Citations 60

Pathology of PD in monozygotic twins with a 20-year discordance interval

Neurology | May 13, 2012 | Volume: 56 | Issue: 7 | Pages: 981-982

10.1212/wnl.56.7.981 | PMID 11294946

Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese

Neurology | May 13, 2012 | Volume: 55 | Issue: 6 | Pages: 800-805

10.1212/wnl.55.6.800 | PMID 10993999

A kindred with Parkinson’s disease not showing genetic linkage to established loci

Neurology | May 13, 2012 | Volume: 54 | Issue: 2 | Pages: 504-504

10.1212/wnl.54.2.504 | PMID 10668726

Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson’s disease

Neurology | May 13, 2012 | Volume: 53 | Issue: 8 | Pages: 1858-1858

10.1212/wnl.53.8.1858 | PMID 10563640

A family with parkinsonism, essential tremor, restless legs syndrome, and depression

Neurology | May 9, 2011 | Volume: 76 | Issue: 19 | Pages: 1623-1630

10.1212/wnl.0b013e318219fb42 | PMID 21555728

MAPT H1 haplotype is a risk factor for essential tremor and multiple system atrophy

Neurology | February 15, 2011 | Volume: 76 | Issue: 7 | Pages: 670-672

10.1212/wnl.0b013e31820c30c1 | PMID 21321341

An independent replication of PARK16 in Asian samples

Neurology | December 14, 2010 | Volume: 75 | Issue: 24 | Pages: 2248-2249

10.1212/wnl.0b013e318202031f | PMID 21172849

O1‐07‐06: A genome‐wide association study of progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD)

Alzheimer's & Dementia | July 11, 2010 | Volume: 6 | Issue: 4S_Part_3 | Pages: No page available

10.1016/j.jalz.2010.05.254

MEIS1 p.R272H IN FAMILIAL RESTLESS LEGS SYNDROME

Neurology | July 20, 2009 | Volume: 73 | Issue: 3 | Pages: 243-245

10.1212/wnl.0b013e3181ae7c79 | PMID 19620614

Characterization of DCTN1 genetic variability in neurodegeneration

Neurology | June 8, 2009 | Volume: 72 | Issue: 23 | Pages: 2024-2028

10.1212/wnl.0b013e3181a92c4c | PMID 19506225