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
1378 1141

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
2104 1078

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
927 830

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
1066 959

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
1586 1100

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 1037

Cockayne Syndrome as a Rare Cause of Hemiplegia: Review of the Literature Accompanied by a Case Report

Beşir Şahin İnceer, Onur Bulut, Yılmaz Savaş

DOI: 10.4274/tnd.2018.49827

Issue: 2019, Volume 25 - Issue 1
0 843

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
0 976

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
0 752

Cerebral Palsy and Genetics

Nihan Hande Akçakaya, Zuhal Yapıcı, Uğur Özbek

DOI: 10.4274/tnd.67864

Issue: 2018, Volume 24 - Issue 1
0 708

Transthyretin-Related Familial Amyloid Polyneuropathy: In the Light of New Developments

Arman Çakar, Hacer Durmuş Tekçe, Feza Deymeer, Piraye Oflazer Serdaroğlu, Yeşim G Parman

DOI: 10.4274/tnd.03206

Issue: 2017, Volume 23 - Issue 3
0 1182

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
0 815

Colchicine-Related Polyneuropathy and Multiple Organ Failure

Ersel Dağ, Yakup Türkel, Burcu Gökçe

DOI: 10.4274/Tnd.04557

Issue: 2013, Volume 19 - Issue 2
0 1182

Neurosyphilis: Various Presentations

Kezban Aslan, Hacer Bozdemir, Şebnem Bıçakcı, Turgay Demir, İlker Öztürk, Tamer Çelik

DOI: 10.4274/Tnd.46794

Issue: 2012, Volume 18 - Issue 4
0 759

POEMS Syndrome: Report of Three Cases with Review of the Literature

Somanath Padhi, Tara Roshni Paul, Rajlaxmi Sarangi, Shantveer Uppin, Sundaram Challa, Putcha Deekshanti Narayan

Issue: 2011, Volume 17 - Issue 2
0 703

Early Diagnosis of Distal Peripheral Polyneuropathy Due to Glucose Metabolism Disorders via Intraepidermal Nerve Fiber Analysis

Oğuzhan Kurşun, Hülya Karataş, Kayıhan Uluç, Sevim Erdem Özdamar, Tomris Erbaş, Ersin Tan

Issue: 2009, Volume 15 - Issue 1
0 719

Van der Knaap Leukoencephalopathy Case Report

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

Issue: 2008, Volume 14 - Issue 1
0 683

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

Nazan SANER, A. Nazlı BAŞAK

Issue: 2006, Volume 12 - Issue 3
0 726

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
0 624

Androgen lnsensitivity Syndrome Associated with Sensory-Motor Polyneuropathy

A. Filiz KOÇ, Yakup SARICA, Cansun DEMİR

Issue: 2004, Volume 10 - Issue 6
0 513