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
668 414

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
347 315

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
337 429

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
416 335

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
0 371

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
0 290

Cerebral Palsy and Genetics

Nihan Hande Akçakaya, Zuhal Yapıcı, Uğur Özbek

DOI: 10.4274/tnd.67864

Issue: 2018, Volume 24 - Issue 1
0 230

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
0 309

Repetitive Transcranial Magnetic Stimulation in Patients with Hereditary Spastic Paraplegia

Mehmet Ağırman, Beyhan Eren, Evrim Karadağ Saygı

Issue: 2011, Volume 17 - Issue 2
0 1048

Van der Knaap Leukoencephalopathy Case Report

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

Issue: 2008, Volume 14 - Issue 1
0 279

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

Nazan SANER, A. Nazlı BAŞAK

Issue: 2006, Volume 12 - Issue 3
0 276

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
0 242

Trichothiodystrophy with neurologic involvement: an adult and fertil case

Hulusi KEÇECİ, Fatma SILAN, Ayşe KAVAK

Issue: 2004, Volume 10 - Issue 1
0 170

Joubert Syndrome: A Report of Three Cases

F. GENEL, D. ÖZDEMİR, N. URAN, F. ATLIHAN

Issue: 2000, Volume 6 - Issue 4
0 203

Sporadic Late Onset Cereberallar Ataxia with Photosensitive Myoclonus and Electrophysiological Evalution

Burhanettin ULUDAĞ, Sultan TARLACI

Issue: 1998, Volume 4 - Issue 3-4
0 249

Diagnostic Difficulties in a Case With Spinocerebellar Ataxia

Macit SELEKLER, Arif ÇELEBİ, Mefküre ERAKSOY

Issue: 1996, Volume 2 - Issue 1-2
0 191

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
0 168

Classification Of Hereditary Ataxias

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

Issue: 1995, Volume 1 - Issue 4
0 210

The role of spastin and paraplegin genes in primary progressive multiple sclerosis

Burak Çopuroğlu, Ali Ulvi Uca, Ayse Gul Zamani, Mahmut Selman Yıldırım, Mustafa Altaş, Betül Okur Altındaş

DOI: 10.55697/tnd.2024.12

Issue: 2024, Volume 30 - Issue 4
105 244