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Pediatric Neurology

Volumn 26, Issue 1, 2002, Pages 51-54

Juvenile dentatorubral-pallidoluysian atrophy: New clinical features

(2) Licht, Daniel J a Lynch, David R a,b

a CHILDREN S HOSPITAL OF PHILADELPHIA (United States)

b UNIVERSITY OF PENNSYLVANIA (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; ATAXIA; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CEREBELLUM ATROPHY; CHROMOSOME 12; CLINICAL FEATURE; DENTATORUBROPALLIDOLUYSIAN ATROPHY; DISEASE ASSOCIATION; DISEASE COURSE; FEMALE; GEOGRAPHIC DISTRIBUTION; HEREDITY; HUMAN; HUNTINGTON CHOREA; INFANTILE AUTISM; LABORATORY TEST; MALE; MENTAL DEFICIENCY; MYOCLONUS EPILEPSY; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PATERNITY; PEDIGREE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; RACE DIFFERENCE; SEIZURE; SYMPTOMATOLOGY; TRINUCLEOTIDE REPEAT;

ADOLESCENT; ADULT; AUTISTIC DISORDER; CEREBELLUM; CHILD; ELECTROENCEPHALOGRAPHY; EPILEPSIES, MYOCLONIC; FEMALE; HUMANS; MALE; MENTAL RETARDATION; MYOCLONIC EPILEPSIES, PROGRESSIVE; NERVE TISSUE PROTEINS; PEDIGREE; PHOTIC STIMULATION; SEVERITY OF ILLNESS INDEX; SPINOCEREBELLAR DEGENERATIONS; TRINUCLEOTIDE REPEAT EXPANSION;

EID: 0036157660 PISSN: 08878994 EISSN: None Source Type: Journal
DOI: 10.1016/S0887-8994(01)00346-0 Document Type: Article

Times cited : (34)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.