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Position statement on the diagnosis and management of premature/primary ovarian insufficiency (except Turner Syndrome).
Christin-Maitre S, Givony M, Albarel F, Bachelot A, Bidet M, Blanc JV, Bouvattier C, Brac de la Perrière A, Catteau-Jonard S, Chevalier N, Carel JC, Coutant R, Donadille B, Duranteau L, El-Khattabi L, Hugon-Rodin J, Houang M, Grynberg M, Kerlan V, Leger J, Misrahi M, Pienkowski C, Plu-Bureau G, Polak M, Reynaud R, Siffroi JP, Sonigo C, Touraine P, Zenaty D. Christin-Maitre S, et al. Among authors: houang m. Ann Endocrinol (Paris). 2021 Dec;82(6):555-571. doi: 10.1016/j.ando.2021.09.001. Epub 2021 Sep 8. Ann Endocrinol (Paris). 2021. PMID: 34508691
Phenotypic variation of SF1 gene mutations.
Philibert P, Paris F, Audran F, Kalfa N, Polak M, Thibaud E, Pinto G, Houang M, Zenaty D, Leger J, Mas JC, Pienkowski C, Einaudi S, Damiani D, Ten S, Sinha S, Poulat F, Sultan C. Philibert P, et al. Among authors: houang m. Adv Exp Med Biol. 2011;707:67-72. doi: 10.1007/978-1-4419-8002-1_16. Adv Exp Med Biol. 2011. PMID: 21691958 No abstract available.
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. 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.
82 results