Invited Review

Redefining multiple sclerosis: 2024 McDonald diagnostic criteria

Hazal Ceren Manazoğlu, Murat Kürtüncü

Pages: 255-269 · DOI: 10.55697/tnd.2025.500
4024 2788

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
575 307

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
536 305

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
1818 327

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
496 288

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
591 421

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
490 375

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
420 249

Fenestration of the superior sagittal sinus in a ring configuration

Anton Ivanov, Sergey Kim

Pages: 362-369 · DOI: 10.55697/tnd.2025.353
467 320

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
494 272

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
572 304

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
506 232

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
492 292

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
492 237

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
499 236