Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2014 | 1 |
2015 | 3 |
2019 | 1 |
2021 | 1 |
2022 | 1 |
2023 | 0 |
Search Results
6 results
Results by year
Filters applied: . Clear all
Page 1
Child Brides and Forced Marriages: An Aspect of Child Abuse and Neglect.
J Pediatr. 2022 Nov;250:116-117.e2. doi: 10.1016/j.jpeds.2022.07.043. Epub 2022 Aug 5.
J Pediatr. 2022.
PMID: 35940291
No abstract available.
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.
Item in Clipboard
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.
Item in Clipboard
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.
Item in Clipboard
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
Item in Clipboard
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
Item in Clipboard
Cite
Cite