Vorgerd M - Search Results

1

Myofibrillar instability exacerbated by acute exercise in filaminopathy.

Chevessier F, Schuld J, Orfanos Z, Plank AC, Wolf L, Maerkens A, Unger A, Schlötzer-Schrehardt U, Kley RA, Von Hörsten S, Marcus K, Linke WA, Vorgerd M, van der Ven PF, Fürst DO, Schröder R. Chevessier F, et al. Among authors: vorgerd m. Hum Mol Genet. 2015 Dec 20;24(25):7207-20. doi: 10.1093/hmg/ddv421. Epub 2015 Oct 15. Hum Mol Genet. 2015. PMID: 26472074

2

Effect of high-dose creatine therapy on symptoms of exercise intolerance in McArdle disease: double-blind, placebo-controlled crossover study.

Vorgerd M, Zange J, Kley R, Grehl T, Hüsing A, Jäger M, Müller K, Schröder R, Mortier W, Fabian K, Malin JP, Luttmann A. Vorgerd M, et al. Arch Neurol. 2002 Jan;59(1):97-101. doi: 10.1001/archneur.59.1.97. Arch Neurol. 2002. PMID: 11790236 Clinical Trial.

3

Consequences of a novel caveolin-3 mutation in a large German family.

Fischer D, Schroers A, Blümcke I, Urbach H, Zerres K, Mortier W, Vorgerd M, Schröder R. Fischer D, et al. Among authors: vorgerd m. Ann Neurol. 2003 Feb;53(2):233-41. doi: 10.1002/ana.10442. Ann Neurol. 2003. PMID: 12557291

4

Immune-mediated rippling muscle disease.

Schulte-Mattler WJ, Kley RA, Rothenfusser-Korber E, Böhm S, Brüning T, Hackemann J, Steinbrecher A, Düring MV, Voss B, Vorgerd M. Schulte-Mattler WJ, et al. Among authors: vorgerd m. Neurology. 2005 Jan 25;64(2):364-7. doi: 10.1212/01.WNL.0000149532.52938.5B. Neurology. 2005. PMID: 15668444

5

Pathogenic effects of a novel heterozygous R350P desmin mutation on the assembly of desmin intermediate filaments in vivo and in vitro.

Bär H, Fischer D, Goudeau B, Kley RA, Clemen CS, Vicart P, Herrmann H, Vorgerd M, Schröder R. Bär H, et al. Among authors: vorgerd m. Hum Mol Genet. 2005 May 15;14(10):1251-60. doi: 10.1093/hmg/ddi136. Epub 2005 Mar 30. Hum Mol Genet. 2005. PMID: 15800015

6

Creatine has no beneficial effect on skeletal muscle energy metabolism in patients with single mitochondrial DNA deletions: a placebo-controlled, double-blind 31P-MRS crossover study.

Kornblum C, Schröder R, Müller K, Vorgerd M, Eggers J, Bogdanow M, Papassotiropoulos A, Fabian K, Klockgether T, Zange J. Kornblum C, et al. Among authors: vorgerd m. Eur J Neurol. 2005 Apr;12(4):300-9. doi: 10.1111/j.1468-1331.2004.00970.x. Eur J Neurol. 2005. PMID: 15804248 Clinical Trial.

7

A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy.

Vorgerd M, van der Ven PF, Bruchertseifer V, Löwe T, Kley RA, Schröder R, Lochmüller H, Himmel M, Koehler K, Fürst DO, Huebner A. Vorgerd M, et al. Am J Hum Genet. 2005 Aug;77(2):297-304. doi: 10.1086/431959. Epub 2005 May 31. Am J Hum Genet. 2005. PMID: 15929027 Free PMC article.

8

Hsp27-2D-gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathies.

Clemen CS, Fischer D, Roth U, Simon S, Vicart P, Kato K, Kaminska AM, Vorgerd M, Goldfarb LG, Eymard B, Romero NB, Goudeau B, Eggermann T, Zerres K, Noegel AA, Schröder R. Clemen CS, et al. Among authors: vorgerd m. FEBS Lett. 2005 Jul 4;579(17):3777-82. doi: 10.1016/j.febslet.2005.05.051. FEBS Lett. 2005. PMID: 15978589 Free article.

9

Gentamicin treatment in McArdle disease: failure to correct myophosphorylase deficiency.

Schroers A, Kley RA, Stachon A, Horvath R, Lochmüller H, Zange J, Vorgerd M. Schroers A, et al. Among authors: vorgerd m. Neurology. 2006 Jan 24;66(2):285-6. doi: 10.1212/01.wnl.0000194212.31318.fc. Neurology. 2006. PMID: 16434679 No abstract available.

10

Muscle pain in myophosphorylase deficiency (McArdle's disease): the role of gender, genotype, and pain-related coping.

Rommel O, Kley RA, Dekomien G, Epplen JT, Vorgerd M, Hasenbring M. Rommel O, et al. Among authors: vorgerd m. Pain. 2006 Oct;124(3):295-304. doi: 10.1016/j.pain.2006.04.017. Epub 2006 Jun 21. Pain. 2006. PMID: 16793208

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