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Year Number of Results
2014 1
2015 3
2019 1
2020 0
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Page 1
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.
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
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