PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE

Known as: Parkinson Disease Autosomal Recessive, Early Onset, Parkinsonism, Early Onset, with Diurnal Fluctuation, Chromosome 6 Linked Autosomal Recessive Parkinsonism 
 
National Institutes of Health

Papers overview

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Review
2013
Review
2013
The past 15 years has witnessed tremendous progress in our understanding of the genetic basis for Parkinson's disease (PD… (More)
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Highly Cited
2013
Highly Cited
2013
Cerebral ischemia-reperfusion (I-R) is a complex pathological process. Although autophagy can be evoked by ischemia, its… (More)
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Review
2012
Review
2012
Several forms of autosomal recessive parkinsonism are known. In three forms, caused by mutations in parkin (PARK2), PINK1 (PARK6… (More)
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Review
2012
Review
2012
There has been tremendous progress toward understanding the genetic basis of Parkinson’s disease and related movement disorders… (More)
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Highly Cited
2010
Highly Cited
2010
Mutation of the gene PARK2, which encodes an E3 ubiquitin ligase, is the most common cause of early-onset Parkinson's disease. In… (More)
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Highly Cited
2009
Highly Cited
2009
Missense mutations in park2, encoding the parkin protein, account for approximately 50% of autosomal recessive juvenile Parkinson… (More)
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Highly Cited
2009
Highly Cited
2009
Mutations in PINK1 and PARK2 cause autosomal recessive parkinsonism, a neurodegenerative disorder that is characterized by the… (More)
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Highly Cited
2004
Highly Cited
2004
In many temporary wetlands such as those on the Northern Tablelands of New South Wales Australia, the development of plant… (More)
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Highly Cited
2004
Highly Cited
2004
BACKGROUND Mutations in the Parkin gene (PARK2) are the most commonly identified cause of recessively inherited early-onset… (More)
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Highly Cited
2003
Highly Cited
2003
Characterization of FRA6E (6q26), the third most frequently observed common fragile site (CFS) in the human population… (More)
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