Knoers NV - Search Results

1

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. Among authors: knoers nv. J Neurol. 2001 Oct;248(10):911-4. doi: 10.1007/s004150170082. J Neurol. 2001. PMID: 11697534 No abstract available.

2

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. Among authors: knoers nv. Arch Neurol. 2001 Nov;58(11):1839-44. doi: 10.1001/archneur.58.11.1839. Arch Neurol. 2001. PMID: 11708993

3

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: knoers nv. Arch Neurol. 2004 Feb;61(2):257-61. doi: 10.1001/archneur.61.2.257. Arch Neurol. 2004. PMID: 14967775 Clinical Trial.

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

5

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: knoers nv. Neurology. 2003 Dec 23;61(12):1760-5. doi: 10.1212/01.wnl.0000098883.79421.73. Neurology. 2003. PMID: 14694043

6

Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations.

de Bot ST, van den Elzen RT, Mensenkamp AR, Schelhaas HJ, Willemsen MA, Knoers NV, Kremer HP, van de Warrenburg BP, Scheffer H. de Bot ST, et al. Among authors: knoers nv. J Neurol Neurosurg Psychiatry. 2010 Oct;81(10):1073-8. doi: 10.1136/jnnp.2009.201103. Epub 2010 Jun 20. J Neurol Neurosurg Psychiatry. 2010. PMID: 20562464 Free article.

7

[Friedrich's ataxia: clinical difficulties and genetic possibilities].

van de Warrenburg BP, Knoers NV, Kremer HP. van de Warrenburg BP, et al. Among authors: knoers nv. Ned Tijdschr Geneeskd. 2002 Sep 7;146(36):1669-72. Ned Tijdschr Geneeskd. 2002. PMID: 12244768 Dutch.

8

[Neurodegenerative disorders and the role of trinucleotide repeat expansion. I. The diseases].

Kremer HP, Knoers NV. Kremer HP, et al. Among authors: knoers nv. Ned Tijdschr Geneeskd. 1996 Nov 23;140(47):2325-9. Ned Tijdschr Geneeskd. 1996. PMID: 8984394 Review. Dutch. No abstract available.

9

[Neurodegenerative disorders and the role of trinucleotide repeat expansion. III. Molecular pathophysiology].

Kremer HP, Knoers NV. Kremer HP, et al. Among authors: knoers nv. Ned Tijdschr Geneeskd. 1996 Nov 23;140(47):2333-6. Ned Tijdschr Geneeskd. 1996. PMID: 8984396 Dutch. No abstract available.

10

ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia.

Vermeer S, Meijer RP, Pijl BJ, Timmermans J, Cruysberg JR, Bos MM, Schelhaas HJ, van de Warrenburg BP, Knoers NV, Scheffer H, Kremer B. Vermeer S, et al. Among authors: knoers nv. Neurogenetics. 2008 Jul;9(3):207-14. doi: 10.1007/s10048-008-0131-7. Epub 2008 May 9. Neurogenetics. 2008. PMID: 18465152 Free PMC article.

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