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Paternal inheritance of mitochondrial DNA.
Schwartz M, Vissing J. Schwartz M, et al. N Engl J Med. 2002 Aug 22;347(8):576-80. doi: 10.1056/NEJMoa020350. N Engl J Med. 2002. PMID: 12192017 No abstract available.
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: schwartz m. Eur J Hum Genet. 2004 Sep;12(9):738-43. doi: 10.1038/sj.ejhg.5201218. Eur J Hum Genet. 2004. PMID: 15162127
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: schwartz m. Neurology. 2002 Sep 24;59(6):926-9. doi: 10.1212/wnl.59.6.926. Neurology. 2002. PMID: 12297582
An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome.
Ravn K, Wibrand F, Hansen FJ, Horn N, Rosenberg T, Schwartz M. Ravn K, et al. Among authors: schwartz m. Eur J Hum Genet. 2001 Oct;9(10):805-9. doi: 10.1038/sj.ejhg.5200712. Eur J Hum Genet. 2001. PMID: 11781695
Short- and long-term effects of endurance training in patients with mitochondrial myopathy.
Jeppesen TD, Dunø M, Schwartz M, Krag T, Rafiq J, Wibrand F, Vissing J. Jeppesen TD, et al. Among authors: schwartz m. Eur J Neurol. 2009 Dec;16(12):1336-9. doi: 10.1111/j.1468-1331.2009.02660.x. Epub 2009 May 27. Eur J Neurol. 2009. PMID: 19486129 Clinical Trial.
Leukocyte cDNA analysis of NSD1 derived from confirmed Sotos syndrome patients.
Duno M, Skovby F, Schwartz M. Duno M, et al. Among authors: schwartz m. Ann Hum Genet. 2007 Nov;71(Pt 6):713-8. doi: 10.1111/j.1469-1809.2007.00376.x. Epub 2007 Jun 11. Ann Hum Genet. 2007. PMID: 17561922
Mitochondrial DNA variant 11719G is a marker for the mtDNA haplogroup cluster HV.
Saillard J, Magalhães PJ, Schwartz M, Rosenberg T, Nørby S. Saillard J, et al. Among authors: schwartz m. Hum Biol. 2000 Dec;72(6):1065-8. Hum Biol. 2000. PMID: 11236862
Variable clinical expression in a family with OI type IV due to deletion of three base pairs in COL1A1.
Lund AM, Schwartz M, Skovby F. Lund AM, et al. Among authors: schwartz m. Clin Genet. 1996 Nov;50(5):304-9. doi: 10.1111/j.1399-0004.1996.tb02379.x. Clin Genet. 1996. PMID: 9007315
Detection of ten new mutations by screening the gene encoding factor IX of Danish hemophilia B patients.
Nielsen LR, Scheibel E, Ingerslev J, Schwartz M. Nielsen LR, et al. Among authors: schwartz m. Thromb Haemost. 1995 May;73(5):774-8. Thromb Haemost. 1995. PMID: 7482402
Frequency of the delta F508 mutation on cystic fibrosis chromosomes in Denmark.
Schwartz M, Johansen HK, Koch C, Brandt NJ. Schwartz M, et al. Hum Genet. 1990 Sep;85(4):427-8. doi: 10.1007/BF02428297. Hum Genet. 1990. PMID: 2210762
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