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BMC Neurology|June 27, 2019
Towards seeing the visual impairments in Parkinson's disease: protocol for a multicentre observational, cross-sectional studyCarlijn D J M Borm, Mario Werkmann, Femke Visser, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 7, 2011
The Movement Disorders task force review of dysautonomia rating scales in Parkinson's disease with regard to symptoms of orthostatic hypotensionAnne Pavy-Le Traon, Gerard Amarenco, Susanne Duerr, et al.Movement Disorders Clinical Practice|April 25, 2024
Early Screening for the Parkinson Variant of Multiple System Atrophy: A 6-Item ScoreAlessandra Fanciulli, Iva Stankovic, Omer Avraham, et al.The Lancet. Neurology|June 21, 2020
Safety and immunogenicity of the α-synuclein active immunotherapeutic PD01A in patients with Parkinson's disease: a randomised, single-blinded, phase 1 trialDieter Volc, Werner Poewe, Alexandra Kutzelnigg, et al.Neuroimage|February 22, 2003
Echogenicity of the substantia nigra in relatives of patients with sporadic Parkinson's diseasePetra Ruprecht-Dörfler, Daniela Berg, Oliver Tucha, et al.Plos One|February 19, 2013
Illicit stimulant use is associated with abnormal substantia nigra morphology in humansGabrielle Todd, Carolyn Noyes, Stanley C Flavel, et al.Journal of Alzheimer'S Disease : JAD|July 19, 2011
Serum and cerebrospinal fluid uric acid levels in lewy body disorders: associations with disease occurrence and amyloid-β pathwayWalter Maetzler, Anne Kathrin Stapf, Claudia Schulte, et al.Journal of Alzheimer'S Disease : JAD|February 17, 2010
The CST3 BB genotype and low cystatin C cerebrospinal fluid levels are associated with dementia in Lewy body diseaseWalter Maetzler, Benjamin Schmid, Matthis Synofzik, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 29, 2008
Autonomic dysfunction in different subtypes of multiple system atrophyClaudia Schmidt, Birgit Herting, Silke Prieur, et al.Acta Neurochirurgica|June 24, 2010
Polymorphisms in TGFB1 and PDGFRB are associated with Moyamoya disease in European patientsConstantin Roder, Vera Peters, Hidetoshi Kasuya, et al.Pageof 100