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The Turkish Journal of Pediatrics|April 1, 1993
Iminoglycinuria: a benign type of inherited aminoaciduriaT Coşkun, I Ozalp, A Tokatli
The Turkish Journal of Pediatrics|October 1, 1994
Inborn errors of biotin metabolism. Clinical and laboratory features of eight casesT Coşkun, A Tokatli, I Ozalp
The Turkish Journal of Pediatrics|April 1, 1997
Hypophosphatemic vitamin-D resistant rickets associated with epidermal nevus syndrome. A case reportA Tokatli, T Coşkun, I Ozalp
The Turkish Journal of Pediatrics|July 25, 1998
Citrullinemia. Clinical experience with 23 casesA Tokatli, T Coşkun, I Ozalp
The Turkish Journal of Pediatrics|July 23, 1998
Isovaleric acidemia. Clinical presentation of 6 casesA Tokatli, T Coşkun, I Ozalp
The Turkish Journal of Pediatrics|July 1, 1997
Acute pancreatitis in a patient with glutaric acidemia type IIT Coşkun, S Göğüş, Z Akçören, et al.
The Turkish Journal of Pediatrics|April 1, 1994
Classical phenylketonuria associated with Goldenhar's syndrome. A case reportA Tokatli, T Coşkun, C N Kocabaş, et al.
The Turkish Journal of Pediatrics|April 19, 2000
Guanosine triphosphate cyclohydrolase I deficiency: a rare cause of hyperphenylalaninemiaT Coşkun, T Karagöz, S Kalkanoğlu, et al.
The Turkish Journal of Pediatrics|July 1, 1991
Hereditary fructose intolerance in a patient with phenylketonuriaT Coşkun, I Ozalp, G Tekinalp
The Turkish Journal of Pediatrics|July 4, 2001
Newborn PKU screening in Turkey: at present and organization for futureI Ozalp, T Coşkun, A Tokatli, et al.
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