Yazar "Kotan, Dilcan" için listeleme
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Bilateral vertebral artery stenosis present with vertigo
Of ischaemic stroke patients, about 25% rise from the posterior or vertebrobasilar system. The ischaemia of vertebral arteries may emerge for different vascular pathological reasons, at different localisations and with ... -
A database for screening and registering late onset Pompe disease in Turkey
Çelik Gökyiğit, Münevver; Ekmekçi, Hakan; Durmuş, Hacer; Karlı, Necdet; Köseoğlu, Emel; Aysal, Fikret; Kotan, Dilcan; Ali, Asuman; Kahraman Koytak, Pınar; Karasoy, Hatice; Yaman, Aylin; Şengün, İhsan Şükrü; Sayın, Refah; Tiftikcioğlu, Bedile Irem; Soysal, Aysun; Tutkavul, Kemal; Oytun Bayrak, Ayşe; Kısabay, Ayşın; Elçi, Mehmet Ali; Yayla, Vildan; Yılmaz, İbrahim Arda; Özdamar, Sevim Erdem; Erdoğan, Çağdaş; Taşdemir, Nebahat; Oflazer, Zehra Piraye (Pergamon-Elsevier Science Ltd, 2018)The aim of this study was to search for the frequency of late onset Pompe disease (LOPD) among patients who had a myopathy with unknown diagnosis registered in the pre-diagnostic part of a novel registry for LOPD within a ... -
Dev i̇nternal karoti̇d arter anevri̇zmali bi̇r olgu
Kotan, Dilcan; Ünal, Gözde; Sayan, Saadet; Polat, Pınar; Bölük, Ayhan (Turkish Society of Cerebrovascular Diseases, 2013)Çapı 2,5 cm den büyük olan anevrizmalar, dev anevrizma olarak sınıflandırılır ve bütün intrakranyal anevrizmaların yaklaşık %5-8’ini oluşturur. Dev intrakranyal anevrizmalar subaraknoid kanama, kitle etkisi, nöbet ve ... -
A rare case, diagnosed as calcified callosal lipoma, when the patient presented with acute stroke
Özözen Ayas, Zeynep; Kotan, Dilcan; Polat, Pınar (2016)Intracranial lipomas are rare and generally located at pericallosal midline lesions. They are usually asymptomatic; when symptoms occur, they may depend on localization and include headache, seizure, psychomotor retardation, ... -
A rare cause of young stroke: Cerebral venous thrombosis
Kotan, Dilcan; Polat, Pınar (Sage Publications Ltd, 2014)... -
Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database
Tunca, Ceren; Şeker, Tuncay; Akçimen, Fulya; Coşkun, Cemre; Bayraktar, Elif; Palvadeau, Robin; Zor, Seyit; Koçoğlu, Cemile; Kartal, Ece; Şen, Nesli Ece; Hamzeiy, Hamid; Özoğuz Erimiş, Aslıhan; Norman, Utku; Karakahya, Oğuzhan; Olgun, Gülden; Akgün, Tahsin; Durmuş, Hacer; Şahin, Erdi; Çakar, Arman; Başar Gürsoy, Esra; Babacan Yıldız, Gülşen; İşak, Barış; Uluç, Kayıhan; Hanağası, Haşmet; Bilgiç, Başar; Turgut, Nilda; Aysal, Fikret; Ertaş, Mustafa; Boz, Cavit; Kotan, Dilcan; İdrisoğlu, Halil; Soysal, Aysun; Uzun Adatepe, Nurten; Akalın, Mehmet Ali; Koç, Filiz; Tan, Ersin; Oflazer, Piraye; Deymeer, Feza; Taştan, Öznur; Çiçek, Ercüment; Kavak, Ersen; Parman, Yeşim; Başak, Nazlı (Wiley, 2020)The last decade has proven that amyotrophic lateral sclerosis (ALS) is clinically and genetically heterogeneous, and that the genetic component in sporadic cases might be stronger than expected. This study investigates ... -
A spontaneous ruptured intracranial dermoid cyst in an older patient
Kotan, Dilcan; Sayan, Saadet; Polat, Pınar; Özözen Ayas, Zeynep (Wolters Kluwer Health, 2015)Dermoid cysts are rare cystic tumors originating from ectodermic cells within the intracranial region. These cysts emerge during closure of the neural tube during embryological development. The symptoms are generally ...