Sezen Güntekin Ergün

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 7

Top Topics

Computed Tomography

Dna Methylation

Regulatory T Cells

Top Venues

Turkish journal of ophthalmology

Turkish journal of medical sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Fulya Yaylacıoğlu Tuncay, Kübra Serbest Ceylanoğlu, Sezen Güntekin Ergün, Güntekin Ergün, Onur Konuk
The Role of FOXP3 Polymorphisms in Graves' Disease with or without Ophthalmopathy in a Turkish Population. Turkish journal of ophthalmology 54 (2) (2024)
Fulya Yaylacıoğlu Tuncay, Kübra Serbest Ceylanoğlu, Sezen Güntekin Ergün, Güntekin Ergün, Onur Konuk
The Role of FOXP3 Polymorphisms in Graves' Disease with or without Ophthalmopathy in a Turkish Population. Turkish journal of ophthalmology 54 (2) (2024)
Fulya Yaylacıoğlu Tuncay, Kübra Serbest Ceylanoğlu, Sezen Güntekin Ergün, Güntekin Ergün, Onur Konuk
Reply. Turkish journal of ophthalmology 54 (4) (2024)
Fulya Yaylacıoğlu Tuncay, Kübra Serbest Ceylanoğlu, Sezen Güntekin Ergün, Güntekin Ergün, Onur Konuk
The Role of FOXP3 Polymorphisms in Graves' Disease with or without Ophthalmopathy in a Turkish Population. Turkish journal of ophthalmology 54 (2) (2024)
Fulya Yaylacıoğlu Tuncay, Kübra Serbest Ceylanoğlu, Sezen Güntekin Ergün, Güntekin Ergün, Onur Konuk
The Role of FOXP3 Polymorphisms in Graves' Disease with or without Ophthalmopathy in a Turkish Population. Turkish journal of ophthalmology 54 (2) (2024)
Fulya Yaylacıoğlu Tuncay, Kübra Serbest Ceylanoğlu, Sezen Güntekin Ergün, Güntekin Ergün, Onur Konuk
The Role of FOXP3 Polymorphisms in Graves' Disease with or without Ophthalmopathy in a Turkish Population. Turkish journal of ophthalmology 54 (2) (2024)
Erkan Yurtcu, Deniz Karçaaltıncaba, Hasan Hüseyin Kazan, Halis Özdemir, Meral Yirmibes Karaoguz, Pinar Calis, Gulsum Kayhan, Sezen Güntekin Ergün, Ferda Emriye Percin, Merih Bayram, Mustafa Necmi İlhan, Gamze Bilgili, Tuğrul Kaymak, Mehmet Ali Ergün
Is cervical swab an efficient method for developing a new noninvasive prenatal diagnostic test for numerical and structural chromosome anomalies? Turkish journal of medical sciences 51 (3) (2021)