Clinical features of Friedreich's ataxia: classical and atypical phenotypes-Reference-Cited by-同舟云学术

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Clinical features of Friedreich's ataxia: classical and atypical phenotypes

Published:2013-07-17 Issue: Volume:126 Page:103-117
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:J. Neurochem.

Author:

Parkinson Michael H.¹,Boesch Sylvia²,Nachbauer Wolfgang²,Mariotti Caterina³,Giunti Paola¹

Affiliation:

1. Department of Molecular Neuroscience; UCL Institute of Neurology; London UK

2. Department of Neurology; Medical University Innsbruck; Innsbruck Austria

3. Unit of Genetics of Neurodegenerative and Metabolic Disorders; Istituto Neurologico C Besta; Milan Italy

Funder

European Commission

Department of Health's National Institute for Health Research Biomedical Research Centres funding scheme

Dementias and Neurodegenerative Diseases Research Network

l'Associazione Italiana per la lotta alle Sindromi Atassiche

Deutsche Heredo-Ataxie Gesellschaft (DHAG), Ataxia UK and Ataxia Ireland

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jnc.12317/fullpdf

Reference113 articles.

1. Friedreich's ataxia: a clinical review with neurophysiological and echocardiographic findings;Ackroyd;Arch. Dis. Child.,1984

2. Superior cerebellar peduncle atrophy in Friedreich's ataxia correlates with disease symptoms;Akhlaghi;Cerebellum,2011

3. Genetic and family studies in Friedreuch's ataxia;Andermann;Can. J. Neurol. Sci.,1976

4. Exonic deletions of FXN and early-onset Friedreich ataxia;Anheim;Arch. Neurol.,2012

5. Expanding view of phenotype and oxidative stress in Friedreich's ataxia patients with and without idebenone;Arnold;Schweiz. Archiv. Neurol. Psychiatr.,2006

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