Genetic Dystonia-ataxia Syndromes: Clinical Spectrum, Diagnostic Approach, and Treatment Options

Author:

Rossi Malco1ORCID,Balint Bettina234,Millar Vernetti Patricio1,Bhatia Kailash P.2ORCID,Merello Marcelo15ORCID

Affiliation:

1. Movement Disorders Section, Neuroscience Department; Raul Carrea Institute for Neurological Research (FLENI); Buenos Aires Argentina

2. Sobell Department of Motor Neuroscience and Movement Disorders UCL Institute of Neurology, Queen Square; London WC1N3BG UK

3. Department of Neurology; University Hospital; Heidelberg Germany

4. Neuroimmunology Group, Nuffield Department of Clinical Neurosciences; John Radcliffe Hospital; Oxford UK

5. Argentine National Scientific and Technological Research Council (CONICET)

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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1. α‐Methylacyl‐CoA Racemase Deficiency in a Patient with Ataxia, Spasticity, and Segmental Dystonia;Movement Disorders Clinical Practice;2024-08-12

2. Canine paroxysmal dyskinesia—a review;Frontiers in Veterinary Science;2024-07-18

3. A Novel Variant in SQSTM1 Gene Causing Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy in a Peruvian Family;Movement Disorders Clinical Practice;2024-03-26

4. Inherited Dystonias;Reference Module in Neuroscience and Biobehavioral Psychology;2024

5. Dystonia Phenomenology;Reference Module in Neuroscience and Biobehavioral Psychology;2024

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