Nonimmune hydrops fetalis in two cases of consanguineous parents and associated with hereditary spherocytosis and hemophagocytic hystiocytosis von Yetgin, S, Aytac, S, Gurakan, F, Yurdakok, M

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232 ACUTE LIVER FAILURE IN CHILDREN: 20 YEARS RESULTS OF A TERTIARY CENTER FROM CENTRAL ANATOLIA von Saltik-Temizel, I.N, Baris, Z, Usta, Y, Uslu, N, Demir, H, Gurakan, F, Ozen, H, Yuce, A

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P318 Unusual presentations in Niemann Pick disease type C: Clues for early diagnosis von Topcu, M, Haliloglu, G, Kaya, U, Oguz, K. Karlı, Gurakan, F, Yuce, A

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Phenotypic and Genetic Heterogeneity in Congenital Generalized Lipodystrophy von Agarwal, Anil K., Simha, Vinaya, Oral, Elif Arioglu, Moran, Stephanie A., Gorden, Phillip, O’Rahilly, Stephen, Zaidi, Zohra, Gurakan, Figen, Arslanian, Silva A., Klar, Aharon, Ricker, Alyne, White, Neil H., Bindl, Lutz, Herbst, Karen, Kennel, Kurt, Patel, Shailesh B., Al-Gazali, Lihadh, Garg, Abhimanyu

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Comparison of standard and high dosage recombinant interferon alpha 2b for treatment of children with chronic hepatitis B infection von GÜRAKAN, FIGEN, KOÇAK, NURTEN, ÖZEN, HASAN, YÜCE, AYSEL

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Subnormal growth in children with Helicobacter pylori infection von DEMIR, HÜLYA, SALTIK, INCI NUR, KOÇAK, NURTEN, YÜCE, AYSEL, ÖZEN, HASAN, GÜRAKAN, FIGEN

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MLP09 Evaluation of central nervous system in patients with glycogen storage disease type Ia von Gurakan, F, Aydemir, Y, Yuce, A, Temizel, I.S, Demir, H, Yalnizoglu, D, Topcu, M, Usta, Y, Erdogan, E, Ozen, H, Erbas, B, Lay, E

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Lamivudine (LMV) versus LMV+interferon (IFN) alpha as initial therapy for children with chronic hepatitis B (first year results) von Gurakan, F

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P264 – 1791 Evolution of the disease under Miglustat treatment: timeline in two patients with early-infantile NPC in the Turkish cohort von Haliloglu, G, Duzgun, G, Oguz, KK, Yuce, A, Gurakan, F, Topcu, M

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A Gene for Congenital Generalized Lipodystrophy Maps to Human Chromosome 9q34 von Garg, Abhimanyu, Wilson, Ross, Barnes, Robert, Arioglu, Elif, Zaidi, Zohra, Gurakan, Figen, Kocak, Nurten, O’Rahilly, Stephen, Taylor, Simeon I, Patel, Shailendra B, Bowcock, Anne M

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P05.11 Miglustat treatment in Niemann-Pick disease type C (NP-C): Clinical experience in two patients von Haliloglu, G., Yuce, A., Gurakan, F., Topcu, M.

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Lansoprazole Triple Therapy for Turkish Children With Helicobacter pylori Infections von Koçak, Nurten, Saltik, Inci Nur, Özen, Hasan, Yüce, Aysel, Gürakan, Figen

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Retreatment with higher dose interferon alpha in children with chronic hepatitis B infection von ÖZEN, HASAN, KOÇAK, NURTEN, YÜCE, AYSEL, GÜRAKAN, FIGEN

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Bone Mineral Density in Children With Untreated and Treated Celiac Disease von Kavak, Umut S., Yüce, Aysel, Koçak, Nurten, Demir, Hülya, Saltik, İnci Nur, Gürakan, Figen, Özen, Hasan

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Helicobacter pylori Infection in Turkish Children with Recurrent Abdominal Pain von Saltik, Inci Nur, Koçak, Nurten, Özen, Hasan, Yüce, Aysel, Gürakan, Figen, Demir, Hülya

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A Zinc Sulphate-Resistant Acrodermatitis Enteropathica Patient with a Novel Mutation in SLC39A4 Gene von Kilic, M., Taskesen, M., Coskun, T., Gürakan, F., Tokatli, A., Sivri, H. S., Dursun, A., Schmitt, S., Küry, S.

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Homozygous Factor V Leiden Mutation in a Child With Budd‐Chiari Syndrome von Gürakan, Figen, Gürgey, Aytemiz, Bakkaloğlu, Ayşin, Koçak, Nurten

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Obliteration of maxillary and sphenoid sinuses in Gaucher's disease von Karabulut, N, Ahmetoglu, A, Ariyürek, M, Erol, C, Gürakan, F

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51. The identification of relationship between GC genotype and Gaucher disease with proteomic analysis von Emre, Serap, Demiralp, Duygu Ozel, Gurakan, Figen, Gumustekin, Cagr1, Altuner, Meral, Yuce, Aysel

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Amanita poisoning in a child treated with plasma exchange von Saltik, I N, Soysal, A, Sarikayalar, F, Topalglu, R, Gurakan, F

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