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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2007 1
2008 2
2009 3
2010 6
2011 5
2012 3
2013 4
2014 4
2015 1
2016 1
2017 3
2018 2
2019 2
2020 2
2022 0
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31 results
Results by year
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Page 1
[Short QT syndrome as an inherited condition].
Møller DV, Hedley PL, Olesen M, Kanters J, Svendsen JH, Christiansen M. Møller DV, et al. Ugeskr Laeger. 2011 Feb 7;173(6):420-4. Ugeskr Laeger. 2011. PMID: 21299935 Review. Danish.
Causes of hypereosinophilia in 100 consecutive patients.
Moller D, Tan J, Gauiran DTV, Medvedev N, Hudoba M, Carruthers MN, Dehghan N, van den Berghe J, Bruyère H, Chen LYC. Moller D, et al. Eur J Haematol. 2020 Sep;105(3):292-301. doi: 10.1111/ejh.13437. Epub 2020 May 18. Eur J Haematol. 2020. PMID: 32364630
Long QT syndrome - a genetic cardiac channelopathy.
Szeliga MA, Hedley PL, Green CP, Møller DV, Christiansen M. Szeliga MA, et al. Among authors: moller dv. Kardiol Pol. 2010 May;68(5):575-83. Kardiol Pol. 2010. PMID: 20491026 Review. No abstract available.
MT-CYB mutations in hypertrophic cardiomyopathy.
Hagen CM, Aidt FH, Havndrup O, Hedley PL, Jespersgaard C, Jensen M, Kanters JK, Moolman-Smook JC, Møller DV, Bundgaard H, Christiansen M. Hagen CM, et al. Among authors: moller dv. Mol Genet Genomic Med. 2013 May;1(1):54-65. doi: 10.1002/mgg3.5. Epub 2013 Apr 12. Mol Genet Genomic Med. 2013. PMID: 24498601 Free PMC article.
31 results