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Journal of Medical Genetics|December 14, 2004
Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's diseaseM Martinez, A Brice, J R Vaughan, et al.
Neuroscience Letters|August 24, 1999
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's diseaseB S Harhangi, M J Farrer, S Lincoln, et al.
Rivista Di Neurologia|March 1, 1981
[Cerebral phospholipids and Parkinson's disease: cross-over double-blind study versus placebo]M Casacchia, G Meco, R Corona, et al.
European Journal of Physical and Rehabilitation Medicine|May 27, 2008
Exploring the use of ''Protocollo di Minima per l'ictus - PMIC'': preliminary data in two Italian rehabilitation unitsL Pratesi, S Paolucci, M Albuzza, et al.
Mechanisms of Ageing and Development|April 1, 1987
Enzyme histochemistry of monoamine oxidase in the heart of aged ratsM Meco, V Bonifati, W L Collier, et al.
Gait & Posture|January 21, 2014
Can overestimation of walking ability increase the risk of falls in people in the subacute stage after stroke on their return home?G Morone, M Iosa, L Pratesi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1986
Fast complex arm movements in Parkinson's diseaseA Berardelli, N Accornero, M Argenta, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseV Bonifati, G De Michele, C B Lücking, et al.
Annals of Neurology|August 26, 1998
The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's DiseaseJ Vaughan, A Durr, J Tassin, et al.
American Journal of Human Genetics|February 17, 2001
Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effectsM Periquet, C Lücking, J Vaughan, et al.
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