Renier WO - Search Results

1

A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome.

De Coo IF, Renier WO, Ruitenbeek W, Ter Laak HJ, Bakker M, Schägger H, Van Oost BA, Smeets HJ. De Coo IF, et al. Among authors: renier wo. Ann Neurol. 1999 Jan;45(1):130-3. doi: 10.1002/1531-8249(199901)45:1<130::aid-art21>3.3.co;2-q. Ann Neurol. 1999. PMID: 9894888

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: renier wo. Neuropediatrics. 1991 Feb;22(1):10-4. doi: 10.1055/s-2008-1071408. Neuropediatrics. 1991. PMID: 1903852 Review.

3

A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscle.

Van Erven PM, Gabreëls FJ, Ruitenbeek W, Renier WO, Ter Laak HJ, Stadhouders AM. Van Erven PM, et al. Among authors: renier wo. J Neurol Neurosurg Psychiatry. 1988 May;51(5):704-8. doi: 10.1136/jnnp.51.5.704. J Neurol Neurosurg Psychiatry. 1988. PMID: 2841425 Free PMC article.

4

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

5

Hypokinesia and rigidity as clinical manifestations of mitochondrial encephalomyopathy: report of three cases.

van Erven PM, Renier WO, Gabreëls FJ, Thijssen HO, Ruitenbeek W, Horstink MW. van Erven PM, et al. Among authors: renier wo. Dev Med Child Neurol. 1989 Feb;31(1):81-91. doi: 10.1111/j.1469-8749.1989.tb08415.x. Dev Med Child Neurol. 1989. PMID: 2537772

6

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

7

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.

8

Leigh syndrome, a mitochondrial encephalo(myo)pathy. A review of the literature.

van Erven PM, Cillessen JP, Eekhoff EM, Gabreëls FJ, Doesburg WH, Lemmens WA, Slooff JL, Renier WO, Ruitenbeek W. van Erven PM, et al. Among authors: renier wo. Clin Neurol Neurosurg. 1987;89(4):217-30. doi: 10.1016/s0303-8467(87)80020-3. Clin Neurol Neurosurg. 1987. PMID: 3319345 Review.

9

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

10

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

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