Schoser B - Search Results

1

Congenital myopathy and epidermolysis bullosa due to PLEC variant.

Walter MC, Reilich P, Krause S, Hiebeler M, Gehling S, Goebel HH, Schoser B, Abicht A. Walter MC, et al. Among authors: schoser b. Neuromuscul Disord. 2021 Nov;31(11):1212-1217. doi: 10.1016/j.nmd.2021.09.009. Epub 2021 Sep 30. Neuromuscul Disord. 2021. PMID: 34702657

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

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

5

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

6

Homozygosity for CCTG mutation in myotonic dystrophy type 2.

Schoser BG, Kress W, Walter MC, Halliger-Keller B, Lochmüller H, Ricker K. Schoser BG, et al. Brain. 2004 Aug;127(Pt 8):1868-77. doi: 10.1093/brain/awh210. Epub 2004 Jul 1. Brain. 2004. PMID: 15231584

7

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

8

Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophy.

Müller JS, Piko H, Schoser BG, Schlotter-Weigel B, Reilich P, Gürster S, Born C, Karcagi V, Pongratz D, Lochmüller H, Walter MC. Müller JS, et al. Among authors: schoser bg. Neuromuscul Disord. 2006 Jul;16(7):432-6. doi: 10.1016/j.nmd.2006.04.006. Epub 2006 May 26. Neuromuscul Disord. 2006. PMID: 16730439

9

Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350P.

Walter MC, Reilich P, Huebner A, Fischer D, Schröder R, Vorgerd M, Kress W, Born C, Schoser BG, Krause KH, Klutzny U, Bulst S, Frey JR, Lochmüller H. Walter MC, et al. Among authors: schoser bg. Brain. 2007 Jun;130(Pt 6):1485-96. doi: 10.1093/brain/awm039. Epub 2007 Apr 17. Brain. 2007. PMID: 17439987

10

Accuracy of botulinum toxin injections in myofascial pain. Response to Gobel et al. Pain 2006;125:82-8.

Reilich P, Schoser BGH. Reilich P, et al. Pain. 2007 Aug;130(3):299. doi: 10.1016/j.pain.2007.04.020. Epub 2007 May 25. Pain. 2007. PMID: 17532140 No abstract available.

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