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Page 1
A multidisciplinary and structured investigation of three suspected clusters of transverse upper limb reduction defects in France.
Boudet-Berquier J, Demattei C, Guldner L, Gallay A, Manouvrier S, Botton J, Philippat C, Delva F, Bloch J, Semaille C, Odent S, Perthus I, Randrianaivo H, Babajko S, Barjat T, Beneteau C, Brennetot N, Garne E, Haddad G, Hocine M, Lacroix I, Leuraud K, Mench M, Morris J, Patrier S, Sartelet A, Verloes A, Bonaldi C, Le Barbier M, Gagnière B, Pépin P, Ollivier R, Bitoun M, King L, Guajardo-Villar A, Gomes E, Desenclos JC, Regnault N, Benachi A. Boudet-Berquier J, et al. Among authors: patrier s. Eur J Epidemiol. 2024 Apr 27. doi: 10.1007/s10654-024-01125-5. Online ahead of print. Eur J Epidemiol. 2024. PMID: 38671254
Risk factors for placenta accreta spectrum disorders in women with any prior cesarean and a placenta previa or low lying: a prospective population-based study.
Kayem G, Seco A, Vendittelli F, Crenn Hebert C, Dupont C, Branger B, Huissoud C, Fresson J, Winer N, Langer B, Rozenberg P, Morel O, Bonnet MP, Perrotin F, Azria E, Carbillon L, Chiesa C, Raynal P, Rudigoz RC, Patrier S, Beucher G, Dreyfus M, Sentilhes L, Deneux-Tharaux C. Kayem G, et al. Among authors: patrier s. Sci Rep. 2024 Mar 19;14(1):6564. doi: 10.1038/s41598-024-56964-9. Sci Rep. 2024. PMID: 38503816 Free PMC article.
Correction to: Practical guidelines of the EOTTD for pathological and genetic diagnosis of hydatidiform moles.
Bartosch C, Nadal A, Braga AC, Salerno A, Rougemont AL, Van Rompuy AS, Fitzgerald B, Joyce C, Allias F, Maher GJ, Turowski G, Tille JC, Alsibai KD, Van de Vijver K, McMahon L, Sunde L, Pyzlak M, Downey P, Wessman S, Patrier S, Kaur B, Fisher R. Bartosch C, et al. Among authors: patrier s. Virchows Arch. 2024 Mar;484(3):539-548. doi: 10.1007/s00428-023-03715-2. Virchows Arch. 2024. PMID: 38421406 No abstract available.
Impact of molecular genotyping on the diagnosis and treatment of human chorionic gonadotropin-producing tumors.
Peyle M, Massoud M, Patrier S, Gaillot-Durand L, Side G, Devouassoux-Shisheboran M, Massardier J, Descargues P, Msika A, Hajri T, Rousset P, Haesebaert J, Lotz JP, Jamelot M, You B, Golfier F, Eiriksson L, Allias F, Bolze PA. Peyle M, et al. Among authors: patrier s. J Gynecol Obstet Hum Reprod. 2024 Jan;53(1):102704. doi: 10.1016/j.jogoh.2023.102704. Epub 2023 Nov 29. J Gynecol Obstet Hum Reprod. 2024. PMID: 38040333
Practical guidelines of the EOTTD for pathological and genetic diagnosis of hydatidiform moles.
Bartosch C, Nadal A, Braga AC, Salerno A, Rougemont AL, Van Rompuy AS, Fitzgerald B, Joyce C, Allias F, Maher GJ, Turowski G, Tille JC, Alsibai KD, Van de Vijver K, McMahon L, Sunde L, Pyzlak M, Downey P, Wessman S, Patrier S, Kaur B, Fisher R. Bartosch C, et al. Among authors: patrier s. Virchows Arch. 2024 Mar;484(3):401-422. doi: 10.1007/s00428-023-03658-8. Epub 2023 Oct 19. Virchows Arch. 2024. PMID: 37857997 Review.
Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort.
van der Sluijs PJ, Joosten M, Alby C, Attié-Bitach T, Gilmore K, Dubourg C, Fradin M, Wang T, Kurtz-Nelson EC, Ahlers KP, Arts P, Barnett CP, Ashfaq M, Baban A, van den Born M, Borrie S, Busa T, Byrne A, Carriero M, Cesario C, Chong K, Cueto-González AM, Dempsey JC, Diderich KEM, Doherty D, Farholt S, Gerkes EH, Gorokhova S, Govaerts LCP, Gregersen PA, Hickey SE, Lefebvre M, Mari F, Martinovic J, Northrup H, O'Leary M, Parbhoo K, Patrier S, Popp B, Santos-Simarro F, Stoltenburg C, Thauvin-Robinet C, Thompson E, Vulto-van Silfhout AT, Zahir FR, Scott HS, Earl RK, Eichler EE, Vora NL, Wilnai Y, Giordano JL, Wapner RJ, Rosenfeld JA, Haak MC, Santen GWE. van der Sluijs PJ, et al. Among authors: patrier s. Genet Med. 2023 Feb;25(2):100004. doi: 10.1016/j.gim.2022.100004. Genet Med. 2023. PMID: 36745127 Free PMC article. No abstract available.
The human placenta as a model for training and research in mechanical thrombectomy: Clarifications and use of the chorionic plate veins.
Burel J, Cornacchini J, Garnier M, Patrier S, Guigné A, Gerardin E, Papagiannaki C, Sourour N, Shotar E, Premat K, Laporte C, Clarençon F. Burel J, et al. Among authors: patrier s. Front Neurol. 2022 Sep 20;13:925763. doi: 10.3389/fneur.2022.925763. eCollection 2022. Front Neurol. 2022. PMID: 36203983 Free PMC article.
Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort.
van der Sluijs PJ, Joosten M, Alby C, Attié-Bitach T, Gilmore K, Dubourg C, Fradin M, Wang T, Kurtz-Nelson EC, Ahlers KP, Arts P, Barnett CP, Ashfaq M, Baban A, van den Born M, Borrie S, Busa T, Byrne A, Carriero M, Cesario C, Chong K, Cueto-González AM, Dempsey JC, Diderich KEM, Doherty D, Farholt S, Gerkes EH, Gorokhova S, Govaerts LCP, Gregersen PA, Hickey SE, Lefebvre M, Mari F, Martinovic J, Northrup H, O'Leary M, Parbhoo K, Patrier S, Popp B, Santos-Simarro F, Stoltenburg C, Thauvin-Robinet C, Thompson E, Vulto-van Silfhout AT, Zahir FR, Scott HS, Earl RK, Eichler EE, Vora NL, Wilnai Y, Giordano JL, Wapner RJ, Rosenfeld JA, Haak MC, Santen GWE. van der Sluijs PJ, et al. Among authors: patrier s. Genet Med. 2022 Aug;24(8):1753-1760. doi: 10.1016/j.gim.2022.04.010. Epub 2022 May 18. Genet Med. 2022. PMID: 35579625 Free PMC article.
53 results