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Presence of specific SARS-COV2 antibodies in hemodialysis patients and their caregivers after the first wave of COVID-19.
Robert T, Lano G, Resseguier N, Bobot M, Bouchouareb D, Burtey S, de Lamballerie X, Dhorne J, Dussol B, Duval A, Faraut J, Fourié T, Giaime P, Hallah M, Jaubert D, Jéhel O, Legris T, Liotatis S, Moal V, Ninove L, Pedinielli N, Pelletier M, Romeu-Giannoli M, Saba M, Sallée M, Samson L, Saveanu A, Scarfoglière V, Sebahoun P, Vial R, Von Kotze C, Brunet P, Lebrun G, Bataille S, Jourde-Chiche N. Robert T, et al. Among authors: saveanu a. Sci Rep. 2022 Jul 13;12(1):11972. doi: 10.1038/s41598-022-15913-0. Sci Rep. 2022. PMID: 35831388 Free PMC article.
Diagnosis and management of congenital hypopituitarism in children.
Castets S, Thomas-Teinturier C, Villanueva C, Amsellem J, Barat P, Brun G, Quoc EB, Carel JC, De Filippo GP, Kipnis C, Martinerie L, Vergier J, Saveanu A, Teissier N, Coutant R, Léger J, Reynaud R. Castets S, et al. Among authors: saveanu a. Arch Pediatr. 2024 Apr;31(3):165-171. doi: 10.1016/j.arcped.2024.01.003. Epub 2024 Mar 27. Arch Pediatr. 2024. PMID: 38538470 Free article.
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: saveanu a. Ann Endocrinol (Paris). 2024 Mar 5:S0003-4266(24)00035-0. doi: 10.1016/j.ando.2024.03.001. Online ahead of print. Ann Endocrinol (Paris). 2024. PMID: 38452869 Free article.
Heterozygous pathogenic variants in POMC are not responsible for monogenic obesity: Implication for MC4R agonist use.
Le Collen L, Delemer B, Poitou C, Vaxillaire M, Toussaint B, Dechaume A, Badreddine A, Boissel M, Derhourhi M, Clément K, Petit JM, Mau-Them FT, Bruel AL, Thauvin-Robinet C, Saveanu A, Cherifi BG, Le Beyec-Le Bihan J, Froguel P, Bonnefond A. Le Collen L, et al. Among authors: saveanu a. Genet Med. 2023 Jul;25(7):100857. doi: 10.1016/j.gim.2023.100857. Epub 2023 Apr 21. Genet Med. 2023. PMID: 37092539
IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency.
Fourneaux R, Reynaud R, Mougel G, Castets S, Bretones P, Dauriat B, Edouard T, Raverot G, Barlier A, Brue T, Castinetti F, Saveanu A. Fourneaux R, et al. Among authors: saveanu a. Eur J Endocrinol. 2022 Nov 3;187(6):787-795. doi: 10.1530/EJE-22-0520. Print 2022 Dec 1. Eur J Endocrinol. 2022. PMID: 36201163
89 results