Sevim Turay (Sevim Türay)

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 4

Top Topics

Pseudomonas Aeruginosa

Mitochondrial Dna

Intellectual Disability

Chronic Kidney Disease

Top Venues

Acta neurologica Belgica

Neuropediatrics

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

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

Publications

Çağatay Günay, Duygu Aykol, Özlem Özsoy, Ece Sönmezler, Yaren Sena Hanci, Bulent Kara, Deniz Akkoyunlu Sünnetçi, Naci Cine, Adnan Deniz, Tolgahan Özer, Cemile Büşra Ölçülü, Özlem Yilmaz, Seda Kanmaz, Sanem Yilmaz, Hasan Tekgül, Nihal Yildiz, Elif Acar Arslan, Ali Cansu, Nihal Olgaç Dündar, Fatma Kusgoz, Elif Didinmez, Pinar Gencpinar, Tuğçe Aksu Uzunhan, Biray Ertürk, Alper Gezdirici, Akif Ayaz, Akgün Ölmez, Müge Ayanoğlu, Ayşe Fahriye Tosun, Yasemin Topçu, Betül Kılıç, Kursad Aydin, Ezgi Çağlar, Özlem Ersoy Kosvali, Cetin Okuyaz, Şeyda Besen, Leman Tekin Orgun, İlknur Erol, Deniz Yüksel, Abdullah Sezer, Ergin Atasoy, Ülkühan Öztoprak, Serdal Güngör, Bilge Ozgor, Meral Karadağ, Cengiz Dilber, Bahtiyar Şahinoğlu, Emek Uyur Yalçın, Nilüfer Eldes Hacifazlioglu, Ahmet Yaramiş, Pinar Edem, Hande Gazeteci Tekin, Ünsal Yilmaz, Aycan Ünalp, Sevim Turay, Didem Biçer, Gülen Gül Mert, İpek Dokurel Çetin, Serkan Kırık, Gülten Öztürk, Yasemin Karal, Aslıhan Sanri, Ayşe Aksoy, Muzaffer Polat, Nezir Özgün, Didem Soydemir, Gamze Sarikaya Uzan, Döndü Ülker Üstebay, Ayşen Gök, Mehmet Can Yeşilmen, Uluç Yaş, Gökhan Karakülah, Ahmet Bursali, Yavuz Oktay, A Semra Hiz
Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study. Neuropediatrics (2023)
Sevim Turay, Recep Eröz, A Nazlı Başak
A novel pathogenic variant in the 3' end of the AGTPBP1 gene gives rise to neurodegeneration without cerebellar atrophy: an expansion of the disease phenotype? Neurogenetics 22 (2) (2021)
Sevim Turay, Recep Eröz
White-Sutton syndrome with hot water epilepsy and coexistence of SHOX gene variations. Acta neurologica Belgica 121 (3) (2021)
Sevim Turay, Nimet Kabakuş, Fatma Hancı, Fatih Ulaş, Mustafa Dilek, Büşra Cihan
The role of clinical signs in the diagnosis of papilledema: development of an algorithm. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 37 (2) (2020)