Hünermund G - Search Results

1

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: hunermund g. J Neurol. 2002 Dec;249(12):1629-50. doi: 10.1007/s00415-002-0946-3. J Neurol. 2002. PMID: 12529785 Review.

2

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: hunermund g. J Neurol. 2001 Oct;248(10):861-5. doi: 10.1007/s004150170070. J Neurol. 2001. PMID: 11697522

3

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: hunermund g. Neurology. 2002 Apr 23;58(8):1273-6. doi: 10.1212/wnl.58.8.1273. Neurology. 2002. PMID: 11971098

4

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: hunermund g. Neurology. 2004 Jun 22;62(12):2203-8. doi: 10.1212/01.wnl.0000130485.89814.10. Neurology. 2004. PMID: 15210883

5

Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophy.

Hünermund G, Schirmacher A, Ringelstein B, Young P, Watts GD, Meuleman J, Nelis E, Chance PF, Timmerman V, Stögbauer F, Kuhlenbäumer G. Hünermund G, et al. Muscle Nerve. 2004 Apr;29(4):601-4. doi: 10.1002/mus.20009. Muscle Nerve. 2004. PMID: 15052627

6

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: hunermund g. J Neurol. 2004 Mar;251(3):357-9. doi: 10.1007/s00415-004-0335-1. J Neurol. 2004. PMID: 15015022 No abstract available.

7

Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA).

Meuleman J, Kuhlenbäumer G, Audenaert D, Hünermund G, Hor H, Young P, Stögbauer F, Ringelstein EB, Van Broeckhoven C, De Jonghe P, Timmerman V. Meuleman J, et al. Among authors: hunermund g. Hum Genet. 2001 May;108(5):390-3. doi: 10.1007/s004390100510. Hum Genet. 2001. PMID: 11409865

8

[The reliability of the german version of the barthel-index and the development of a postal and telephone version for the application on stroke patients].

Heuschmann PU, Kolominsky-Rabas PL, Nolte CH, Hünermund G, Ruf HU, Laumeier I, Meyrer R, Alberti T, Rahmann A, Kurth T, Berger K. Heuschmann PU, et al. Among authors: hunermund g. Fortschr Neurol Psychiatr. 2005 Feb;73(2):74-82. doi: 10.1055/s-2004-830172. Fortschr Neurol Psychiatr. 2005. PMID: 15685491 German.

9

[The battle against cattle tuberculosis in Germany].

Hünermund G, Kropp R. Hünermund G, et al. Pneumologie. 2006 Dec;60(12):772-6. doi: 10.1055/s-2006-944284. Pneumologie. 2006. PMID: 17163317 German. No abstract available.

10

[Rapidly progressive glomerulonephritis in a child. Clinical and histological observation over 3 1/2 years (author's transl)].

Brandis M, Krause PH, Hünermund G, Bahlmann J. Brandis M, et al. Among authors: hunermund g. Monatsschr Kinderheilkd (1902). 1976 Feb;124(2):85-9. Monatsschr Kinderheilkd (1902). 1976. PMID: 1256457 German.

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