Okur İ - Search Results

1

Neonates with inborn errors of metabolism: spectrum and short-term outcomes at a tertiary care hospital.

Gündüz M, Ünal S, Okur İ, Ayrancı Sucaklı İ, Güzel F, Koç N. Gündüz M, et al. Among authors: okur i. Turk J Pediatr. 2015 Jan-Feb;57(1):45-52. Turk J Pediatr. 2015. PMID: 26613220

2

Management of phenylketonuria in Europe: survey results from 19 countries.

Blau N, Bélanger-Quintana A, Demirkol M, Feillet F, Giovannini M, MacDonald A, Trefz FK, van Spronsen F; European PKU centers. Blau N, et al. Mol Genet Metab. 2010 Feb;99(2):109-15. doi: 10.1016/j.ymgme.2009.09.005. Epub 2009 Sep 13. Mol Genet Metab. 2010. PMID: 19800826

3

Endocrinological and metabolic profile of Gaucher disease patients treated with enzyme replacement therapy.

Kilic A, Emecen Sanli M, Ozsaydı Aktasoglu E, Gokalp S, Biberoğlu G, Inci A, Okur I, Suheyl Ezgu F, Tumer L. Kilic A, et al. Among authors: okur i. J Pediatr Endocrinol Metab. 2024 Apr 17;37(5):413-418. doi: 10.1515/jpem-2023-0504. Print 2024 May 27. J Pediatr Endocrinol Metab. 2024. PMID: 38624096

4

Vitamin D intoxication and hypercalcaemia in an infant treated with pamidronate infusions.

Ezgu FS, Buyan N, Gündüz M, Tümer L, Okur I, Hasanoglu A. Ezgu FS, et al. Among authors: okur i. Eur J Pediatr. 2004 Mar;163(3):163-5. doi: 10.1007/s00431-003-1387-4. Epub 2004 Jan 9. Eur J Pediatr. 2004. PMID: 14714183

5

An infantile case of Zellweger syndrome presented with Kabuki-like phenotype.

Ezgu F, Eminoglu T, Okur I, Gunduz M, Tumer L, Hasanoglu A, Dalgic B. Ezgu F, et al. Among authors: okur i. Genet Couns. 2011;22(2):217-20. Genet Couns. 2011. PMID: 21848015

6

The levels of asymmetric dimethylarginine, homocysteine and carotid intima-media thickness in hypercholesterolemic children.

Hasanoğlu A, Okur I, Oren AC, Biberoğlu G, Oktar S, Eminoğlu FT, Tümer L. Hasanoğlu A, et al. Among authors: okur i. Turk J Pediatr. 2011 Sep-Oct;53(5):522-7. Turk J Pediatr. 2011. PMID: 22272452

7

Autism: Screening of inborn errors of metabolism and unexpected results.

İnci A, Özaslan A, Okur İ, Biberoğlu G, Güney E, Ezgü FS, Tümer L, İşeri E. İnci A, et al. Among authors: okur i. Autism Res. 2021 May;14(5):887-896. doi: 10.1002/aur.2486. Epub 2021 Feb 19. Autism Res. 2021. PMID: 33605552

8

N-carbamylglutamate treatment for acute neonatal hyperammonemia in isovaleric acidemia.

Kasapkara CS, Ezgu FS, Okur I, Tumer L, Biberoglu G, Hasanoglu A. Kasapkara CS, et al. Among authors: okur i. Eur J Pediatr. 2011 Jun;170(6):799-801. doi: 10.1007/s00431-010-1362-9. Epub 2011 Jan 5. Eur J Pediatr. 2011. PMID: 21207059

9

Hypercalcemia in glycogen storage disease type I patients of Turkish origin.

Kasapkara CS, Tümer L, Okur I, Eminoğlu T, Ezgü FS, Hasanoğlu A. Kasapkara CS, et al. Among authors: okur i. Turk J Pediatr. 2012 Jan-Feb;54(1):35-7. Turk J Pediatr. 2012. PMID: 22397040

10

Hematologic Findings of Inherited Metabolic Disease: They are More Than Expected.

Sal E, Yenicesu I, Okur I, Kaya Z, Ezgu FS, Kocak U, Tumer L, Gursel T, Hasanoglu A. Sal E, et al. Among authors: okur i. J Pediatr Hematol Oncol. 2018 Jul;40(5):355-359. doi: 10.1097/MPH.0000000000001206. J Pediatr Hematol Oncol. 2018. PMID: 29746437

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