Filiz Tutunculer
Overview
Explore the profile of Filiz Tutunculer including associated specialties, affiliations and a list of published articles.
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Articles
32
Citations
159
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0
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Recent Articles
1.
Magnotto J, Mancini A, Bird K, Montenegro L, Tutunculer F, Pereira S, et al.
J Clin Endocrinol Metab
. 2023 Mar;
108(7):1646-1656.
PMID: 36916482
Context: Loss-of-function mutations in the maternally imprinted genes, MKRN3 and DLK1, are associated with central precocious puberty (CPP). Mutations in MKRN3 are the most common known genetic etiology of CPP....
2.
Kiral E, Kirel B, Havan M, Keskin M, Karaoglan M, Yildirim A, et al.
Front Pediatr
. 2022 Jul;
10:926013.
PMID: 35844756
Introduction: There have been some significant changes regarding healthcare utilization during the COVID-19 pandemic. Majority of the reports about the impact of the COVID-19 pandemic on diabetes care are from...
3.
Comlek F, Karal Y, Tutunculer F
Paediatr Int Child Health
. 2022 Apr;
42(2):105-107.
PMID: 35389821
Diabetic neuropathy in children and adolescents with Type 1 diabetes mellitus is rare and is usually subclinical and a complication of the late diabetes period. A 17-year-old boy admitted with...
4.
Comlek F, Celik H, Keskin B, Sut N, Dilek E, Tutunculer F
Indian J Endocrinol Metab
. 2021 Nov;
25(3):202-205.
PMID: 34760674
Background And Aims: Many diseases, especially chronic diseases, can lead to sleep disturbances. Our study aimed to evaluate sleep characteristics and the relationship between sleep disorders and diabetes-related variables in...
5.
Hatun S, Dalgic B, Goksen D, Aydogdu S, Savas Erdeve S, Kulogu Z, et al.
J Clin Res Pediatr Endocrinol
. 2021 Sep;
14(1):1-9.
PMID: 34538045
It is well-known that in children with type 1 diabetes (T1D), the frequency of Celiac disease (CD) is increased due to mechanisms which are not fully elucidated but include autoimmune...
6.
Comlek F, Yildiz R, Seyrek F, Tutunculer F
Oxf Med Case Reports
. 2021 May;
2021(4):omab015.
PMID: 33948188
Leydig cell aplasia/hypoplasia is an autosomal recessive condition. In its complete form, these patients are 46XY but are cryptorchid and phenotypically female. Most cases reported in literature presented with in...
7.
Demir S, Yalcintepe S, Ikbal Atli E, Sanri A, Yildirim R, Tutunculer F, et al.
Genet Test Mol Biomarkers
. 2021 Jan;
25(1):59-67.
PMID: 33470886
Osteogenesis imperfecta (OI) includes a group of disorders characterized by susceptibility to bone fractures with different severities. The increasing number of genes that may underlie the disorder, along with the...
8.
Guran T, Kara C, Yildiz M, Bitkin E, Haklar G, Lin J, et al.
J Clin Endocrinol Metab
. 2020 Jan;
105(3).
PMID: 31950145
Context: The clinical effects of classical 3β-hydroxysteroid dehydrogenase 2 (3βHSD2) deficiency are insufficiently defined due to a limited number of published cases. Objective: To evaluate an integrated steroid metabolome and...
9.
Sonmez A, Arifoglu I, Yildirim A, Tutunculer F
Turk Pediatri Ars
. 2018 Aug;
53(2):120-123.
PMID: 30116134
Benign transient hyperphosphatasemia is characterized by a significant increase in alkaline phosphatase levels, which is detected incidentally in infancy and children without underlying bone and liver disease. This condition is...
10.
Poyrazoglu S, Bundak R, Yavas Abali Z, Onal H, Sarikaya S, Akgun A, et al.
J Clin Res Pediatr Endocrinol
. 2018 May;
10(4):336-342.
PMID: 29789274
Objective: To assess the incidence of type 1 diabetes mellitus (T1DM) in children under 18 years of age in the northwest region of Turkey during 2013-2015. Methods: All newly diagnosed...