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

Year Number of Results
1971 2
1977 1
1978 1
1979 1
1980 1
1989 1
1990 1
1991 2
1992 1
1993 2
1994 1
2003 1
2006 2
2007 3
2008 4
2009 5
2010 10
2011 4
2012 2
2013 3
2014 3
2015 8
2016 9
2017 3
2018 7
2019 3
2020 3
2021 1
2022 4
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Search Results

73 results
Results by year
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Page 1
DMD and West syndrome.
Cardas R, Iliescu C, Butoianu N, Seferian A, Gataullina S, Gargaun E, Nectoux J, Bienvenu T, Craiu D, Gidaro T, Servais L. Cardas R, et al. Among authors: nectoux j. Neuromuscul Disord. 2017 Oct;27(10):911-913. doi: 10.1016/j.nmd.2017.07.008. Epub 2017 Jul 19. Neuromuscul Disord. 2017. PMID: 28802771
[Development of digital PCR molecular tests for clinical practice: principles, practical implementation and recommendations].
Denis JA, Nectoux J, Lamy PJ, Rouillac Le Sciellour C, Guermouche H, Alary AS, Kosmider O, Sarafan-Vasseur N, Jovelet C, Busser B, Nizard P, Taly V, Fina F. Denis JA, et al. Among authors: nectoux j. Ann Biol Clin (Paris). 2018 Oct 1;76(5):505-523. doi: 10.1684/abc.2018.1372. Ann Biol Clin (Paris). 2018. PMID: 30226193 Free article. Review. French.
Detection and monitoring of circulating tumor DNA in adrenocortical carcinoma.
Garinet S, Nectoux J, Neou M, Pasmant E, Jouinot A, Sibony M, Orhant L, Pipoli da Fonseca J, Perlemoine K, Bricaire L, Groussin L, Soubrane O, Dousset B, Libe R, Letourneur F, Bertherat J, Assié G. Garinet S, et al. Among authors: nectoux j. Endocr Relat Cancer. 2018 Mar;25(3):L13-L17. doi: 10.1530/ERC-17-0467. Epub 2017 Dec 6. Endocr Relat Cancer. 2018. PMID: 29212777 No abstract available.
A FOXG1 mutation in a boy with congenital variant of Rett syndrome.
Le Guen T, Bahi-Buisson N, Nectoux J, Boddaert N, Fichou Y, Diebold B, Desguerre I, Raqbi F, Daire VC, Chelly J, Bienvenu T. Le Guen T, et al. Among authors: nectoux j. Neurogenetics. 2011 Feb;12(1):1-8. doi: 10.1007/s10048-010-0255-4. Epub 2010 Aug 24. Neurogenetics. 2011. PMID: 20734096 Review.
MeCP2 is involved in random mono-allelic expression for a subset of human autosomal genes.
Brousseau M, Nectoux J, Saintpierre B, Lebrun N, Cagnard N, Izac B, Olivier E, Letourneur F, Bienvenu T. Brousseau M, et al. Among authors: nectoux j. Biochim Biophys Acta Mol Basis Dis. 2020 Jun 1;1866(6):165730. doi: 10.1016/j.bbadis.2020.165730. Epub 2020 Feb 15. Biochim Biophys Acta Mol Basis Dis. 2020. PMID: 32070770 Free article.
73 results