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PARKINSON DISEASE, LATE-ONSET

Known as: PARK, PD 
 
National Institutes of Health

Papers overview

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2018
2018
Given the rapidly increasing number of reported movement disorder genes and clinical-genetic desciptions of mutation carriers… Expand
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2016
2016
Objective: To assess whether Parkinson disease (PD) genes are somatically mutated in cutaneous melanoma (CM) tissue, because CM… Expand
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2016
2016
A new electron density profile reconstruction procedure based on the PARK-matrix method has been firstly exploited for the multi… Expand
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2014
2014
BACKGROUND Tremulous Parkinson's disease (PD) and essential tremor are well known to be associated, but characteristics of… Expand
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Highly Cited
2014
Highly Cited
2014
Kufor–Rakeb syndrome (KRS) is caused by loss-of-function mutations in ATP13A2 (PARK9) and characterized by juvenile-onset… Expand
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Review
2012
Review
2012
  • N. Hattori
  • Parkinsonism & related disorders
  • 2012
  • Corpus ID: 40490577
Recently, several genes for parkinsonism have been identified. Among them, familial Parkinson's disease (PD) could be assigned… Expand
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Highly Cited
2012
Highly Cited
2012
  • F. Coppedè
  • TheScientificWorldJournal
  • 2012
  • Corpus ID: 17719325
In 1997 a mutation in the a-synuclein (SNCA) gene was associated with familial autosomal dominant Parkinson's disease (PD). Since… Expand
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Review
2008
Review
2008
BACKGROUND The early recognition of stroke signs and symptoms is of great relevance concerning the outcome, since it enhances the… Expand
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Highly Cited
2008
Highly Cited
2008
Mutations in five PARK genes (SNCA, PARKIN, DJ-1, PINK1, and LRRK2) are well-established genetic causes of Parkinson disease (PD… Expand
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Review
1999
Review
1999
  • H. Matsumine
  • Rinsho shinkeigaku = Clinical neurology
  • 1999
  • Corpus ID: 25638429
We identified a PARK 2 (AR-JP) family with a patient presenting with homozygous deletion of D 6 S305--a marker within the 17cM… Expand
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