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Results: 26-30/30
Authors:
COSKUN T
OZALP I
TOKATLI A
BLAU N
NIEDERWIESER A
Citation: T. Coskun et al., HYPERPHENYLALANINEMIA DUE TO TETRAHYDROBIOPTERIN DEFICIENCY - A REPORT OF 16 CASES, Journal of inherited metabolic disease, 16(3), 1993, pp. 605-607
Authors:
YUCE A
COSKUN T
KOCAK N
OZSOYLU S
OZALP I
GOGUS S
Citation: A. Yuce et al., TYPE-I GLYCOGENOSIS WITH RENAL TUBULAR DYSFUNCTION - (PRESENTATION OF2 CASES), Turkish Journal of Pediatrics, 35(3), 1993, pp. 201-204
Authors:
COSKUN T
OZALP I
TOKATLI A
Citation: T. Coskun et al., IMINOGLYCINURIA - A BENIGN TYPE OF INHERITED AMINOACIDURIA, Turkish Journal of Pediatrics, 35(2), 1993, pp. 121-125
Authors:
COSKUN T
TOPCU M
USTUNDAG I
OZALP I
RENDA Y
CIGER A
NURLU G
Citation: T. Coskun et al., NEUROPHYSIOLOGICAL STUDIES OF PATIENTS WITH CLASSICAL PHENYLKETONURIA- EVALUATION OF RESULTS OF IQ SCORES, EEG AND EVOKED-POTENTIALS, Turkish Journal of Pediatrics, 35(1), 1993, pp. 1-10
Authors:
OZGUC M
OZALP I
COSKUN T
YILMAZ E
ERDEM H
AYTER S
Citation: M. Ozguc et al., FREQUENCY OF THE IVS-10NT546 MUTATION IN 44 TURKISH PHENYLKETONURIA PATIENTS, Turkish Journal of Pediatrics, 35(1), 1993, pp. 11-14