1. Benefits of 11C-methionine PET/MRI and intraoperative fluorescence in treating hyperparathyroidism. (29th July 2020) Authors: Luong, Thien Vinh; Rejnmark, Lars; Arveschoug, Anne Kirstine; Iversen, Peter; Rolighed, Lars Journal: Endocrinology, diabetes & metabolism case reports Issue: (2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Benefits of 11C-methionine PET/MRI and intraoperative fluorescence in treating hyperparathyroidism. (29th July 2020) Authors: Luong, Thien Vinh; Rejnmark, Lars; Arveschoug, Anne Kirstine; Iversen, Peter; Rolighed, Lars Journal: Endocrinology, diabetes & metabolism case reports Issue: (2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Brachydactyly mental retardation syndrome with growth hormone deficiency. (21st July 2018) Authors: Arefzadeh, Alireza; Khalighinejad, Pooyan; Ataeinia, Bahar; Parvar, Pegah Journal: Endocrinology, diabetes & metabolism case reports Issue: (2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Growth hormone deficiency as a cause for short stature in Wiedemann–Steiner Syndrome. (23rd August 2018) Authors: Stoyle, George; Banka, Siddharth; Langley, Claire; Jones, Elizabeth A; Banerjee, Indraneel Journal: Endocrinology, diabetes & metabolism case reports Issue: (2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Growth hormone treatment for short stature associated with duplication of the NSD1 Sotos syndrome gene. (5th March 2021) Authors: Bernhardt, Isaac T; Gunn, Alistair J; Carter, Philippa J Journal: Endocrinology, diabetes & metabolism case reports Issue: (2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Non classic presentations of a genetic mutation typically associated with transient neonatal diabetes. (26th February 2020) Authors: Devaraja, Janani; Elder, Charlotte; Scott, Adrian Journal: Endocrinology, diabetes & metabolism case reports Issue: (2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Non classic presentations of a genetic mutation typically associated with transient neonatal diabetes. (26th February 2020) Authors: Devaraja, Janani; Elder, Charlotte; Scott, Adrian Journal: Endocrinology, diabetes & metabolism case reports Issue: (2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗