Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

52 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Functional divergence of the two Elongator subcomplexes during neurodevelopment.
Gaik M, Kojic M, Stegeman MR, Öncü-Öner T, Kościelniak A, Jones A, Mohamed A, Chau PYS, Sharmin S, Chramiec-Głąbik A, Indyka P, Rawski M, Biela A, Dobosz D, Millar A, Chau V, Ünalp A, Piper M, Bellingham MC, Eichler EE, Nickerson DA, Güleryüz H, Abbassi NEH, Jazgar K, Davis MJ, Mercimek-Andrews S, Cingöz S, Wainwright BJ, Glatt S. Gaik M, et al. Among authors: guleryuz h. EMBO Mol Med. 2022 Jul 7;14(7):e15608. doi: 10.15252/emmm.202115608. Epub 2022 Jun 13. EMBO Mol Med. 2022. PMID: 35698786 Free PMC article.
GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria.
Öncü-Öner T, Ünalp A, Porsuk-Doru İ, Ağılkaya S, Güleryüz H, Saraç A, Ergüner B, Yüksel B, Hız-Kurul S, Cingöz S. Öncü-Öner T, et al. Among authors: guleryuz h. Turk J Pediatr. 2018;60(3):229-237. doi: 10.24953/turkjped.2018.03.001. Turk J Pediatr. 2018. PMID: 30511534 Free article.
Oncu-Oner T, Unalp A, Porsuk-Doru I, Agilkaya S, Guleryuz H, Sarac A, Erguner B, Yuksel B, Hiz-Kurul S, Cingoz S. GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria. ...
Oncu-Oner T, Unalp A, Porsuk-Doru I, Agilkaya S, Guleryuz H, Sarac A, Erguner B, Yuksel B, Hiz-Kurul S, Cingoz S. GPR56 homozy …
Atypical Presentation and Course of ACTH-independent Cushing's Syndrome in Two Families.
Yüksek Acinikli K, Acar S, Paketçi A, Kırbıyık Ö, Erbaş M, Besci Ö, Akın Kağızmanlı G, Kızmazoğlu D, Ulusoy O, Özer E, Yörükoğlu K, Abacı A, Güleryüz H, Böber E, Demir K. Yüksek Acinikli K, et al. Among authors: guleryuz h. J Clin Res Pediatr Endocrinol. 2023 Dec 12. doi: 10.4274/jcrpe.galenos.2023.2023-9-15. Online ahead of print. J Clin Res Pediatr Endocrinol. 2023. PMID: 38084047 Free article.
Chronic spinal epidural hematoma.
Yiş U, Kalemci O, Polat I, Karaoğlu P, Oztura I, Güleryüz H, Kurul SH. Yiş U, et al. Among authors: guleryuz h. J Pediatr. 2014 Jan;164(1):215-215.e1. doi: 10.1016/j.jpeds.2013.08.043. Epub 2013 Oct 8. J Pediatr. 2014. PMID: 24119875 No abstract available.
A newborn with monosomy X in association with corpus callosum agenesis.
Onur Cura D, Iscan B, Gursoy S, Guleryuz H, Cankaya T, Ozturk T, Giray Bozkaya O. Onur Cura D, et al. Among authors: guleryuz h. Pediatr Neonatol. 2017 Oct;58(5):455-457. doi: 10.1016/j.pedneo.2016.05.006. Epub 2016 Nov 28. Pediatr Neonatol. 2017. PMID: 28117231 Free article. No abstract available.
52 results