Kose E - Search Results

1

Changes of thyroid hormonal status in patients receiving ketogenic diet due to intractable epilepsy.

Kose E, Guzel O, Demir K, Arslan N. Kose E, et al. J Pediatr Endocrinol Metab. 2017 Apr 1;30(4):411-416. doi: 10.1515/jpem-2016-0281. J Pediatr Endocrinol Metab. 2017. PMID: 28076316

2

Is ketogenic diet treatment hepatotoxic for children with intractable epilepsy?

Arslan N, Guzel O, Kose E, Yılmaz U, Kuyum P, Aksoy B, Çalık T. Arslan N, et al. Among authors: kose e. Seizure. 2016 Dec;43:32-38. doi: 10.1016/j.seizure.2016.10.024. Epub 2016 Nov 13. Seizure. 2016. PMID: 27866088 Free article.

3

The Effect of Ketogenic Diet on Serum Selenium Levels in Patients with Intractable Epilepsy.

Arslan N, Kose E, Guzel O. Arslan N, et al. Among authors: kose e. Biol Trace Elem Res. 2017 Jul;178(1):1-6. doi: 10.1007/s12011-016-0897-7. Epub 2016 Nov 21. Biol Trace Elem Res. 2017. PMID: 27873289

4

Identification of three novel mutations in fourteen patients with citrullinemia type 1.

Kose E, Unal O, Bulbul S, Gunduz M, Häberle J, Arslan N. Kose E, et al. Clin Biochem. 2017 Aug;50(12):686-689. doi: 10.1016/j.clinbiochem.2017.01.011. Epub 2017 Jan 27. Clin Biochem. 2017. PMID: 28132756

5

A novel mutation in the glycine decarboxylase gene in patient with non-ketotic hyperglycinemia.

Kose E, Yis U, Hiz S, Arslan N. Kose E, et al. Neurosciences (Riyadh). 2017 Apr;22(2):131-133. doi: 10.17712/nsj.2017.2.20160468. Neurosciences (Riyadh). 2017. PMID: 28416785 Free PMC article.

6

First report of carglumic acid in a patient with citrullinemia type 1 (argininosuccinate synthetase deficiency).

Kose E, Kuyum P, Aksoy B, Häberle J, Arslan N, Ozturk Y. Kose E, et al. J Clin Pharm Ther. 2018 Feb;43(1):124-128. doi: 10.1111/jcpt.12593. Epub 2017 Jul 25. J Clin Pharm Ther. 2018. PMID: 28741715

7

Analysis of hematological parameters in patients treated with ketogenic diet due to drug-resistant epilepsy.

Kose E, Guzel O, Arslan N. Kose E, et al. Neurol Sci. 2018 Jan;39(1):85-89. doi: 10.1007/s10072-017-3152-x. Epub 2017 Oct 16. Neurol Sci. 2018. PMID: 29038947

8

The Effects of Breastfeeding in Infants With Phenylketonuria.

Kose E, Aksoy B, Kuyum P, Tuncer N, Arslan N, Ozturk Y. Kose E, et al. J Pediatr Nurs. 2018 Jan-Feb;38:27-32. doi: 10.1016/j.pedn.2017.10.009. Epub 2017 Oct 19. J Pediatr Nurs. 2018. PMID: 29167077

9

Identification of the largest homozygous glycine decarboxylase gene deletion in a Turkish infant.

Gürsoy S, Ataman E, Bozkaya ÖG, Köse E, Ayanoğlu M, Polat Aİ, Arslan N, Kurul SH, Erçal D. Gürsoy S, et al. Among authors: kose e. Pediatr Neonatol. 2018 Dec;59(6):632-633. doi: 10.1016/j.pedneo.2018.01.011. Epub 2018 Jan 31. Pediatr Neonatol. 2018. PMID: 29398553 Free article. No abstract available.

10

Vitamin/mineral and micronutrient status in patients with classical phenylketonuria.

Kose E, Arslan N. Kose E, et al. Clin Nutr. 2019 Feb;38(1):197-203. doi: 10.1016/j.clnu.2018.01.034. Epub 2018 Feb 15. Clin Nutr. 2019. PMID: 29433755

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