A Rare Cause of Ataxia: SPG7 Mutation

Afra Çelik, Banu Özen Barut, Rahsan İnan

DOI: 10.4274/tnd.2021.22804

Issue: 2022, Volume 28 - Issue 3
228 302

Diagnostic Delay and Clinical Features in Friedreich’s Ataxia

Mehmet Fatih Yetkin, Murat Gültekin, Merve Akçakoyunlu, Recep Baydemir, Ayşe Sarılar, Mehmet Canpolat, Hüseyin Per

DOI: 10.4274/tnd.2022.26780

Issue: 2022, Volume 28 - Issue 2
424 296

Mild Encephalitis with Reversible Splenial Lesion Associated with COVID-19

Esra Demir, Berna Arlı

DOI: 10.4274/tnd.2021.24022

Issue: 2021, Volume 27 - Issue 3
183 249

Results of Special Neck Exercises in a Patient with Cerebellar Ataxia and Axial Myoclonus Due to ADCK3 Mutation

Özlem Menevşe, Sevil Bilgin, Murat Gültekin

DOI: 10.4274/tnd.2021.24196

Issue: 2021, Volume 27 - Issue 3
210 310

Family History of Headache and Epistaxis Associated with Ischemic Stroke

Eu Jene Choi, Dong Goo Lee, Do-Hyung Kim, Sang Hyun Jang

DOI: 10.4274/tnd.2020.48902

Issue: 2020, Volume 26 - Issue 4
0 272

Neurological Manifestation of Legionnaire’s Disease

Burcu Işık, Ferhat Arslan

DOI: 10.4274/tnd.2019.04317

Issue: 2019, Volume 25 - Issue 2
0 267

Inotersen Treatment for Patients with Hereditary Transthyretin Amyloidosis

Faruk Uğur Doğan, Murat Kürtüncü

DOI: 10.4274/tnd.2019.57224

Issue: 2019, Volume 25 - Issue 1
0 263

A Rare Presentation of Spontaneous Intracranial Hypotension

Cihat Uzunköprü, Volkan Çakır, Şehnaz Arıcı, Yeşim Beckmann

DOI: 10.4274/tnd.98624

Issue: 2018, Volume 24 - Issue 1
0 245

The Neurophysiologic Frequency of Hereditary Neuropathy with Liability to Pressure Palsy in Entrapment Neuropathies

F Gökçem Yıldız, Gülay Nurlu, Sevim Erdem Özdamar, Çağrı Mesut Temuçin

DOI: 10.4274/tnd.70446

Issue: 2016, Volume 22 - Issue 4
0 229

A Family with Vocal Cord Paralysis Associated with GDAP1 Mutation in Giresun, Turkey

Nilgün Erten, Esra Battaloğlu, Alperen Erdogan, Erdal Seren

DOI: 10.4274/tnd.38358

Issue: 2015, Volume 21 - Issue 3
0 217

Repetitive Transcranial Magnetic Stimulation in Patients with Hereditary Spastic Paraplegia

Mehmet Ağırman, Beyhan Eren, Evrim Karadağ Saygı

Issue: 2011, Volume 17 - Issue 2
0 688

Hereditary Neuropathy with Liability to Pressure Palsy: The Clinical and Electrophysiological Features of Four Families**

Ayşe Oytun Bayrak, Esra Battaloğlu, Handan Akar, İbrahim Barış, Musa Kazım Onar

Issue: 2010, Volume 16 - Issue 4
0 209

Hereditary Sensorimotor Neuropathy with Sensorineural Deafness(CMT4D ): A Case Report

Özgür BİLGİN, İpek MİDİ, Geysu KARLIKAYA, Neşe TUNCER ELMACI, Tülin TANRIDAĞ

Issue: 2004, Volume 10 - Issue 5
0 151

Hemiakinesia and ideomotor apraxia: A disconnection case report

Talip ASİL, Yahya ÇELİK, Ceren ELÇİN, Ufuk UTKU

Issue: 2004, Volume 10 - Issue 2
0 114

MRI findings of acute methanol intoxication: Case report

Şebnem ÖRGÜÇ, Serap IŞLAK, Serdar TARHAN, Gönül TEZCAN KELEŞ, Yüksel PABUŞÇU

Issue: 2004, Volume 10 - Issue 2
0 140

Classification Of Hereditary Ataxias

Aysun SOYSAL, Sibel ÇETİN, Feriha ÖZER, Okan DOĞU, Hüseyin SARI, Baki ARPACI

Issue: 1995, Volume 1 - Issue 4
0 163