Meyer T - Search Results

1

NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis.

Blauw HM, van Rheenen W, Koppers M, Van Damme P, Waibel S, Lemmens R, van Vught PW, Meyer T, Schulte C, Gasser T, Cuppen E, Pasterkamp RJ, Robberecht W, Ludolph AC, Veldink JH, van den Berg LH. Blauw HM, et al. Among authors: meyer t. Hum Mol Genet. 2012 Jun 1;21(11):2497-502. doi: 10.1093/hmg/dds064. Epub 2012 Feb 28. Hum Mol Genet. 2012. PMID: 22378146

2

Ifosfamide encephalopathy presenting with asterixis.

Meyer T, Ludolph AC, Münch C. Meyer T, et al. J Neurol Sci. 2002 Jul 15;199(1-2):85-8. doi: 10.1016/s0022-510x(02)00077-1. J Neurol Sci. 2002. PMID: 12084448

3

Differential regulation of 5' splice variants of the glutamate transporter EAAT2 in an in vivo model of chemical hypoxia induced by 3-nitropropionic acid.

Münch C, Zhu BG, Leven A, Stamm S, Einkörn H, Schwalenstöcker B, Ludolph AC, Riepe MW, Meyer T. Münch C, et al. Among authors: meyer t. J Neurosci Res. 2003 Mar 15;71(6):819-25. doi: 10.1002/jnr.10536. J Neurosci Res. 2003. PMID: 12605408

4

Chromosomal translocation t(18;21)(q23;q22.1) indicates novel susceptibility loci for frontotemporal dementia with ALS.

Prudlo J, Alber B, Kalscheuer VM, Roemer K, Martin T, Dullinger J, Sittinger H, Niemann S, Heutink P, Ludolph AC, Ropers HH, Zang K, Meyer T. Prudlo J, et al. Among authors: meyer t. Ann Neurol. 2004 Jan;55(1):134-8. doi: 10.1002/ana.10822. Ann Neurol. 2004. PMID: 14705124

5

Frequency of a tau genotype in amyotrophic lateral sclerosis.

Münch C, Prechter F, Xu R, Linke P, Prudlo J, Kuzma M, Kwiecinski H, Ludolph AC, Meyer T. Münch C, et al. Among authors: meyer t. J Neurol Sci. 2005 Sep 15;236(1-2):13-6. doi: 10.1016/j.jns.2005.04.004. J Neurol Sci. 2005. PMID: 16005901

6

Spastin related hereditary spastic paraplegia with dysplastic corpus callosum.

Alber B, Pernauer M, Schwan A, Rothmund G, Hoffmann KT, Brummer D, Sperfeld AD, Uttner I, Binder H, Epplen JT, Dullinger J, Ludolph AC, Meyer T. Alber B, et al. Among authors: meyer t. J Neurol Sci. 2005 Sep 15;236(1-2):9-12. doi: 10.1016/j.jns.2005.03.040. J Neurol Sci. 2005. PMID: 16009377

7

Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD.

Münch C, Rosenbohm A, Sperfeld AD, Uttner I, Reske S, Krause BJ, Sedlmeier R, Meyer T, Hanemann CO, Stumm G, Ludolph AC. Münch C, et al. Among authors: meyer t. Ann Neurol. 2005 Nov;58(5):777-80. doi: 10.1002/ana.20631. Ann Neurol. 2005. PMID: 16240349

8

Guidelines for the preclinical in vivo evaluation of pharmacological active drugs for ALS/MND: report on the 142nd ENMC international workshop.

Ludolph AC, Bendotti C, Blaugrund E, Hengerer B, Löffler JP, Martin J, Meininger V, Meyer T, Moussaoui S, Robberecht W, Scott S, Silani V, Van Den Berg LH; ENMC Group for the Establishment of Guidelines for the Conduct of Preclinical and Proof of Concept Studies in ALS/MND Models. Ludolph AC, et al. Among authors: meyer t. Amyotroph Lateral Scler. 2007 Aug;8(4):217-23. doi: 10.1080/17482960701292837. Amyotroph Lateral Scler. 2007. PMID: 17653919

9

Chemical hypoxia facilitates alternative splicing of EAAT2 in presymptomatic APP23 transgenic mice.

Münch C, Zhu BG, Mink A, Seefried U, Riepe MW, Ludolph AC, Meyer T. Münch C, et al. Among authors: meyer t. Neurochem Res. 2008 Jun;33(6):1005-10. doi: 10.1007/s11064-007-9540-5. Epub 2007 Nov 13. Neurochem Res. 2008. PMID: 17999180

10

Heterozygous S44L missense change of the spastin gene in amyotrophic lateral sclerosis.

Münch C, Rolfs A, Meyer T. Münch C, et al. Among authors: meyer t. Amyotroph Lateral Scler. 2008 Aug;9(4):251-3. doi: 10.1080/17482960801900172. Amyotroph Lateral Scler. 2008. PMID: 18608088

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