Autosomal recessive early-onset parkinsonism with diurnal fluctuation: Clinicopathologic characteristics and molecular genetic identification

Brain and Development

Volumn 22, Issue SUPPL. 1, 2000, Pages 87-91

  Yamamura, Yasuhiro ^a   Hattori, Nobutaka ^b   Matsumine, Hiroto ^b   Kuzuhara, Shigeki ^c   Mizuno, Yoshikuni ^b  

^a HIROSHIMA UNIV SCHOOL OF MEDICINE   (Japan)

^b JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c MIE UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Autosomal recessive parkinsonism; Diurnal fluctuation; Early onset parkinsonism; Nigral neuronal death; Parkin gene

Indexed keywords

AMANTADINE; ANTIPARKINSON AGENT; BROMOCRIPTINE; DOPA DECARBOXYLASE INHIBITOR; LEVODOPA; NEUROLEPTIC AGENT; PERGOLIDE; TRIHEXYPHENIDYL;

AUTOSOMAL RECESSIVE INHERITANCE; CIRCADIAN RHYTHM; CLINICAL ARTICLE; CLINICAL TRIAL; CONFERENCE PAPER; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DELETION MUTANT; DISEASE COURSE; DYSKINESIA; DYSTONIA; FAMILY; FEMALE; GENETIC ANALYSIS; GENETIC LINKAGE; HALLUCINATION; HUMAN; LOCUS CERULEUS; MALE; NERVE CELL LESION; ONSET AGE; PARKINSONISM; SUBSTANTIA NIGRA; TENDON REFLEX;

EID: 0033849550     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0387-7604(00)00130-3     Document Type: Conference Paper

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