Genetics of movement disorders and ataxia

Neurology in Practice

Volumn 73, Issue 2, 2002, Pages

  Jarman, Paul R ^a   Wood, Nicholas W ^a  

^a NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA SYNUCLEIN; PARKIN; NEUROLEPTIC AGENT; POLYGLUTAMINE; SULPIRIDE;

ARTICLE; ATAXIA; DYSKINESIA; DYSTONIA; ESSENTIAL TREMOR; GENE MUTATION; HUMAN; HUNTINGTON CHOREA; MOTOR DYSFUNCTION; NEUROACANTHOCYTOSIS; PARKINSON DISEASE; PARKINSONISM; PRIORITY JOURNAL; WILSON DISEASE; CHOREA; CLINICAL FEATURE; DRUG RESPONSE; GENE MAPPING; GENETIC ANALYSIS; HETEROZYGOTE DETECTION; MOLECULAR CLONING; PERSONALITY DISORDER; PHENOTYPE; PRENATAL DIAGNOSIS; REVIEW; SACCADIC EYE MOVEMENT;

AGE OF ONSET; ATAXIA; DYSTONIA; GENETIC SCREENING; HUMANS; HUNTINGTON DISEASE; MOVEMENT DISORDERS;

EID: 0036897477     PISSN: 14737086     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

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2. Valente EM, Warner TT, Jarman PR, et al. The role of DYT1 in primary torsion dystonia in Europe. Brain 1998;121:2335-9. Phenotype-genotype study of DYT1 dystonia in Europe.
3. Gasser T. Genetics of Parkinson's disease. J Neurol 2001;248:833-40.
4. Harding AE. Friedreich's ataxia: A clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features. Brain 1981;104:589-620.
5. Harding AE. The Hereditary Ataxias and Related Disorders. Edinburgh: Churchill Livingstone, 1984.