Zeybek AC[Author] - Search Results

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Year	Number of Results
2014	1
2015	3
2019	1
2021	1
2022	0

Page 1

Long-term N-carbamylglutamate treatment of hyperammonemia in patients with classic organic acidemias.

Kiykim E, Oguz O, Duman C, Zubarioglu T, Cansever MS, Zeybek ACA. Kiykim E, et al. Among authors: zeybek aca. Mol Genet Metab Rep. 2021 Jan 30;26:100715. doi: 10.1016/j.ymgmr.2021.100715. eCollection 2021 Mar. Mol Genet Metab Rep. 2021. PMID: 33552909 Free PMC article.

Hereditary tyrosinemia type 1 in Turkey: twenty year single-center experience.

Zeybek AC, Kiykim E, Soyucen E, Cansever S, Altay S, Zubarioglu T, Erkan T, Aydin A. Zeybek AC, et al. Pediatr Int. 2015 Apr;57(2):281-9. doi: 10.1111/ped.12503. Epub 2014 Dec 11. Pediatr Int. 2015. PMID: 25223216

Evaluation of the effect of chenodeoxycholic acid treatment on skeletal system findings in patients with cerebrotendinous xanthomatosis.

Zübarioğlu T, Bilen İP, Kıykım E, Doğan BB, Enver EÖ, Cansever MŞ, Zeybek AÇA. Zübarioğlu T, et al. Among authors: zeybek aca. Turk Pediatri Ars. 2019 Jul 11;54(2):113-118. doi: 10.14744/TurkPediatriArs.2019.23281. eCollection 2019. Turk Pediatri Ars. 2019. PMID: 31384146 Free PMC article.

A NOVEL ASPARTYLGLUCOSAMINURIA MUTATION IN A PATIENT WITH CO-EXISTENCE OF GAUCHER DISEASE.

Kiykim E, Zubarioglu T, Gorukmez O, Gunes S, Cansever MS, Zeybek AC. Kiykim E, et al. Among authors: zeybek ac. Genet Couns. 2015;26(4):463-6. Genet Couns. 2015. PMID: 26852520 No abstract available.

CITRIN DEFICIENCY: AN INFANT INCIDENTALLY DETECTED BY PHENYLKETONURIA SCREENING WITH A NOVEL MUTATION IN SLC25A13 GENE.

Zeybek AC, Kiykim E, Zubarioglu T, Cansever MS, Ceylaner S, Erkan T. Zeybek AC, et al. Genet Couns. 2015;26(4):409-13. Genet Couns. 2015. PMID: 26852511

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