Schelhaas HJ - Search Results

1

Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxia.

Schelhaas HJ, Ippel PF, Hageman G, Sinke RJ, van der Laan EN, Beemer FA. Schelhaas HJ, et al. J Neurol. 2001 Feb;248(2):113-20. doi: 10.1007/s004150170245. J Neurol. 2001. PMID: 11284128

2

Cerebellar ataxia, dementia, pyramidal signs, cortical cataract of the posterior pole and a raised IgG index in a patient with a sporadic form of olivopontocerebellar atrophy.

Schelhaas HJ, Hageman G, Post JG. Schelhaas HJ, et al. Clin Neurol Neurosurg. 1997 May;99(2):99-101. doi: 10.1016/s0303-8467(97)00604-5. Clin Neurol Neurosurg. 1997. PMID: 9213052

3

Early onset cerebellar ataxia with retained tendon reflexes: foot deformity in a first grade family member.

Schelhaas HJ, Hulst MV, Ippel E, Prevo RL, Hageman G. Schelhaas HJ, et al. Clin Neurol Neurosurg. 1999 Dec;101(4):253-5. doi: 10.1016/s0303-8467(99)00051-7. Clin Neurol Neurosurg. 1999. PMID: 10622455

4

Schelhaas HJ, Ippel PF, Beemer FA, Hageman G. Schelhaas HJ, et al. Eur J Neurol. 2000 May;7(3):309-14. doi: 10.1046/j.1468-1331.2000.00067.x. Eur J Neurol. 2000. PMID: 10886315 Review.

5

Transient cerebral white matter lesions in a patient with connexin 32 missense mutation.

Schelhaas HJ, Van Engelen BG, Gabreëls-Festen AA, Hageman G, Vliegen JH, Van Der Knaap MS, Zwarts MJ. Schelhaas HJ, et al. Neurology. 2002 Dec 24;59(12):2007-8. doi: 10.1212/01.wnl.0000038390.29853.46. Neurology. 2002. PMID: 12499506 No abstract available.

6

The "split hand" phenomenon: evidence of a spinal origin.

Schelhaas HJ, van de Warrenburg BP, Kremer HP, Zwarts MJ. Schelhaas HJ, et al. Neurology. 2003 Dec 9;61(11):1619-20. doi: 10.1212/01.wnl.0000096009.50213.6c. Neurology. 2003. PMID: 14663056

7

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.

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. Among authors: schelhaas hj. 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

Clinical, psychological, and genetic characteristics of spinocerebellar ataxia type 19 (SCA19).

Schelhaas HJ, van de Warrenburg BP. Schelhaas HJ, et al. Cerebellum. 2005;4(1):51-4. doi: 10.1080/14734220510007888. Cerebellum. 2005. PMID: 15895560 Review.

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