Knoers NV - Search Results

1

[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.

2

[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.

3

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

4

[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.

5

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

6

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

7

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.

8

Autosomal recessive cerebellar ataxias: the current state of affairs.

Vermeer S, van de Warrenburg BP, Willemsen MA, Cluitmans M, Scheffer H, Kremer BP, Knoers NV. Vermeer S, et al. Among authors: knoers nv. J Med Genet. 2011 Oct;48(10):651-9. doi: 10.1136/jmedgenet-2011-100210. Epub 2011 Aug 19. J Med Genet. 2011. PMID: 21856962 Review.

9

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.

10

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.

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