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Volumn 68, Issue 24, 2007, Pages 2157-
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Predominant dystonia with marked cerebellar atrophy: A rare phenotype in familial dystonia [3]
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NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
ADULT;
ATAXIA;
CASE REPORT;
CEREBELLUM;
CEREBELLUM ATROPHY;
CORRELATION ANALYSIS;
DISEASE COURSE;
DYSTONIA;
FEMALE;
GLUCOSE METABOLISM;
HUMAN;
LETTER;
MORPHOLOGY;
MORPHOMETRICS;
NUCLEAR MAGNETIC RESONANCE IMAGING;
PHENOTYPE;
PRIORITY JOURNAL;
ADULT;
ATROPHY;
CEREBELLAR ATAXIA;
CEREBELLAR DISEASES;
CEREBELLUM;
DYSTONIC DISORDERS;
FEMALE;
GENETIC PREDISPOSITION TO DISEASE;
GENOTYPE;
HUMANS;
MAGNETIC RESONANCE IMAGING;
MUTATION;
PHENOTYPE;
TATA-BOX BINDING PROTEIN;
VOICE DISORDERS;
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EID: 34250363020
PISSN: 00283878
EISSN: None
Source Type: Journal
DOI: 10.1212/01.wnl.0000269478.69285.7e Document Type: Letter |
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Times cited : (11)
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References (0)
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