Schoser B - Search Results

1

Immune-mediated rippling muscle disease with myasthenia gravis: a report of seven patients with long-term follow-up in two.

Schoser B, Jacob S, Hilton-Jones D, Müller-Felber W, Kubisch C, Claus D, Goebel HH, Vita G, Vincent A, Toscano A, Van den Bergh P. Schoser B, et al. Neuromuscul Disord. 2009 Mar;19(3):223-8. doi: 10.1016/j.nmd.2009.01.002. Epub 2009 Feb 8. Neuromuscul Disord. 2009. PMID: 19208478

2

Tenascin in denervated human muscle.

Schoser BG, Goebel HH. Schoser BG, et al. J Neurol Sci. 1996 Aug;139(2):203-9. J Neurol Sci. 1996. PMID: 8856654

3

Immunolocalization of tenascin-C in human type II fiber atrophy.

Schoser BG, Faissner A, Goebel HH. Schoser BG, et al. J Mol Neurosci. 1999 Aug-Oct;13(1-2):167-75. doi: 10.1385/JMN:13:1-2:167. J Mol Neurosci. 1999. PMID: 10691303

4

Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease.

Betz RC, Schoser BG, Kasper D, Ricker K, Ramírez A, Stein V, Torbergsen T, Lee YA, Nöthen MM, Wienker TF, Malin JP, Propping P, Reis A, Mortier W, Jentsch TJ, Vorgerd M, Kubisch C. Betz RC, et al. Among authors: schoser bg. Nat Genet. 2001 Jul;28(3):218-9. doi: 10.1038/90050. Nat Genet. 2001. PMID: 11431690

5

A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutation.

Vorgerd M, Ricker K, Ziemssen F, Kress W, Goebel HH, Nix WA, Kubisch C, Schoser BG, Mortier W. Vorgerd M, et al. Among authors: schoser bg. Neurology. 2001 Dec 26;57(12):2273-7. doi: 10.1212/wnl.57.12.2273. Neurology. 2001. PMID: 11756609

6

Homozygous mutations in caveolin-3 cause a severe form of rippling muscle disease.

Kubisch C, Schoser BG, von Düring M, Betz RC, Goebel HH, Zahn S, Ehrbrecht A, Aasly J, Schroers A, Popovic N, Lochmüller H, Schröder JM, Brüning T, Malin JP, Fricke B, Meinck HM, Torbergsen T, Engels H, Voss B, Vorgerd M. Kubisch C, et al. Among authors: schoser bg. Ann Neurol. 2003 Apr;53(4):512-20. doi: 10.1002/ana.10501. Ann Neurol. 2003. PMID: 12666119

7

Muscle pathology in 57 patients with myotonic dystrophy type 2.

Schoser BG, Schneider-Gold C, Kress W, Goebel HH, Reilich P, Koch MC, Pongratz DE, Toyka KV, Lochmüller H, Ricker K. Schoser BG, et al. Muscle Nerve. 2004 Feb;29(2):275-81. doi: 10.1002/mus.10545. Muscle Nerve. 2004. PMID: 14755494

8

Novel missense mutation in the caveolin-3 gene in a Belgian family with rippling muscle disease.

Van den Bergh PY, Gérard JM, Elosegi JA, Manto MU, Kubisch C, Schoser BG. Van den Bergh PY, et al. Among authors: schoser bg. J Neurol Neurosurg Psychiatry. 2004 Sep;75(9):1349-51. doi: 10.1136/jnnp.2003.028217. J Neurol Neurosurg Psychiatry. 2004. PMID: 15314133 Free PMC article.

9

Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy.

Horváth R, Schoser BG, Müller-Höcker J, Völpel M, Jaksch M, Lochmüller H. Horváth R, et al. Among authors: schoser bg. Neuromuscul Disord. 2005 Dec;15(12):851-7. doi: 10.1016/j.nmd.2005.09.005. Epub 2005 Nov 8. Neuromuscul Disord. 2005. PMID: 16288875

10

Prediction of response to IVIg treatment in patients with lower motor neurone disorders.

Strigl-Pill N, König A, Schröder M, Beranek H, Schoser BG, Spaeth M, Pongratz D, Müller-Felber W. Strigl-Pill N, et al. Among authors: schoser bg. Eur J Neurol. 2006 Feb;13(2):135-40. doi: 10.1111/j.1468-1331.2006.01142.x. Eur J Neurol. 2006. PMID: 16490043 Clinical Trial.

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