Heves Kirmizibekmez
Overview
Explore the profile of Heves Kirmizibekmez including associated specialties, affiliations and a list of published articles.
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Articles
42
Citations
139
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Recent Articles
1.
Yuksel O, Atmaca F, Dursun F, Seymen G, Atla P, Altun E, et al.
J Clin Res Pediatr Endocrinol
. 2025 Jan;
PMID: 39885768
Introduction: Obesity is associated with an increased risk of PCOS. It can be difficult to differentiate between PCOS and physiological oligomenorrhoea/anovulation in adolescent girls. To date, studies of the prevalence...
2.
Yeter B, Kendir Demirkol Y, Eser M, Akgulle A, Sozeri B, Kirmizibekmez H
J Clin Res Pediatr Endocrinol
. 2025 Jan;
PMID: 39849673
Objective: Heterozygous COL2A1 gene mutations are associated with type 2 collagenopathies, characterized by a wide, diverse, and overlapping clinical spectrum in related diseases. Our goal is to describe the clinical,...
3.
Yasar A, Altun E, Kirmizibekmez H, Dursun F
J Pediatr Endocrinol Metab
. 2024 Aug;
37(10):885-891.
PMID: 39189676
Objectives: Subclinical hypothyroidism (SH) is defined by normal free triiodothyronine (fT3) and free thyroxine (fT4) levels, elevated thyroid-stimulating hormone levels, and the absence of overt clinical signs of hypothyroidism. The ...
4.
Karakus K, Sakarya S, Yildirim R, Ozalkak S, Ozbek M, Yildirim N, et al.
J Clin Res Pediatr Endocrinol
. 2024 Jul;
PMID: 38953734
Objective: To determine inequalities in access to diabetes technologies and the effect of socioeconomic factors on families with children with type 1 diabetes. Methods: In this multicenter cross-sectional study, parents...
5.
Altun E, Yasar A, Dursun F, Seymen G, Kirmizibekmez H
J Clin Res Pediatr Endocrinol
. 2024 Jun;
16(4):426-430.
PMID: 38828891
Objective: Central precocious puberty (CPP) is treated with long-acting gonadotropin releasing hormone (GnRH) analogues (GnRHa). Some adult patients undergoing GnRHa treatment experienced prolonged QT syndrome, which is associated with an...
6.
Dursun F, Turan I, Bitkin E, Bayramoglu E, Cayir A, Savas Erdeve S, et al.
Clin Endocrinol (Oxf)
. 2024 Feb;
101(5):475-484.
PMID: 38324408
Objective: Autosomal-recessive hypophosphataemic rickets type 2 (ARHR2) is a rare disease that is reported in survivors of generalized arterial calcification of infancy (GACI). Design, Patients And Measurement: The objective of...
7.
Atmaca F, Akgun Dogan O, Kutlubay B, Kirmizibekmez H
J Clin Res Pediatr Endocrinol
. 2024 Jan;
PMID: 38212959
Schwartz-Jampel Syndrome (SJS) type-1 (OMIM; #255800), a rare cause of skeletal dysplasia, is characterized by myotonic myopathy, chondrodystrophy, short stature, facial and eye abnormalities. SJS Type-1 develops due to variations...
8.
Aykanat Girgin B, Gol I, Gozen D, Carikci F, Kirmizibekmez H
J Pediatr Nurs
. 2023 Aug;
73:84-90.
PMID: 37651942
Background: Pain and fear associated with insulin injections can cause children with type 1 diabetes mellitus to avoid insulin injections and skip doses. Objective: To evaluate and compare pain and...
9.
Guran O, Guven S, Kirmizibekmez H, Akgun Dogan O, Bilgin L
J Clin Res Pediatr Endocrinol
. 2023 Feb;
PMID: 36815512
Congenital nephrogenic diabetes insipidus (NDI) is a rare cause of hypernatremia in newborns. Central diabetes insipidus (CDI) is the main differential diagnosis of NDI. NDI responds poorly to desmopressin acetate...
10.
Dursun F, Ilce Z, Tosun I, Atla P, Kalin S, Guvenc F, et al.
J Pediatr Endocrinol Metab
. 2022 Nov;
36(1):96-100.
PMID: 36330765
Adrenocortical tumor (ACT) is a rare malignant tumor which usually present with Cushing syndrome and virilization. Paraneoplastic syndromes (PNS) due to neoplasms can occur with peptides or cytokines secreted by...