Arslan N - Search Results

1

Frequency and status of depression and anxiety in mothers of children with inborn errors of metabolism with restricted diet, with and without risk of metabolic crises.

Kisa PT, Uzun OU, Gunduz M, Bulbul FS, Kose E, Arslan N. Kisa PT, et al. Among authors: arslan n. Arch Pediatr. 2021 Nov;28(8):702-706. doi: 10.1016/j.arcped.2021.09.008. Epub 2021 Oct 5. Arch Pediatr. 2021. PMID: 34620546

2

Depression and anxiety in chronic hepatitis B: effect of hepatitis B virus infection on psychological state in childhood.

Arslan N, Büyükgebiz B, Oztürk Y, Akay AP. Arslan N, et al. Turk J Pediatr. 2003 Jan-Mar;45(1):26-8. Turk J Pediatr. 2003. PMID: 12718367

3

Comparison of atherogenic risk factors among poorly controlled and well-controlled adolescent phenylketonuria patients.

Gündüz M, Çakar S, Kuyum P, Makay B, Arslan N. Gündüz M, et al. Among authors: arslan n. Cardiol Young. 2016 Jun;26(5):901-8. doi: 10.1017/S104795111500150X. Epub 2015 Aug 17. Cardiol Young. 2016. PMID: 26278115

4

Depression and anxiety among parents of phenylketonuria children.

Gunduz M, Arslan N, Unal O, Cakar S, Kuyum P, Bulbul SF. Gunduz M, et al. Among authors: arslan n. Neurosciences (Riyadh). 2015 Oct;20(4):350-6. doi: 10.17712/nsj.2015.4.20150319. Neurosciences (Riyadh). 2015. PMID: 26492114 Free PMC article.

5

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. Seizure. 2016 Dec;43:32-38. doi: 10.1016/j.seizure.2016.10.024. Epub 2016 Nov 13. Seizure. 2016. PMID: 27866088 Free article.

6

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

Arslan N, Kose E, Guzel O. Arslan N, et al. 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

7

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. Among authors: arslan n. J Pediatr Endocrinol Metab. 2017 Apr 1;30(4):411-416. doi: 10.1515/jpem-2016-0281. J Pediatr Endocrinol Metab. 2017. PMID: 28076316

8

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. Among authors: arslan n. 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

9

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. Among authors: arslan n. Neurosciences (Riyadh). 2017 Apr;22(2):131-133. doi: 10.17712/nsj.2017.2.20160468. Neurosciences (Riyadh). 2017. PMID: 28416785 Free PMC article.

10

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. Among authors: arslan n. 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

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