Meltem Tayfun
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Explore the profile of Meltem Tayfun including associated specialties, affiliations and a list of published articles.
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10
Citations
81
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Recent Articles
1.
Molecular Diagnosis of Monogenic Diabetes and Their Clinical/Laboratory Features in Turkish Children
Goksen D, Yesilkaya E, Ozen S, Kor Y, Eren E, Korkmaz O, et al.
J Clin Res Pediatr Endocrinol
. 2021 Jul;
13(4):433-438.
PMID: 34250910
Objective: Monogenic diabetes is a heterogeneous disease that causes functional problems in pancreatic beta cells and hyperglycemia. The aim of this study was to determine the clinical and laboratory features,...
2.
Koksoy A, Kurtul M, Kantar Ozsahin A, Cayci F, Tayfun M, Bayrakci U
J Pediatr Pharmacol Ther
. 2019 Jan;
23(6):494-498.
PMID: 30697137
Hyponatremia is one of the most common electrolyte abnormalities encountered in the clinical setting in hospitalized patients. The syndrome of inappropriate antidiuretic hormone secretion (SIADH) is the leading cause of...
3.
Kara O, Esen I, Tepe D, Gulleroglu N, Tayfun M
Med Sci Monit
. 2018 Dec;
24:9473-9478.
PMID: 30594946
BACKGROUND The present study investigated the relationship between detection of organic pathologies with magnetic resonance imaging of the pituitary gland, clinical and laboratory findings, and treatment response. MATERIAL AND METHODS...
4.
Cetinkaya S, Poyrazoglu S, Bas F, Ercan O, Yildiz M, Adal E, et al.
J Pediatr Endocrinol Metab
. 2018 Jan;
31(2):175-184.
PMID: 29353264
Background: The aim of the study was to assess the response to growth hormone (GH) treatment in very young patients with GH deficiency (GHD) through a national, multi-center study. Possible...
5.
Elmaogullari S, Ucakturk S, Elbeg S, Doger E, Tayfun M, Gurbuz F, et al.
J Clin Res Pediatr Endocrinol
. 2017 Sep;
10(2):108-112.
PMID: 28943512
Objective: Zinc transporter 8 protein (ZnT8A) is a transmembrane protein which functions to transfer zinc to insulin vesicles. Antibodies formed against ZnT8A (ZnT8A) are regarded as an independent autoimmunity demonstrator...
6.
Tepe D, Demirel F, Dag Seker E, Arhan E, Tayfun M, Esen I, et al.
J Pediatr Endocrinol Metab
. 2016 Jul;
29(8):907-14.
PMID: 27464033
Background: Idiopathic intracranial hypertension (IIH) is one of the most important and rare complications of obesity. Prevalence of IIH in childhood obesity is not known. The purpose of this study...
7.
Unal S, Gonulal D, Ucakturk A, Siyah Bilgin B, Flanagan S, Gurbuz F, et al.
J Clin Res Pediatr Endocrinol
. 2016 May;
8(4):478-481.
PMID: 27181099
Congenital hyperinsulinism (CHI) is the most common cause of neonatal persistent hypoglycemia caused by mutations in nine known genes. Early diagnosis and treatment are important to prevent brain injury. The...
8.
Atay Z, Yesilkaya E, Savas Erdeve S, Turan S, Akin L, Eren E, et al.
J Clin Endocrinol Metab
. 2016 Mar;
101(5):1980-8.
PMID: 26964727
Aim: The causes of gonadotropin-independent precocious puberty are diverse, and often have overlapping clinical and biochemical features. With the exception of congenital adrenal hyperplasia (CAH), disorders that cause gonadotropin-independent precocious...
9.
Topcu S, Orhon F, Tayfun M, Ucakturk S, Demirel F
J Pediatr Endocrinol Metab
. 2015 Nov;
29(3):357-61.
PMID: 26565543
Background: Obesity is a global health problem affecting all age groups. Childhood obesity, which may cause chronic diseases including diabetes mellitus, cardiovascular disease and cancer, etc., deserves more attention. However,...
10.
Oden Akman A, Tayfun M, Demirel F, Ucakturk S, Gungor A
J Pediatr Adolesc Gynecol
. 2015 Jul;
28(6):e161-3.
PMID: 26165912
Background: Van Wyk Grumbach syndrome (VWGS) and Kocher-Debre Semelaigne syndrome (KDSS) are rare forms of pseudo-precocious puberty and myopathy in patients with longstanding untreated hypothyroidism. We present the case of...