Frequency of the LRRK2 G2019S mutation in late-onset sporadic patients with Parkinson’s disease

Olfactory dysfunction in LRRK2 G2019S mutation carriers

(2011) R. Saunders-Pullman et al.   NEUROLOGY

Clinical and molecular neuroimaging characteristics of Brazilian patients with Parkinson's disease and mutations in PARK2 or PARK8 genes

(2010) Orlando G.P. Barsottini et al.   ARQUIVOS DE NEURO-PSIQUIATRIA

Genetic analysis of LRRK2 functional domains in Brazilian patients with Parkinson’s disease

(2010) C. B. Abdalla-Carvalho et al.   EUROPEAN JOURNAL OF NEUROLOGY

Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: Phenotypic characterization and frequency ofSNCA,PRKN,PINK1, andLRRK2mutations

(2009) Sarah Teixeira Camargos et al.   MOVEMENT DISORDERS

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

(2008) Daniel G Healy et al.   LANCET NEUROLOGY

Genetic and environmental findings in early-onset Parkinson's disease Brazilian patients

(2008) Patricia de Carvalho Aguiar et al.   MOVEMENT DISORDERS