Dunø M - Search Results

1

Improved molecular diagnosis of dystrophin gene mutations using the multiplex ligation-dependent probe amplification method.

Schwartz M, Dunø M. Schwartz M, et al. Among authors: duno m. Genet Test. 2004 Winter;8(4):361-7. doi: 10.1089/gte.2004.8.361. Genet Test. 2004. PMID: 15684864 Clinical Trial.

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. Among authors: duno m. 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: duno m. 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: duno m. 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. Eur J Hum Genet. 2004 Sep;12(9):738-43. doi: 10.1038/sj.ejhg.5201218. Eur J Hum Genet. 2004. PMID: 15162127

6

Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletion.

Dunø M, Hove H, Kirchhoff M, Devriendt K, Schwartz M. Dunø M, et al. Hum Genet. 2004 Nov;115(6):459-67. doi: 10.1007/s00439-004-1174-y. Epub 2004 Sep 18. Hum Genet. 2004. PMID: 15378350

7

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: duno m. Ann Neurol. 2005 Jan;57(1):60-6. doi: 10.1002/ana.20320. Ann Neurol. 2005. PMID: 15622536

8

Multiplex ligation-dependent probe amplification is superior for detecting deletions/duplications in Duchenne muscular dystrophy.

Schwartz M, Dunø M. Schwartz M, et al. Among authors: duno m. Clin Genet. 2005 Feb;67(2):189-91. doi: 10.1111/j.1399-0004.2004.00382.x. Clin Genet. 2005. PMID: 15679833 No abstract available.

9

dHPLC screening of the NSD1 gene identifies nine novel mutations--summary of the first 100 Sotos syndrome mutations.

Melchior L, Schwartz M, Duno M. Melchior L, et al. Among authors: duno m. Ann Hum Genet. 2005 Mar;69(Pt 2):222-6. doi: 10.1046/j.1529-8817.2004.00150.x. Ann Hum Genet. 2005. PMID: 15720303

10

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: duno m. Brain. 2006 Dec;129(Pt 12):3402-12. doi: 10.1093/brain/awl149. Epub 2006 Jun 30. Brain. 2006. PMID: 16815877

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