Etiology and pathogenesis of Parkinson's disease: From mitochondrial dysfunctions to familial Parkinson's disease

Clinical Neurology

Volumn 44, Issue 4-5, 2004, Pages 241-262

  Hattori, Nobutaka ^a  

^a JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINOPURINE; 4 HYDROXYNONENAL; 8 HYDROXYDEOXYGUANOSINE; ALPHA SYNUCLEIN; ALPHA SYNUCLEIN 22; CELL PROTEIN; MITOCHONDRIAL DNA; OXOGLUTARATE DEHYDROGENASE; PAEL RECEPTOR; PROTEIN CDCREL1; RECEPTOR PROTEIN; SUPEROXIDE DISMUTASE; UBIQUITIN PROTEIN LIGASE; UNCLASSIFIED DRUG;

ADULT; AGED; ALZHEIMER DISEASE; AMYOTROPHIC LATERAL SCLEROSIS; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 6; CLINICAL ARTICLE; CONFERENCE PAPER; CONTROLLED STUDY; DEGENERATIVE DISEASE; DENTATORUBROPALLIDOLUYSIAN ATROPHY; ENDOPLASMIC RETICULUM; ENVIRONMENTAL FACTOR; FAMILIAL DISEASE; FEMALE; GENE; GENE LOCATION; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC DISORDER; GENETIC LINKAGE; GENETIC POLYMORPHISM; GENETIC RISK; HUMAN; HUNTINGTON CHOREA; MACHADO JOSEPH DISEASE; MALE; MICROSATELLITE MARKER; MITOCHONDRIAL DNA DISORDER; MITOCHONDRIAL RESPIRATION; MOLECULAR CLONING; NERVE CELL LESION; NEUROPROTECTION; OXIDATION; PARKIN GENE; PARKINSON DISEASE; PATHOGENESIS; PROTEIN FUNCTION; RESPIRATORY FAILURE; RISK FACTOR; STRIATONIGRAL DEGENERATION; SYNAPSE VESICLE; TELOMERE; UBIQUITINATION;

CHROMOSOMES, HUMAN, PAIR 6; ELECTRON TRANSPORT COMPLEX I; FAMILY; FEMALE; HUMANS; MALE; MITOCHONDRIAL DISEASES; MUTATION; PARKINSON DISEASE; SUPEROXIDE DISMUTASE; UBIQUITIN-PROTEIN LIGASES;

EID: 3142585176     PISSN: 0009918X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

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