van de Warrenburg BP - Search Results

1

Genotype-phenotype correlations in spastic paraplegia type 7: a study in a large Dutch cohort.

van Gassen KL, van der Heijden CD, de Bot ST, den Dunnen WF, van den Berg LH, Verschuuren-Bemelmans CC, Kremer HP, Veldink JH, Kamsteeg EJ, Scheffer H, van de Warrenburg BP. van Gassen KL, et al. Among authors: van der heijden cd, van den berg lh, van de warrenburg bp, de bot st. Brain. 2012 Oct;135(Pt 10):2994-3004. doi: 10.1093/brain/aws224. Epub 2012 Sep 10. Brain. 2012. PMID: 22964162

2

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

3

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.

4

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

5

[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.

6

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.

7

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

8

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

9

Neuromuscular transmission in SCA6.

Schelhaas HJ, Van de Warrenburg BP, Kremer HP, Zwarts MJ. Schelhaas HJ, et al. Among authors: van de warrenburg bp. Ann Neurol. 2004 Mar;55(3):451-2. doi: 10.1002/ana.20015. Ann Neurol. 2004. PMID: 14991832 No abstract available.

10

[From gene to disease; autosomal dominant cerebellar ataxias].

Kremer HP, van de Warrenburg BP, Sinke RJ. Kremer HP, et al. Among authors: van de warrenburg bp. Ned Tijdschr Geneeskd. 2004 Mar 27;148(13):614-6. Ned Tijdschr Geneeskd. 2004. PMID: 15083626 Review. Dutch.

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