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Article

Differentiating symptomatic Parkin mutations carriers from patients with idiopathic Parkinson's disease: contribution of automated segmentation neuroimaging method.

Parkinsonism & related disorders - 1 Jun 2012

Bilgic Basar, Bayram Ali, Arslan Ali Bilgin, Hanagasi Hasmet, Dursun Burcu, Gurvit Hakan, Emre Murat, Lohmann Ebba

Abstract excerpt

BACKGROUND: Parkin (PARK2) gene mutations are the predominant cause of autosomal recessive parkinsonism. Characteristic features include: early onset symptoms with slow clinical course, good response to low doses of levodopa, and frequently treatment-induced dyskinesia. Studies using a voxel-base...

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PMID: 22445249
DOI: 10.1016/j.parkreldis.2012.02.017

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22445249-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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