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Turkish Journal of Neurology
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Current Issue: 2025, Volume 31 - Issue 4

• Antiquity, past, present, and future of in vivo diagnosis of Alzheimer’s disease

  Hakan Gürvit

• 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

• 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

• 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

• 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