Coşkun T - Search Results

1

Mutation analysis in Turkish patients with hereditary fructose intolerance.

Dursun A, Kalkanoğlu HS, Coşkun T, Tokatli A, Bittner R, Koçak N, Yüce A, Ozalp I, Boehme HJ. Dursun A, et al. Among authors: coskun t. J Inherit Metab Dis. 2001 Oct;24(5):523-6. doi: 10.1023/a:1012423624993. J Inherit Metab Dis. 2001. PMID: 11757579

2

Cerebrospinal fluid glutamine level in the differential diagnosis of a "bloody tap" in newborn infants.

Yurdakök M, Göktoğan S, Erdem G, Ozalp I, Tekinalp G, Coşkun T, Cağlar M. Yurdakök M, et al. Among authors: coskun t. Brain Dev. 1992 Nov;14(6):428-9. doi: 10.1016/s0387-7604(12)80357-3. Brain Dev. 1992. PMID: 1492661 No abstract available.

3

Beta-ketothiolase deficiency. A case report.

Altintaş B, Teziç T, Coşkun T, Ozalp I, Kükner S, Kaya A. Altintaş B, et al. Among authors: coskun t. Turk J Pediatr. 1992 Jan-Mar;34(1):43-6. Turk J Pediatr. 1992. PMID: 1509529 Review.

4

The major presenting symptom in a biotinidase-deficient patient: laryngeal stridor.

Tokatli A, Coşkun T, Ozalp I, Günay M. Tokatli A, et al. Among authors: coskun t. J Inherit Metab Dis. 1992;15(2):281-2. doi: 10.1007/BF01799644. J Inherit Metab Dis. 1992. PMID: 1527996 No abstract available.

5

Type I hereditary tyrosinaemia: presentation of 11 cases.

Coşkun T, Ozalp I, Koçak N, Yüce A, Caglar M, Berger R. Coşkun T, et al. J Inherit Metab Dis. 1991;14(5):765-70. doi: 10.1007/BF01799947. J Inherit Metab Dis. 1991. PMID: 1664010

6

Fifteen years' experience with 212 hyperammonaemic cases at a metabolic unit.

Tokatli A, Coşkun T, Ozalp I. Tokatli A, et al. Among authors: coskun t. J Inherit Metab Dis. 1991;14(5):698-706. doi: 10.1007/BF01799938. J Inherit Metab Dis. 1991. PMID: 1779617 No abstract available.

7

Valproate-induced lethal hyperammonaemic coma in a carrier of ornithine carbamoyltransferase deficiency.

Tokatli A, Coşkun T, Cataltepe S, Ozalp I. Tokatli A, et al. Among authors: coskun t. J Inherit Metab Dis. 1991;14(5):836-7. doi: 10.1007/BF01799961. J Inherit Metab Dis. 1991. PMID: 1779634 No abstract available.

8

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

9

Prenatal diagnosis of cystic fibrosis in a Turkish family.

Yilmaz E, Ozgüç M, Coşkun T, Beksaç S, Cakar N, Ayter S, Ozalp I. Yilmaz E, et al. Among authors: coskun t. Turk J Pediatr. 1991 Apr-Jun;33(2):79-84. Turk J Pediatr. 1991. PMID: 1844185

10

Intracranial calcification in dihydropteridine reductase deficiency.

Coşkun T, Besim A, Ozalp I, Eryilmaz M. Coşkun T, et al. Turk J Pediatr. 1990 Oct-Dec;32(4):259-64. Turk J Pediatr. 1990. PMID: 2135679

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