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The Turkish Journal of Pediatrics|July 1, 1993
Type I glycogenosis with renal tubular dysfunction (presentation of two cases)A Yüce, T Coşkun, N Koçak, et al.Acta Paediatrica Japonica : Overseas Edition|December 1, 1995
Cerebrospinal fluid amino acid levels in newborn infants with intracranial hemorrhageM Yurdakök, T Coşkun, G Erdem, et al.The Turkish Journal of Pediatrics|January 1, 1995
Nonketotic hyperglycinemia in a newborn infantG Tekinalp, T Coşkun, O Oran, et al.Journal of Inherited Metabolic Disease|August 7, 2001
Factor V Leiden mutation in Turkish patients with homozygous cystathionine beta-synthase deficiencyH S Kalkanoğlu, T Coşkun, S D Aydoğdu, et al.Human Heredity|May 1, 1995
Study of 12 mutations in Turkish cystic fibrosis patientsE Yilmaz, H Erdem, M Ozgüç, et al.The Turkish Journal of Pediatrics|April 1, 1991
Prenatal diagnosis of cystic fibrosis in a Turkish familyE Yilmaz, M Ozgüç, T Coşkun, et al.The Turkish Journal of Pediatrics|January 1, 1993
Neurophysiological studies of patients with classical phenylketonuria: evaluation of results of IQ scores, EEG and evoked potentialsT Coşkun, M Topçu, I Ustündağ, et al.Journal of Pediatric Gastroenterology and Nutrition|March 3, 1998
The effect of zinc-supplemented bread consumption on school children with asymptomatic zinc deficiencyI Kiliç, I Ozalp, T Coŝkun, et al.The Journal of Pediatrics|January 1, 1994
Infantile spasms as the initial symptom of biotinidase deficiencyO Kalayci, T Coskun, A Tokatli, et al.Journal of Inherited Metabolic Disease|May 9, 2000
Novel mutations cause biotinidase deficiency in Turkish childrenR J Pomponio, T Coskun, M Demirkol, et al.Pageof 11