Sinke RJ - Search Results

1

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

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

2

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. Among authors: sinke rj. Neurology. 2002 Mar 12;58(5):702-8. doi: 10.1212/wnl.58.5.702. Neurology. 2002. PMID: 11889231

3

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. Among authors: sinke rj. Neurology. 2003 Dec 23;61(12):1760-5. doi: 10.1212/01.wnl.0000098883.79421.73. Neurology. 2003. PMID: 14694043

4

Age at onset variance analysis in spinocerebellar ataxias: a study in a Dutch-French cohort.

van de Warrenburg BP, Hendriks H, Dürr A, van Zuijlen MC, Stevanin G, Camuzat A, Sinke RJ, Brice A, Kremer BP. van de Warrenburg BP, et al. Among authors: sinke rj. Ann Neurol. 2005 Apr;57(4):505-12. doi: 10.1002/ana.20424. Ann Neurol. 2005. PMID: 15747371

5

Recent advances in hereditary spinocerebellar ataxias.

van de Warrenburg BP, Sinke RJ, Kremer B. van de Warrenburg BP, et al. Among authors: sinke rj. 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.

6

Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3.

Verbeek DS, van de Warrenburg BP, Wesseling P, Pearson PL, Kremer HP, Sinke RJ. Verbeek DS, et al. Among authors: sinke rj. Brain. 2004 Nov;127(Pt 11):2551-7. doi: 10.1093/brain/awh276. Epub 2004 Aug 11. Brain. 2004. PMID: 15306549

7

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. Among authors: sinke rj. Arch Neurol. 2004 Feb;61(2):257-61. doi: 10.1001/archneur.61.2.257. Arch Neurol. 2004. PMID: 14967775 Clinical Trial.

8

Functional analysis helps to define KCNC3 mutational spectrum in Dutch ataxia cases.

Duarri A, Nibbeling EA, Fokkens MR, Meijer M, Boerrigter M, Verschuuren-Bemelmans CC, Kremer BP, van de Warrenburg BP, Dooijes D, Boddeke E, Sinke RJ, Verbeek DS. Duarri A, et al. Among authors: sinke rj. PLoS One. 2015 Mar 10;10(3):e0116599. doi: 10.1371/journal.pone.0116599. eCollection 2015. PLoS One. 2015. PMID: 25756792 Free PMC article.

9

Clinical and molecular correlations in spinocerebellar ataxia type 6: a study of 24 Dutch families.

Sinke RJ, Ippel EF, Diepstraten CM, Beemer FA, Wokke JH, van Hilten BJ, Knoers NV, van Amstel HK, Kremer HP. Sinke RJ, et al. Arch Neurol. 2001 Nov;58(11):1839-44. doi: 10.1001/archneur.58.11.1839. Arch Neurol. 2001. PMID: 11708993

10

Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population.

Verbeek DS, Warrenburg BP, Hennekam FA, Dooijes D, Ippel PF, Verschuuren-Bemelmans CC, Kremer HP, Sinke RJ. Verbeek DS, et al. Among authors: sinke rj. Hum Genet. 2005 Jun;117(1):88-91. doi: 10.1007/s00439-005-1278-z. Epub 2005 Apr 20. Hum Genet. 2005. PMID: 15841389

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