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
289 346

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
511 340

Ophthalmic Features in SPA-8 with a Homozygous Missense Variant in the Homeobox Domain of the NKX6-2

Hidayet Şener, Duygu Gülmez Sevim, Murat Gültekin, Gülşah Şimşir, Ayşe Nazlı Başak

DOI: 10.4274/tnd.2022.00483

Issue: 2022, Volume 28 - Issue 1
283 248

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
254 357

Glucose Transporter Type 1 Deficiency Syndrome: A Single-Center Case Series

Miraç Yıldırım, Ömür Babayiğit, Fatma Ilgaz, Dilek Yalnızoğlu, Meral Topçu

DOI: 10.4274/tnd.2021.12979

Issue: 2021, Volume 27 - Issue 3
303 270

Anti-glutamic Acid Decarboxylase Antibody-associated Cerebellar Ataxia: A Case Report

Miray Atacan Yaşgüçlükal, Cansu Tunç, Muhammet Duran Bayar, Birgül Baştan, Sefer Günaydın, Belgin Petek Balcı, Özlem Çokar

DOI: 10.4274/tnd.2020.93457

Issue: 2021, Volume 27 - Issue 1
0 300

Diffusion Tensor Imaging in a Patient with Joubert Syndrome

Mehmet Haydar Atalar, Bülent Yıldız, Özlem Kayım Yıldız

DOI: 10.4274/tnd.2019.90912

Issue: 2019, Volume 25 - Issue 3
0 242

Posterior Reversible Encephalopathy Syndrome in the Late Postpartum Period: A Case Report

Merve Melodi Çakar, Sezgin Kehaya, Hülya Özkan, Babürhan Feyzullah Güldiken

DOI: 10.4274/tnd.65481

Issue: 2018, Volume 24 - Issue 4
0 242

Cerebral Palsy and Genetics

Nihan Hande Akçakaya, Zuhal Yapıcı, Uğur Özbek

DOI: 10.4274/tnd.67864

Issue: 2018, Volume 24 - Issue 1
0 187

Late-onset Tremor and Ataxia Syndrome: Fragile X-Associated Tremor/Ataxia Syndrome and Neuroimaging Findings

Levent Öcek, Onural Tümer, Figen Tokuçoğlu, Özgür Öztekin, Yaşar Zorlu

DOI: 10.4274/tnd.68878

Issue: 2017, Volume 23 - Issue 1
0 250

Van der Knaap Leukoencephalopathy Case Report

Çağla Soysüren, Ufuk Şener, Süleyman Men, Uğur Kulu, Yaşar Zorlu

Issue: 2008, Volume 14 - Issue 1
0 228

A Heterogeneous Group of Disorders: Spinocerebellar Ataxias, Their Genetic Bases and Molecular Diagnoses

Nazan SANER, A. Nazlı BAŞAK

Issue: 2006, Volume 12 - Issue 3
0 208

Ataxic Hemiparesis with Good Prognosis After Giant Pontine Hemorrhage

Necmettin YILDIZ, Hilmi UYSAL, Meltem DALYAN ARAS, Betül ORBAY, Füsun KÖSEOĞLU

Issue: 2005, Volume 11 - Issue 2
0 202

Trichothiodystrophy with neurologic involvement: an adult and fertil case

Hulusi KEÇECİ, Fatma SILAN, Ayşe KAVAK

Issue: 2004, Volume 10 - Issue 1
0 137

Sporadic Late Onset Cereberallar Ataxia with Photosensitive Myoclonus and Electrophysiological Evalution

Burhanettin ULUDAĞ, Sultan TARLACI

Issue: 1998, Volume 4 - Issue 3-4
0 192

Diagnostic Difficulties in a Case With Spinocerebellar Ataxia

Macit SELEKLER, Arif ÇELEBİ, Mefküre ERAKSOY

Issue: 1996, Volume 2 - Issue 1-2
0 152

EMG And Evoked Responses in Friedreicb's Ataxia

Abdullah ÖZKARDEŞ, Turgay GÜL, Fatih ÖZDAĞ, Hikmet DOLU, Okay VURAL, Muzaffer YARDIM

Issue: 1995, Volume 1 - Issue 4
0 139

Classification Of Hereditary Ataxias

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

Issue: 1995, Volume 1 - Issue 4
0 180