Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1993 1
1995 1
1999 1
2000 2
2001 1
2002 1
2003 3
2004 5
2005 5
2006 3
2007 9
2008 2
2009 4
2010 5
2011 5
2012 17
2013 22
2014 22
2015 19
2016 13
2017 14
2018 13
2019 15
2020 18
2021 10
2022 8
Text availability
Article attribute
Article type
Publication date

Search Results

183 results
Results by year
Filters applied: . Clear all
Page 1
Myotonia Congenita.
Dunø M, Vissing J. Dunø M, et al. 2005 Aug 3 [updated 2021 Feb 25]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2005 Aug 3 [updated 2021 Feb 25]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301529 Free Books & Documents. Review.
Response.
Witting N, Duno M, Vissing J. Witting N, et al. Among authors: duno m. Neuromuscul Disord. 2013 Feb;23(2):193. doi: 10.1016/j.nmd.2012.12.006. Epub 2013 Jan 26. Neuromuscul Disord. 2013. PMID: 23357682 No abstract available.
[Preimplantation genetic testing for aneuploidy].
Holmqvist V, Roos LKS, Kjartansdottir KR, Dunø M, Petersen MR, Hnida C, Pedersen IS, Ernst A, Toft CLF, Diemer T, Ingerslev HJ, Pinborg A, Løssl K. Holmqvist V, et al. Among authors: duno m. Ugeskr Laeger. 2019 May 13;181(20):V12180849. Ugeskr Laeger. 2019. PMID: 31124451 Free article. Review. Danish.
Permanent muscle weakness in hypokalemic periodic paralysis.
Holm-Yildiz S, Witting N, Dahlqvist J, de Stricker Borch J, Solheim T, Fornander F, Eisum AS, Duno M, Soerensen T, Vissing J. Holm-Yildiz S, et al. Among authors: duno m. Neurology. 2020 Jul 28;95(4):e342-e352. doi: 10.1212/WNL.0000000000009828. Epub 2020 Jun 24. Neurology. 2020. PMID: 32580975
[Exome sequencing for syndrome diagnostics].
Østergaard E, Risom L, Ek J, Grønborg S, Dunø M, Skovby F. Østergaard E, et al. Among authors: duno m. Ugeskr Laeger. 2017 Apr 24;179(17):V10160762. Ugeskr Laeger. 2017. PMID: 28473029 Free article. Review. Danish.
Successful treatment with dupilumab of an adult with Netherton syndrome.
Andreasen TH, Karstensen HG, Duno M, Lei U, Zachariae C, Thyssen JP. Andreasen TH, et al. Among authors: duno m. Clin Exp Dermatol. 2020 Oct;45(7):915-917. doi: 10.1111/ced.14317. Epub 2020 Jul 22. Clin Exp Dermatol. 2020. PMID: 32472705 No abstract available.
Cardiac Involvement in Women With Pathogenic Dystrophin Gene Variants.
Solheim TÅ, Fornander F, Raja AA, Møgelvang R, Poulsen NS, Dunø M, Bundgaard H, Vissing J. Solheim TÅ, et al. Among authors: duno m. Front Neurol. 2021 Jul 27;12:707838. doi: 10.3389/fneur.2021.707838. eCollection 2021. Front Neurol. 2021. PMID: 34385974 Free PMC article.
Use of Molecular Genetic Analyses in Danish Routine Newborn Screening.
Lund AM, Wibrand F, Skogstrand K, Bækvad-Hansen M, Gregersen N, Andresen BS, Hougaard DM, Dunø M, Olsen RKJ. Lund AM, et al. Among authors: duno m. Int J Neonatal Screen. 2021 Jul 26;7(3):50. doi: 10.3390/ijns7030050. Int J Neonatal Screen. 2021. PMID: 34449524 Free PMC article.
183 results