1. A truncating TPO mutation (Y55X) in patients with hypothyroidism and total iodide organification defect. (August 2015) Authors: Cangul, Hakan; Darendeliler, Feyza; Saglam, Yaman; Kucukemre, Banu; Kendall, Michaela; Boelaert, Kristien; Barrett, Timothy G.; Maher, Eamonn R. Journal: Endocrine research Issue: Volume 40:Number 3(2015:Aug.) Page Start: 146 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. An effective and cost‐saving structured education program teaching dynamic glucose management strategies to a socio‐economically deprived cohort with type 1 diabetes in a VIRTUAL setting. Issue 7 (12th July 2022) Authors: Pemberton, John S.; Barrett, Timothy G.; Dias, Renuka P.; Kershaw, Melanie; Krone, Ruth; Uday, Suma Journal: Pediatric diabetes Issue: Volume 23:Issue 7(2022) Page Start: 1045 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Metabolic syndrome: unravelling or unravelled?. Issue 7 (July 2019) Authors: Baranowski, Elizabeth S.; Barrett, Timothy G. Journal: Paediatrics and child health Issue: Volume 29:Issue 7(2019) Page Start: 297 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Metabolic syndrome: unravelling or unravelled?. Issue 7 (July 2019) Authors: Baranowski, Elizabeth S.; Barrett, Timothy G.; Parsons, Leonard Journal: Paediatrics and child health Issue: Volume 29:Issue 7(2019) Page Start: 297 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Monogenic diabetes syndromes: Locus‐specific databases for Alström, Wolfram, and Thiamine‐responsive megaloblastic anemia. Issue 7 (1st June 2017) Authors: Astuti, Dewi; Sabir, Ataf; Fulton, Piers; Zatyka, Malgorzata; Williams, Denise; Hardy, Carol; Milan, Gabriella; Favaretto, Francesca; Yu‐Wai‐Man, Patrick; Rohayem, Julia; López de Heredia, Miguel; Hershey, Tamara; Tranebjaerg, Lisbeth; Chen, Jian‐Hua; Chaussenot, Annabel; Nunes, Virginia; Marshal... Journal: Human mutation Issue: Volume 38:Issue 7(2017) Page Start: 764 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Refining genotype–phenotype correlation in Alström syndrome through study of primary human fibroblasts. Issue 4 (15th May 2017) Authors: Chen, Jian‐Hua; Geberhiwot, Tarekegn; Barrett, Timothy G.; Paisey, Richard; Semple, Robert K. Journal: Molecular genetics & genomic medicine Issue: Volume 5:Issue 4(2017) Page Start: 390 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community. (6th May 2013) Authors: Cangul, Hakan; Aycan, Zehra; Olivera‐Nappa, Alvaro; Saglam, Halil; Schoenmakers, Nadia A.; Boelaert, Kristien; Cetinkaya, Semra; Tarim, Omer; Bober, Ece; Darendeliler, Feyza; Bas, Veysel; Demir, Korcan; Aydin, Banu K.; Kendall, Michaela; Cole, Trevor; Högler, Wolfgang; Chatterjee, V. Krishna K.; ... Journal: Clinical endocrinology Issue: Volume 79:Number 2(2013:Aug.) Page Start: 275 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Treatment adherence and BMI reduction are key predictors of HbA1c 1 year after diagnosis of childhood type 2 diabetes in the United Kingdom. Issue 8 (11th October 2018) Authors: Candler, Toby P.; Mahmoud, Osama; Lynn, Richard M.; Majbar, Abdalmonen A.; Barrett, Timothy G.; Shield, Julian P. H. Journal: Pediatric diabetes Issue: Volume 19:Issue 8(2018) Page Start: 1393 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗