| Primary intracranial germ cell tumors in children : A report of eight cases and review of the literature | Canan AKYÜZ, Münevver BÜYÜKPAMUKÇU, Vural BERTAN, Figen SÖYLEMEZOĞLU, Vedat KÖSEOĞLU, M. Tezer KUTLUK | 161–172 |
| Associated brain abnormalities in patients with corpus callosum anomalies | Hasan TEKGÜL, Osman YALMAN, Nuri ŞENER, Nilgün YÜNTEN, Sarenur TÜTÜNCÜOĞLU, Gülşen DİZDARER | 173–180 |
| Human leukocyte antigens in Turkish pediatric celiac patients | Tülay ERKAN, Fügen ÇULLU, Güngör T. TÜMAY, Tufan KUTLU, Erkan YILMAZ | 181–188 |
| Cryptosporidium parvum prevalence in a group of Turkish children | Yakut AKYÖN, Sibel ERGÜVEN, Kadriye YURDAKÖK, Sevtap ARIKAN, Ayfer GÜNALP | 189–196 |
| Methylenetetrahydrofolate reductase (MTHFR) C677T mutation in Turkish patients with thrombosis | Günay BALTA, Aytemiz GÜRGEY | 197–199 |
| Tropisetron in the prevention of chemotherapy-induced acute emesis in pediatric patients | Mutafoğlu Kamer UYSAL, Faik SARIALİOĞLU, Nur OLGUN | 207–218 |
| Biphenotypic characteristics, cell size and prognosis in childhood acute myeloblastic leukemia | Gönül HİÇSÖNMEZ, A. Murat TUNCER, Lale OLCAY, Ulya ERTEM, Hamza OKUR | 219–224 |
| Cyclosporin A plus prednisone treatment of steroid-sensitive frequently relapsing nephrotic syndrome in children | Nejat AKSU, Savaş KANSOY, Meral TÜRKER, Sema ÖZİNEL, Hakan ERDOĞAN | 225–230 |
| Guanosine triphosphate cyclohydrolase I deficiency: A rare cause of hyperphenylalaninemia | Nenad BLAU, İmran ÖZALP, Serap KALKANOĞLU, Beat THONY, Ayşegül TOKATLI, Tevfik KARAGÖZ, Turgay COŞKUN | 231–237 |
| A warm antibody mediated acute hemolytic anemia with reticulocytopenia in a four-month-old girl requiring immunosuppressive therapy | Lale OLCAY, Ali DÜZOVA, Fatma GÜMRÜK | 239–244 |
| Rhabdomyosarcoma of the biliary tree | İrfan KIRIŞTIOĞLU, Emin BALKAN, Tanju ÖZKAN, Arif GÜRPINAR, Kutluğ SINMAZ, Hasan DOĞRUYOL | 245–248 |
| Cerebrospinal fluid pleocytosis in acute lymphoblastic leukemia without central nervous system relapse: A report of three cases |