An X-Linked Hyper-IgM Patient Followed Successfully for 23 Years without Hematopoietic Stem Cell Transplantation

nork Kutukculer, Necil, Karaca, Neslihan Edeer, Aksu, Guzide, Aykut, Ayca, Pariltay, Erhan, Cogulu, Ozgur
Argitaratua izan da Case Reports Immunol (2018)

DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo

nork Bolat, Hilmi, Ercan, Eyüp S., Ünsel-Bolat, Gül, Tahillioğlu, Akin, Yazici, Kemal U., Bacanli, Ali, Pariltay, Erhan, Aygüneş Jafari, Duygu, Kosova, Buket, Özgül, Semiha, Rohde, Luis A., Akin, Haluk
Argitaratua izan da Braz J Psychiatry (2020)

The phenotypic and molecular genetic spectrum of Alström Syndrome in 44 Turkish kindreds and a literature review of Alström Syndrome in Turkey

nork Ozantürk, Ayşegül, Marshall, Jan D, Collin, Gayle B, Düzenli, Selma, Marshall, Robert P, Candan, Şükrü, Tos, Tülay, Esen, İhsan, Taşkesen, Mustafa, Çayır, Atilla, Öztürk, Şükrü, Üstün, İhsan, Ataman, Esra, Karaca, Emin, Özdemir, Taha Reşid, Erol, İlknur, Eroğlu, Fehime Kara, Torun, Deniz, Parıltay, Erhan, Yılmaz-Güleç, Elif, Karaca, Ender, Atabek, M. Emre, Elçioğlu, Nursel, Satman, İlhan, Möller, Claes, Müller, Jean, Naggert, Jürgen K, Özgül, Rıza Köksal
Argitaratua izan da J Hum Genet (2014)