Aysel Tekmenuray-Unal
Overview
Explore the profile of Aysel Tekmenuray-Unal including associated specialties, affiliations and a list of published articles.
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4
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Recent Articles
1.
Unal E, Tekmenuray-Unal A, Cayir A, Papatya Cakir E, Beyazit N, Kolbasi B, et al.
J Clin Endocrinol Metab
. 2025 Jan;
PMID: 39812180
Context: Duplications occurring upstream of the SOX9 gene have been identified in a limited subset of patients with 46,XX testicular/ovotesticular differences/disorders of sex development (DSD). However, comprehensive understanding regarding their...
2.
Celmeli F, Oz A, Kihtir H, Ongun E, Tekmenuray-Unal A, Ceylaner S, et al.
J Clin Immunol
. 2024 Oct;
45(1):25.
PMID: 39404985
Inborn errors of immunity (IEI) are a heterogeneous group of genetic diseases characterized by impaired immune system function. This prospective study aimed to determine the frequency, characteristics, and clinical course...
3.
Durmaz C, Tekmenuray-Unal A
Int J Dermatol
. 2023 Jun;
62(10):1295-1299.
PMID: 37387535
No abstract available.
4.
Tekmenuray-Unal A, Durmaz C
Mol Syndromol
. 2023 Feb;
14(1):80-87.
PMID: 36777703
Introduction: -related cutis laxa is a very rare, autosomal recessive syndrome that is characterized by loose, wrinkled, and redundant skin, sagging cheeks, emphysema, aortic or pulmonary artery abnormalities, inguinal hernia,...
5.
Yildirim R, Unal E, Tekmenuray-Unal A, Tas F, Ozalkak S, Cayir A, et al.
Endocrine
. 2022 Oct;
79(2):376-383.
PMID: 36194344
Aim: Triple-A Syndrome (TAS) is a rare autosomal recessive disorder characterized by adrenal insufficiency, achalasia, and alacrimia. This disorder is caused by mutations in the AAAS gene. The aim of...