Associated Papers
Cognitive Decline in Parkinsonism: From Clinical Phenotypes to the Genetic Background.
Koros C et al.
Biomedicines, 2025
The novel p.A30G SNCA pathogenic variant in Greek patients with familial and sporadic Parkinson's disease.
Alefanti I et al.
European Journal of Neurology, 2025
Monogenic Parkinson's Disease: Genotype, Phenotype, Pathophysiology, and Genetic Testing.
Jia F et al.
Genes, 2022
Screening LRRK2 gene mutations in patients with Parkinson's disease in Ghana.
Cilia R et al.
Journal of Neurology, 2012
A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients.
Shojaee S et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2009
Select a paper to view details