Coşkun T - Search Results

1

Diagnostic and management practices for phenylketonuria in 19 countries of the South and Eastern European Region: survey results.

Giżewska M, MacDonald A, Bélanger-Quintana A, Burlina A, Cleary M, Coşkun T, Feillet F, Muntau AC, Trefz FK, van Spronsen FJ, Blau N. Giżewska M, et al. Among authors: coskun t. Eur J Pediatr. 2016 Feb;175(2):261-72. doi: 10.1007/s00431-015-2622-5. Epub 2015 Sep 8. Eur J Pediatr. 2016. PMID: 26350228 Free PMC article.

2

Hereditary fructose intolerance in a patient with phenylketonuria.

Coşkun T, Ozalp I, Tekinalp G. Coşkun T, et al. Turk J Pediatr. 1991 Jul-Sep;33(3):181-4. Turk J Pediatr. 1991. PMID: 1792698

3

Scleroderma-like skin lesions in two patients with phenylketonuria.

Coşkun T, Ozalp I, Kale G, Göğüş S. Coşkun T, et al. Eur J Pediatr. 1990 Dec;150(2):109-10. doi: 10.1007/BF02072050. Eur J Pediatr. 1990. PMID: 2279504

4

DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish population.

Lichter-Konecki U, Schlotter M, Yaylak C, Ozgüç M, Coskun T, Ozalp I, Wendel U, Batzler U, Trefz FK, Konecki D. Lichter-Konecki U, et al. Among authors: coskun t. Hum Genet. 1989 Mar;81(4):373-6. doi: 10.1007/BF00283695. Hum Genet. 1989. PMID: 2564839

5

Hyperphenylalaninaemia due to tetrahydrobiopterin deficiency: a report of 16 cases.

Coskun T, Ozalp I, Tokatli A, Blau N, Niederwieser A. Coskun T, et al. J Inherit Metab Dis. 1993;16(3):605-7. doi: 10.1007/BF00711694. J Inherit Metab Dis. 1993. PMID: 7609463 No abstract available.

6

Frequency of the IVS-10nt546 mutation in 44 Turkish phenylketonuria patients.

Ozgüç M, Ozalp I, Coşkun T, Yilmaz E, Erdem H, Ayter S. Ozgüç M, et al. Among authors: coskun t. Turk J Pediatr. 1993 Jan-Mar;35(1):11-4. Turk J Pediatr. 1993. PMID: 7901929

7

Neurophysiological studies of patients with classical phenylketonuria: evaluation of results of IQ scores, EEG and evoked potentials.

Coşkun T, Topçu M, Ustündağ I, Ozalp I, Renda Y, Ciğer A, Nurlu G. Coşkun T, et al. Turk J Pediatr. 1993 Jan-Mar;35(1):1-10. Turk J Pediatr. 1993. PMID: 8236512

8

Infantile spasms as the initial symptom of biotinidase deficiency.

Kalayci O, Coskun T, Tokatli A, Demir E, Erdem G, Güngör C, Yükselen A, Ozalp I. Kalayci O, et al. Among authors: coskun t. J Pediatr. 1994 Jan;124(1):103-4. doi: 10.1016/s0022-3476(94)70263-2. J Pediatr. 1994. PMID: 8283357

9

Phenylketonuria and cystic fibrosis in the same patient.

Kalkanoğlu HS, Anadol D, Yilmaz E, Coşkun T. Kalkanoğlu HS, et al. Among authors: coskun t. Pediatr Int. 2000 Feb;42(1):92-3. doi: 10.1046/j.1442-200x.2000.01160.x. Pediatr Int. 2000. PMID: 10703245 No abstract available.

10

Guanosine triphosphate cyclohydrolase I deficiency: a rare cause of hyperphenylalaninemia.

Coşkun T, Karagöz T, Kalkanoğlu S, Tokatli A, Ozalp I, Thöny B, Blau N. Coşkun T, et al. Turk J Pediatr. 1999 Apr-Jun;41(2):231-7. Turk J Pediatr. 1999. PMID: 10770663

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