Invited Review

Redefining multiple sclerosis: 2024 McDonald diagnostic criteria

Hazal Ceren Manazoğlu, Murat Kürtüncü

Pages: 255-269 · DOI: 10.55697/tnd.2025.500
2623 1510

Original Article

Digital transformation of the Turkish national neurology board examination: Implementation and candidates’ feedback

S. Ayhan Çalışkan, Gülşen Taşdelen Teker, Hatice Mavioğlu, Özgül Ekmekci, Figen Gökçay, Figen Eşmeli, Semiha Kurt, Füsun Ferda Erdoğan, Meltem Demirkiran, Bijen Nazlıel, Esen Saka

Pages: 270-277 · DOI: 10.55697/tnd.2025.383
389 217

The impact of COVID-19 pandemic on adult individuals with neuromuscular disease

Muhammed Kılınç, Ender Ayvat, Özge Onursal Kılınç, Fatma Ayvat, Mert Doğan, Gülşah Sütçü Uçmak, Can Ebru Bekircan Kurt, Sevim Erdem Özdamar, Sibel Aksu Yıldırım, Ersin Tan

Pages: 294-300 · DOI: 10.55697/tnd.2025.358
334 202

Liquid embolization agents for arteriovenous malformations: A preliminary experience from a tertiary care teaching hospital

Himanshu Kaushal, Gourav Goyal, Yogesh Kaushik, Ira Chaudhary, Jatinkumar Vijaykumar Jain

Pages: 301-309 · DOI: 10.55697/tnd.2025.365
1494 205

Ventral striatal dopaminergic loss drives dopamine dysregulation syndrome-like behaviors in an experimental model of parkinsonism

Esra Özkan, Gül Yalçın Çakmakli, Özgür Öztop Çakmak, Esen Saka Topçuoğlu

Pages: 310-318 · DOI: 10.55697/tnd.2025.487
304 191

Monocytes and systemic inflammation in Guillain-Barré syndrome: Subtypes and relationship with prognosis

Memet Aslanyavrusu, Fahrettin Ege, Gülhan Sarıçam

Pages: 334-340 · DOI: 10.55697/tnd.2025.508
379 310

Case Report

Long-term cladribine experience in relapsing-remitting multiple sclerosis

Ömer Faruk Turan, Furkan Sarıdaş, Emine Rabia Koç

Pages: 354-358 · DOI: 10.55697/tnd.2025.293
283 233

An uncommon case with coexistence of Down syndrome and Duchenne muscular dystrophy

Abdulkerim Elmas, Mustafa Akçam

Pages: 359-361 · DOI: 10.55697/tnd.2025.309
271 157

Fenestration of the superior sagittal sinus in a ring configuration

Anton Ivanov, Sergey Kim

Pages: 362-369 · DOI: 10.55697/tnd.2025.353
287 194

Letter to the Editor

A novel mutation of the NKX2-1 gene: A late-onset diagnosis of benign hereditary chorea

Buse Çağla Ari, Sezin Canbek, Gülay Kenangil

Pages: 370-374 · DOI: 10.55697/tnd.2025.443
323 193

A case of stroke with epilepsy, drug-induced encephalopathy, and movement disorder

Murat Mert Atmaca, Candan Gürses

Pages: 375-379 · DOI: 10.55697/tnd.2025.245
373 237

Paroxysmal kinesigenic dyskinesia arising from isolated thalamic infarction: A rare convergence

İsmail Koç, Serap Kökoğlu, Nuriye Kayalı Şendur

Pages: 380-382 · DOI: 10.55697/tnd.2025.317
329 165

A rare case of subclavian steal phenomenon with anterograde vertebral artery flow

Ahmet Yabalak, Osman Kayapınar

Pages: 383-385 · DOI: 10.55697/tnd.2025.313
341 213

Comment to the article: Methyl alcohol intoxication in İzmir

Tuğçe Mengi, Hüseyin Özkök, Özlem Öner, Erdem Yaka, Bilgin Cömert, Ali Necati Gökmen

Pages: 386-387 · DOI: 10.55697/tnd.2025.274
347 154

Response to the comment on: Methyl Alcohol Intoxication in İzmir

Hasan Armağan Uysal, Halil Güllüoğlu, Müge Kuzu Kumcu, Fatma Nazlı Durmaz Çelik

Pages: 388-389 · DOI: 10.55697/tnd.2025.148
336 170