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Issue DateTitleAuthor(s)
2002Osteochondritis dissecans in a patient with hyperimmunoglobulin E syndromeSanal, Özden; Tezcan, İlhan; Ersoy, Figen; Uludağ Üniversitesi/Tıp Fakültesi/Pediatri Bölümü.; Kılıç, Sara Şebnem; 34975059200
2001-12Common variable immunodeficiency in a patient with neurofibromatosisİlhan, Tezcan; Sanal, Özden; Ersoy, Feyzi; Uludağ Üniversitesi/Tıp Fakültesi/Pediatri Anabilim Dalı.; Kılıç, Sara Şebnem; AAH-1658-2021; 34975059200
2010-02Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndromeWoellner, Cristina; Gertz, Edward Michael; Schaffer, Alejandro A.; Lagos, Macarena; Perro, Mario; Glocker, Erik Oliver; Pietrogrande, Maria Cristina; Cossu, Fausto; Franko, Josè Luis; Matamoros, Núria; Pietrucha, Barbara Maria; Heropolitańska-Pliszka, Edyta; Yeganeh, Mehdi; Moin, Mostafa; Español, Theresa; Ehl, Stephan; Gennery, Andrew R.; Abinun, Mario A.; Brȩborowicz, Anna; Niehues, Tim; Junker, Anne K.; Turvey, Stuart E.; Plebani, Alessandro; Sánchez, Berta; Garty, Ben Zion; Pignata, Claudio; Cancrini, Caterina; Litzman, Jiří; Sanal, Özden; Baumann, Ulrich; Bacchetta, Rosa; Hsu, Amy P.; Davis, Joie N.; Hammarström, Lennart L.G.; Davis, Edward Graham; Eren, Efrem; Arkwright, Peter D.; Moilanen, Jukka S.; Viemann, Dorothee; Khan, Sujoy; Máródi, László D.R.; Cant, Andrew James; Freeman, Alexandra F.; Puck, Jennifer M.; Holland, Steven M.; Grimbacher, Bodo; Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı.; 0000-0001-8571-2581; Kılıç, Sara Şebnem; AAH-1658-2021; 34975059200
2013-11Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patientsKöker, Mustafa Yavuz; Camcıoğlu, Yıldız; van Leeuwen, Karin; Barlan, Işıl; Yılmaz, Mustafa; Metin, Ayşe; de Boer, Martin; Avcılar, Hüseyin; Patıroğlu, Türkan; Yıldıran, Alişan; Yeğin, Olcay; Tezcan, İlhan; Sanal, Özden; Roos, Dirk; Uludağ Üniversitesi/Tıp Fakültesi/Pediatrik Alerji ve İmmünoloji Anabilim Dalı.; 0000-0001-8571-2581; Kılıç, Sara Şebnem; AAH-1658-2021; 34975059200
2015-12STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutationHalaçlı, Sevil Oskay; Çağdaş, Deniz; Tan, Çağman; Erman, Baran; Yılmaz, Didem Yücel; Özgül, Rıza Koksal; Tezcan, İlhan; Sanal, Özden; Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Moleküler Biyoloji ve Genetik Bölümü.; 0000-0002-1459-5485; Uz, Elif; 13807893000
2011-08Accounting for genetic heterogeneity in homozygosity mapping: Application to Mendelian susceptibility to mycobacterial diseaseGrant, Audrey V.; Dupuis, Stephanie Boisson; Herquelot, Eleonore; de Beaucoudrey, Ludovic; Santos, Orchidee Filipe; Nolan, Daniel K.; Feinberg, Jacqueline; Boland, Anne; Al-Muhsen, Saleh; Sanal, Özden; Çamcıoğlu, Yıldız; Palanduz, Ayşe; Bustamante, Jacinta; Casanova, Jean-Laurent; Abel, Laurent; Uludağ Üniversitesi/Tıp Fakültesi/Pediatri Anabilim Dalı.; 0000-0001-8571-2581; Kılıç, Sara Şebnem; AAH-1658-2021; 34975059200