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Movement Disorders : Official Journal of the Movement Disorder Society|May 13, 2010
Safety and efficacy of perampanel in advanced Parkinson's disease: a randomized, placebo-controlled studyKarla Eggert, David Squillacote, Paolo Barone, et al.
Acta Neuropathologica Communications|November 21, 2013
Rapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity?Gabor G Kovacs, Alexander Peden, Serge Weis, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 8, 2025
Update on Treatments for Parkinson's Disease Motor Fluctuations - An International Parkinson and Movement Disorder Society Evidence-Based Medicine ReviewRob M A de Bie, Regina Katzenschlager, Bart E K S Swinnen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 11, 2014
EuroInf: a multicenter comparative observational study of apomorphine and levodopa infusion in Parkinson's diseasePablo Martinez-Martin, Prashanth Reddy, Regina Katzenschlager, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 3, 2014
The onset of nonmotor symptoms in Parkinson's disease (the ONSET PD study)Claustre Pont-Sunyer, Anna Hotter, Carles Gaig, et al.
Parkinsonism & Related Disorders|July 21, 2015
Expert Consensus Group report on the use of apomorphine in the treatment of Parkinson's disease--Clinical practice recommendationsClaudia Trenkwalder, K Ray Chaudhuri, Pedro J García Ruiz, et al.
Brain : a Journal of Neurology|November 8, 2005
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic dataNaheed L Khan, Shushant Jain, John M Lynch, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 5, 2023
Levodopa Dose Equivalency in Parkinson's Disease: Updated Systematic Review and ProposalsStefanie T Jost, Marie-Ann Kaldenbach, Angelo Antonini, et al.
American Journal of Human Genetics|July 19, 2011
A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson diseaseAlexander Zimprich, Anna Benet-Pagès, Walter Struhal, et al.
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