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IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency.
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
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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Acromegaly in remission: a view from the partner.
Fourneaux R, Vermalle M, Albarel F, Morange I, Graillon T, Amodru V, Cuny T, Dufour H, Brue T, Castinetti F.
Fourneaux R, et al.
Eur J Endocrinol. 2021 Oct 21;185(6):K19-K23. doi: 10.1530/EJE-21-0537.
Eur J Endocrinol. 2021.
PMID: 34586080
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