Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Elif Karakoç Aydıner"'
Autor:
Esra Karabiber, Elif Karakoç Aydıner
Publikováno v:
The Journal of Pediatric Academy, Vol 3, Iss 2, Pp 37-46 (2022)
Abstract Hereditary angioedema (HAE) is a rare, mostly inherited disorder however 25% of patients have de novo mutations. Although it’s rarity, it can be life threatening due to laryngeal involvement. Along with understanding the basis of swelli
Externí odkaz:
https://doaj.org/article/b68713c1c96e46709d8720034cd62e4c
Autor:
Ahmet Özen, Perran Boran, Fatih Torlak, Elif Karakoç Aydıner, Safa Barış, Melda Karavuş, Işıl Barlan
Publikováno v:
Balkan Medical Journal, Vol 33, Iss 5, Pp 539-542 (2016)
Aims: This study was carried out to identify the current status of prevention and management of anaphylaxis in school children with the main goal of establishing such an action plan. Study Design: Cross-sectional study. Methods: Schools were ra
Externí odkaz:
https://doaj.org/article/d10af973cb1543f792b67b0648bb323f
Autor:
Safa Baris, Hülya Ellidokuz, Ismail Ogulur, Goncagül Haklar, Eren Özek, Tolga Besci, Asım Leblebici, Perran Boran, Ayşe Cansu Berberoglu, Dilek Baser, Elif Karakoç Aydıner, Özge Besci, Ayca Kiykim, Ahmet Ozen
Publikováno v:
Turkish Journal of Medical Sciences
Background/aim Established reference values are critical for the interpretation of immunologic assessments. In particular, the proportion and absolute counts of T- and B- cell subpopulations are subject to change with age and ethnicity. We aimed to e
Autor:
Dilara Fatma Kocacık Uygun, Vedat Uygun, Yuk Yin Ng, Ismail Reisli, Safa Baris, Serdar Nepesov, Esra Hazar Sayar, Yildiz Camcioglu, Funda Erol Cipe, Tuba Cogurlu, Elif Karakoç Aydıner, Selda Hançerli Törün, Ozden Hatirnaz Ng, Ahmet Ozen, Muge Sayitoglu, Ugur Ozbek, Ayca Kiykim, Aysenur Kaya, Şükrü Çekiç, Deniz Cagdas, Isil Eser Simsek, Sinem Firtina, Esra Yücel
Publikováno v:
International Journal of Immunogenetics. 47:529-538
Severe combined immunodeficiency (SCID) has a diverse genetic aetiology, where a clinical phenotype, caused by single and/or multiple gene variants, can give rise to multiple presentations. The advent of next-generation sequencing (NGS) has recently
Autor:
Esra Özek, Ismail Reisli, Esra Hazar Sayar, Manolya Kara, Muge Sayitoglu, Ugur Ozbek, Ezgi Yalcin Gungoren, Serdar Nepesov, Elif Karakoç Aydıner, Sule Haskologlu, Safa Baris, Ayşenur Kaya, Selda Hançerli Törün, Ayca Kiykim, Şükrü Çekiç, Ahmet Ozen, Yildiz Camcioglu, Sinem Firtina, Tuba Cogurlu, Yuk Yin Ng, Ozden Hatirnaz Ng
Primary antibody deficiencies (PAD) are the most common subtype of primary immunodeficiencies, characterized by increased susceptibility to infections and autoimmunity, allergy, or malignancy predisposition. PAD syndromes comprise of immune system ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::745fd6ee4abe9af80ae811154510499d
https://aperta.ulakbim.gov.tr/record/232722
https://aperta.ulakbim.gov.tr/record/232722
Autor:
Ahmet Ozen, Ismail Ogulur, Safa Baris, Sehnaz Olgun Yildizeli, Berrin Ceyhan, Elif Karakoç Aydıner, Melahat Bekir, Derya Kocakaya, Emel Eryuksel
Publikováno v:
Turk Thorac J
Objective Bronchiectasis is characterized by chronic respiratory infection. The role of immunodeficiency in this disease is poorly studied in relation to clinical indices. The primary aim of this study was to determine the frequency of these neglecte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::643ee79299c14417c59fff212626fd32
https://europepmc.org/articles/PMC7919424/
https://europepmc.org/articles/PMC7919424/
Autor:
Öner Özdemir, Safa Baris, Omer Aydiner, Sevgi Bilgic Eltan, Haluk Cokugras, Burcu Kolukisa, Esra Yücel, Elif Karakoç Aydıner, Ezgi Yalcin Gungoren, Asena Pinar Sefer, Koray Yalcin, Fazil Orhan, Mehmet Akif Yesilipek, Ayca Kiykim, Ahmet Ozen, Hasibe Artac, Royale Babayeva, Nalan Yakıcı, Tülin Tiraje Celkan, Esra Karabiber, Eda Kepenekli
Publikováno v:
Allergy
Background Genetic deficiencies of immune system, referred to as inborn errors of immunity (IEI), serve as a valuable model to study human immune responses. In a multicenter prospective cohort, we evaluated the outcome of SARS‐CoV‐2 infection amo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73acdb7b7a427b594034f06d6ddec16a
https://hdl.handle.net/20.500.12831/6497
https://hdl.handle.net/20.500.12831/6497
Autor:
Fatih Çelmeli, Elif Karakoç Aydıner, Suar Çakı Kılıç, Ayşen Bingöl, Vedat Uygun, Safa Baris, Volkan Hazar, Dilara Fatma Kocacık Uygun, Hayriye Daloğlu, Ahmet Ozen, Seda Öztürkmen, Selda Hançerli Törün, Koray Yalcin, Akif Yeşilipek, Gülsün Karasu
Publikováno v:
Pediatric transplantationREFERENCES. 24(6)
Uygun, Vedat ; Karasu, Gulsun Tezcan (isu author) Deficiency of the CD40L, expressed on the surface of T lymphocytes, is caused by mutations in the glycoproteinCD40L (CD154)gene. Resulting defective humoral and cellular responses cause a clinical pre
Autor:
Safa Baris, Elif Karakoç Aydıner, Ahmet Selçuk Özen, Ayca Kiykim, Hatice Ezgi Baris, Perran Boran
Publikováno v:
Türk Pediatri Arşivi.
Aim In the presence of food allergies, especially egg allergies, primary physicians in Turkey avoid vaccine administration and refer children to a hospital setting. We aimed to evaluate children who had allergies or suspected allergies and were refer