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The Turkish Journal of Pediatrics|September 9, 2022
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infantBurak Deliloğlu, Özlem Tüfekçi, Funda Tüzün, et al.
The Turkish Journal of Pediatrics|September 9, 2022
Rare cause of ketolysis: Monocarboxylate transporter 1 deficiencyAyşe Ergül Bozacı, Aysel Tekmenuray Ünal
The Turkish Journal of Pediatrics|September 9, 2022
Fucosidosis: clinical and molecular findings of Turkish patientsMerve Emecen Şanlı, Serap Uysal
The Turkish Journal of Pediatrics|July 1, 1994
The epidemiology of juvenile-onset insulin-dependent diabetes mellitus in Turkish children. A retrospective analysis of 477 casesN Kandemir, E Açikgöz, N Yordam
The Turkish Journal of Pediatrics|July 1, 1994
A study on enzyme activities of some sphingolipidosesH A Ozkara, M C Arikan, M Topçu, et al.
The Turkish Journal of Pediatrics|January 1, 1995
Eosinophilic gastroenteritis presenting as protein--losing enteropathy (case report)S Karademir, A Akçayöz, K Bek, et al.
The Turkish Journal of Pediatrics|January 1, 1995
Nonketotic hyperglycinemia in a newborn infantG Tekinalp, T Coşkun, O Oran, et al.
The Turkish Journal of Pediatrics|January 1, 1995
Renal replacement therapies for critically ill pediatric patientsA Sakarcan, M Karaböcüoğlu
The Turkish Journal of Pediatrics|January 1, 1995
Fatal agranulocytosis developed in the course of carbamazepine therapy. A case report and review of the literatureL Olcay, S Pekcan, D Yalnizoğlu, et al.
The Turkish Journal of Pediatrics|January 1, 1994
Ocular involvement in childhood leukemiasM Soylu, A Tanyeli, N Ozdemir, et al.
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