Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Pinar Tekturk"'
Autor:
Gulistan HALAC, Pinar TEKTURK, Cigdem DENIZ, Mehmet KOLUKISA, Muhammet Emin OZCAN, Talip ASIL
Publikováno v:
Bezmiâlem Science, Vol 3, Iss 1, Pp 18-20 (2015)
Bilateral thalamic infarction is a rare cerebral vascular disease. The most common findings are acute impairment of consciousness, vertical gaze paresis, cognitive disturbances, and abnormal behavioral symptoms. In this paper, we report a case of bil
Externí odkaz:
https://doaj.org/article/566e37c2617c480a9f68942bf28a4593
Publikováno v:
Namık Kemal Tıp Dergisi, Vol 4, Iss 1, Pp 43-44 (2016)
In this presentation we report a case of seizures following the administration of pethidine.
Externí odkaz:
https://doaj.org/article/d5c958f4c2f6445e902e21ad5436b020
Publikováno v:
Child's Nervous System. 35:2405-2409
Tuberous sclerosis (TSC) is an autosomal dominantly inherited genetic disorder that chiefly affects the central nervous system, along with the other multiple systems. While phenomenology and symptom severity may vary greatly from one individual to an
Autor:
Hülya Kayserili, Haluk Topaloglu, Ayaz Aghayev, Zehra Oya Uyguner, Sahin Avci, Hacer Durmus, Zuhal Yapici, Pinar Tekturk, Seher Başaran, Yesim Parman, Umut Altunoglu, Piraye Oflazer-Serdaroglu, B Sevinc Rustemoglu, Gulendam Bagirova, Feza Deymeer, Güven Toksoy, Birsen Karaman
Publikováno v:
Neuromuscular Disorders. 29:601-613
We genetically evaluated 260 dystrophinopathy patients from Turkey. Karyotyping as an initial test in female patients, followed stepwise by multiplex ligation-dependent probe amplification and by targeted next-generation sequencing of DMD revealed de
Autor:
Erdem Tüzün, Ebru Yilmaz, Ece Erdağ, Gokçen Gundogdu-Unverengil, Mine Sezgin, Betül Baykan, Ebru Nur Vanlı-Yavuz, Esme Ekizoglu, Pinar Tekturk, Nerses Bebek
Publikováno v:
Epilepsy & Behavior. 92:103-107
Objective The long-term follow-up of patients with epilepsy harboring autoantibodies against the glycine receptor (also glycine receptor antibodies or GlyR-Ab) is not well-known. Our aim was to investigate the 5-year prognosis and treatment response
Autor:
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
Background The genetic and epidemiological features of hereditary ataxias have been reported in several populations; however, Turkey is still unexplored. Due to high consanguinity, recessive ataxias are more common in Turkey than in Western European
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bd268a54a7c084aa9507fb520b75a7d
https://avesis.gazi.edu.tr/publication/details/dc537293-2ef2-4fdc-932d-c75876075839/oai
https://avesis.gazi.edu.tr/publication/details/dc537293-2ef2-4fdc-932d-c75876075839/oai
Autor:
Esra Battaloglu, Nihan Hande Akçakaya, Murat Gultekin, Hasmet Hanagasi, Mefkure Eraksoy, Zuhal Yapici, Recep Alp, Pinar Tekturk, Gokcen Akar, Birdal Bilir, Remzi Yigiter, Ugur Ozbek, Sibel Aylin Ugur Iseri, Sultan Cagirici
Publikováno v:
Clinical Neurology and Neurosurgery. 154:34-42
Objective Pantothenate kinase-associated neurodegeneration (PKAN) is caused by mutations of the pantothenate kinase 2 ( PANK2 ) gene. The major clinical sign of PKAN is dystonia and the eye-of-the-tiger pattern on the MRI has been a clue for the diag
Autor:
Candan Gürses, Nerses Bebek, Zuhal Yapici, Sacit Karamürsel, Aysen Gokyigit, Z. Küçük, Esme Ekizoglu, Serkan Aksu, Pinar Tekturk, Ezgi Tuna Erdogan, Adnan Kurt, Ebru Nur Vanlı-Yavuz, Ece Kocagoncu, Betül Baykan
Publikováno v:
Clinical Neurology and Neurosurgery. 149:27-32
Objectives Transcranial direct current stimulation (tDCS) is a non-invasive and safe method tried in drug-resistant epilepsies, in recent years. Our aim was to evaluate the effect of tDCS in patients diagnosed with mesial temporal lobe epilepsy with
Publikováno v:
Brain and Development. 38:755-758
Pantothenate kinase-associated neurodegeneration (PKAN) is a rare neurodegenerative condition. Major clinical features include progressive dystonia, pigmentary retinopathy, spasticity, and cognitive decline. The typical MRI sign of the disease, known
Publikováno v:
Seizure. 42:49-51