The curious case of phenocopies in families with genetic Parkinson's disease

Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease

(2010) Suzanne Lesage et al.   HUMAN MOLECULAR GENETICS

Prevalence and clinical features ofLRRK2mutations in patients with Parkinson’s disease in southern Spain

(2009) L. Gao et al.   EUROPEAN JOURNAL OF NEUROLOGY

Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease

(2009) S Lesage et al.   JOURNAL OF MEDICAL GENETICS

Pathogenesis of familial Parkinson’s disease: new insights based on monogenic forms of Parkinson’s disease

(2009) Taku Hatano et al.   JOURNAL OF NEUROCHEMISTRY

Neuropathological assessment of Parkinson's disease: refining the diagnostic criteria

(2009) Dennis W Dickson et al.   LANCET NEUROLOGY

Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

(2009) E. Sidransky et al.   NEW ENGLAND JOURNAL OF MEDICINE

Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2

(2008) Jose Bras et al.   BMC Neurology

Significance of the parkin and PINK1gene in Jordanian families with incidences of young-onset and juvenile parkinsonism

(2008) Ronny Myhre et al.   BMC Neurology

Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients

(2008) Karen Nuytemans et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Transcranial sonography findings in a large family with homozygous and heterozygous PINK1 mutations

(2008) J M Hagenah et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

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

(2008) Daniel G Healy et al.   LANCET NEUROLOGY