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

Year Number of Results
1977 1
1983 1
1984 1
1988 1
1993 1
1995 1
1999 2
2004 1
2005 2
2006 2
2007 2
2008 3
2009 1
2014 1
2015 1
2016 1
2020 1
2022 1
2023 2
2024 1

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23 results

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Page 1
Formulation of Sunscreens for Optimal Efficacy.
Dominique M, Thierry P, Martin J, StÉphane D, VÉronique D, Sophie S. Dominique M, et al. Among authors: thierry p. J Cosmet Sci. 2020 Jul/Aug;71(4):199-208. J Cosmet Sci. 2020. PMID: 33022204
Unusual recurrence of sacrococcygeal mature teratoma: A case report.
Delehaye F, Damien B, Anne D, Céline B, Andreea A, Thierry P, Julien R. Delehaye F, et al. Among authors: thierry p. Pediatr Blood Cancer. 2023 Apr;70(4):e30048. doi: 10.1002/pbc.30048. Epub 2022 Oct 10. Pediatr Blood Cancer. 2023. PMID: 36215198 No abstract available.
Homozygous truncating PTPRF mutation causes athelia.
Borck G, de Vries L, Wu HJ, Smirin-Yosef P, Nürnberg G, Lagovsky I, Ishida LH, Thierry P, Wieczorek D, Nürnberg P, Foley J, Kubisch C, Basel-Vanagaite L. Borck G, et al. Among authors: thierry p. Hum Genet. 2014 Aug;133(8):1041-7. doi: 10.1007/s00439-014-1445-1. Epub 2014 Apr 30. Hum Genet. 2014. PMID: 24781087
Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome.
Kortüm F, Caputo V, Bauer CK, Stella L, Ciolfi A, Alawi M, Bocchinfuso G, Flex E, Paolacci S, Dentici ML, Grammatico P, Korenke GC, Leuzzi V, Mowat D, Nair LD, Nguyen TT, Thierry P, White SM, Dallapiccola B, Pizzuti A, Campeau PM, Tartaglia M, Kutsche K. Kortüm F, et al. Among authors: thierry p. Nat Genet. 2015 Jun;47(6):661-7. doi: 10.1038/ng.3282. Epub 2015 Apr 27. Nat Genet. 2015. PMID: 25915598
Endoscopic submucosal dissection with adaptive traction strategy: first prospective multicenter study.
Grimaldi J, Louis-Jean M, Lafeuille P, de Cristofaro E, Jérôme R, Thierry P, Clara Y, Timothée W, Alexandru L, Romain L, Florian R, Jérémie J, Mathieu P. Grimaldi J, et al. Among authors: thierry p. Gastrointest Endosc. 2024 Mar 6:S0016-5107(24)00148-2. doi: 10.1016/j.gie.2024.02.032. Online ahead of print. Gastrointest Endosc. 2024. PMID: 38458261 Free article.
No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome.
Abo-Dalo B, Roes M, Canún S, Delatycki M, Gillessen-Kaesbach G, Hrytsiuk I, Jung C, Kerr B, Mowat D, Seemanova E, Steiner CE, Stewart H, Thierry P, van Buggenhout G, White S, Zenker M, Kutsche K. Abo-Dalo B, et al. Among authors: thierry p. Clin Dysmorphol. 2008 Jul;17(3):181-185. doi: 10.1097/MCD.0b013e3282f2514c. Clin Dysmorphol. 2008. PMID: 18541964 No abstract available.
A new large deletion in the DFNB1 locus causes nonsyndromic hearing loss.
Feldmann D, Le Maréchal C, Jonard L, Thierry P, Czajka C, Couderc R, Ferec C, Denoyelle F, Marlin S, Fellmann F. Feldmann D, et al. Among authors: thierry p. Eur J Med Genet. 2009 Jul-Aug;52(4):195-200. doi: 10.1016/j.ejmg.2008.11.006. Epub 2008 Dec 13. Eur J Med Genet. 2009. PMID: 19101659
23 results