Urinary 24-hour copper excretion at the time of diagnosis in children with Wilson's disease von Aksu, A Ü, Sarı, S, Gürkan, Ö E, Dalgıç, B

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Detection of adenovirus in diarrheal children between 0 and 5 years old and except adenovirus serotype 40/41 by DNA sequencing, and phylogenetic analysis von Colak, M, Bozdayi, G, Altay, A, Dalgic, B, Ahmed, K

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Investigation of malignancy associated with EBV (Epstein-barr virus) in paediatric patients with liver transplant von Colak, M, Altay, A, Bozbulut, N. Eksi, Dalgic, B, Fidan, I, Ozkan, S, Bozdayi, G

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330 Hepatopulmonary syndrome may mask cystic fibrosis von Aslan, A, Sismanlar, T, Sarı, S, Dalgic, B, Oguz, D, Ezgu, F.S

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P13—A Case of Fabry Disease With Unexplained Abdominal Pain von Küçükçongar, A, Ezgü, F.S, Tümer, L, Dalgıç, B, Hasanoğlu, A

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P184 Epidemiology and molecular characteristics of diarrheal viruses detected in children from Bangladesh and Turkey von Matsumoto, T, Mitui, M.T, Bozdayi, G, Ahmed, S, Dalgic, B, Kabir, L, Bostanci, I, Nishizono, A, Ahmed, K

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A case with rare type of congenital disorder of glycosylation: PGM1-CDG von Küçükçongar, A, Tümer, L, Ezgü, F. Süheyl, Kasapkara, Ç. Seher, Jaeken, Jaak, Matthijs, Gert, Rymen, Daisy, Dalgiç, B, Bıdecı, A, Hasanoğlu, A

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Odevixibat treatment in progressive familial intrahepatic cholestasis: a randomised, placebo-controlled, phase 3 trial von Thompson, Richard J, Arnell, Henrik, Artan, Reha, Baumann, Ulrich, Calvo, Pier Luigi, Czubkowski, Piotr, Dalgic, Buket, D'Antiga, Lorenzo, Durmaz, Özlem, Fischler, Björn, Gonzalès, Emmanuel, Grammatikopoulos, Tassos, Gupte, Girish, Hardikar, Winita, Houwen, Roderick H J, Kamath, Binita M, Karpen, Saul J, Kjems, Lise, Lacaille, Florence, Lachaux, Alain, Lainka, Elke, Mack, Cara L, Mattsson, Jan P, McKiernan, Patrick, Özen, Hasan, Rajwal, Sanjay R, Roquelaure, Bertrand, Shagrani, Mohammad, Shteyer, Eyal, Soufi, Nisreen, Sturm, Ekkehard, Tessier, Mary Elizabeth, Verkade, Henkjan J, Horn, Patrick

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PVII-14 Molecular analysis of genes encoding the NSP4, VP4, VP6, AND VP7 of human group C rotavirus from Turkey von Mitui, M.T, Bozdayi, G, Dalgic, B, Bostanci, I, Nishizono, A, Ahmed, K

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Detection of adenovirus in diarrheal children between 0 and 5 years old and except adenovirus serotype 40/41 by DNA sequencing, and phylogenetic analysis: Presentation at ESCV 2016... von Colak, M, Bozdayi, G, Altay, A, Dalgic, B, Ahmed, K

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OP1-7 Molecular epidemiology of rotavirus in children aged between 0–5 years old in Turkey von Bozdayi, G, Dinc, B, Dogan, B, Dallar, Y, Dalgic, B, Rota, S, Nishizono, A, Ahmed, K

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Multisystem involvement in a patient due to accumulation of amylopectin-like material with diminished branching enzyme activity von Eminoglu, T. F., Tumer, L., Okur, I., Olgunturk, R., Hasanoglu, A., Gonul, I. I., Dalgic, B.

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P0372 OXIDATIVE STRESS IN WILSON’S DISEASE von Dalgiç, B., Sönmez, N., Biberoglu, G., Erbaþ, D., Hasanoglu, A.

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FACTORS RELATED TO NON‐ALCOHOLIC FATTY LIVER DISEASE IN OBESE CHILDREN von Dalgiç, B, Çamurdan, MO, Eminoglu, FT, Oktar, SÖ, Özer, Ç, Gülbahar, Ö

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Investigation of malignancy associated with EBV (Epstein-barr virus) in paediatric patients with liver transplant: Presentation at ESCV 2016: Poster 247 von Colak, M, Altay, A, Bozbulut, NEksi, Dalgic, B, Fidan, I, Ozkan, S, Bozdayi, G

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Gastric emptying time in renal transplant recipients treated with cyclosporine von Ozkaya, O, Derici, U, Buyan, N, Dalgic, A, Dalgic, B, Cingi, E, Kitapci, M, Sindel, S, Hasanoglu, E

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Serum Prohepcidin Levels in Children with Solid Tumors, Inflammatory Bowel Disease and Iron Deficiency Anemia von KAYA, Zühre, YILDIZ, Ejderhan, GURSEL, Turkiz, ALBAYRAK, Meryem, KOCAK, Ulker, KARADENIZ, Ceyda, DALGIC, Buket

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Partial Hepatectomy for the Resistant Fasciola Hepatica Infection in a Child von Belgin, Gülhan, S, Kanık Yüksek, H, Tezer, A, Özkaya Parlakay, B, Dalgıç, A, Dalgıç, G, Yilmaz

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ACOX2 deficiency: A disorder of bile acid synthesis with transaminase elevation, liver fibrosis, ataxia, and cognitive impairment von Vilarinho, S, Sari, S, Mazzacuva, F, Bilgüvar, K, Esendagli-Yilmaz, G, Jain, D, Akyol, G, Dalgiç, B, Günel, M, Clayton, PT, Lifton, RP

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GRISCELLI SYNDROME: Description of a Case with Rab27A Mutation von Aslan, Deniz, Sari, Sinan, Derinöz, Ok an, Dalgiç, Buket

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