Browsing by Author "Emre, Murat"
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Differentiating symptomatic Parkin mutations carriers from patients with idiopathic Parkinson’s disease: Contribution of automated segmentation neuroimaging method
Bilgic, Basar; Bayram, Ali; Arslan, Ali Bilgin; Hanagasi, Hasmet; Dursun, Burcu; Gurvit, Hakan; Emre, Murat; Lohmann, Ebba (2012-02-20)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, ...