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Year Number of Results
1998 1
1999 2
2000 1
2001 2
2002 1
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2004 3
2005 7
2006 4
2007 3
2008 10
2009 3
2010 1
2011 8
2012 6
2013 2
2014 4
2015 3
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2017 4
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2022 12
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91 results

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Page 1
Phenotype and genotype of 23 patients with hypopituitarism and pathogenic GLI2 variants.
Aouchiche K, Charmensat C, Morgane P, Teinturier C, Bretones P, Brac de la Perriere A, Layet V, Bouhours-Nouet N, Vantyghem MC, Haine E, Nunes-Sanchez ML, Camard O, Baron S, Castinetti F, Barlier A, Brue T, Reynaud R, Saveanu A; Genhypopit Network. Aouchiche K, et al. Among authors: saveanu a. Eur J Endocrinol. 2025 Feb 1;192(2):110-118. doi: 10.1093/ejendo/lvaf015. Eur J Endocrinol. 2025. PMID: 39938560
CSNK2B Mutation: A Rare Cause of IGHD.
Aouchiche K, Romanet P, Barlier A, Brue T, Pertuit M, Reynaud R, Saveanu A. Aouchiche K, et al. Among authors: saveanu a. Clin Endocrinol (Oxf). 2025 Apr;102(4):421-426. doi: 10.1111/cen.15174. Epub 2024 Dec 15. Clin Endocrinol (Oxf). 2025. PMID: 39676320 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 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.
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 Free article.
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
91 results