van de Warrenburg BPC - Search Results

1

Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia.

Nibbeling EAR, Duarri A, Verschuuren-Bemelmans CC, Fokkens MR, Karjalainen JM, Smeets CJLM, de Boer-Bergsma JJ, van der Vries G, Dooijes D, Bampi GB, van Diemen C, Brunt E, Ippel E, Kremer B, Vlak M, Adir N, Wijmenga C, van de Warrenburg BPC, Franke L, Sinke RJ, Verbeek DS. Nibbeling EAR, et al. Among authors: de boer bergsma jj, van diemen c, van der vries g, van de warrenburg bpc. Brain. 2017 Nov 1;140(11):2860-2878. doi: 10.1093/brain/awx251. Brain. 2017. PMID: 29053796

2

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.

3

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

4

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.

5

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

6

SCA19 and SCA22: evidence for one locus with a worldwide distribution.

Schelhaas HJ, Verbeek DS, Van de Warrenburg BP, Sinke RJ. Schelhaas HJ, et al. Brain. 2004 Jan;127(Pt 1):E6; author reply E7. doi: 10.1093/brain/awh036. Brain. 2004. PMID: 14679032 Free article. No abstract available.

7

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

8

Peripheral nerve involvement in spinocerebellar ataxias.

van de Warrenburg BP, Notermans NC, Schelhaas HJ, van Alfen N, Sinke RJ, Knoers NV, Zwarts MJ, Kremer BP. van de Warrenburg BP, et al. Arch Neurol. 2004 Feb;61(2):257-61. doi: 10.1001/archneur.61.2.257. Arch Neurol. 2004. PMID: 14967775 Clinical Trial.

9

Cognitive impairment in SCA-19.

Schelhaas HJ, van de Warrenburg BP, Hageman G, Ippel EE, van Hout M, Kremer B. Schelhaas HJ, et al. Acta Neurol Belg. 2003 Dec;103(4):199-205. Acta Neurol Belg. 2003. PMID: 15008504

10

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

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

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