Výsledky vyhledávání - "Aylin Kont Ozhan"

Akademický článek

Lower Arginine Bioavailability, Increased FeNO Levels, and Airway Resistance on Impulse Oscillometry Are Characteristics of Asthma in Children and Young Adults with Sickle Cell Disease

Autor: Aylin Kont Ozhan, Tugba Arikoglu, Melih Er, Selma Unal, Didem Derici Yıldırım, Funda Erkasar, Şenay Balcı, Lulufer Tamer, Semanur Kuyucu

Publikováno v: Medicina, Vol 60, Iss 3, p 446 (2024)

Background and Objectives: Data on characteristics of asthma in children with sickle cell disease (SCD) is conflicting. Recently, the L-arginine pathway has gained attention in the pathogenesis of asthma and SCD. This study aimed to determine the dis

Externí odkaz: https://doaj.org/article/efe43d9b39214a46916fd581c649f907

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Akademický článek

The cumulative effects of MEFV gene polymorphisms and mutations in patients with inflammatory bowel diseases

Autor: Mehmet Agin, Atil Bisgin, Mustafa Yilmaz, Aylin Kont Ozhan, Ferid Mammadov, Gokhan Tumgor

Publikováno v: Journal of the Pakistan Medical Association, Vol 71, Iss 2 (2020)

Objective: To determine the cumulative effects of Mediterranean fever gene polymorphisms and mutations in patients with ?nflammatory bowel diseases. Methods: The case-control study was conducted from January, 2012, to January, 2016,at Cukurova Univ

Externí odkaz: https://doaj.org/article/00381c5e3cb6472c92dfbe4848a6246f

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Management Of Anaphylaxıs In Pedıatrıc Populatıon

Autor: Semanur Kuyucu, Tuğba Arıkoğlu, Aylin Kont Ozhan

Publikováno v: Current pharmaceutical design.

Abstract: Although an increase in the incidence of childhood anaphylaxis has been reported, it remains underdiagnosed. Foods are the most common triggers for anaphylaxis, particularly cow’s milk, hen’s egg, and nuts. Other common causes of anaphy

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6844163a4ca210d8a6e5e3fb711b9b0a
https://pubmed.ncbi.nlm.nih.gov/36281867

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Investigation of causative genetic defects in patients with primary immunodeficiency by next generation sequencing

Autor: Aylin Kont Ozhan, Nazan Tokmeci, Caner Aytekin, Baran Erman, Tugba Arikoglu, Ali Demirhan, Cigdem Aydogmus

Publikováno v: Annals of Medical Research. 28:1038

Aim: Inborn errors of immunity are rare diseases presented with a broad range of clinical symptoms. There are more than 450 causative genetic defects and the genetic diagnosis is very important for the patients. Use of next generation sequencing faci

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ba64f0da5a2245d1d63c3bf7543b3ae7
https://doi.org/10.5455/annalsmedres.2021.03.201

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