Evaluation of apolipoprotein A5 variants: A cohort of patients with severe hypertriglyceridemia from Turkiye von Cakmak, B., Yeral, S., Ozcan, B., Pariltay, E., Ozgul, S., Simsir, I.Y., Hegele, R.A.

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A Novel TTC37 Mutation Causing Clinical Symptoms of Trichohepatoenteric Syndrome Such as Pyoderma Gangrenosum and Immunodeficiency Without Severe Diarrhea von Karaca Edeer, N, Aykut, A, Pariltay, E, Aksu, G, Cogulu, O, Kutukculer, N

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TdT Negativity and ETP Phenotype in Young Patients with Acute T- Lymphoid Leukemia: A Case Report von D, Cetin, MM, Midik, FK, Karadag, N, Ozsan, E, Pariltay, H, Akin, G, Saydam

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The evaluation of the referral reasons of patients at a tertiary pediatric genetic center in Izmir, Turkey von Durmaz, Burak, Alpman, Asude, Pariltay, Erhan, Akgul, Mehmet, Ataman, Esra, Kirbiyik, Ozgur, Cogulu, Ozgur, Ozkinay, Ferda

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Chronic granulamatous disease: Two decades of experience from a paediatric immunology unit in a country with high rate of consangineous marriages von Kutukculer, Necil, Aykut, Ayca, Karaca, Neslihan E., Durmaz, Asude, Aksu, Guzide, Genel, Ferah, Pariltay, Erhan, Cogulu, Özgür, Azarsız, Elif

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The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey von 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, Muller, Jean, Naggert, Jürgen K, Özgül, Rıza Köksal

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