Witting N - Search Results

1

A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy.

Vissing J, Barresi R, Witting N, Van Ghelue M, Gammelgaard L, Bindoff LA, Straub V, Lochmüller H, Hudson J, Wahl CM, Arnardottir S, Dahlbom K, Jonsrud C, Duno M. Vissing J, et al. Among authors: witting n. Brain. 2016 Aug;139(Pt 8):2154-63. doi: 10.1093/brain/aww133. Epub 2016 Jun 3. Brain. 2016. PMID: 27259757

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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