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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 10
2023 11
2024 3

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197 results

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Page 1
Cerebellar ataxia-neuropathy-vestibular areflexia-syndrome.
Vinther-Jensen T, Dunø M, Ingolfsdottir HM, Krarup C, Nielsen JE, Jakobsen JK. Vinther-Jensen T, et al. Among authors: duno m. Ugeskr Laeger. 2023 May 8;185(19):V06220383. Ugeskr Laeger. 2023. PMID: 37170740 Free article. Review. Danish.
Myotonia Congenita.
Dunø M, Vissing J. Dunø M, et al. 2005 Aug 3 [updated 2021 Feb 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2005 Aug 3 [updated 2021 Feb 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 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.
ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsy.
Mattison KA, Tossing G, Mulroe F, Simmons C, Butler KM, Schreiber A, Alsadah A, Neilson DE, Naess K, Wedell A, Wredenberg A, Sorlin A, McCann E, Burghel GJ, Menendez B, Hoganson GE, Botto LD, Filloux FM, Aledo-Serrano Á, Gil-Nagel A, Tatton-Brown K, Verbeek NE, van der Zwaag B, Aleck KA, Fazenbaker AC, Balciuniene J, Dubbs HA, Marsh ED, Garber K, Ek J, Duno M, Hoei-Hansen CE, Deardorff MA, Raca G, Quindipan C, van Hirtum-Das M, Breckpot J, Hammer TB, Møller RS, Whitney A, Douglas AGL, Kharbanda M, Brunetti-Pierri N, Morleo M, Nigro V, May HJ, Tao JX, Argilli E, Sherr EH, Dobyns WB; Genomics England Research Consortium; Baines RA, Warwicker J, Parker JA, Banka S, Campeau PM, Escayg A. Mattison KA, et al. Among authors: duno m. Brain. 2023 Apr 19;146(4):1357-1372. doi: 10.1093/brain/awac330. Brain. 2023. PMID: 36074901 Free PMC article.
Cell-free fetal DNA for genetic evaluation in Copenhagen Pregnancy Loss Study (COPL): a prospective cohort study.
Schlaikjær Hartwig T, Ambye L, Gruhn JR, Petersen JF, Wrønding T, Amato L, Chi-Ho Chan A, Ji B, Bro-Jørgensen MH, Werge L, Petersen MMBS, Brinkmann C, Petersen JB, Dunø M, Bache I, Herrgård MJ, Jørgensen FS, Hoffmann ER, Nielsen HS; COPL consortium. Schlaikjær Hartwig T, et al. Among authors: duno m. Lancet. 2023 Mar 4;401(10378):762-771. doi: 10.1016/S0140-6736(22)02610-1. Epub 2023 Feb 2. Lancet. 2023. PMID: 36739882
[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.
[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.
197 results