Turgay Coşkun

High cystine in platelets from patients with nephropathic cystinosis: a chemical, ultrastructural, and functional evaluation

T. Coşkun, M. Kesimer, Y. Buyukasik, 2005, Journal of Clinical Pathology.

Predictors of eventual requirement of phenylalanine-restricted diet in young infants with phenylalanine hydroxylase deficiency initially managed with sapropterin monotherapy.

A. Dursun, A. Tokatlı, S. Sivri, 2023, Molecular genetics and metabolism.

Novel mutations cause biotinidase deficiency in Turkish children

T. Coşkun, B. Wolf, R. Pomponio, 2000, Journal of Inherited Metabolic Disease.

Maple syrup urine disease: Mutation analysis in Turkish patients

T. Coşkun, M. Henneke, K. Özgül, 2002, Journal of Inherited Metabolic Disease.

Newborn PKU screening in Turkey: at present and organization for future.

T. Coşkun, A. Dursun, H. Kalkanoğlu, 2001, The Turkish journal of pediatrics.

Inherited metabolic disorders in Turkey

T. Coşkun, E. Mönch, G. Demircin, 1990, Journal of Inherited Metabolic Disease.

Identification of mutations and evaluation of cardiomyopathy in Turkish patients with primary carnitine deficiency.

T. Coşkun, M. Kılıç, A. Dursun, 2012, JIMD reports.