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Recent advances in hereditary spinocerebellar ataxias.
van de Warrenburg BP, Sinke RJ, Kremer B. van de Warrenburg BP, et al. J Neuropathol Exp Neurol. 2005 Mar;64(3):171-80. doi: 10.1093/jnen/64.3.171. J Neuropathol Exp Neurol. 2005. PMID: 15804048 Review.
Paroxysmal leg weakness and hearing loss in a patient with subarachnoid hemorrhage.
van de Warrenburg B, Vos P, Merx H, Kremer B. van de Warrenburg B, et al. Eur Neurol. 2000;44(3):186-7. doi: 10.1159/000008233. Eur Neurol. 2000. PMID: 11053971 No abstract available.
Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations.
van de Warrenburg BP, Lammens M, Lücking CB, Denèfle P, Wesseling P, Booij J, Praamstra P, Quinn N, Brice A, Horstink MW. van de Warrenburg BP, et al. Neurology. 2001 Feb 27;56(4):555-7. doi: 10.1212/wnl.56.4.555. Neurology. 2001. PMID: 11222808
[Autosomal dominant cerebellar ataxias in the Netherlands: a national inventory].
van de Warrenburg BP. van de Warrenburg BP. Ned Tijdschr Geneeskd. 2001 May 19;145(20):962-7. Ned Tijdschr Geneeskd. 2001. PMID: 11396263 Dutch.
Striking anticipation in spinocerebellar ataxia type 7: the infantile phenotype.
van de Warrenburg BP, Frenken CW, Ausems MG, Kleefstra T, Sinke RJ, Knoers NV, Kremer HP. van de Warrenburg BP, et al. J Neurol. 2001 Oct;248(10):911-4. doi: 10.1007/s004150170082. J Neurol. 2001. PMID: 11697534 No abstract available.
Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis.
van de Warrenburg BP, Sinke RJ, Verschuuren-Bemelmans CC, Scheffer H, Brunt ER, Ippel PF, Maat-Kievit JA, Dooijes D, Notermans NC, Lindhout D, Knoers NV, Kremer HP. van de Warrenburg BP, et al. Neurology. 2002 Mar 12;58(5):702-8. doi: 10.1212/wnl.58.5.702. Neurology. 2002. PMID: 11889231
[Friedrich's ataxia: clinical difficulties and genetic possibilities].
van de Warrenburg BP, Knoers NV, Kremer HP. van de Warrenburg BP, et al. Ned Tijdschr Geneeskd. 2002 Sep 7;146(36):1669-72. Ned Tijdschr Geneeskd. 2002. PMID: 12244768 Dutch.
Langerhans' cell histiocytosis presenting with progressive spinocerebellar ataxia.
van de Warrenburg BP, van der Heijden HF, Pieters G, Kremer HP. van de Warrenburg BP, et al. Among authors: van der heijden hf. J Neurol. 2003 Sep;250(9):1112-4. doi: 10.1007/s00415-003-0126-0. J Neurol. 2003. PMID: 14504976 No abstract available.
The "split hand" phenomenon: evidence of a spinal origin.
Schelhaas HJ, van de Warrenburg BP, Kremer HP, Zwarts MJ. Schelhaas HJ, et al. Among authors: van de warrenburg bp. Neurology. 2003 Dec 9;61(11):1619-20. doi: 10.1212/01.wnl.0000096009.50213.6c. Neurology. 2003. PMID: 14663056
Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family.
van de Warrenburg BP, Verbeek DS, Piersma SJ, Hennekam FA, Pearson PL, Knoers NV, Kremer HP, Sinke RJ. van de Warrenburg BP, et al. Neurology. 2003 Dec 23;61(12):1760-5. doi: 10.1212/01.wnl.0000098883.79421.73. Neurology. 2003. PMID: 14694043
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