Schirmacher A - Search Results

1

Interaction of BDNF and COMT polymorphisms on paired-associative stimulation-induced cortical plasticity.

Witte AV, Kürten J, Jansen S, Schirmacher A, Brand E, Sommer J, Flöel A. Witte AV, et al. Among authors: schirmacher a. J Neurosci. 2012 Mar 28;32(13):4553-61. doi: 10.1523/JNEUROSCI.6010-11.2012. J Neurosci. 2012. PMID: 22457502 Free PMC article.

2

COMT Val158Met Polymorphism Modulates Cognitive Effects of Dietary Intervention.

Witte AV, Jansen S, Schirmacher A, Young P, Flöel A. Witte AV, et al. Among authors: schirmacher a. Front Aging Neurosci. 2010 Nov 5;2:146. doi: 10.3389/fnagi.2010.00146. eCollection 2010. Front Aging Neurosci. 2010. PMID: 21119769 Free PMC article.

3

Enhanced rapid-onset cortical plasticity in CADASIL as a possible mechanism of preserved cognition.

List J, Duning T, Meinzer M, Kürten J, Schirmacher A, Deppe M, Evers S, Young P, Flöel A. List J, et al. Among authors: schirmacher a. Cereb Cortex. 2011 Dec;21(12):2774-87. doi: 10.1093/cercor/bhr071. Epub 2011 Apr 29. Cereb Cortex. 2011. PMID: 21531778

4

A novel splice site mutation in the SPG7 gene causing widespread fiber damage in homozygous and heterozygous subjects.

Warnecke T, Duning T, Schirmacher A, Mohammadi S, Schwindt W, Lohmann H, Dziewas R, Deppe M, Ringelstein EB, Young P. Warnecke T, et al. Among authors: schirmacher a. Mov Disord. 2010 Mar 15;25(4):413-20. doi: 10.1002/mds.22949. Mov Disord. 2010. PMID: 20108356

5

Specific pattern of early white-matter changes in pure hereditary spastic paraplegia.

Duning T, Warnecke T, Schirmacher A, Schiffbauer H, Lohmann H, Mohammadi S, Young P, Deppe M. Duning T, et al. Among authors: schirmacher a. Mov Disord. 2010 Sep 15;25(12):1986-92. doi: 10.1002/mds.23211. Mov Disord. 2010. PMID: 20669295

6

Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women.

Domschke K, Freitag CM, Kuhlenbäumer G, Schirmacher A, Sand P, Nyhuis P, Jacob C, Fritze J, Franke P, Rietschel M, Garritsen HS, Fimmers R, Nöthen MM, Lesch KP, Stögbauer F, Deckert J. Domschke K, et al. Among authors: schirmacher a. Int J Neuropsychopharmacol. 2004 Jun;7(2):183-8. doi: 10.1017/S146114570400416X. Epub 2004 Mar 5. Int J Neuropsychopharmacol. 2004. PMID: 15009906 Free article.

7

Genetic variants of the NOTCH3 gene in migraine--a mutation analysis and association study.

Schwaag S, Evers S, Schirmacher A, Stögbauer F, Ringelstein EB, Kuhlenbäumer G. Schwaag S, et al. Among authors: schirmacher a. Cephalalgia. 2006 Feb;26(2):158-61. doi: 10.1111/j.1468-2982.2005.01007.x. Cephalalgia. 2006. PMID: 16426270 Clinical Trial.

8

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

9

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. Among authors: schirmacher a. Muscle Nerve. 2004 Apr;29(4):601-4. doi: 10.1002/mus.20009. Muscle Nerve. 2004. PMID: 15052627

10

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

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