Kremer HP - Search Results

1

[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.

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: kremer hp. Neurology. 2002 Mar 12;58(5):702-8. doi: 10.1212/wnl.58.5.702. Neurology. 2002. PMID: 11889231

3

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

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

4

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

5

Reviewing the genetic causes of spastic-ataxias.

de Bot ST, Willemsen MA, Vermeer S, Kremer HP, van de Warrenburg BP. de Bot ST, et al. Among authors: kremer hp. Neurology. 2012 Oct 2;79(14):1507-14. doi: 10.1212/WNL.0b013e31826d5fb0. Neurology. 2012. PMID: 23033504 Review.

6

CSF analysis differentiates multiple-system atrophy from idiopathic late-onset cerebellar ataxia.

Abdo WF, van de Warrenburg BP, Munneke M, van Geel WJ, Bloem BR, Kremer HP, Verbeek MM. Abdo WF, et al. Among authors: kremer hp. Neurology. 2006 Aug 8;67(3):474-9. doi: 10.1212/01.wnl.0000227891.25592.8c. Neurology. 2006. PMID: 16894110 Free article.

7

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: kremer hp. Brain. 2012 Oct;135(Pt 10):2994-3004. doi: 10.1093/brain/aws224. Epub 2012 Sep 10. Brain. 2012. PMID: 22964162

8

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: kremer hp. Brain. 2004 Nov;127(Pt 11):2551-7. doi: 10.1093/brain/awh276. Epub 2004 Aug 11. Brain. 2004. PMID: 15306549

9

Pure adult-onset spastic paraplegia caused by a novel mutation in the KIAA0196 (SPG8) gene.

de Bot ST, Vermeer S, Buijsman W, Heister A, Voorendt M, Verrips A, Scheffer H, Kremer HP, van de Warrenburg BP, Kamsteeg EJ. de Bot ST, et al. Among authors: kremer hp. J Neurol. 2013 Jul;260(7):1765-9. doi: 10.1007/s00415-013-6870-x. Epub 2013 Mar 2. J Neurol. 2013. PMID: 23455931

10

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: kremer hp. 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.

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