Detalhe da pesquisa
1.
The filtering of the posturographic signals shows the age related features.
ScientificWorldJournal
; 2014: 403893, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-25587563
2.
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
Neuron
; 44(4): 601-7, 2004 Nov 18.
Artigo
Inglês
| MEDLINE | ID: mdl-15541309
3.
Reply to: "polychlorinated biphenyls in prospectively collected serum and Parkinson's disease risk".
Mov Disord
; 28(9): 1317, 2013 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-23813772
4.
Genes associated with Parkinson syndrome.
J Neurol
; 255 Suppl 5: 8-17, 2008 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-18787878
5.
Role of ethnicity on the association of MAPT H1 haplotypes and subhaplotypes in Parkinson's disease.
Eur J Hum Genet
; 15(11): 1163-8, 2007 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-17637803
6.
Randomized, double-blind, placebo-controlled trial on symptomatic effects of coenzyme Q(10) in Parkinson disease.
Arch Neurol
; 64(7): 938-44, 2007 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-17502459
7.
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2.
Brain
; 129(Pt 8): 2093-102, 2006 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-16714318
8.
Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study.
Arch Neurol
; 63(6): 826-32, 2006 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-16769863
9.
Brain potential signs of slowed stimulus processing following cholecystokinin in Parkinson's disease.
Psychopharmacology (Berl)
; 161(1): 70-6, 2002 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-11967633
10.
The striatal dopaminergic deficit is dependent on the number of mutant alleles in a family with mutations in the parkin gene: evidence for enzymatic parkin function in humans.
Neurosci Lett
; 323(1): 50-4, 2002 Apr 19.
Artigo
Inglês
| MEDLINE | ID: mdl-11911988
11.
Frequency of the D620N mutation in VPS35 in Parkinson disease.
Arch Neurol
; 69(10): 1360-4, 2012 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-22801713
12.
MDR1 variants and risk of Parkinson disease. Association with pesticide exposure?
J Neurol
; 256(1): 115-20, 2009 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-19184162
13.
Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation-dependent probe amplification.
Mov Disord
; 22(12): 1708-14, 2007 Sep 15.
Artigo
Inglês
| MEDLINE | ID: mdl-17674414
14.
Recurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease.
Mov Disord
; 21(9): 1506-10, 2006 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-16758483
15.
Case-control study of multiple system atrophy.
Mov Disord
; 20(2): 158-63, 2005 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-15382209
16.
Premutations in the FMR1 gene as a modifying factor in Parkin-associated Parkinson's disease?
Mov Disord
; 20(8): 1060-2, 2005 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-15929093
17.
Role of parkin mutations in 111 community-based patients with early-onset parkinsonism.
Ann Neurol
; 51(5): 621-5, 2002 May.
Artigo
Inglês
| MEDLINE | ID: mdl-12112109
18.
Distribution, type, and origin of Parkin mutations: review and case studies.
Mov Disord
; 19(10): 1146-57, 2004 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-15390068
19.
PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study.
Am J Hum Genet
; 70(5): 1089-95, 2002 May.
Artigo
Inglês
| MEDLINE | ID: mdl-11920285
20.
NR4A2 mutations are rare among European patients with familial Parkinson's disease.
Ann Neurol
; 54(3): 415, 2003 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-12953278