Renier WO - Search Results

1

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: renier wo. 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.

2

Congenital muscular dystrophy with eye and brain malformations in six Dutch patients.

Leyten QH, Gabreëls FJ, Renier WO, Renkawek K, ter Laak HJ, Mullaart RA. Leyten QH, et al. Among authors: renier wo. Neuropediatrics. 1992 Dec;23(6):316-20. doi: 10.1055/s-2008-1071365. Neuropediatrics. 1992. PMID: 1491751

3

Neuropathological findings in muscle-eye-brain disease (MEB-D). Neuropathological delineation of MEB-D from congenital muscular dystrophy of the Fukuyama type.

Leyten QH, Renkawek K, Renier WO, Gabreëls FJ, Mooy CM, ter Laak HJ, Mullaart RA. Leyten QH, et al. Among authors: renier wo. Acta Neuropathol. 1991;83(1):55-60. doi: 10.1007/BF00294430. Acta Neuropathol. 1991. PMID: 1792864

4

Congenital muscular dystrophy.

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

5

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: renier wo. Acta Neuropathol. 1993;86(4):386-92. doi: 10.1007/BF00369452. Acta Neuropathol. 1993. PMID: 8256590

6

Congenital muscular dystrophy and severe central nervous system atrophy in two siblings.

Leyten QH, Barth PG, Gabreëls FJ, Renkawek K, Renier WO, Gabreëls-Festen AA, ter Laak HJ, Smits MG. Leyten QH, et al. Among authors: renier wo. Acta Neuropathol. 1995;90(6):650-6. doi: 10.1007/BF00318580. Acta Neuropathol. 1995. PMID: 8615088

7

Association of congenital muscular dystrophy with hypoplasia of the lateral abdominal wall musculature and hypoplasia of the external genitalia.

Leyten QH, Renier WO, Gabreëls FJ, Brunner HG, ter Laak HJ, Mullaart RA. Leyten QH, et al. Among authors: renier wo. Neuropediatrics. 1996 Apr;27(2):108-10. doi: 10.1055/s-2007-973759. Neuropediatrics. 1996. PMID: 8737828 Free article. No abstract available.

8

Congenital muscular dystrophy: a review of the literature.

Leyten QH, Gabreëls FJ, Renier WO, ter Laak HJ. Leyten QH, et al. Among authors: renier wo. Clin Neurol Neurosurg. 1996 Nov;98(4):267-80. doi: 10.1016/0303-8467(96)00043-1. Clin Neurol Neurosurg. 1996. PMID: 8930416 Review.

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: renier wo. Clin Neurol Neurosurg. 1998 Mar;100(1):5-10. doi: 10.1016/s0303-8467(97)00109-1. Clin Neurol Neurosurg. 1998. PMID: 9637197

10

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: renier wo. Arch Neurol. 1991 Mar;48(3):334-8. doi: 10.1001/archneur.1991.00530150106028. Arch Neurol. 1991. PMID: 1900413

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