Vissing J - Search Results

1

Phenotypes, genotypes, and prevalence of congenital myopathies older than 5 years in Denmark.

Witting N, Werlauff U, Duno M, Vissing J. Witting N, et al. Among authors: vissing j. Neurol Genet. 2017 Mar 21;3(2):e140. doi: 10.1212/NXG.0000000000000140. eCollection 2017 Apr. Neurol Genet. 2017. PMID: 28357410 Free PMC article.

2

Multiple mtDNA deletions with features of MNGIE.

Vissing J, Ravn K, Danielsen ER, Dunø M, Wibrand F, Wevers RA, Schwartz M. Vissing J, et al. Neurology. 2002 Sep 24;59(6):926-9. doi: 10.1212/wnl.59.6.926. Neurology. 2002. PMID: 12297582

3

Decrement of compound muscle action potential is related to mutation type in myotonia congenita.

Colding-Jørgensen E, DunØ M, Schwartz M, Vissing J. Colding-Jørgensen E, et al. Among authors: vissing j. Muscle Nerve. 2003 Apr;27(4):449-55. doi: 10.1002/mus.10347. Muscle Nerve. 2003. PMID: 12661046

4

Characterization of two new dominant ClC-1 channel mutations associated with myotonia.

Grunnet M, Jespersen T, Colding-Jørgensen E, Schwartz M, Klaerke DA, Vissing J, Olesen SP, Dunø M. Grunnet M, et al. Among authors: vissing j. Muscle Nerve. 2003 Dec;28(6):722-32. doi: 10.1002/mus.10501. Muscle Nerve. 2003. PMID: 14639587 Clinical Trial.

5

Difference in allelic expression of the CLCN1 gene and the possible influence on the myotonia congenita phenotype.

Dunø M, Colding-Jørgensen E, Grunnet M, Jespersen T, Vissing J, Schwartz M. Dunø M, et al. Among authors: vissing j. Eur J Hum Genet. 2004 Sep;12(9):738-43. doi: 10.1038/sj.ejhg.5201218. Eur J Hum Genet. 2004. PMID: 15162127

6

Fuel utilization in subjects with carnitine palmitoyltransferase 2 gene mutations.

Ørngreen MC, Dunø M, Ejstrup R, Christensen E, Schwartz M, Sacchetti M, Vissing J. Ørngreen MC, et al. Among authors: vissing j. Ann Neurol. 2005 Jan;57(1):60-6. doi: 10.1002/ana.20320. Ann Neurol. 2005. PMID: 15622536

7

High prevalence and phenotype-genotype correlations of limb girdle muscular dystrophy type 2I in Denmark.

Sveen ML, Schwartz M, Vissing J. Sveen ML, et al. Among authors: vissing j. Ann Neurol. 2006 May;59(5):808-15. doi: 10.1002/ana.20824. Ann Neurol. 2006. PMID: 16634037

8

Aerobic training is safe and improves exercise capacity in patients with mitochondrial myopathy.

Jeppesen TD, Schwartz M, Olsen DB, Wibrand F, Krag T, Dunø M, Hauerslev S, Vissing J. Jeppesen TD, et al. Among authors: vissing j. Brain. 2006 Dec;129(Pt 12):3402-12. doi: 10.1093/brain/awl149. Epub 2006 Jun 30. Brain. 2006. PMID: 16815877

9

Autosomal dominant monosymptomatic myotonia permanens.

Colding-Jørgensen E, Duno M, Vissing J. Colding-Jørgensen E, et al. Among authors: vissing j. Neurology. 2006 Jul 11;67(1):153-5. doi: 10.1212/01.wnl.0000223838.88872.da. Neurology. 2006. PMID: 16832098

10

Do carriers of PYGM mutations have symptoms of McArdle disease?

Andersen ST, Dunø M, Schwartz M, Vissing J. Andersen ST, et al. Among authors: vissing j. Neurology. 2006 Aug 22;67(4):716-8. doi: 10.1212/01.wnl.0000230154.79933.d7. Neurology. 2006. PMID: 16924035 Clinical Trial.

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