Current Issue: 2025, Volume 31 - Issue 4
Invited Review
Antiquity, past, present, and future of in vivo diagnosis of Alzheimer’s disease
Hakan Gürvit
Original Article
Association between urinary symptoms, quality of life, and pelvic floor function in females diagnosed with multiple sclerosis
Seda Kılıç, Ayşe Neriman Yılmaz, Murat Terzi
Relationship between education status and cerebrovascular disease awareness in patients with ischemic stroke
Gizem Gürsoy, Havva Tuğba Çelik
Digital subtraction angiography as an additional modality in idiopathic intracranial hypertension and its comparison with magnetic resonance venography: A prospective study
Kishor Kumar Paikara, Chandradev Sahu, Arpit Agrawal, Abhijeet Kumar Kohat, Anam Fatima
Audiovestibular findings according to the subtypes of multiple sclerosis
Fatmanur Uysal, Selim S. Erbek, Alper Köycü, Osman Halit Çam, Meliha Güleryüz
Development of restless legs syndrome severity prediction models for people with multiple sclerosis using machine learning
Ergi Kaya, Murat Emeç, Asiye Tuba Özdoğar, Ela Simay Zengin, Hilal Karakaş, Seda Daştan, Cavid Baba, Mehmet Hilal Özcanhan, Serkan Özakbaş
The effect of fingolimod on complete blood count, lipid panel, and relationship with clinicoradiologic features in patients with multiple sclerosis
Furkan Sarıdaş, Sarah Hamide Lazrak, Emine Rabia Koç, Güven Özkaya, Ömer Faruk Turan
Case Report
Isolated foot drop due to cerebral infarction: A rare presentation mimicking peroneal neuropathy
Zamoum Mourad, Kassouri Nora, Ameur El Koudoud Wahiba
Immune checkpoint inhibitor-related myositis with ocular manifestations and fatal outcome
Nuri Tuğra Uslucan, Merve Yavuz, Esra Aşıkdoğan, Emre Kumral
Short Communication
A diagnosis to consider in paralysis aggravated by excessive carbohydrate intake: Hypokalemic periodic paralysis associated with CACNA1S in a pediatric patient
Arife Derda Yücel Şen, Ahmet Baysal, Özlem Uğur Aydın, Kürşat Bora Çarman, Aslı Kavas Tufan, Oğuz Çilingir, Coşkun Yarar
Letter to the Editor
Genetic generalized epilepsy with a heterozygous missense variant in the chloride channel protein 2 gene responsive to perampanel
Murat Mert Atmaca, Candan Gürses
A rare pupillary phenomenon: Tadpole pupil
Cihat Ozguncu, Onur Bulut