Movement Disorders in Autosomal Dominant Cerebellar Ataxias: A Systematic Review-Reference-Cited by-同舟云学术

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Movement Disorders in Autosomal Dominant Cerebellar Ataxias: A Systematic Review

Published:2014-06-06 Issue:3 Volume:1 Page:154-160
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Mov Disord Clin Pract

Author:

Rossi Malco¹,Perez-Lloret Santiago²³,Cerquetti Daniel¹,Merello Marcelo¹³

Affiliation:

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

2. Clinical Pharmacology and Epidemiology Laboratory; Pontifical Catholic University of Argentina; Buenos Aires Argentina

3. Argentine National Scientific and Technological Research Council (CONICET); Buenos Aires Argentina

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mdc3.12042/fullpdf

Reference38 articles.

1. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond;Durr;Lancet Neurol,2010

2. Extrapyramidal motor signs in degenerative ataxias;Schols;Arch Neurol,2000

3. SCA-2 presenting as parkinsonism in an Alberta family: clinical, genetic, and PET findings;Furtado;Neurology,2002

4. Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes;Stevanin;Brain.,2003

5. SCA2 may present as levodopa-responsive parkinsonism;Payami;Mov Disord,2003

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1. Data-Driven Analysis of Patients’ Body Language in Healthcare: A Comprehensive Review;IEEE Access;2024

2. Writer's Cramps as an Initial Symptom of Spinocerebellar Ataxia Type 14: A Case Report;Internal Medicine;2024

3. Parkinsonism in complex neurogenetic disorders: lessons from hereditary dementias, adult-onset ataxias and spastic paraplegias;Neurological Sciences;2023-08-30

4. Deep brain stimulation in Dopa-Responsive Parkinsonism – Look out for red flags: Expert commentary;Parkinsonism & Related Disorders;2023-05

5. Rapidly Progressive Atypical Parkinsonism as a Presenting Feature of ATX‐CACNA1G (SCA42);Movement Disorders Clinical Practice;2023-03-16

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