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Acromegaly in remission: a view from the partner.
Eur J Endocrinol. 2021 Oct 21;185(6):K19-K23. doi: 10.1530/EJE-21-0537.
Eur J Endocrinol. 2021.
PMID: 34586080
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.
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
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Congenital Central Hypothyroidism Caused by a Novel IGSF1 Variant Identified in a French Family.
Fourneaux R, Castets S, Godefroy A, Grelet M, Abeillon-du Payrat J, Saveanu A, Castinetti F, Reynaud R.
Fourneaux R, et al.
Horm Res Paediatr. 2022;95(3):296-303. doi: 10.1159/000524233. Epub 2022 Mar 29.
Horm Res Paediatr. 2022.
PMID: 35350016
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