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Journal of Pediatric Endocrinology & Metabolism : JPEM|September 24, 2025
Clinical insights of the TBX19 C.856 C>T variant: a case report and literature review on neonatal isolated ACTH deficiencySirmen Kizilcan Cetin, Zeynep Siklar, Zehra Aycan, et al.Endocrinologia, Diabetes Y Nutricion|April 23, 2026
Psychopathological aspects of EDs in adolescents with type 1 diabetes: Findings from the DEPS-R and clinical outcomesMeliha Esra Bilici, Hümeyra Altıntaş, Elif Özsu, et al.International Ophthalmology|January 24, 2014
Corneal biomechanical characteristics in children with diabetes mellitusPınar Nalcacioglu-Yuksekkaya, Emine Sen, Semra Cetinkaya, et al.Journal of Clinical Research in Pediatric Endocrinology|July 29, 2025
Long-Term Follow-up of a Case with TBX19 Mutation, a Rare Cause of Isolated ACTH Deficiency and Literature ReviewAysegul Ceran, Zehra Aycan, Zeynep Siklar, et al.Biological Psychology|September 23, 2024
Pupillary dilation response to the auditory food words in adolescents with obesity without binge eating disorderElif Akcay, Özgür Aydın, Veronika Zagvozdkina, et al.BMC Public Health|July 9, 2026
Cyberbullying among medical school students: an examination of the relationship between frequency, sensitivity, and psychological symptoms: a cross-sectional studyCemal Koçak, Zeynep Irmak, Ayşe Gül Güven, et al.Scandinavian Journal of Clinical and Laboratory Investigation|April 24, 2013
Peroxisome proliferator activated receptor (PPAR)-gamma concentrations in childhood obesityNesibe Akyürek, Zehra Aycan, Semra Çetinkaya, et al.Taiwanese Journal of Obstetrics & Gynecology|November 25, 2019
Vitamin D deficiency in adolescent pregnancy and obstetric outcomesDoğa F Öcal, Zehra Aycan, Gülşah Dağdeviren, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|April 21, 2015
17βHSD-3 enzyme deficiency due to novel mutations in the HSD17B3 gene diagnosed in a neonateElif Sagsak, Zehra Aycan, Senay Savas-Erdeve, et al.European Journal of Ophthalmology|May 8, 2014
Decreased retinal nerve fiber layer thickness in patients with congenital isolated growth hormone deficiencyPinar Nalcacioglu-Yuksekkaya, Emine Sen, Sebahat Yilmaz, et al.Pageof 24