Vissing J - Search Results

1

Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy.

Ross JA, Levy Y, Ripolone M, Kolb JS, Turmaine M, Holt M, Lindqvist J, Claeys KG, Weis J, Monforte M, Tasca G, Moggio M, Figeac N, Zammit PS, Jungbluth H, Fiorillo C, Vissing J, Witting N, Granzier H, Zanoteli E, Hardeman EC, Wallgren-Pettersson C, Ochala J. Ross JA, et al. Among authors: vissing j. Acta Neuropathol. 2019 Sep;138(3):477-495. doi: 10.1007/s00401-019-02034-8. Epub 2019 Jun 19. Acta Neuropathol. 2019. PMID: 31218456 Free PMC article.

2

Short- and long-term effects of endurance training in patients with mitochondrial myopathy.

Jeppesen TD, Dunø M, Schwartz M, Krag T, Rafiq J, Wibrand F, Vissing J. Jeppesen TD, et al. Among authors: vissing j. Eur J Neurol. 2009 Dec;16(12):1336-9. doi: 10.1111/j.1468-1331.2009.02660.x. Epub 2009 May 27. Eur J Neurol. 2009. PMID: 19486129 Clinical Trial.

3

Cardiac manifestations of myotonic dystrophy type 1.

Petri H, Vissing J, Witting N, Bundgaard H, Køber L. Petri H, et al. Among authors: vissing j. Int J Cardiol. 2012 Oct 4;160(2):82-8. doi: 10.1016/j.ijcard.2011.08.037. Epub 2011 Sep 13. Int J Cardiol. 2012. PMID: 21917328 Review.

4

Deletion of exon 26 of the dystrophin gene is associated with a mild Becker muscular dystrophy phenotype.

Witting N, Duno M, Vissing J. Witting N, et al. Among authors: vissing j. Acta Myol. 2011 Dec;30(3):182-4. Acta Myol. 2011. PMID: 22616200 Free PMC article.

5

Becker muscular dystrophy with widespread muscle hypertrophy and a non-sense mutation of exon 2.

Witting N, Duno M, Vissing J. Witting N, et al. Among authors: vissing j. Neuromuscul Disord. 2013 Jan;23(1):25-8. doi: 10.1016/j.nmd.2012.07.004. Epub 2012 Aug 28. Neuromuscul Disord. 2013. PMID: 22939275

6

Response letter to "Cardiac involvement in myotonic dystrophy type 1--do not forget the loop recorder!".

Petri H, Vissing J, Witting N, Bundgaard H, Køber L. Petri H, et al. Among authors: vissing j. Int J Cardiol. 2013 Sep 30;168(2):1541. doi: 10.1016/j.ijcard.2012.12.033. Epub 2012 Dec 29. Int J Cardiol. 2013. PMID: 23276392 No abstract available.

7

Response.

Witting N, Duno M, Vissing J. Witting N, et al. Among authors: vissing j. Neuromuscul Disord. 2013 Feb;23(2):193. doi: 10.1016/j.nmd.2012.12.006. Epub 2013 Jan 26. Neuromuscul Disord. 2013. PMID: 23357682 No abstract available.

8

Anoctamin 5 muscular dystrophy in Denmark: prevalence, genotypes, phenotypes, cardiac findings, and muscle protein expression.

Witting N, Duno M, Petri H, Krag T, Bundgaard H, Kober L, Vissing J. Witting N, et al. Among authors: vissing j. J Neurol. 2013 Aug;260(8):2084-93. doi: 10.1007/s00415-013-6934-y. Epub 2013 May 14. J Neurol. 2013. PMID: 23670307

9

Delayed diagnosis of oculopharyngeal muscular dystrophy in Denmark: from initial ptosis to genetic testing.

Mensah A, Witting N, Duno M, Milea D, Vissing J. Mensah A, et al. Among authors: vissing j. Acta Ophthalmol. 2014 May;92(3):e247-9. doi: 10.1111/aos.12243. Epub 2013 Jul 15. Acta Ophthalmol. 2014. PMID: 23848287 Free article. No abstract available.

10

Severe axial myopathy in McArdle disease.

Witting N, Duno M, Piraud M, Vissing J. Witting N, et al. Among authors: vissing j. JAMA Neurol. 2014 Jan;71(1):88-90. doi: 10.1001/jamaneurol.2013.3209. JAMA Neurol. 2014. PMID: 24216972

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