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Journal of Clinical Research in Pediatric Endocrinology|September 28, 2013
Multiple pituitary hormone deficiency due to gunshot injury in a 6-year-old girlHüseyin Demirbilek, Mehmet Nuri Ozbek, Rıza Taner Baran, et al.
Journal of Clinical Research in Pediatric Endocrinology|June 8, 2012
Plasma kisspeptin levels in girls with premature thelarcheAyşehan Akinci, Dilek Cetin, Nevin Ilhan
Journal of Clinical Research in Pediatric Endocrinology|June 8, 2012
Characteristics of children with type 1 diabetes and persistent suboptimal glycemic controlHyuntae Kim, Angelo Elmi, Celia L Henderson, et al.
Journal of Clinical Research in Pediatric Endocrinology|June 8, 2012
SLC34A3 intronic deletion in a new kindred with hereditary hypophosphatemic rickets with hypercalciuriaShirin Hasani-Ranjbar, Mahsa M Amoli, Azadeh Ebrahim-Habibi, et al.
Journal of Clinical Research in Pediatric Endocrinology|August 24, 2016
Safety and Efficacy of Stosstherapy in Nutritional RicketsDaipayan Chatterjee, Mathad K S Swamy, Vikas Gupta, et al.
Journal of Clinical Research in Pediatric Endocrinology|April 18, 2019
Impact of Socioeconomic Characteristics on Metabolic Control in Children with Type 1 Diabetes in a Developing CountryAbeer Alassaf, Rasha Odeh, Lubna Gharaibeh, et al.
Journal of Clinical Research in Pediatric Endocrinology|September 26, 2018
Remarkable Increase in the Prevalence of Overweight and Obesity Among School Age Children in Antalya, Turkey, Between 2003 and 2015Gamze Çelmeli, Yusuf Çürek, Zümrüt Arslan Gülten, et al.
Journal of Clinical Research in Pediatric Endocrinology|May 5, 2018
Under-recognized Hypoparathyroidism in ThalassemiaHataitip Tangngam, Pat Mahachoklertwattana, Preamrudee Poomthavorn, et al.
Journal of Clinical Research in Pediatric Endocrinology|May 30, 2018
The Role of Irisin, Insulin and Leptin in Maternal and Fetal InteractionDeniz Ökdemir, Nihal Hatipoğlu, Selim Kurtoğlu, et al.
Journal of Clinical Research in Pediatric Endocrinology|September 26, 2017
Neonatal Diabetes: Two Cases with Isolated Pancreas Agenesis due to Homozygous PTF1A Enhancer Mutations and One with Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome due to KCNJ11 MutationOlcay Evliyaoğlu, Oya Ercan, Emel Ataoğlu, et al.
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