Kress W - Search Results

1

Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy--double trouble as an explanation for an atypical phenotype.

Rudnik-Schöneborn S, Weis J, Kress W, Häusler M, Zerres K. Rudnik-Schöneborn S, et al. Among authors: kress w. Neuromuscul Disord. 2008 Nov;18(11):881-5. doi: 10.1016/j.nmd.2008.06.387. Epub 2008 Aug 5. Neuromuscul Disord. 2008. PMID: 18684626

2

Anoctamin 5 muscular dystrophy associated with a silent p.Leu115Leu mutation resulting in exon skipping.

Joshi PR, Gläser D, Dreßel C, Kress W, Weis J, Deschauer M. Joshi PR, et al. Among authors: kress w. Neuromuscul Disord. 2014 Jan;24(1):43-7. doi: 10.1016/j.nmd.2013.09.003. Epub 2013 Sep 10. Neuromuscul Disord. 2014. PMID: 24239059

3

Incontinetia pigmenti-related myopathy or unsolved "double trouble"?

Huttner HB, Richter G, Jünemann A, Kress W, Weis J, Schröder JM, Gal A, Doerfler A, Udd B, Schröder R. Huttner HB, et al. Among authors: kress w. Neuromuscul Disord. 2010 Feb;20(2):139-41. doi: 10.1016/j.nmd.2009.12.006. Epub 2010 Jan 12. Neuromuscul Disord. 2010. PMID: 20064724

4

Facioscapulohumeral muscular dystrophy presenting with unusual phenotypes and atypical morphological features of vacuolar myopathy.

Reilich P, Schramm N, Schoser B, Schneiderat P, Strigl-Pill N, Müller-Höcker J, Kress W, Ferbert A, Rudnik-Schöneborn S, Noth J, Lochmüller H, Weis J, Walter MC. Reilich P, et al. Among authors: kress w. J Neurol. 2010 Jul;257(7):1108-18. doi: 10.1007/s00415-010-5471-1. Epub 2010 Feb 10. J Neurol. 2010. PMID: 20146070

5

Clinical utility gene card for: proximal spinal muscular atrophy.

Rudnik-Schöneborn S, Eggermann T, Kress W, Lemmink HH, Cobben JM, Zerres K. Rudnik-Schöneborn S, et al. Among authors: kress w. Eur J Hum Genet. 2012 Jun;20(6). doi: 10.1038/ejhg.2012.62. Epub 2012 Apr 18. Eur J Hum Genet. 2012. PMID: 22510849 Free PMC article. No abstract available.

6

Outcome and effect of pregnancy in myotonic dystrophy type 2.

Rudnik-Schöneborn S, Schneider-Gold C, Raabe U, Kress W, Zerres K, Schoser BG. Rudnik-Schöneborn S, et al. Among authors: kress w. Neurology. 2006 Feb 28;66(4):579-80. doi: 10.1212/01.wnl.0000198227.91131.1e. Neurology. 2006. PMID: 16505316

7

Brugada-like cardiac disease in myotonic dystrophy type 2: report of two unrelated patients.

Rudnik-Schöneborn S, Schaupp M, Lindner A, Kress W, Schulze-Bahr E, Zumhagen S, Elbracht M, Zerres K. Rudnik-Schöneborn S, et al. Among authors: kress w. Eur J Neurol. 2011 Jan;18(1):191-4. doi: 10.1111/j.1468-1331.2010.03077.x. Eur J Neurol. 2011. PMID: 20491895

8

Laing distal myopathy with a novel mutation in exon 34 of the MYH7 gene.

Ferbert A, Zibat A, Rautenstrauß B, Kress W, Hügens-Penzel M, Weis J, Shah Y, Roth C. Ferbert A, et al. Among authors: kress w. Neuromuscul Disord. 2016 Sep;26(9):598-603. doi: 10.1016/j.nmd.2016.06.458. Epub 2016 Jun 22. Neuromuscul Disord. 2016. PMID: 27469267

9

Clinical utility gene card for: Proximal spinal muscular atrophy (SMA) - update 2015.

Rudnik-Schöneborn S, Eggermann T, Kress W, Lemmink HH, Cobben JM, Zerres K. Rudnik-Schöneborn S, et al. Among authors: kress w. Eur J Hum Genet. 2015 Nov;23(11). doi: 10.1038/ejhg.2015.90. Epub 2015 May 20. Eur J Hum Genet. 2015. PMID: 25990799 Free PMC article. No abstract available.

10

The Caveolin-3 G56S sequence variant of unknown significance: Muscle biopsy findings and functional cell biological analysis.

Brauers E, Roos A, Kollipara L, Zahedi RP, Beckmann A, Mohanadas N, Bauer H, Häusler M, Thoma S, Kress W, Senderek J, Weis J. Brauers E, et al. Among authors: kress w. Proteomics Clin Appl. 2017 Jan;11(1-2):1600007. doi: 10.1002/prca.201600007. Epub 2016 Nov 14. Proteomics Clin Appl. 2017. PMID: 27739254 Free PMC article.

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