Witting N - Search Results

1

Autophagy is affected in patients with hypokalemic periodic paralysis: an involvement in vacuolar myopathy?

Krag TO, Holm-Yildiz S, Witting N, Vissing J. Krag TO, et al. Among authors: witting n. Acta Neuropathol Commun. 2021 Jun 13;9(1):109. doi: 10.1186/s40478-021-01212-8. Acta Neuropathol Commun. 2021. PMID: 34120654 Free PMC article.

2

Cardiac manifestations of myotonic dystrophy type 1.

Petri H, Vissing J, Witting N, Bundgaard H, Køber L. Petri H, et al. Among authors: witting n. 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.

3

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. Acta Myol. 2011 Dec;30(3):182-4. Acta Myol. 2011. PMID: 22616200 Free PMC article.

4

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. 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

5

LGMD2L with bone affection: overlapping phenotype of dominant and recessive ANO5-induced disease.

Witting N, Duno M, Born AP, Vissing J. Witting N, et al. Muscle Nerve. 2012 Nov;46(5):829-30. doi: 10.1002/mus.23440. Muscle Nerve. 2012. PMID: 23055322 No abstract available.

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: witting n. 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. 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. 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: witting n. 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. JAMA Neurol. 2014 Jan;71(1):88-90. doi: 10.1001/jamaneurol.2013.3209. JAMA Neurol. 2014. PMID: 24216972

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