المؤلفون: Semiha Kurt, Betul Cevik, Durdane Aksoy, E. Irmak Sahbaz, Aslı Gundogdu Eken, A. Nazli Basak

المصدر: Case Reports in Neurological Medicine, Vol 2016 (2016)

مصطلحات موضوعية: Neurology. Diseases of the nervous system, RC346-429

العلاقة: http://dx.doi.org/10.1155/2016/4515938Test; https://doaj.org/toc/2090-6668Test; https://doaj.org/toc/2090-6676Test; https://doaj.org/article/320c89f746734b55bafa476d04dc0a12Test

الإتاحة: https://doi.org/10.1155/2016/4515938Test
https://doaj.org/article/320c89f746734b55bafa476d04dc0a12Test

المؤلفون: Mefkure Eraksoy, Onder Us, Sibel Ertan, Hacer Durmus, Filiz Koç, Nazan Saner, Şeyma Tekgül, Pinar Tekturk, Cemile Kocoglu, Gençer Genç, Robin Palvadeau, Feza Deymeer, Güneş Kızıltan, Ece Kartal, Hulya Apaydin, Sevda Erer Özbek, Cenk Akbostanci, Suna Lahut, Yesim Parman, Erdi Şahin, Dilcan Kotan, Hülya Tireli, Murat Gultekin, Zeynep Özözen Ayas, Ersin Tan, Sibel Özekmekçi, Irmak Şahbaz, Hamit Acer, Zeynep Tufekcioglu, Dilek Ince Gunal, Hasmet Hanagasi, İhsan Şükrü Şengün, Arman Çakar, Esen Saka Topcuoglu, Gülşah Şimşir, Gülden Akdal, Elif Bayraktar, Fulya Akçimen, Ayşe Bora Tokçaer, Aysegul Gunduz, Uluç Yiş, Gul Serdaroglu, Atay Vural, Ayse Altintas, Hüseyin A. Şahin, Özgür Ömür, Tuğçe Gül, Gül Demet Kaya Özçora, Müge Kovancılar Koç, Vildan Yayla, Aksel Siva, Semra Hiz, Meral Topçu, Piraye Oflazer, Başar Bilgiç, M. Osman Çorbalı, Semiha Kurt, Elçin Bora, Nesli E. Şen, Kadriye Agan, A. Nazli Basak, Halil Güllüoğlu, Ceren Tunca, Sefer Kumandaş, Muhsin Elmas, Özgür Öztop Çakmak, Bulent Elibol, Aysun Soysal, Zeynep E. Kaya Gulec, Caroline Pirkevi Çetinkaya, Dürdane Aksoy, Aslı Gündoğdu Eken

المساهمون: Ege Üniversitesi, Elmas, Muhsin

مصطلحات موضوعية: 0301 basic medicine, Proband, congenital, hereditary, and neonatal diseases and abnormalities, Ataxia, Turkey, Consanguinity, 03 medical and health sciences, symbols.namesake, Wholeexome sequencing, 0302 clinical medicine, medicine, Genetics, Humans, Spinocerebellar Ataxias, genetics, Exome sequencing, Spinocerebellar Degenerations, Sanger sequencing, biology, ataxia, medicine.disease, Optic Atrophy, 030104 developmental biology, Neurology, Muscle Spasticity, whole‐, Spinocerebellar ataxia, symbols, Frataxin, biology.protein, Neurology (clinical), medicine.symptom, Heterogeneity, heterogeneity, Trinucleotide repeat expansion, exome sequencing, 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bd268a54a7c084aa9507fb520b75a7dTest
https://avesis.gazi.edu.tr/publication/details/dc537293-2ef2-4fdc-932d-c75876075839/oaiTest

المؤلفون: Saadet Sayan, Dilcan Kotan, Kotan Dündar, Dilcan, Asli Gundogdu-Eken, Irmak Sahbaz, Cemile Kocoglu, A. Nazli Basak

المساهمون: Sayan, S, Kotan, D, Gundogdu-Eken, A, Sahbaz, I, Kocoglu, C, Basak, AN, Sakarya Üniversitesi/Tıp Fakültesi/Dahili Tıp Bilimleri Bölümü, Kotan Dündar, Dilcan

مصطلحات موضوعية: Neurosciences & Neurology

العلاقة: NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY; Sayan, S; Kotan, D; Gundogdu-Eken, A; Sahbaz, I; Kocoglu, C; Basak, AN; (2019). Phenotypic and Genotypic Analysis of Hereditary Ataxia Patients in Sakarya City, Turkey. NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY, 56, 109-106; https://doi.org/10.5152/npa.2017.20525Test; https://hdl.handle.net/20.500.12619/66033Test; 56; 106; 109; WOS:000503182900005

الإتاحة: https://doi.org/20.500.12619/66033Test
https://doi.org/10.5152/npa.2017.20525Test
https://hdl.handle.net/20.500.12619/66033Test

المؤلفون: Dürdane Aksoy, A. Nazli Basak, Aslı Gündoğdu Eken, Semiha Kurt, Ece Kartal, Betül Çevik, Irmak Şahbaz

المصدر: Journal of the Neurological Sciences. 357:290-291

مصطلحات موضوعية: Spondyloepiphyseal dysplasia, medicine.medical_specialty, Ataxia, business.industry, medicine.disease, Dermatology, Neurology, Spinocerebellar ataxia, medicine, Neurology (clinical), Spasticity, medicine.symptom, Spastic ataxia, business, Novel mutation

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::42a0a6dace26d03049ae41ac8a9317b8Test
https://doi.org/10.1016/j.jns.2015.06.050Test