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Author/Creator Castets, Sarah

1. IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency. Issue 6 (3rd November 2022)

Authors:
Fourneaux, Rachel; Reynaud, Rachel; Mougel, Gregory; Castets, Sarah; Bretones, Patricia; Dauriat, Benjamin; Edouard, Thomas; Raverot, Gerald; Barlier, Anne; Brue, Thierry; Castinetti, Frederic; Saveanu, Alexandru
Journal:
European journal of endocrinology
Issue:
Volume 187:Issue 6(2022)
Page Start:
787
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Reference values for the external genitalia of full-term and pre-term female neonates. Issue 1 (19th June 2020)

Authors:
Castets, Sarah; Nguyen, Kim-An; Plaisant, Franck; Prudon, Malika Baya; Plotton, Ingrid; Kassai, Behrouz; Roche, Sylvain; Ecochard, Rene; Claris, Olivier; Nicolino, Marc; Villanueva, Carine; Gay, Claire-Lise
Journal:
Archives of disease in childhood
Issue:
Volume 106:Issue 1(2021)
Page Start:
39
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗