Ozalp I - 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: ozalp i. J Inherit Metab Dis. 2001 Oct;24(5):523-6. doi: 10.1023/a:1012423624993. J Inherit Metab Dis. 2001. PMID: 11757579

2

Biotinidase deficiency with neurological features resembling multiple sclerosis.

Tokatli A, Coşkun T, Ozalp I. Tokatli A, et al. Among authors: ozalp i. J Inherit Metab Dis. 1997 Sep;20(5):707-8. doi: 10.1023/a:1005334712056. J Inherit Metab Dis. 1997. PMID: 9323568 No abstract available.

3

Molecular basis of mild hyperphenylalaninaemia in Turkey.

Yilmaz E, Cali F, Roman V, Ozalp I, Coşkun T, Tokatli A, Kalkanoğlu HS, Ozgüç M. Yilmaz E, et al. Among authors: ozalp i. J Inherit Metab Dis. 2000 Jul;23(5):523-5. doi: 10.1023/a:1005628717813. J Inherit Metab Dis. 2000. PMID: 10947211 No abstract available.

4

Maple syrup urine disease: mutation analysis in Turkish patients.

Dursun A, Henneke M, Ozgül K, Gartner J, Coşkun T, Tokatli A, Kalkanoğlu HS, Demirkol M, Wendel U, Ozalp I. Dursun A, et al. Among authors: ozalp i. J Inherit Metab Dis. 2002 May;25(2):89-97. doi: 10.1023/a:1015668425004. J Inherit Metab Dis. 2002. PMID: 12118532

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. Among authors: ozalp i. J Inherit Metab Dis. 1991;14(5):765-70. doi: 10.1007/BF01799947. J Inherit Metab Dis. 1991. PMID: 1664010

6

Hereditary fructose intolerance in a patient with phenylketonuria.

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

7

Mutational analysis of Turkish galactosaemia patients.

Coskun T, Erkul E, Seyrantepe V, Ozgüç M, Tokatli A, Ozalp I. Coskun T, et al. Among authors: ozalp i. J Inherit Metab Dis. 1995;18(3):368-9. doi: 10.1007/BF00710438. J Inherit Metab Dis. 1995. PMID: 7474913 Clinical Trial. No abstract available.

8

Association between mutations and the variable number tandem repeat alleles in a sample of Turkish phenylketonuria patients.

Ozgüç M, Yilmaz E, Erdem H, Coşkun T, Tokatli A, Ozalp I. Ozgüç M, et al. Among authors: ozalp i. J Inherit Metab Dis. 1994;17(3):373-4. doi: 10.1007/BF00711836. J Inherit Metab Dis. 1994. PMID: 7807959 No abstract available.

9

Sanfilippo syndrome in Turkey: Identification of novel mutations in subtypes A and B.

Emre S, Terzioglu M, Tokatli A, Coskun T, Ozalp I, Weber B, Hopwood JJ. Emre S, et al. Among authors: ozalp i. Hum Mutat. 2002 Feb;19(2):184-5. doi: 10.1002/humu.9009. Hum Mutat. 2002. PMID: 11793481

10

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: ozalp i. Turk J Pediatr. 1993 Jan-Mar;35(1):11-4. Turk J Pediatr. 1993. PMID: 7901929

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