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Journal of Pediatric Endocrinology & Metabolism : JPEM|October 8, 2020
Treatment response to long term antiresorptive therapy in osteogenesis imperfecta type VI: does genotype matter?Nur Berna Celik, Nazli Gonc, Alev Ozon, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 3, 2007
Inappropriate use of potent topical glucocorticoids in infantsAlev Ozon, Semra Cetinkaya, Ayfer Alikasifoglu, et al.
Pituitary|September 14, 2021
Management of prolactinomas in children and adolescents; which factors define the response to treatment?Ayfer Alikasifoglu, Nur Berna Celik, Zeynep Alev Ozon, et al.
Therapeutic Advances in Endocrinology and Metabolism|December 28, 2023
Dual-basal-insulin regimen for the management of dawn phenomenon in children with type 1 diabetes: a retrospective cohort studyNur Berna Celik, Dicle Canoruc Emet, Merve Canturk, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 15, 2021
Long-term effect of conventional phosphate and calcitriol treatment on metabolic recovery and catch-up growth in children with PHEX mutationAyfer Alikasifoglu, Yagmur Unsal, Elmas Nazli Gonc, et al.
European Journal of Pediatrics|November 30, 2025
Does gonadotropin-releasing hormone analogue treatment alter body mass index in boys with central precocious puberty?Yagmur Unsal, Dogus Vuralli Karaoglan, Elmas Nazli Gonc, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 3, 2011
Two pediatric patients with Von Hippel-Lindau disease type 2b: from patient to screening, from screening to patientNazli Gonc, Ozlem Engiz, Hartmut P H Neumann, et al.
The Journal of Steroid Biochemistry and Molecular Biology|March 10, 2016
Novel and prevalent CYP11B1 gene mutations in Turkish patients with 11-β hydroxylase deficiencyNurgun Kandemir, Didem Yucel Yilmaz, E Nazli Gonc, et al.
Journal of Diabetes and Its Complications|January 4, 2006
Thrombin-activatable fibrinolysis inhibitor activity and global fibrinolytic capacity in Type 1 diabetes: evidence for normal fibrinolytic stateAyla Harmanci, Nurgun Kandemir, Selcuk Dagdelen, et al.
Pediatric Diabetes|July 20, 2011
HNF1B mutation in a Turkish child with renal and exocrine pancreas insufficiency, diabetes and liver diseaseE Nazli Gonc, Burcu Bulum Ozturk, Ingfrid S Haldorsen, et al.
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