Detalhe da pesquisa
1.
Multiple alpha-synuclein gene polymorphisms are associated with Parkinson's disease in a Norwegian population.
Acta Neurol Scand
; 118(5): 320-7, 2008 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-18485051
2.
DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function.
J Med Genet
; 41(3): e22, 2004 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-14985393
3.
Characterization of DCTN1 genetic variability in neurodegeneration.
Neurology
; 72(23): 2024-8, 2009 Jun 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-19506225
4.
PINK1 mutations and parkinsonism.
Neurology
; 71(12): 896-902, 2008 Sep 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-18685134
5.
Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1: redefining DYT14 as DYT5.
Neurology
; 70(16 Pt 2): 1377-83, 2008 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17804835
6.
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.
Neurology
; 70(16 Pt 2): 1456-60, 2008 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18337586
7.
Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication.
Neurology
; 68(12): 916-22, 2007 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-17251522
8.
LRRK2 mutations are a common cause of Parkinson's disease in Spain.
Eur J Neurol
; 13(4): 391-4, 2006 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-16643318
9.
LRRK2 mutations in Parkinson disease.
Neurology
; 65(5): 738-40, 2005 Sep 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-16157908
10.
Clinical and genetic evaluation of 8 Polish families with levodopa-responsive parkinsonism.
J Neural Transm (Vienna)
; 112(11): 1487-502, 2005 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-15785861
11.
alpha-Synuclein locus triplication causes Parkinson's disease.
Science
; 302(5646): 841, 2003 Oct 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-14593171