Abstract:
:The discovery of SNCA mutations pathogenic for autosomal-dominant Lewy body Parkinson's disease (PD) in 1997 heralded a revolution in understanding the molecular and genetic basis of PD. Indeed, it now is clear that Lewy body PD is one of many neurodegenerative parkinsonian disorders that result from nigrostriatal degeneration caused by diverse mechanisms. However, to capitalize on these new insights and facilitate efforts to improve the diagnosis and therapy of neurodegenerative movement disorders, it is timely to define a nosology for these diseases that is based on their genetic and molecular underpinnings, as proposed here.
journal_name
Neuronjournal_title
Neuronauthors
Forman MS,Lee VM,Trojanowski JQdoi
10.1016/j.neuron.2005.07.021subject
Has Abstractpub_date
2005-08-18 00:00:00pages
479-82issue
4eissn
0896-6273issn
1097-4199pii
S0896-6273(05)00641-0journal_volume
47pub_type
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