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Year Number of Results
2000 1
2001 1
2005 1
2006 1
2007 1
2008 1
2010 1
2011 4
2012 3
2013 5
2014 2
2015 3
2016 1
2017 3
2018 5
2019 1
2020 9
2021 3
2022 5
2023 5
2024 3

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54 results

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Page 1
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.
Küry S, van Woerden GM, Besnard T, Proietti Onori M, Latypova X, Towne MC, Cho MT, Prescott TE, Ploeg MA, Sanders S, Stessman HAF, Pujol A, Distel B, Robak LA, Bernstein JA, Denommé-Pichon AS, Lesca G, Sellars EA, Berg J, Carré W, Busk ØL, van Bon BWM, Waugh JL, Deardorff M, Hoganson GE, Bosanko KB, Johnson DS, Dabir T, Holla ØL, Sarkar A, Tveten K, de Bellescize J, Braathen GJ, Terhal PA, Grange DK, van Haeringen A, Lam C, Mirzaa G, Burton J, Bhoj EJ, Douglas J, Santani AB, Nesbitt AI, Helbig KL, Andrews MV, Begtrup A, Tang S, van Gassen KLI, Juusola J, Foss K, Enns GM, Moog U, Hinderhofer K, Paramasivam N, Lincoln S, Kusako BH, Lindenbaum P, Charpentier E, Nowak CB, Cherot E, Simonet T, Ruivenkamp CAL, Hahn S, Brownstein CA, Xia F, Schmitt S, Deb W, Bonneau D, Nizon M, Quinquis D, Chelly J, Rudolf G, Sanlaville D, Parent P, Gilbert-Dussardier B, Toutain A, Sutton VR, Thies J, Peart-Vissers LELM, Boisseau P, Vincent M, Grabrucker AM, Dubourg C; Undiagnosed Diseases Network; Tan WH, Verbeek NE, Granzow M, Santen GWE, Shendure J, Isidor B, Pasquier L, Redon R, Yang Y, State MW, Kleefstra T, Cogné B; GEM HUGO; Deciphering Developmental Disorders Study; Petrovski S, Retterer K… See abstract for full author list ➔ Küry S, et al. Among authors: simonet t. Am J Hum Genet. 2017 Nov 2;101(5):768-788. doi: 10.1016/j.ajhg.2017.10.003. Am J Hum Genet. 2017. PMID: 29100089 Free PMC article.
Combining prehabilitation with enhanced recovery programs in gynecological surgery.
Falandry C, Fauvet R, Alfonsi P, Foulon A, Texier C, Bourdel N, Simonet T, Azaïs H, Lambaudie E. Falandry C, et al. Among authors: simonet t. J Gynecol Obstet Hum Reprod. 2022 May;51(5):102376. doi: 10.1016/j.jogoh.2022.102376. Epub 2022 Apr 6. J Gynecol Obstet Hum Reprod. 2022. PMID: 35398373 Review.
H2A.Z is involved in premature aging and DSB repair initiation in muscle fibers.
Belotti E, Lacoste N, Iftikhar A, Simonet T, Papin C, Osseni A, Streichenberger N, Mari PO, Girard E, Graies M, Giglia-Mari G, Dimitrov S, Hamiche A, Schaeffer L. Belotti E, et al. Among authors: simonet t. Nucleic Acids Res. 2024 Apr 12;52(6):3031-3049. doi: 10.1093/nar/gkae020. Nucleic Acids Res. 2024. PMID: 38281187 Free PMC article.
[Iron deficiency anemia and pregnancy. Prevention and treatment].
Beucher G, Grossetti E, Simonet T, Leporrier M, Dreyfus M. Beucher G, et al. Among authors: simonet t. J Gynecol Obstet Biol Reprod (Paris). 2011 May;40(3):185-200. doi: 10.1016/j.jgyn.2011.01.004. Epub 2011 Feb 17. J Gynecol Obstet Biol Reprod (Paris). 2011. PMID: 21333465 Free article. Review. French.
[Management of the HELLP syndrome].
Beucher G, Simonet T, Dreyfus M. Beucher G, et al. Among authors: simonet t. Gynecol Obstet Fertil. 2008 Dec;36(12):1175-90. doi: 10.1016/j.gyobfe.2008.08.015. Epub 2008 Nov 12. Gynecol Obstet Fertil. 2008. PMID: 19008144 Review. French.
Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons.
Jacquier A, Risson V, Simonet T, Roussange F, Lacoste N, Ribault S, Carras J, Theuriet J, Girard E, Grosjean I, Le Goff L, Kröger S, Meltoranta J, Bauché S, Sternberg D, Fournier E, Kostera-Pruszczyk A, O'Connor E, Eymard B, Lochmüller H, Martinat C, Schaeffer L. Jacquier A, et al. Among authors: simonet t. Acta Neuropathol. 2022 Oct;144(4):707-731. doi: 10.1007/s00401-022-02475-8. Epub 2022 Aug 10. Acta Neuropathol. 2022. PMID: 35948834 Free PMC article.
54 results