Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Aylin Kont Ozhan"'
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
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
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
https://pubmed.ncbi.nlm.nih.gov/36281867
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
https://doi.org/10.5455/annalsmedres.2021.03.201
Autor:
Aylin Kont Özhan, Tuğba Arıkoğlu
Publikováno v:
Children, Vol 11, Iss 1, p 86 (2024)
Pediatric data on the clinical and etiologic features, treatment response, and use of omalizumab for chronic urticaria (CU) are quite limited. The aim of this study was to evaluate the clinical and demographic characteristics, laboratory findings, an
Externí odkaz:
https://doaj.org/article/4b7553d4a28b4627a1d957f0ed2bb139
Publikováno v:
Genel Tıp Dergisi, Vol 31, Iss 3, Pp 321-323 (2021)
Konjenital lober amfizem, alt solunum yollarında hiperinflasyon ile karakterize nadir rastlanan akciğerin doğumsal bir anomalisidir. Konjenital lober amfizemli hastalarda klinik seyir, hastalığın ortaya çıktığı yaşa, etkilenen loba veya n
Externí odkaz:
https://doaj.org/article/2115efdc1d14496490bfca2e507aa42a
Publikováno v:
Cukurova Medical Journal, Vol 44, Iss 4, Pp 1317-1322 (2019)
Purpose: Regular transfusions cause progressive iron deposition in critical organs such as heart, liver and lungs in transfusion-dependent thalassemia (TDT). We aimed to evaluate respiratory dysfunction and factors affecting respiratory dysfunction i
Externí odkaz:
https://doaj.org/article/14ae7750365845a7a181f89858675494