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

Year Number of Results
2005 2
2008 2
2009 3
2010 2
2012 2
2013 1
2014 1
2015 3
2016 8
2017 4
2018 2
2019 2
2020 1
2021 1
2022 4
2023 2
2024 4
2025 0

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38 results

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Page 1
[Neuro-Langerhans cell histiocytosis].
Le Guennec L, Martin-Duverneuil N, Mokhtari K, Santiago-Ribeiro M, Bayen E, Del Cul A, Delgadillo D, Kas A, Courtillot C, Haroche J, Cohen F, Donadieu J, Hoang-Xuan K, Idbaih A. Le Guennec L, et al. Among authors: courtillot c. Presse Med. 2017 Jan;46(1):79-84. doi: 10.1016/j.lpm.2016.09.014. Epub 2016 Nov 2. Presse Med. 2017. PMID: 27816346 Review. French.
Erratum à l'article « Un programme d'éducation thérapeutique centré sur la transition des patients, avec endocrinopathie chronique, entre les services d'endocrinologie pédiatrique et adulte » [Presse Med. 45 (5) (2016) e119-e129].
Malivoir S, Courtillot C, Bachelot A, Chakhtoura Z, Téjédor I, Touraine P; Les référents pédiatres. Malivoir S, et al. Among authors: courtillot c. Presse Med. 2016 Jul-Aug;45(7-8P1):718. doi: 10.1016/j.lpm.2016.06.012. Epub 2016 Jul 27. Presse Med. 2016. PMID: 27476021 French. No abstract available.
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
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, Leclercq D, 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;86(1):101631. doi: 10.1016/j.ando.2024.07.002. Online ahead of print. Ann Endocrinol (Paris). 2024. PMID: 39002896 Free article. No abstract available.
Benign breast diseases.
Courtillot C, Plu-Bureau G, Binart N, Balleyguier C, Sigal-Zafrani B, Goffin V, Kuttenn F, Kelly PA, Touraine P. Courtillot C, et al. J Mammary Gland Biol Neoplasia. 2005 Oct;10(4):325-35. doi: 10.1007/s10911-006-9006-4. J Mammary Gland Biol Neoplasia. 2005. PMID: 16900392 Review.
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.
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
Hypoglycaemia revealing heterozygous insulin receptor mutations.
Preumont V, Feincoeur C, Lascols O, Courtillot C, Touraine P, Maiter D, Vigouroux C. Preumont V, et al. Among authors: courtillot c. Diabetes Metab. 2017 Feb;43(1):95-96. doi: 10.1016/j.diabet.2016.07.001. Epub 2016 Jul 26. Diabetes Metab. 2017. PMID: 27474196 Free PMC article. No abstract available.
38 results