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Thalamic T2 hypointensity: a diagnostic clue for Tay-Sachs disease.
Güngör O, Güngör G, Yurttutan N, Dilber C. Güngör O, et al. Among authors: dilber c. Acta Neurol Belg. 2016 Jun;116(2):195-7. doi: 10.1007/s13760-015-0538-5. Epub 2015 Sep 4. Acta Neurol Belg. 2016. PMID: 26338066 No abstract available.
Vanishing white matter disease with different faces.
Güngör G, Güngör O, Çakmaklı S, Maraş Genç H, İnce H, Yeşil G, Dilber C, Aydın K. Güngör G, et al. Among authors: dilber c. Childs Nerv Syst. 2020 Feb;36(2):353-361. doi: 10.1007/s00381-019-04334-6. Epub 2019 Aug 5. Childs Nerv Syst. 2020. PMID: 31385086
Novel mutation in SUCLA2 identified on sequencing analysis.
Güngör O, Özkaya AK, Güngör G, Karaer K, Dilber C, Aydin K. Güngör O, et al. Among authors: dilber c. Pediatr Int. 2016 Jul;58(7):659-61. doi: 10.1111/ped.12921. Epub 2016 Mar 8. Pediatr Int. 2016. PMID: 26952923
Acute Mercury Poisoning in a Group of School Children.
Güngör O, Özkaya AK, Kirik S, Dalkiran T, Güngör G, Işikay S, Davutoğlu M, Dilber C. Güngör O, et al. Among authors: dilber c. Pediatr Emerg Care. 2019 Oct;35(10):696-699. doi: 10.1097/PEC.0000000000001011. Pediatr Emerg Care. 2019. PMID: 27977534
Muscular Dystrophy: A Retrospective Evaluation of 15 Cases.
Güngör O, Dilber C. Güngör O, et al. Among authors: dilber c. Sisli Etfal Hastan Tip Bul. 2018 Mar 26;52(1):47-50. doi: 10.14744/SEMB.2017.53496. eCollection 2018. Sisli Etfal Hastan Tip Bul. 2018. PMID: 32595371 Free PMC article.
43 results