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Page 1
Diagnosis and management of children and adult craniopharyngiomas: a French Endocrine Society/French Society for Paediatric Endocrinology & Diabetes Consensus Statement.
Cuny T, Reynaud R, Raverot G, Coutant R, Chanson P, Kariyawasam D, Poitou C, Thomas-Teinturier C, Baussart B, Samara-Boustani D, Feuvret L, Villanueva C, Villa C, Bouillet B, Tauber M, Espiard S, Castets S, Beckers A, Amsellem J, Vantyghem MC, Delemer B, Chevalier N, Brue T, André N, Kerlan V, Graillon T, Raingeard I, Alapetite C, Raverot V, Salenave S, Boulin A, Appay R, Dalmas F, Fodil S, Coppin L, Buffet C, Thuillier P, Castinetti F, Vogin G, Cazabat L, Kuhn E, Haissaguerre M, Reznik Y, Goichot B, Bachelot A, Kamenicky P, Decoudier B, Planchon C, Micoulaud-Franchi JA, Romanet P, Jacobi D, Faucher P, Carette C, Bihan H, Drui D, Rossignol S, Gonin L, Sokol E, Wiard L, Courtillot C, Nicolino M, Grunenwald S, Chabre O, Christin-Maître S, Desailloud R, Maiter D, Guignat L, Brac de la Perrière A, Salva P, Scavarda D, Bonneville F, Caron P, Vasiljevic A, Cortet C, Gaillard S, Albarel F, Clément K, Jouanneau E, Dufour H, Barat P, Gatta-Cherifi B. Cuny T, et al. Among authors: courtillot c. Ann Endocrinol (Paris). 2024 Jul 11:S0003-4266(24)00108-2. doi: 10.1016/j.ando.2024.07.002. Online ahead of print. Ann Endocrinol (Paris). 2024. PMID: 39002896 Free article.
Shifting the landscape: Dominant C-terminal rare missense FOXL2 variants in non-syndromic primary ovarian failure etiology.
Jordan P, Verebi C, Hervé B, Perol S, Chakhtoura Z, Courtillot C, Bachelot A, Karila D, Renard C, Grouthier V, de la Croix SM, Bernard V, Fouveaut C, de la Perrière AB, Jonard-Catteau S, Touraine P, Plu-Bureau G, Dupont JM, Christin-Maitre S, Bienvenu T. Jordan P, et al. Among authors: courtillot c. Clin Genet. 2024 Jul;106(1):102-108. doi: 10.1111/cge.14526. Epub 2024 Apr 1. Clin Genet. 2024. PMID: 38558253
Position statement on the diagnosis and management of congenital pituitary deficiency in adults: The French National Diagnosis and Treatment Protocol (NDTP).
Castets S, Albarel F, Bachelot A, Brun G, Bouligand J, Briet C, Bui Quoc E, Cazabat L, Chabbert-Buffet N, Christin-Maitre S, Courtillot C, Cuny T, De Filippo G, Donadille B, Illouz F, Pellegrini I, Reznik Y, Saveanu A, Teissier N, Touraine P, Vantyghem MC, Vergier J, Léger J, Brue T, Reynaud R. Castets S, et al. Among authors: courtillot c. Ann Endocrinol (Paris). 2024 Jul;85(4):327-339. doi: 10.1016/j.ando.2024.03.001. Epub 2024 Mar 5. Ann Endocrinol (Paris). 2024. PMID: 38452869 Free article.
Pituitary surgery outcome in patients 75 years and older: a retrospective study.
Garvayo M, Villa C, Jouinot A, Messerer M, Reina V, Hage M, Raffin-Sanson ML, Courtillot C, Bachelot A, Kamenicky P, Chanson P, Vatier C, Christin-Maitre S, Bertherat J, Assié G, Gaillard S, Baussart B. Garvayo M, et al. Among authors: courtillot c. Acta Neurochir (Wien). 2023 Nov;165(11):3409-3420. doi: 10.1007/s00701-023-05809-x. Epub 2023 Sep 22. Acta Neurochir (Wien). 2023. PMID: 37736839
Treatment patterns and unmet needs in adults with classic congenital adrenal hyperplasia: A modified Delphi consensus study.
Auchus RJ, Courtillot C, Dobs A, El-Maouche D, Falhammar H, Lacroix A, Farrar M, O'Donoghue C, Anatchkova M, Cutts K, Taylor N, Yonan C, Lamotte M, Touraine P. Auchus RJ, et al. Among authors: courtillot c. Front Endocrinol (Lausanne). 2022 Nov 18;13:1005963. doi: 10.3389/fendo.2022.1005963. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36465641 Free PMC article.
Fertility and pregnancy outcomes in women with nonclassic 21-hydroxylase deficiency.
Carrière C, Nguyen LS, Courtillot C, Tejedor I, Chakhtoura Z, Bellanné-Chantelot C, Tardy V, Leban M, Touraine P, Bachelot A. Carrière C, et al. Among authors: courtillot c. Clin Endocrinol (Oxf). 2023 Mar;98(3):315-322. doi: 10.1111/cen.14842. Epub 2022 Nov 17. Clin Endocrinol (Oxf). 2023. PMID: 36325983
Age at diagnosis in patients with chronic congenital endocrine conditions: a regional cohort study from a reference center for rare diseases.
Kallali W, Messiaen C, Saïdi R, Lessim S, Viaud M, Dulon J, Nedelcu M, Samara D, Houang M, Donadille B, Courtillot C, de Filippo G, Carel JC, Christin-Maitre S, Touraine P, Netchine I, Polak M, Léger J. Kallali W, et al. Among authors: courtillot c. Orphanet J Rare Dis. 2021 Nov 4;16(1):469. doi: 10.1186/s13023-021-02099-3. Orphanet J Rare Dis. 2021. PMID: 34736502 Free PMC article.
38 results