Sengers RC - Search Results

1

MELAS syndrome. Report of two patients, and comparison with data of 24 patients derived from the literature.

van Hellenberg Hubar JL, Gabreëls FJ, Ruitenbeek W, Sengers RC, Renier WO, Thijssen HO, ter Laak HJ. van Hellenberg Hubar JL, et al. Among authors: sengers rc. Neuropediatrics. 1991 Feb;22(1):10-4. doi: 10.1055/s-2008-1071408. Neuropediatrics. 1991. PMID: 1903852 Review.

2

Mitochondrial creatine kinase containing crystals, creatine content and mitochondrial creatine kinase activity in chronic progressive external ophthalmoplegia.

Smeitink J, Stadhouders A, Sengers R, Ruitenbeek W, Wevers R, ter Laak H, Trijbels F. Smeitink J, et al. Neuromuscul Disord. 1992;2(1):35-40. doi: 10.1016/0960-8966(92)90024-z. Neuromuscul Disord. 1992. PMID: 1525556

3

Mitochondrial creatine kinase activity in patients with disturbed energy generation in muscle mitochondria.

Smeitink J, Ruitenbeek W, Sengers R, Wevers R, van Lith T, Trijbels F. Smeitink J, et al. J Inherit Metab Dis. 1994;17(1):67-73. doi: 10.1007/BF00735397. J Inherit Metab Dis. 1994. PMID: 8051938

4

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: sengers rc. Eur J Pediatr. 1992 Mar;151(3):192-5. doi: 10.1007/BF01954382. Eur J Pediatr. 1992. PMID: 1601011

5

Successful treatment of pure myopathy, associated with complex I deficiency, with riboflavin and carnitine.

Bernsen PL, Gabreëls FJ, Ruitenbeek W, Sengers RC, Stadhouders AM, Renier WO. Bernsen PL, et al. Among authors: sengers rc. Arch Neurol. 1991 Mar;48(3):334-8. doi: 10.1001/archneur.1991.00530150106028. Arch Neurol. 1991. PMID: 1900413

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: sengers rc. Eur J Pediatr. 1990 Dec;150(2):104-8. doi: 10.1007/BF02072049. Eur J Pediatr. 1990. PMID: 2279503

7

Congenital muscular dystrophy.

Leyten QH, Gabreëls FJ, Renier WO, Ter Laak HJ, Sengers RC, Mullaart RA. Leyten QH, et al. Among authors: sengers rc. J Pediatr. 1989 Aug;115(2):214-21. doi: 10.1016/s0022-3476(89)80068-x. J Pediatr. 1989. PMID: 2754551

8

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: sengers rc. Eur J Pediatr. 1988 Nov;148(2):92-7. doi: 10.1007/BF00445910. Eur J Pediatr. 1988. PMID: 3069472 Review.

9

White matter abnormalities in congenital muscular dystrophy.

Leyten QH, Gabreëls FJ, Renier WO, van Engelen BG, ter Laak HJ, Sengers RC, Thijssen HO. Leyten QH, et al. Among authors: sengers rc. J Neurol Sci. 1995 Apr;129(2):162-9. doi: 10.1016/0022-510x(94)00264-o. J Neurol Sci. 1995. PMID: 7608731 Free article.

10

Congenital muscular dystrophy. A study on the variability of morphological changes and dystrophin distribution in muscle biopsies.

Leyten QH, ter Laak HJ, Gabreëls FJ, Renier WO, Renkawek K, Sengers RC. Leyten QH, et al. Among authors: sengers rc. Acta Neuropathol. 1993;86(4):386-92. doi: 10.1007/BF00369452. Acta Neuropathol. 1993. PMID: 8256590

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