Atypical tauopathy in a patient with LRRK2-G2019S mutation and tremor-dominant Parkinsonism.

Ruffmann, C; Giaccone, G; Canesi, M; Bramerio, M; Goldwurm, S; Gambacorta, M; Rossi, G; Tagliavini, F; Pezzoli, G

Ruffmann, C; Giaccone, G; Canesi, M; Bramerio, M; Goldwurm, S; Gambacorta, M; Rossi, G; Tagliavini, F; Pezzoli, G.

Neuropathol Appl Neurobiol ; 38(4): 382-6, 2012 Jun.

Article in En | MEDLINE | ID: mdl-21883375

Subject(s)

Mutation; Parkinsonian Disorders/genetics; Parkinsonian Disorders/pathology; Protein Serine-Threonine Kinases/genetics; Tauopathies/genetics; Tauopathies/pathology; Aged; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Parkinsonian Disorders/complications; Tauopathies/complications; Tomography, Emission-Computed, Single-Photon; Tremor/etiology; Tremor/genetics; Tremor/pathology

Fulltext

XML

PubMed Links

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein Serine-Threonine Kinases / Parkinsonian Disorders / Tauopathies / Mutation Type of study: Etiology_studies Limits: Aged / Humans / Male Language: En Journal: Neuropathol Appl Neurobiol Year: 2012 Document type: Article

Fulltext

XML

PubMed Links

Search on Google