Nazli Gonc
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Explore the profile of Nazli Gonc including associated specialties, affiliations and a list of published articles.
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Articles
43
Citations
271
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Recent Articles
1.
Emet D, Helhel E, Portakal O, Gonc N
Horm Res Paediatr
. 2025 Jan;
:1-10.
PMID: 39864412
Introduction: Carboxypeptidase E (CPE) is an enzyme involved in the neuropeptides/hormones processing. Its deficiency is associated with endocrinopathies comparable to those caused by proprotein convertase 1/3(PC1/3) deficiency. In this case...
2.
Cavusoglu G, Boynuyogun E, Erek N, Calis M, Emet D, Gonc N, et al.
Turk J Pediatr
. 2025 Jan;
66(6):703-712.
PMID: 39807744
Background: Any impediment to the development of midline structures i.e. hypothalamus, pituitary and oral cavity may cause anatomical and functional issues. We aimed to determine the association of endocrine disorders...
3.
Kandemir N, Vuralli D, Ozon A, Gonc N, Ardicli D, Jalilova L, et al.
J Diabetes
. 2024 Apr;
16(5):e13562.
PMID: 38664892
Background: Global variations in epidemiology of type 1 diabetes mellitus (T1DM) exist. This study is designed to examine demographic and clinical features of T1DM over the past 3 decades as...
4.
Mete Yesil A, Kayaoglu B, Gul E, Gonc N, Ozon A, Tezcan I, et al.
Turk J Pediatr
. 2023 Jul;
65(3):536-541.
PMID: 37395973
Background: Hyperimmunoglobulin E syndrome (HIES) due to dedicator of cytokinesis8 (DOCK8) deficiency may present in infancy and childhood with different clinical features involving recurrent infections, allergic dysregulation, and autoimmunity. Case:...
5.
Emet D, Mete Yesil A, Celik B, Sencan B, Unsal Y, Gonc N, et al.
Turk Arch Pediatr
. 2023 Jun;
58(4):418-424.
PMID: 37357456
Objective: Governments have enforced restrictions to prevent the spread of coronavirus dis- ease 2019, which has affected lifestyle and psychosocial well-being. The aim of this study is to examine the...
6.
Vuralli D, Yildiz Y, Ozon A, Dursun A, Gonc N, Tokatli A, et al.
J Clin Res Pediatr Endocrinol
. 2022 Mar;
14(3):275-286.
PMID: 35308014
Objective: Phosphomannomutase 2 deficiency (PMM2-CDG) is a disorder of protein N-glycosylation with a wide clinical spectrum. Hypoglycemia is rarely reported in PMM2-CDG. In this study, we evaluated cause, treatment options...
7.
Gulhan B, Unsal Y, Baltu D, Celik Ertas N, Ozdemir G, Utine E, et al.
Blood Press Monit
. 2022 Jan;
27(3):208-211.
PMID: 35044984
A genetic defect of 11 β-hydroxysteroid dehydrogenase causes apparent mineralocorticoid excess syndrome. Since 50 days of life, our patient was hospitalized several times for various reasons including hypokalemia. At the...
8.
Vuralli D, Gonc N, Ozon A, Ekinci S, Dogan H, Tekgul S, et al.
J Clin Res Pediatr Endocrinol
. 2021 Aug;
14(1):17-28.
PMID: 34380293
Objective: Estrogen-secreting adrenocortical tumors (ACTs) are quite rare with feminizing adrenocortical tumors (FATs) accounting for 0.37-2% of all ACTs. The aim was to evaluate clinical and hormonal characteristics of FATS...
9.
Ardicli B, User I, Ciftci A, Akyuz C, Kutluk M, Gonc N, et al.
J Pediatr Urol
. 2021 Feb;
17(3):400.e1-400.e7.
PMID: 33593626
Aim: Pheochromocytoma (PCC) and paraganglioma (PGL) are rare tumors in childhood. They are catecholamine secreting tumors and present with signs or symptoms related to their excess. Most common signs and...
10.
Emet D, Ozon A, Alikasifoglu A, Kandemir N, Gonc N
Obesity (Silver Spring)
. 2021 Jan;
29(2):402-408.
PMID: 33491320
Objective: The purpose of this study was to investigate the peripheral concentrations of leptin and neuropeptides taking part in the melanocortin pathway in hypothalamic obesity (HO) associated with craniopharyngioma (CP)...