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Angelman syndrome without detectable chromosome 15q11-13 anomaly: clinical study of familial and isolated cases.
Laan LA, Halley DJ, den Boer AT, Hennekam RC, Renier WO, Brouwer OF. Laan LA, et al. Among authors: renier wo. Am J Med Genet. 1998 Mar 19;76(3):262-8. Am J Med Genet. 1998. PMID: 9508247 Review.
The linear naevus sebaceus syndrome.
van de Warrenburg BP, van Gulik S, Renier WO, Lammens M, Doelman JC. van de Warrenburg BP, et al. Among authors: renier wo. Clin Neurol Neurosurg. 1998 Jun;100(2):126-32. doi: 10.1016/s0303-8467(98)00012-2. Clin Neurol Neurosurg. 1998. PMID: 9746301 Review.
Early infantile form of neuronal ceroid lipofuscinosis. Four Dutch cases and review of the literature.
Jongen PJ, Gabreëls FJ, Stekhoven JH, Renier WO, le Coultre R, Begeer JH. Jongen PJ, et al. Among authors: renier wo. Clin Neurol Neurosurg. 1987;89(3):161-7. doi: 10.1016/s0303-8467(87)80049-5. Clin Neurol Neurosurg. 1987. PMID: 3311523 Review.
Evolution of epilepsy and EEG findings in Angelman syndrome.
Laan LA, Renier WO, Arts WF, Buntinx IM, vd Burgt IJ, Stroink H, Beuten J, Zwinderman KH, van Dijk JG, Brouwer OF. Laan LA, et al. Among authors: renier wo. Epilepsia. 1997 Feb;38(2):195-9. doi: 10.1111/j.1528-1157.1997.tb01097.x. Epilepsia. 1997. PMID: 9048672
Epilepsy treatment in The Netherlands. Comparison of two medical centres.
Wijsman DJ, Lammers MW, Hekster YA, Keyser A, Renier WO, Meinardi H, van Lier H. Wijsman DJ, et al. Among authors: renier wo. Acta Neurol Scand. 1993 Jun;87(6):438-42. doi: 10.1111/j.1600-0404.1993.tb04132.x. Acta Neurol Scand. 1993. PMID: 8356871
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
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
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.
2-Hydroxyglutaric aciduria: a case report on an infant with the D-isomeric form with review of the literature.
Geerts Y, Renier WO, Bakkeren J, de Jong J. Geerts Y, et al. Among authors: renier wo. J Neurol Sci. 1996 Nov;143(1-2):166-9. doi: 10.1016/s0022-510x(96)00179-7. J Neurol Sci. 1996. PMID: 8981317 Review.
Serologic HLA typing in cryptogenic Lennox-Gastaut syndrome.
van Engelen BG, de Waal LP, Weemaes CM, Renier WO. van Engelen BG, et al. Among authors: renier wo. Epilepsy Res. 1994 Jan;17(1):43-7. doi: 10.1016/0920-1211(94)90078-7. Epilepsy Res. 1994. PMID: 8174524
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