Janssen AJ - Search Results

1

Estimation of pyruvate dehydrogenase (E1) activity in human skeletal muscle; three cases with E1 deficiency.

van Laack HL, Ruitenbeek W, Trijbels JM, Sengers RC, Gabreëls FJ, Janssen AJ, Kerkhof CM. van Laack HL, et al. Among authors: janssen aj. Clin Chim Acta. 1988 Jan 15;171(1):109-18. doi: 10.1016/0009-8981(88)90296-3. Clin Chim Acta. 1988. PMID: 3127087

2

Postnatal development of pyruvate oxidation in quadriceps muscle of the rat.

Sperl W, Sengers RC, Trijbels JM, Ruitenbeek W, De Graaf R, Ter Laak H, Van Lith T, Kerkhoff C, Janssen A. Sperl W, et al. Biol Neonate. 1992;61(3):188-200. doi: 10.1159/000243742. Biol Neonate. 1992. PMID: 1319216

3

Deficiency of the alpha and beta subunits of pyruvate dehydrogenase in a patient with lactic acidosis and unexpected sudden death.

Sperl W, Ruitenbeek W, Kerkhof CM, Sengers RC, Trijbels JM, Guggenbichler JP, Janssen AJ, Bakkeren JA. Sperl W, et al. Among authors: janssen aj. Eur J Pediatr. 1990 Apr;149(7):487-92. doi: 10.1007/BF01959401. Eur J Pediatr. 1990. PMID: 2189731 Review.

4

Differential investigation of the capacity of succinate oxidation in human skeletal muscle.

Fischer JC, Ruitenbeek W, Berden JA, Trijbels JM, Veerkamp JH, Stadhouders AM, Sengers RC, Janssen AJ. Fischer JC, et al. Among authors: janssen aj. Clin Chim Acta. 1985 Nov 29;153(1):23-36. doi: 10.1016/0009-8981(85)90135-4. Clin Chim Acta. 1985. PMID: 3000647

5

Estimation of NADH oxidation in human skeletal muscle mitochondria.

Fischer JC, Ruitenbeek W, Trijbels JM, Veerkamp JH, Stadhouders AM, Sengers RC, Janssen AJ. Fischer JC, et al. Among authors: janssen aj. Clin Chim Acta. 1986 Mar 28;155(3):263-73. doi: 10.1016/0009-8981(86)90246-9. Clin Chim Acta. 1986. PMID: 3011316

6

Measurement of totally activated pyruvate dehydrogenase complex activity in human muscle: evaluation of a useful assay.

Sperl W, Trijbels JM, Ruitenbeek W, van Laack HL, Janssen AJ, Kerkhof CM, Sengers RC. Sperl W, et al. Among authors: janssen aj. Enzyme Protein. 1993;47(1):37-46. doi: 10.1159/000468654. Enzyme Protein. 1993. PMID: 8012500

7

The use of chorionic villi in prenatal diagnosis of mitochondriopathies.

Ruitenbeek W, Sengers RC, Trijbels JM, Janssen AJ, Bakkeren JA. Ruitenbeek W, et al. Among authors: janssen aj. J Inherit Metab Dis. 1992;15(3):303-6. doi: 10.1007/BF02435962. J Inherit Metab Dis. 1992. PMID: 1328761 No abstract available.

8

Pyruvate metabolism in Lafora disease.

Busard HL, Renier WO, Gabreëls FJ, Trijbels JM, Janssen AJ, Lamers KJ. Busard HL, et al. Among authors: janssen aj. Epilepsia. 1989 May-Jun;30(3):314-7. doi: 10.1111/j.1528-1157.1989.tb05303.x. Epilepsia. 1989. PMID: 2498072

9

Mitochondrial myopathies: multiple enzyme defects in the respiratory chain.

Ruitenbeek W, Trijbels JM, Fischer JC, Sengers RC, Janssen AJ, Kerkhof CM. Ruitenbeek W, et al. Among authors: janssen aj. J Inherit Metab Dis. 1989;12 Suppl 2:352-4. doi: 10.1007/BF03335420. J Inherit Metab Dis. 1989. PMID: 2512442 No abstract available.

10

Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach.

Trijbels JM, Sengers RC, Ruitenbeek W, Fischer JC, Bakkeren JA, Janssen AJ. Trijbels JM, et al. Among authors: janssen aj. Eur J Pediatr. 1988 Nov;148(2):92-7. doi: 10.1007/BF00445910. Eur J Pediatr. 1988. PMID: 3069472 Review.

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