Tokatli A - Search Results

1

Evaluation and identification of IDUA gene mutations in Turkishpatients with mucopolysaccharidosis type I.

Atçeken N, Özgül RK, Yücel Yilmaz D, Tokatli A, Coşkun T, Sivri HS, Dursun A, Karaca M. Atçeken N, et al. Among authors: tokatli a. Turk J Med Sci. 2016 Feb 17;46(2):404-8. doi: 10.3906/sag-1411-160. Turk J Med Sci. 2016. PMID: 27511503 Free article.

2

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

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

3

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

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

4

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

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

5

Mutational analysis of Turkish galactosaemia patients.

Coskun T, Erkul E, Seyrantepe V, Ozgüç M, Tokatli A, Ozalp I. Coskun T, et al. Among authors: tokatli a. 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.

6

Iminoglycinuria: a benign type of inherited aminoaciduria.

Coşkun T, Ozalp I, Tokatli A. Coşkun T, et al. Among authors: tokatli a. Turk J Pediatr. 1993 Apr-Jun;35(2):121-5. Turk J Pediatr. 1993. PMID: 7504361

7

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

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

8

Genetic and neurological evaluation of untreated and late-treated patients with phenylketonuria.

Ozalp I, Coşkun T, Ozgüç M, Tokatli A, Yalaz K, Vanli L, Yilmaz E, Erbay A. Ozalp I, et al. Among authors: tokatli a. J Inherit Metab Dis. 1994;17(3):371. doi: 10.1007/BF00711834. J Inherit Metab Dis. 1994. PMID: 7807957 No abstract available.

9

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: tokatli a. J Inherit Metab Dis. 1994;17(3):373-4. doi: 10.1007/BF00711836. J Inherit Metab Dis. 1994. PMID: 7807959 No abstract available.

10

Inborn errors of biotin metabolism. Clinical and laboratory features of eight cases.

Coşkun T, Tokatli A, Ozalp I. Coşkun T, et al. Among authors: tokatli a. Turk J Pediatr. 1994 Oct-Dec;36(4):267-78. Turk J Pediatr. 1994. PMID: 7825232

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

160 results

Search Page

Filters