Guanosine triphosphate cyclohydrolase I deficiency: A rare cause of hyperphenylalaninemia
Nenad BLAU, İmran ÖZALP, Serap KALKANOĞLU, Beat THONY, Ayşegül TOKATLI, Tevfik KARAGÖZ, Turgay COŞKUN
Associated brain abnormalities in patients with corpus callosum anomalies
Hasan TEKGÜL, Osman YALMAN, Nuri ŞENER, Nilgün YÜNTEN, Sarenur TÜTÜNCÜOĞLU, Gülşen DİZDARER
Tropisetron in the prevention of chemotherapy-induced acute emesis in pediatric patients
Mutafoğlu Kamer UYSAL, Faik SARIALİOĞLU, Nur OLGUN
Ahmet Faik ÖNER, Duygu UÇKAN, Sevgi YETGİN
Ayşe AKSOY, Yakup ASLAN, Ayşenur ÖKTEN, Yusuf GEDİK, Nurcihan ARİ, Gülseren ÇİMŞİT
Tracheal rupture: A rare complication related to foreign body aspiration
Bilge ÇELEBİOĞLU, F. Cahit TANYEL, Hanife ALTUNKAYA
Stenotrophomonas maltophilia pneumonia in a premature infant
Hasan ÖZKAN, Güven PAŞAOĞLU, Nihal OLGAÇ, Ruhi GÜNEL, Ayşe YÜCE, Zeynep GÜLAY
Rhabdomyosarcoma of the biliary tree
İrfan KIRIŞTIOĞLU, Emin BALKAN, Tanju ÖZKAN, Arif GÜRPINAR, Kutluğ SINMAZ, Hasan DOĞRUYOL
Methylenetetrahydrofolate reductase (MTHFR) C677T mutation in Turkish patients with thrombosis
Nejat AKSU, Savaş KANSOY, Meral TÜRKER, Sema ÖZİNEL, Hakan ERDOĞAN