Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Caner Aytekin"'
Autor:
Sule Haskologlu, Kubra Baskin, Caner Aytekin, Candan Islamoglu, Serdar Ceylaner, Figen Dogu, Nurdan Tacyildiz, Emel Unal, Aydan Ikinciogullari
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 21, Iss 1 (2022)
Loss-of-function mutations in magnesium transporter 1 (MAGT1) gene cause X-linked magnesium deficiency with Epstein–Barr virus (EBV) infection and neoplasm (X-MEN), a disease with quite diverse clinical and immunological consequences. The phenotypi
Externí odkaz:
https://doaj.org/article/e5bce7290bbf4c9b94e46f226d7403e6
Autor:
Stéphanie Boisson-Dupuis, Jamila El Baghdadi, Nima Parvaneh, Aziz Bousfiha, Jacinta Bustamante, Jacqueline Feinberg, Arina Samarina, Audrey V Grant, Lucile Janniere, Naima El Hafidi, Amal Hassani, Daniel Nolan, Jilali Najib, Yildiz Camcioglu, Nevin Hatipoglu, Cigdem Aydogmus, Gonul Tanir, Caner Aytekin, Melike Keser, Ayper Somer, Guside Aksu, Necil Kutukculer, Davood Mansouri, Alireza Mahdaviani, Setareh Mamishi, Alexandre Alcais, Laurent Abel, Jean-Laurent Casanova
Publikováno v:
PLoS ONE, Vol 6, Iss 4, p e18524 (2011)
In the last decade, autosomal recessive IL-12Rβ1 deficiency has been diagnosed in four children with severe tuberculosis from three unrelated families from Morocco, Spain, and Turkey, providing proof-of-principle that tuberculosis in otherwise healt
Externí odkaz:
https://doaj.org/article/371611f76da547a09747d5270c01ce63
Autor:
Murat OZER, Caner AYTEKIN
Publikováno v:
Asthma Allergy Immunology. 21:59-63
Autor:
Zeynep Güneş Tepe, Yılmaz Yücehan Yazıcı, Umut Tank, Ladin Işık Köse, Murat Özer, Caner Aytekin, Serkan Belkaya
Publikováno v:
Journal of Clinical Immunology
Human herpesvirus-6 (HHV-6) infection can rarely cause life-threatening conditions, such as encephalitis, in otherwise healthy children, with unclear pathogenesis. We studied a child who presented with acute HHV-6 encephalitis at the age of 10 months
Autor:
Zeynelabidin Ozturk, Merve Duman Küçükkuray, Suna Özdem, Hasibe Gökçe Çınar, Caner Aytekin, Özgür Çağlar
Publikováno v:
Pediatric Allergy, Immunology, and Pulmonology. 35:120-123
Autor:
Özlem Bayram, Ismail Reisli, Sevgi Köstel Bal, Gunseli Bozdogan, Kaan Boztug, Klara Dalva, Aydan Ikinciogullari, Tanıl Kendirli, Caner Aytekin, Mutlu Yuksek, Nazmiye Kurşun, Candan Islamoglu, Şükrü Nail Güner, Sule Haskologlu, Alisan Yildiran, Deniz Bayrakoğlu, Figen Dogu, Funda Erol Cipe
Publikováno v:
Journal of Clinical Immunology. 41:1563-1573
Severe combined immunodeficiency is an inborn error of immunity characterized by impairments in the numbers and functions of T and B lymphocytes due to various genetic causes, and if it remains untreated, patients succumb to infections during the fir
Autor:
Dilara Beşli, Figen Doğu, Avniye Baskin, Aydan Ikincioğullari, Sevgi Köstel Bal, Candan Islamoğlu, Zehra Şule Haskoloğlu, Caner Aytekin
Publikováno v:
Volume: 14, Issue: 4 286-294
Türkiye Çocuk Hastalıkları Dergisi
Türkiye Çocuk Hastalıkları Dergisi
Giriş-Amaç: Lökosit Adezyon Defekti (LAD), lökositlerin adezyon, migrasyon, kemotaksis ve ekstravazasyonunda rol alan moleküllerin eksikliklerine bağlı gelişen, nadir görülen, otozomal resesif katılımlı, üç ayrı tipi olan (LAD-I, LAD-
Autor:
Sevgi Köstel Bal, Caner Aytekin, Figen Dogu, Serdar Ceylaner, Kubra Baskin, Zehra Şule Haskoloğlu, Aydan Ikinciogullari, Zeynep Yavuz, Candan Islamoglu, Demet Altun
Publikováno v:
Asthma Allergy Immunology. 18:38-46
Objective: To evaluate the characteristics of the patients who were followed-up with the diagnosis of ataxia telangiectasia (AT) and to assess the relationship between the hyper IgM (HIGM) phenotype and their prognosis. Materials and Methods: From 20
Publikováno v:
Molecular Syndromology. 11:157-161
Renpenning syndrome is an X-linked intellectual disability syndrome caused by mutations in the human polyglutamine binding protein 1 (PQBP1) gene characterized by intellectual disability (ID), microcephaly, and dysmorphic facial features. We report a
Autor:
Tuğçe Kandemir, Caner Aytekin, Ebru Azapağası, Mutlu Uysal Yazici, Ali Fettah, Emre Ocak, Fatma Nur Öz
Publikováno v:
Klinische Padiatrie. 233(6)