, et al.
QJM : Monthly Journal of the Association of Physicians|March 22, 2001
Reduced vitamin B12 binding by transcobalamin II increases the risk of neural tube defectsL A Afman, N M Van Der Put, C M Thomas, et al.
Acta Paediatrica Scandinavica|November 1, 1971
Concentration of purine nucleotides in erythrocytes of patients with the Lesch-Nyhan syndrome before and during oral administration of adenineE J Lommen, G D Vogels, S P van der Zee, et al.
Archives of Disease in Childhood|December 1, 1971
Citrullinaemia with rapidly fatal neonatal courseS P Van Der Zee, J M Trijbels, L A Monnens, et al.
Journal of Inherited Metabolic Disease|January 1, 1980
Biochemical studies in the cerebro-hepato-renal syndrome of Zellweger: a disturbance in the metabolism of pipecolic acidJ M Trijbels, L A Monnens, J A Bakkeren, et al.
Pageof 18

Showing results (71-80 of 177) with videos related to

Sort By:
Pageof 18
Neurology|July 1, 1996
Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscleH A Bentlage, U Wendel, H Schägger, et al.
The International Journal of Biochemistry|January 1, 1979
Reconstitution of malate-aspartate and alpha-glycerophosphate shuttle activity in rat skeletal muscle mitochondriaH Bookelman, J M Trijbels, R C Sengers, et al.
European Journal of Pediatrics|November 1, 1988
Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approachJ M Trijbels, R C Sengers, W Ruitenbeek, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Mitochondrial myopathies: multiple enzyme defects in the respiratory chainW Ruitenbeek, J M Trijbels, J C Fischer, et al.
Nephron|January 1, 1987
The urinary excretion of total hydroxylysine and its glycosides in normal persons, and in patients suffering from Alport's syndrome--contribution of the peptide-bound fractionC H Schröder, L A Monnens, H M van Lith-Zanders, et al.
Biochemical Medicine|December 1, 1978
The effect of exogenous cytochrome c on pyruvate oxidation by rat skeletal muscle mitochondria isolated in sucrose or KCI mediumH Bookelman, J M Trijbels, R C Sengers, et al.
QJM : Monthly Journal of the Association of Physicians|March 22, 2001
Reduced vitamin B12 binding by transcobalamin II increases the risk of neural tube defectsL A Afman, N M Van Der Put, C M Thomas, et al.
Acta Paediatrica Scandinavica|November 1, 1971
Concentration of purine nucleotides in erythrocytes of patients with the Lesch-Nyhan syndrome before and during oral administration of adenineE J Lommen, G D Vogels, S P van der Zee, et al.
Archives of Disease in Childhood|December 1, 1971
Citrullinaemia with rapidly fatal neonatal courseS P Van Der Zee, J M Trijbels, L A Monnens, et al.
Journal of Inherited Metabolic Disease|January 1, 1980
Biochemical studies in the cerebro-hepato-renal syndrome of Zellweger: a disturbance in the metabolism of pipecolic acidJ M Trijbels, L A Monnens, J A Bakkeren, et al.
Pageof 18