Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Nesrin Gulez"'
Autor:
Sultan Aydin Koker, Nesrin Gulez, Frederic Rieux-Laucat, Ferah Genel, Canan Vergin, Capucine Picard
Publikováno v:
Iranian Journal of Immunology, Vol 17, Iss 2, Pp 172-174 (2020)
Autoimmune lymphoproliferative syndrome (ALPS) is a rare inherited disorder of apoptosis, most commonly due to mutations in the FAS (TNFRSF6) gene. ALPS caused by defective lymphocyte homeostasis is characterized by non-malignant lymphoproliferation
Externí odkaz:
https://doaj.org/article/552a59cad534410eb99af7bdb7a42092
Publikováno v:
Central European Journal of Immunology, Vol 44, Iss 2, Pp 119-126 (2019)
Externí odkaz:
https://doaj.org/article/dd448d4004f44324b1bbcd0a1da47696
Autor:
Neslihan Edeer Karaca, Guzide Aksu, Ezgi Ulusoy, Serap Aksoylar, Salih Gozmen, Ferah Genel, Sanem Akarcan, Nesrin Gulez, Tatjana Hirschmugl, Savas Kansoy, Kaan Boztug, Necil Kutukculer
Publikováno v:
Case Reports in Immunology, Vol 2016 (2016)
Alterations of immune homeostasis in the gut may result in development of inflammatory bowel disease. A five-month-old girl was referred for recurrent respiratory and genitourinary tract infections, sepsis in neonatal period, chronic diarrhea, perian
Externí odkaz:
https://doaj.org/article/24f33638aca6411597516cb55960fca3
Autor:
Nesrin Gulez, Guzide Aksu, Afig Berdeli, Neslihan Karaca, Sema Tanrıverdi, Necil Kutukculer, Elif Azarsiz
Publikováno v:
Case Reports in Medicine, Vol 2011 (2011)
The X-linked lymphoproliferative syndrome (XLP) is a rare, inherited immunodeficiency characterized by recurrent episodes of hemophagocytic lymphohistiocytosis, hypogammaglobulinemia, and/or lymphomas. Recently, X-linked inhibitor of apoptosis (XIAP/
Externí odkaz:
https://doaj.org/article/202664f712e64df09417153076386f1a
Autor:
Neslihan Edeer Karaca, Guzide Aksu, Nesrin Gulez, Basak Yildiz, Elif Azarsiz, Necil Kutukculer
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Iss No. 4 (2010)
Transient hypogammaglobulinemia (THI) of infancy is a common primary immunodeficiency usually resolves by 3 years of age. In this study, clinical, immunological data and outcome of 101 retrospectively diagnosed THI patients were evaluated. Majority o
Externí odkaz:
https://doaj.org/article/ef0c5e7c1ed14ba2896621db601d6ee4
Autor:
Nurhan Kasap, Altan Kara, Velat Celik, Sevgi Bilgic Eltan, Idil Akay Haci, Hulya Kose, Ayse Aygun, Emre Akkelle, Nalan Yakici, Sukru Nail Guner, Ismail Reisli, Sevgi Keles, Sukru Cekic, Sara Sebnem Kilic, Neslihan Edeer Karaca, Nesrin Gulez, Ferah Genel, Ahmet Ozen, Ayse Deniz Yucelten, Elif Karakoc Aydiner, Klaus Schmitz-Abe, Safa Baris
Purpose: Autosomal recessive dedicator of cytokinesis 8 (DOCK8-/-) and autosomal dominant signal transducer and activator of transcription 3 (STAT3+/-) deficiencies are inborn errors of immunity (IEI) disorders present with the classic features of ec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::174e1b2311f83958b9eaf179eecf6076
https://doi.org/10.21203/rs.3.rs-2921301/v1
https://doi.org/10.21203/rs.3.rs-2921301/v1
Autor:
Hasan Kapakli, ESRA HAZAR, Seyma Celikbilek Celik, Huseyin Tokgoz, Selma Erol Aytekin, Yahya Gul, Hasibe Artac, Nesrin Gulez, Ferah Genel, Sukru Guner, Ayca Kıykım, Vedat Uygun, Ismail Reisli, Sevgi Keles
Background: Serine/threonine kinase 4 (STK4) deficiency is a combined immunodeficiency with overlapping features with the autosomal dominant (AD)– and recessive (AR) forms of the Hyper IgE syndrome (HIES), including recurrent infections, eczema, eo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff21dcd0175ee5a0d4a639aa4e681f7e
https://doi.org/10.21203/rs.3.rs-2805048/v1
https://doi.org/10.21203/rs.3.rs-2805048/v1
Autor:
Mehmet C. Catak, Bengu Akcam, Sevgi Bilgic Eltan, Royala Babayeva, Ibrahim S. Karakus, Gamze Akgun, Dilek Baser, Alper Bulutoglu, Feyza Bayram, Nurhan Kasap, Ayca Kiykim, Gonca Hancioglu, Sefika I. Kokcu Karadag, Yasemin kendir Demirkol, Selime Ozen, Sukru Cekic, Dilek Ozcan, Neslihan Edeer Karaca, Ayse S. Sasihuseyinoglu, Murat Cansever, Esra Ozek Yucel, Zeynep Tamay, Derya U. Altintas, Cigdem Aydogmus, Fatih Celmeli, Haluk Cokugras, Nesrin Gulez, Ferah Genel, Ayse Metin, Sukru N. Guner, Necil Kutukculer, Sevgi Keles, Ismail Reisli, Sara S. Kilic, Alisan Yildiran, Elif Karakoc‐Aydiner, Bernice Lo, Ahmet Ozen, Safa Baris
© 2022 EAACI and John Wiley and Sons A/S. Published by John Wiley and Sons Ltd.Background: Lipopolysaccharide-responsive beige-like anchor protein (LRBA) deficiency and cytotoxic T-lymphocyte protein-4 (CTLA-4) insufficiency are recently described d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90d0b7664b5951635514430e6e5152d4
https://hdl.handle.net/11424/289151
https://hdl.handle.net/11424/289151
Autor:
Selime Ozen Boluk, Ilke Taskirdi, Omer Akcal, Mehmet Sirin Kaya, Idil Akay Haci, Ozgen Soyoz, Figen Celebi Celik, Canan Sule Karkiner, Fahri Yuce Ayhan, Nesrin Gulez, Ferah Genel, Demet Can
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology.
Acute asthma exacerbations (AAE) are episodes characterized by potentially life-threatening and rapidly deteriorating asthma symptoms. Viral respiratory infections are one of the major triggers in the pathophysiology of childhood asthma exacerbations
Autor:
Ayca Aykut, Asude Durmaz, Neslihan Karaca, Nesrin Gulez, Ferah Genel, Fatih Celmeli, Gulyuz Ozturk, Didem Atay, Cigdem Aydogmus, Ayca Kiykim, Guzide Aksu, Necil Kutukculer
Publikováno v:
Scandinavian Journal of Immunology. 95
Human Inborn Errors of Immunity (IEIs) are clinically and genetically heterogeneous group of diseases, with relatively mild clinical course or severe types that can be life-threatening. Severe combined immunodeficiency (SCID) is the most severe form