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Hormone Research in Paediatrics|March 29, 2022
Congenital Central Hypothyroidism Caused by a Novel IGSF1 Variant Identified in a French FamilyRachel Fourneaux, Sarah Castets, Alice Godefroy, et al.European Journal of Endocrinology|September 29, 2021
Acromegaly in remission: a view from the partnerRachel Fourneaux, Marie Vermalle, Frederique Albarel, et al.European Journal of Endocrinology|October 6, 2022
IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiencyRachel Fourneaux, Rachel Reynaud, Gregory Mougel, et al.Pageof 1