Hageman G - Search Results

1

Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19.

Duarri A, Jezierska J, Fokkens M, Meijer M, Schelhaas HJ, den Dunnen WF, van Dijk F, Verschuuren-Bemelmans C, Hageman G, van de Vlies P, Küsters B, van de Warrenburg BP, Kremer B, Wijmenga C, Sinke RJ, Swertz MA, Kampinga HH, Boddeke E, Verbeek DS. Duarri A, et al. Among authors: hageman g. Ann Neurol. 2012 Dec;72(6):870-80. doi: 10.1002/ana.23700. Ann Neurol. 2012. PMID: 23280838

2

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. Among authors: hageman g. J Neurol. 2001 Feb;248(2):113-20. doi: 10.1007/s004150170245. J Neurol. 2001. PMID: 11284128

3

First patho-anatomical investigation of the brain of a SCA19 patient.

Seidel K, Küsters B, den Dunnen WF, Bouzrou M, Hageman G, Korf HW, Schelhaas HJ, Verbeek D, Rüb U. Seidel K, et al. Among authors: hageman g. Neuropathol Appl Neurobiol. 2014 Aug;40(5):640-4. doi: 10.1111/nan.12128. Neuropathol Appl Neurobiol. 2014. PMID: 24612451 No abstract available.

4

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. Among authors: hageman g. Clin Neurol Neurosurg. 1997 May;99(2):99-101. doi: 10.1016/s0303-8467(97)00604-5. Clin Neurol Neurosurg. 1997. PMID: 9213052

5

Cognitive impairment in SCA-19.

Schelhaas HJ, van de Warrenburg BP, Hageman G, Ippel EE, van Hout M, Kremer B. Schelhaas HJ, et al. Among authors: hageman g. Acta Neurol Belg. 2003 Dec;103(4):199-205. Acta Neurol Belg. 2003. PMID: 15008504

6

Schelhaas HJ, Ippel PF, Beemer FA, Hageman G. Schelhaas HJ, et al. Among authors: hageman g. 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.

7

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. Among authors: hageman g. Neurology. 2002 Dec 24;59(12):2007-8. doi: 10.1212/01.wnl.0000038390.29853.46. Neurology. 2002. PMID: 12499506 No abstract available.

8

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. Among authors: hageman g. Clin Neurol Neurosurg. 1999 Dec;101(4):253-5. doi: 10.1016/s0303-8467(99)00051-7. Clin Neurol Neurosurg. 1999. PMID: 10622455

9

A Pyramidal Cause of a Cerebellar Ataxia: HSP-7.

Lagrand TJ, Hageman G. Lagrand TJ, et al. Among authors: hageman g. Case Rep Neurol. 2020 Oct 2;12(3):329-333. doi: 10.1159/000509346. eCollection 2020 Sep-Dec. Case Rep Neurol. 2020. PMID: 33173492 Free PMC article.

10

Sensitivity and specificity of the 'Awaji' electrodiagnostic criteria for amyotrophic lateral sclerosis: retrospective comparison of the Awaji and revised El Escorial criteria for ALS.

Boekestein WA, Kleine BU, Hageman G, Schelhaas HJ, Zwarts MJ. Boekestein WA, et al. Among authors: hageman g. Amyotroph Lateral Scler. 2010 Dec;11(6):497-501. doi: 10.3109/17482961003777462. Epub 2010 Jun 11. Amyotroph Lateral Scler. 2010. PMID: 20536375

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