Ludolph AC - Search Results

1

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: ludolph ac. Neurochem Res. 2008 Jun;33(6):1005-10. doi: 10.1007/s11064-007-9540-5. Epub 2007 Nov 13. Neurochem Res. 2008. PMID: 17999180

2

Differential RNA cleavage and polyadenylation of the glutamate transporter EAAT2 in the human brain.

Münch C, Schwalenstöcker B, Hermann C, Cirovic S, Stamm S, Ludolph A, Meyer T. Münch C, et al. Brain Res Mol Brain Res. 2000 Sep 15;80(2):244-51. doi: 10.1016/s0169-328x(00)00139-x. Brain Res Mol Brain Res. 2000. PMID: 11038258

3

Ifosfamide encephalopathy presenting with asterixis.

Meyer T, Ludolph AC, Münch C. Meyer T, et al. Among authors: ludolph ac. 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

4

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: ludolph ac. J Neurosci Res. 2003 Mar 15;71(6):819-25. doi: 10.1002/jnr.10536. J Neurosci Res. 2003. PMID: 12605408

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: ludolph ac. 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: ludolph ac. 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: ludolph ac. Ann Neurol. 2005 Nov;58(5):777-80. doi: 10.1002/ana.20631. Ann Neurol. 2005. PMID: 16240349

8

Tau isoforms expression in transgenic mouse model of amyotrophic lateral sclerosis.

Usarek E, Kuźma-Kozakiewicz M, Schwalenstöcker B, Kaźmierczak B, Münch C, Ludolph AC, Barańczyk-Kuźma A. Usarek E, et al. Among authors: ludolph ac. Neurochem Res. 2006 May;31(5):597-602. doi: 10.1007/s11064-006-9057-3. Epub 2006 May 23. Neurochem Res. 2006. PMID: 16770730

9

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. Amyotroph Lateral Scler. 2007 Aug;8(4):217-23. doi: 10.1080/17482960701292837. Amyotroph Lateral Scler. 2007. PMID: 17653919

10

Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis.

Fernández-Santiago R, Hoenig S, Lichtner P, Sperfeld AD, Sharma M, Berg D, Weichenrieder O, Illig T, Eger K, Meyer T, Anneser J, Münch C, Zierz S, Gasser T, Ludolph A. Fernández-Santiago R, et al. J Neurol. 2009 Aug;256(8):1337-42. doi: 10.1007/s00415-009-5124-4. Epub 2009 Apr 12. J Neurol. 2009. PMID: 19363631 Free PMC article.

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