Sengers RC - Search Results

1

Preterm birth in Sjögren-Larsson syndrome.

Willemsen MA, Rotteveel JJ, van Domburg PH, Gabreëls FJ, Mayatepek E, Sengers RC. Willemsen MA, et al. Among authors: sengers rc. Neuropediatrics. 1999 Dec;30(6):325-7. doi: 10.1055/s-2007-973513. Neuropediatrics. 1999. PMID: 10706028

2

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.

3

GM2-gangliosidosis. Clinical and biochemical aspects of four cases.

Praamstra P, Wevers RA, Gabreëls FJ, Rotteveel JJ, Renier WO, Sengers RC, Lamers KJ. Praamstra P, et al. Among authors: sengers rc. Clin Neurol Neurosurg. 1990;92(2):143-8. doi: 10.1016/0303-8467(90)90090-r. Clin Neurol Neurosurg. 1990. PMID: 2163796

4

Multicore myopathy with restrictive cardiomyopathy.

Willemsen MA, van Oort AM, ter Laak HJ, Sengers RC, Gabreëls FJ. Willemsen MA, et al. Among authors: sengers rc. Acta Paediatr. 1997 Nov;86(11):1271-4. doi: 10.1111/j.1651-2227.1997.tb14862.x. Acta Paediatr. 1997. PMID: 9401528 Review.

5

Clinical heterogeneity in respiratory chain complex III deficiency in childhood.

Mourmans J, Wendel U, Bentlage HA, Trijbels JM, Smeitink JA, de Coo IF, Gabreëls FJ, Sengers RC, Ruitenbeek W. Mourmans J, et al. Among authors: sengers rc. J Neurol Sci. 1997 Jul;149(1):111-7. doi: 10.1016/s0022-510x(97)05379-3. J Neurol Sci. 1997. PMID: 9168175

6

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

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

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

9

Laminin-alpha2 (merosin), beta-dystroglycan, alpha-sarcoglycan (adhalin), and dystrophin expression in congenital muscular dystrophies: an immunohistochemical study.

ter Laak HJ, Leyten QH, Gabreëls FJ, Kuppen H, Renier WO, Sengers RC. ter Laak HJ, et al. Among authors: sengers rc. Clin Neurol Neurosurg. 1998 Mar;100(1):5-10. doi: 10.1016/s0303-8467(97)00109-1. Clin Neurol Neurosurg. 1998. PMID: 9637197

10

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

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