Meyer T - Search Results

1

Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosis.

Ruf WP, Boros M, Freischmidt A, Brenner D, Grozdanov V, de Meirelles J, Meyer T, Grehl T, Petri S, Grosskreutz J, Weyen U, Guenther R, Regensburger M, Hagenacker T, Koch JC, Emmer A, Roediger A, Steinbach R, Wolf J, Weishaupt JH, Lingor P, Deschauer M, Cordts I, Klopstock T, Reilich P, Schoeberl F, Schrank B, Zeller D, Hermann A, Knehr A, Günther K, Dorst J, Schuster J, Siebert R, Ludolph AC, Müller K. Ruf WP, et al. Among authors: meyer t. Brain Commun. 2023 May 9;5(3):fcad152. doi: 10.1093/braincomms/fcad152. eCollection 2023. Brain Commun. 2023. PMID: 37223130 Free PMC article.

2

Studies of the coding region of the neuronal glutamate transporter gene in amyotrophic lateral sclerosis.

Meyer T, Lenk U, Küther G, Weindl A, Speer A, Ludolph AC. Meyer T, et al. Ann Neurol. 1995 Jun;37(6):817-9. doi: 10.1002/ana.410370618. Ann Neurol. 1995. PMID: 7778858

3

The glial glutamate transporter complementary DNA in patients with amyotrophic lateral sclerosis.

Meyer T, Speer A, Meyer B, Sitte W, Küther G, Ludolph AC. Meyer T, et al. Among authors: meyer b. Ann Neurol. 1996 Sep;40(3):456-9. doi: 10.1002/ana.410400317. Ann Neurol. 1996. PMID: 8797537

4

Genomic organization of the human excitatory amino acid transporter gene GLT-1.

Meyer T, Ludolph AC, Morkel M, Hagemeier C, Speer A. Meyer T, et al. Neuroreport. 1997 Feb 10;8(3):775-7. doi: 10.1097/00001756-199702100-00039. Neuroreport. 1997. PMID: 9106765

5

[Molecular biology findings in amyotrophic lateral sclerosis].

Bachus R, Claus A, Meyer T, Riepe M, Ludolph AC. Bachus R, et al. Among authors: meyer t. Nervenarzt. 1997 Oct;68(10):785-91. doi: 10.1007/s001150050195. Nervenarzt. 1997. PMID: 9441250 Review. German.

6

Alternative splicing of the glutamate transporter EAAT2 (GLT-1).

Meyer T, Münch C, Knappenberger B, Liebau S, Völkel H, Ludolph AC. Meyer T, et al. Neurosci Lett. 1998 Jan 23;241(1):68-70. doi: 10.1016/s0304-3940(97)00973-7. Neurosci Lett. 1998. PMID: 9502218

7

5'-heterogeneity of the human excitatory amino acid transporter cDNA EAAT2 (GLT-1).

Münch C, Schwalenstöcker B, Knappenberger B, Liebau S, Völkel H, Ludolph AC, Meyer T. Münch C, et al. Among authors: meyer t. Neuroreport. 1998 May 11;9(7):1295-7. doi: 10.1097/00001756-199805110-00007. Neuroreport. 1998. PMID: 9631416

8

The EAAT2 (GLT-1) gene in motor neuron disease: absence of mutations in amyotrophic lateral sclerosis and a point mutation in patients with hereditary spastic paraplegia.

Meyer T, Münch C, Völkel H, Booms P, Ludolph AC. Meyer T, et al. J Neurol Neurosurg Psychiatry. 1998 Oct;65(4):594-6. doi: 10.1136/jnnp.65.4.594. J Neurol Neurosurg Psychiatry. 1998. PMID: 9771796 Free PMC article.

9

Antiglutamate therapy of ALS--which is the next step?

Ludolph AC, Meyer T, Riepe MW. Ludolph AC, et al. Among authors: meyer t. J Neural Transm Suppl. 1999;55:79-95. doi: 10.1007/978-3-7091-6369-6_8. J Neural Transm Suppl. 1999. PMID: 10335495 Review.

10

The RNA of the glutamate transporter EAAT2 is variably spliced in amyotrophic lateral sclerosis and normal individuals.

Meyer T, Fromm A, Münch C, Schwalenstöcker B, Fray AE, Ince PG, Stamm S, Grön G, Ludolph AC, Shaw PJ. Meyer T, et al. J Neurol Sci. 1999 Nov 15;170(1):45-50. doi: 10.1016/s0022-510x(99)00196-3. J Neurol Sci. 1999. PMID: 10540035

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