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

Year Number of Results
1969 1
1990 2
1991 1
1993 3
1994 1
1995 2
1996 6
1997 4
1998 5
1999 5
2000 2
2001 2
2002 3
2003 8
2004 8
2005 9
2006 8
2007 4
2008 7
2009 5
2010 8
2011 10
2012 14
2013 7
2014 9
2015 11
2016 16
2017 14
2018 17
2019 10
2020 12
2021 18
2022 21
2023 15

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241 results

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Page 1
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Faure-Bardon V, Isnard P, Roux N, Leruez-Ville M, Molina T, Bessieres B, Ville Y. Faure-Bardon V, et al. Among authors: roux n. Ultrasound Obstet Gynecol. 2021 Feb;57(2):352-353. doi: 10.1002/uog.23583. Ultrasound Obstet Gynecol. 2021. PMID: 33524233 Free article. No abstract available.
Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment.
Boehm U, Bouloux PM, Dattani MT, de Roux N, Dodé C, Dunkel L, Dwyer AA, Giacobini P, Hardelin JP, Juul A, Maghnie M, Pitteloud N, Prevot V, Raivio T, Tena-Sempere M, Quinton R, Young J. Boehm U, et al. Among authors: de roux n. Nat Rev Endocrinol. 2015 Sep;11(9):547-64. doi: 10.1038/nrendo.2015.112. Epub 2015 Jul 21. Nat Rev Endocrinol. 2015. PMID: 26194704 Review.
Anemonefish, a model for Eco-Evo-Devo.
Roux N, Salis P, Lee SH, Besseau L, Laudet V. Roux N, et al. Evodevo. 2020 Oct 7;11:20. doi: 10.1186/s13227-020-00166-7. eCollection 2020. Evodevo. 2020. PMID: 33042514 Free PMC article. Review.
Best practices for burnout self-care.
Roux N, Benita T. Roux N, et al. Nurs Manage. 2020 Oct;51(10):30-35. doi: 10.1097/01.NUMA.0000698116.82355.0d. Nurs Manage. 2020. PMID: 33003061 No abstract available.
Neglected but amazingly diverse type IVb pili.
Roux N, Spagnolo J, de Bentzmann S. Roux N, et al. Res Microbiol. 2012 Nov-Dec;163(9-10):659-73. doi: 10.1016/j.resmic.2012.10.015. Epub 2012 Oct 25. Res Microbiol. 2012. PMID: 23103334 Review.
GnRH receptor mutations in isolated gonadotropic deficiency.
Chevrier L, Guimiot F, de Roux N. Chevrier L, et al. Among authors: de roux n. Mol Cell Endocrinol. 2011 Oct 22;346(1-2):21-8. doi: 10.1016/j.mce.2011.04.018. Epub 2011 Apr 30. Mol Cell Endocrinol. 2011. PMID: 21645587 Review.
FGFR1 mutations in Kallmann syndrome.
Villanueva C, de Roux N. Villanueva C, et al. Among authors: de roux n. Front Horm Res. 2010;39:51-61. doi: 10.1159/000312693. Epub 2010 Apr 8. Front Horm Res. 2010. PMID: 20389085 Review.
241 results