Stögbauer F - Search Results

1

Autosomal dominant striatal degeneration (ADSD): clinical description and mapping to 5q13-5q14.

Kuhlenbäumer G, Lüdemann P, Schirmacher A, De Vriendt E, Hünermund G, Young P, Hund-Georgiadis M, Schuierer G, Möller H, Ringelstein EB, Van Broeckhoven C, Timmerman V, Stögbauer F. Kuhlenbäumer G, et al. Among authors: stogbauer f. Neurology. 2004 Jun 22;62(12):2203-8. doi: 10.1212/01.wnl.0000130485.89814.10. Neurology. 2004. PMID: 15210883

2

Clinical features and molecular genetics of hereditary peripheral neuropathies.

Kuhlenbäumer G, Young P, Hünermund G, Ringelstein B, Stögbauer F. Kuhlenbäumer G, et al. Among authors: stogbauer f. J Neurol. 2002 Dec;249(12):1629-50. doi: 10.1007/s00415-002-0946-3. J Neurol. 2002. PMID: 12529785 Review.

3

Autosomal dominant burning feet syndrome.

Stögbauer F, Young P, Kuhlenbäumer G, Kiefer R, Timmerman V, Ringelstein EB, Wang JF, Schröder JM, Van Broeckhoven C, Weis J. Stögbauer F, et al. J Neurol Neurosurg Psychiatry. 1999 Jul;67(1):78-81. doi: 10.1136/jnnp.67.1.78. J Neurol Neurosurg Psychiatry. 1999. PMID: 10369826 Free PMC article.

4

Hereditary recurrent focal neuropathies: clinical and molecular features.

Stögbauer F, Young P, Kuhlenbäumer G, De Jonghe P, Timmerman V. Stögbauer F, et al. Neurology. 2000 Feb 8;54(3):546-51. doi: 10.1212/wnl.54.3.546. Neurology. 2000. PMID: 10680781

5

Thirty-seven CAG repeats in the androgen receptor gene in two healthy individuals.

Kuhlenbäumer G, Kress W, Ringelstein EB, Stögbauer F. Kuhlenbäumer G, et al. Among authors: stogbauer f. J Neurol. 2001 Jan;248(1):23-6. doi: 10.1007/s004150170265. J Neurol. 2001. PMID: 11266016

6

Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous.

Kuhlenbäumer G, Meuleman J, De Jonghe P, Falck B, Young P, Hünermund G, Van Broeckhoven C, Timmerman V, Stögbauer F. Kuhlenbäumer G, et al. Among authors: stogbauer f. J Neurol. 2001 Oct;248(10):861-5. doi: 10.1007/s004150170070. J Neurol. 2001. PMID: 11697522

7

Giant axonal neuropathy (GAN): case report and two novel mutations in the gigaxonin gene.

Kuhlenbäumer G, Young P, Oberwittler C, Hünermund G, Schirmacher A, Domschke K, Ringelstein B, Stögbauer F. Kuhlenbäumer G, et al. Among authors: stogbauer f. Neurology. 2002 Apr 23;58(8):1273-6. doi: 10.1212/wnl.58.8.1273. Neurology. 2002. PMID: 11971098

8

Late onset postpartum eclampsia: a rare and difficult diagnosis.

Dziewas R, Stögbauer F, Freund M, Lüdemann P, Imai T, Holzapfel C, Ringelstein PB. Dziewas R, et al. Among authors: stogbauer f. J Neurol. 2002 Sep;249(9):1287-91. doi: 10.1007/s00415-002-0840-z. J Neurol. 2002. PMID: 12242555

9

Cervical artery dissection--clinical features, risk factors, therapy and outcome in 126 patients.

Dziewas R, Konrad C, Dräger B, Evers S, Besselmann M, Lüdemann P, Kuhlenbäumer G, Stögbauer F, Ringelstein EB. Dziewas R, et al. Among authors: stogbauer f. J Neurol. 2003 Oct;250(10):1179-84. doi: 10.1007/s00415-003-0174-5. J Neurol. 2003. PMID: 14586598

10

Neither collagen 8A1 nor 8A2 mutations play a major role in cervical artery dissection. A mutation analysis and linkage study.

Kuhlenbäumer G, Müller US, Besselmann M, Rauterberg J, Robenek H, Hünermund G, Brandt T, Ringelstein EB, Stögbauer F, Hausser I. Kuhlenbäumer G, et al. Among authors: stogbauer f. J Neurol. 2004 Mar;251(3):357-9. doi: 10.1007/s00415-004-0335-1. J Neurol. 2004. PMID: 15015022 No abstract available.

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