Vissing J - Search Results

1

Deletion of exon 16 of the dystrophin gene is not associated with disease.

Schwartz M, Dunø M, Palle AL, Krag T, Vissing J. Schwartz M, et al. Among authors: vissing j. Hum Mutat. 2007 Feb;28(2):205. doi: 10.1002/humu.9477. Hum Mutat. 2007. PMID: 17226814

2

Multisystem disorder associated with a missense mutation in the mitochondrial cytochrome b gene.

Wibrand F, Ravn K, Schwartz M, Rosenberg T, Horn N, Vissing J. Wibrand F, et al. Among authors: vissing j. Ann Neurol. 2001 Oct;50(4):540-3. doi: 10.1002/ana.1224. Ann Neurol. 2001. PMID: 11601507

3

Paternal inheritance of mitochondrial DNA.

Schwartz M, Vissing J. Schwartz M, et al. Among authors: vissing j. N Engl J Med. 2002 Aug 22;347(8):576-80. doi: 10.1056/NEJMoa020350. N Engl J Med. 2002. PMID: 12192017 Free article. No abstract available.

4

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

5

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

6

Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy.

Van Goethem G, Schwartz M, Löfgren A, Dermaut B, Van Broeckhoven C, Vissing J. Van Goethem G, et al. Among authors: vissing j. Eur J Hum Genet. 2003 Jul;11(7):547-9. doi: 10.1038/sj.ejhg.5201002. Eur J Hum Genet. 2003. PMID: 12825077

7

Oxidative capacity correlates with muscle mutation load in mitochondrial myopathy.

Jeppesen TD, Schwartz M, Olsen DB, Vissing J. Jeppesen TD, et al. Among authors: vissing j. Ann Neurol. 2003 Jul;54(1):86-92. doi: 10.1002/ana.10594. Ann Neurol. 2003. PMID: 12838523

8

Late onset of stroke-like episode associated with a 3256C-->T point mutation of mitochondrial DNA.

Jeppesen TD, Schwartz M, Hansen K, Danielsen ER, Wibrand F, Vissing J. Jeppesen TD, et al. Among authors: vissing j. J Neurol Sci. 2003 Oct 15;214(1-2):17-20. doi: 10.1016/s0022-510x(03)00168-0. J Neurol Sci. 2003. PMID: 12972383

9

New patterns of inheritance in mitochondrial disease.

Schwartz M, Vissing J. Schwartz M, et al. Among authors: vissing j. Biochem Biophys Res Commun. 2003 Oct 17;310(2):247-51. doi: 10.1016/j.bbrc.2003.09.037. Biochem Biophys Res Commun. 2003. PMID: 14521902 Review.

10

[Paternal inheritance of mitochondrial DNA].

Schwartz M, Vissing J. Schwartz M, et al. Among authors: vissing j. Ugeskr Laeger. 2003 Sep 15;165(38):3627-30. Ugeskr Laeger. 2003. PMID: 14556396 Danish. No abstract available.

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