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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
11
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pubmed:dateCreated |
2010-11-9
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pubmed:abstractText |
Mitochondrial diseases are characterized by wide phenotypic and genetic variability, but presentations in adults with akinetic rigidity and hyperkinetic movement disorders are rare.
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pubmed:grant |
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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 |
Nov
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pubmed:issn |
1538-3687
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
67
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1399-402
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pubmed:dateRevised |
2011-1-5
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pubmed:meshHeading |
pubmed-meshheading:21060018-Atrophy,
pubmed-meshheading:21060018-Brain,
pubmed-meshheading:21060018-Dementia,
pubmed-meshheading:21060018-Disease Progression,
pubmed-meshheading:21060018-Female,
pubmed-meshheading:21060018-Humans,
pubmed-meshheading:21060018-Magnetic Resonance Imaging,
pubmed-meshheading:21060018-Middle Aged,
pubmed-meshheading:21060018-Mitochondrial Diseases,
pubmed-meshheading:21060018-Muscle Rigidity,
pubmed-meshheading:21060018-Mutation,
pubmed-meshheading:21060018-Neurodegenerative Diseases,
pubmed-meshheading:21060018-Neuropsychological Tests,
pubmed-meshheading:21060018-Phenylalanine,
pubmed-meshheading:21060018-RNA, Transfer
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pubmed:year |
2010
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pubmed:articleTitle |
Mitochondrial transfer RNA(Phe) mutation associated with a progressive neurodegenerative disorder characterized by psychiatric disturbance, dementia, and akinesia-rigidity.
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pubmed:affiliation |
Essex Centre for Neurological Sciences, Queen's Hospital, Romford RM7 0AG, United Kingdom.
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
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