Browsing by Author "Karakoç Aydıner, Elif"
Now showing items 1-4 of 4
-
Characteristics of food allergy in children: National multicenter study
Bingöl, Ayşen; Uygun, Kocacık; Akdemir, Meltem; Erengin, Hakan; Bozdoğan, Günseli; Bingöl, Gülbin; Orhan, Fazıl; Büyüktiryaki, Betül; Şekerel, Bülent Enis; Kılıç, Mehmet; Saçkesen, Cansin; Eren Akarcan, Sanem; Demir, Esen; Köse, Şirin; Asilsoy, Suna; Kan, Ahmet; Türktaş, İpek; Arikoğlu, Tuğba; Kuyucu, Semanur; Sipahi, Seyhan; Tamay, Zeynep; Nacaroğlu, Tekin; Özdemir, Pınar Gökmirza; Yazıcıoğlu, Mehtap; Çekiç, Şükrü; Sapan, Nihat; Zeyrek, Dost; Doğruel, Dilek; Karakoç Aydıner, Elif; Özen, Ahmet Oğuzhan; Can, Ceren; Ertuğrul, Ayşin; Birol Bostancı, İlknur; Akçal, Ömer; Can, Demet; Arik Yılmaz, Ebru; Anıl, Hülya; Harmancı, Koray; Külhaş Çelik, İlknur; Civelek, Ersoy; Çokuğraş, Haluk; Şenol, Handan Duman; Tuncel, Tuba; Ufuk Altıntaş, Derya (Wiley, 2019)Background : Food allergies impose a significant burden on the life of the child and the family. In this study, to determine the demographic characteristics of food allergies, we investigated the characteristics of patients ... -
Evolution and long-term outcomes of combined immunodeficiency due to CARMIL2 deficiency
Kolukısa, Burcu; Başer, Dilek; Akçam, Bengü; Danielson, Jeffrey; Bilgiç Eltan, Sevgi; Haliloğlu, Yeşim; Sefer, Asena Pınar; Babayeva, Royale; Akgün, Gamze; Charbonnier, Louis-Marie; Schmitz-Abe, Klaus; Kendir Demirkol, Yasemin; Zhang, Yu; Gonzaga-Jauregui, Claudia; Heredia, Raul Jimenez; Kasap, Nurhan; Kıykım, Ayça; Özek Yücel, Esra; Gök, Veysel; Ünal, Ekrem; Paç Kısaarslan, Ayşenur; Nepesov, Serdar; Baysoy, Gökhan; Önal, Zerrin; Yeşil, Gözde; Celkan, Tülin Tiraje; Çokuğraş, Haluk; Camcıoğlu, Yıldız; Eken, Ahmet; Boztug, Kaan; Lo, Bernice; Karakoç Aydıner, Elif; Su, Helen C.; Özen, Ahmet; Chatila, Talal A.; Barış, Safa (Wiley, 2022)Background Biallelic loss-of-function mutations in CARMIL2 cause combined immunodeficiency associated with dermatitis, inflammatory bowel disease (IBD), and EBV-related smooth muscle tumors. Clinical and immunological ... -
Genomic investigation into early onset protein-losing enteropathies: Therapeutic implications and insights into clusters of shared pathomechanisms
Sefer, Asena Pınar; Karakoç Aydıner, Elif; Urgancı, Nafiye; Kıykım, Ertuğrul; Baysoy, Gökhan; Fisher, Megan; Ertem, Deniz; Bayrak, Aykut; Varol, Fatma İlknur; İşlek, Ali; Çullu Çokuğraş, Fügen; Beşer, Ömer Faruk; Baştürk, Ahmet; Güller, Dilek; Çavuşoğlu, Mustafa; Zhang, Yu; Hubrack, Satanay; Lyons, Jonathan; Demirbaş Ar, Fatma; Kutlu, Tufan; Barış, Safa; Lo, Bernice; Özen, Ahmet (Wiley, 2021)... -
Inflammatory bowel disease and guillain barre syndrome in FCHO1 deficiency
Aydemir, Sezin; İşlek, Ali; Nepesov, Serdar; Yaman, Yöntem; Baysoy, Gökhan; Beşer, Ömer Faruk; Çullu Çokuğraş, Fügen; Barış, Safa; Karakoç Aydıner, Elif; Çokuğraş, Haluk; Hubrack, Satanay Z.; Kendir Demirkol, Yasemin; Lo, Bernice; Kıykım, Ayça; Özen, Ahmet (Springer, 2021)To the Editor: FCH And Mu Domain Containing Endocytic Adaptor 1 (FCHO1) gene encodes a protein that plays a critical role in clathrin-mediated endocytosis, a biological process that maintains cellular functions in signaling, ...
