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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2007-4-10
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pubmed:abstractText |
Friedreich ataxia (FA) is the most frequent autosomal recessive cerebellar ataxia. Although the phenotype is well known, disease progression has not been evaluated in a prospective manner.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0003-9942
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pubmed:author |
pubmed-author:BéraudAnne-SophieAS,
pubmed-author:BriceAlexisA,
pubmed-author:CharlesPerrineP,
pubmed-author:DürrAlexandraA,
pubmed-author:GaspariniFranchescaF,
pubmed-author:KoenigMichelM,
pubmed-author:Le BerIsabelleI,
pubmed-author:MalletAlainA,
pubmed-author:PoussetFrançoiseF,
pubmed-author:RibaïPascaleP,
pubmed-author:Rivaud-PechouxSophieS,
pubmed-author:SchmittMicheleM,
pubmed-author:TanguyMarie-LaureML
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pubmed:issnType |
Print
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pubmed:volume |
64
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
558-64
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:17420319-Adolescent,
pubmed-meshheading:17420319-Adult,
pubmed-meshheading:17420319-Aged,
pubmed-meshheading:17420319-Antioxidants,
pubmed-meshheading:17420319-Benzoquinones,
pubmed-meshheading:17420319-Disease Progression,
pubmed-meshheading:17420319-Echocardiography,
pubmed-meshheading:17420319-Electrocardiography, Ambulatory,
pubmed-meshheading:17420319-Electrooculography,
pubmed-meshheading:17420319-Follow-Up Studies,
pubmed-meshheading:17420319-Friedreich Ataxia,
pubmed-meshheading:17420319-Humans,
pubmed-meshheading:17420319-Iron-Binding Proteins,
pubmed-meshheading:17420319-Middle Aged,
pubmed-meshheading:17420319-Neurologic Examination,
pubmed-meshheading:17420319-Paris,
pubmed-meshheading:17420319-Prospective Studies,
pubmed-meshheading:17420319-Time Factors,
pubmed-meshheading:17420319-Treatment Outcome,
pubmed-meshheading:17420319-Trinucleotide Repeat Expansion,
pubmed-meshheading:17420319-Ubiquinone
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pubmed:year |
2007
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pubmed:articleTitle |
Neurological, cardiological, and oculomotor progression in 104 patients with Friedreich ataxia during long-term follow-up.
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pubmed:affiliation |
Department of Genetics, Salpêtrière Medical School, Pierre and Marie Curie University, Paris, France.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, Non-U.S. Gov't
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