Nazli E. Gonc
Ankara, Turkey
Last Updated: 09/26/2026
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Found 13 publications
Apparent mineralocorticoid excess: A diagnosis beyond classical causes of severe hypertension in a child.
Journal: Blood pressure monitoring
Published: January 19, 2022
Adrenocortical tumours in children: a review of surgical management at a tertiary care centre.
Journal: ANZ journal of surgery
Published: September 17, 2020
Which parameters predict the beneficial effect of GnRHa treatment on height in girls with central precocious puberty?
Journal: Clinical endocrinology
Published: September 16, 2020
Approach to pheochromocytoma and paraganglioma in children and adolescents: A retrospective clinical study from a tertiary care center.
Journal: Journal of pediatric urology
Published: July 09, 2020
Treatment response to long term antiresorptive therapy in osteogenesis imperfecta type VI: does genotype matter?
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: May 11, 2020
Erratum to 'Response to early coenzyme Q10 supplementation is not sustained in CoQ10 deficiency caused by CoQ2 mutation' [Pediatric Neurology 88 (2018) 71-74].
Journal: Pediatric neurology
Published: February 20, 2019
Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: February 24, 2017
Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes.
Journal: Journal of human genetics
Published: December 08, 2016
Prevalence of nasal carriage of methicillin-resistant Staphylococcus aureus in children with diabetes mellitus: Trends between 2005 and 2013.
Journal: American journal of infection control
Published: February 15, 2015
Evaluation of hypothalamic-pituitary function in children following acute bacterial meningitis.
Journal: Pituitary
Published: December 21, 2013
Clinical characteristics of type 1 diabetes over a 40 year period in Turkey: secular trend towards earlier age of onset.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: August 02, 2013
17beta-hydroxysteroid dehydrogenase type 3 deficiency as a result of a homozygous 7 base pair deletion in 17betaHSD3 gene.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: August 11, 2012
Last Updated: 09/26/2026