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Journal of Neurology|August 25, 1999
Absence of mutations in ATM, the gene responsible for ataxia telangiectasia in patients with cerebellar ataxiaS Hassin-Baer, A Bar-Shira, S Gilad, et al.Neurology|June 27, 2001
The nigrostriatal dopaminergic system in familial early onset parkinsonism with parkin mutationsA T Portman, N Giladi, K L Leenders, et al.European Journal of Neurology|January 16, 2007
Progression of dysautonomia in multiple system atrophy: a prospective study of self-perceived impairmentM Köllensperger, M Stampfer-Kountchev, K Seppi, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|March 7, 2013
A cross-sectional multicenter study of cognitive and behavioural features in multiple system atrophy patients of the parkinsonian and cerebellar typeC Siri, S Duerr, M Canesi, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|February 8, 2011
High prevalence of malignant melanoma in Israeli patients with Parkinson's diseaseR Inzelberg, J M Rabey, E Melamed, et al.European Journal of Neurology|January 31, 2016
Management of dystonia in Europe: a survey of the European network for the study of the dystonia syndromesA Valadas, M-F Contarino, A Albanese, et al.Parkinsonism & Related Disorders|November 5, 2013
Mobility, mood and site of care impact health related quality of life in Parkinson's diseaseJ G Nutt, A D Siderowf, M Guttman, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|July 29, 2005
The European Multiple System Atrophy-Study Group (EMSA-SG)F Geser, K Seppi, M Stampfer-Kountchev, et al.The New England Journal of Medicine|October 23, 2009
Multicenter analysis of glucocerebrosidase mutations in Parkinson's diseaseE Sidransky, M A Nalls, J O Aasly, et al.Pageof 11