1. Germinal defects of SDHx genes in patients with isolated pituitary adenoma. Issue 4 (October 2020) Authors: Mougel, Grégory; Lagarde, Arnaud; Albarel, Frédérique; Essamet, Wassim; Luigi, Perrine; Mouly, Céline; Vialon, Magaly; Cuny, Thomas; Castinetti, Frédéric; Saveanu, Alexandru; Brue, Thierry; Barlier, Anne; Romanet, Pauline Journal: European journal of endocrinology Issue: Volume 183:Issue 4(2020) Page Start: 369 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Germinal defects of SDHx genes in patients with isolated pituitary adenoma. Issue 4 (October 2020) Authors: Mougel, Grégory; Lagarde, Arnaud; Albarel, Frédérique; Essamet, Wassim; Luigi, Perrine; Mouly, Céline; Vialon, Magaly; Cuny, Thomas; Castinetti, Frédéric; Saveanu, Alexandru; Brue, Thierry; Barlier, Anne; Romanet, Pauline Journal: European journal of endocrinology Issue: Volume 183:Issue 4(2020) Page Start: 369 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Gestational diabetes and acromegaly: Single‐centre experience of 14 pregnancies. (14th October 2019) Authors: Vialon, Magaly; Grunenwald, Solange; Mouly, Céline; Vezzosi, Delphine; Bennet, Antoine; Gourdy, Pierre; Caron, Philippe J. Journal: Clinical endocrinology Issue: Volume 91:Number 6(2019) Page Start: 805 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Impact of transition on quality of life in patients with congenital adrenal hyperplasia diagnosed during childhood. Issue 7 (October 2017) Authors: Bachelot, Anne; Vialon, Magaly; Baptiste, Amandine; Tejedor, Isabelle; Elie, Caroline; Polak, Michel; Touraine, Philippe Journal: Endocrine connections Issue: Volume 6:Issue 7(2017) Page Start: 422 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Severe thyrotoxicosis in an infant revealing familial nonautoimmune hyperthyroidism with a novel (C672W) stimulating thyrotropin receptor germline mutation. Issue 12 (25th October 2017) Authors: Oliver‐Petit, Isabelle; Savagner, Frédérique; Grunenwald, Solange; Vialon, Magaly; Edouard, Thomas; Caron, Philippe Journal: Clinical case reports Issue: Volume 5:Issue 12(2017) Page Start: 1980 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗