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The Turkish Journal of Pediatrics|July 1, 1996
Superior mesenteric artery syndrome. A case reportG Tatar, T Coşkun, H SimşekScandinavian Journal of Haematology|September 1, 1984
High dose intravenous glucocorticoid in the treatment of childhood acquired aplastic anaemiaS Ozsoylu, T Coşkun, S MinassaziHuman Heredity|May 9, 2000
Fine mapping of the human biotinidase gene and haplotype analysis of five common mutationsS H Blanton, A Pandya, B L Landa, et al.Biological Trace Element Research|October 1, 1995
Aluminum content of infant formulas used in TurkeyG Sahin, A Aydin, A Işimer, et al.Journal of Inherited Metabolic Disease|September 1, 2004
Early cirrhosis in a patient with type I citrullinaemia (CTLN1)S Güçer, E Aşan, P Atilla, et al.Human Mutation|April 29, 1999
Identification of mutations in the galactose-1-phosphate uridyltransferase (GALT) gene in 16 Turkish patients with galactosemia, including a novel mutation of F294Y. Mutation in brief no. 235. OnlineV Seyrantepe, M Ozguc, T Coskun, et al.The Turkish Journal of Pediatrics|February 24, 2001
Carnitinuria in rickets due to vitamin D deficiencyA Dursun, D Aliefendioğlu, B Ozkan, et al.The Turkish Journal of Pediatrics|April 1, 1992
Neuroblastoma presenting as protein-losing enteropathyT Coşkun, H Ozen, M Büyükpamukçu, et al.The Turkish Journal of Pediatrics|April 1, 1994
I-cell disease. A case report and review of the literatureN Güngör, T Coşkun, Z Akçören, et al.The Turkish Journal of Pediatrics|July 23, 1998
Recurrent meningitis associated with congenital paravertebral dermal sinus tractN Andiran, T Coşkun, E Ozaydin, et al.Pageof 11