Trijbels JM - Search Results

1

Myopathology and a mitochondrial DNA deletion in the Pearson marrow and pancreas syndrome.

de Vries DD, Buzing CJ, Ruitenbeek W, van der Wouw MP, Sperl W, Sengers RC, Trijbels JM, van Oost BA. de Vries DD, et al. Among authors: trijbels jm. Neuromuscul Disord. 1992;2(3):185-95. doi: 10.1016/0960-8966(92)90005-q. Neuromuscul Disord. 1992. PMID: 1483044

2

Enzymological versus DNA investigations in mitochondrial (encephalo-) myopathies.

de Vries DD, Ruitenbeek W, de Wijs IJ, Trijbels JM, van Oost BA. de Vries DD, et al. Among authors: trijbels jm. J Inherit Metab Dis. 1993;16(3):534-6. doi: 10.1007/BF00711674. J Inherit Metab Dis. 1993. PMID: 7609445 Clinical Trial. No abstract available.

3

Combined deficiencies of the pyruvate dehydrogenase complex and enzymes of the respiratory chain in mitochondrial myopathies.

Sperl W, Ruitenbeek W, Sengers RC, Trijbels JM, Bentlage H, Wraith JE, Heilmann C, Stöckler S, Binder C, Korenke GC, et al. Sperl W, et al. Among authors: trijbels jm. Eur J Pediatr. 1992 Mar;151(3):192-5. doi: 10.1007/BF01954382. Eur J Pediatr. 1992. PMID: 1601011

4

Heterogeneous tissue expression of enzyme defects in mitochondrial myopathies.

Sperl W, Ruitenbeek W, Trijbels JM, Korenke GC, Sengers RC. Sperl W, et al. Among authors: trijbels jm. J Inherit Metab Dis. 1990;13(3):359-62. doi: 10.1007/BF01799395. J Inherit Metab Dis. 1990. PMID: 2172646 No abstract available.

5

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: trijbels jm. Eur J Pediatr. 1990 Apr;149(7):487-92. doi: 10.1007/BF01959401. Eur J Pediatr. 1990. PMID: 2189731 Review.

6

Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathies.

Korenke GC, Bentlage HA, Ruitenbeek W, Sengers RC, Sperl W, Trijbels JM, Gabreels FJ, Wijburg FA, Wiedermann V, Hanefeld F, et al. Korenke GC, et al. Among authors: trijbels jm. Eur J Pediatr. 1990 Dec;150(2):104-8. doi: 10.1007/BF02072049. Eur J Pediatr. 1990. PMID: 2279503

7

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: trijbels jm. J Inherit Metab Dis. 1989;12 Suppl 2:352-4. doi: 10.1007/BF03335420. J Inherit Metab Dis. 1989. PMID: 2512442 No abstract available.

8

[Mitochondrial defects].

Sengers RC, Stadhouders AM, Trijbels JM. Sengers RC, et al. Among authors: trijbels jm. Monatsschr Kinderheilkd. 1989 Jun;137(6):308-11. Monatsschr Kinderheilkd. 1989. PMID: 2668741 Review. German.

9

Fatal neonatal cardiomyopathy associated with cataract and mitochondrial myopathy.

Smeitink JA, Sengers RC, Trijbels JM, Ruitenbeek W, Daniëls O, Stadhouders AM, Kock-Jansen MJ. Smeitink JA, et al. Among authors: trijbels jm. Eur J Pediatr. 1989 Jun;148(7):656-9. doi: 10.1007/BF00441527. Eur J Pediatr. 1989. PMID: 2744041

10

[Mitochondrial myopathies].

Sengers RC, Stadhouders AM, Trijbels JM. Sengers RC, et al. Among authors: trijbels jm. Tijdschr Kindergeneeskd. 1988 Jun;56(3):110-5. Tijdschr Kindergeneeskd. 1988. PMID: 2842888 Dutch.

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