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Movement Disorders Clinical Practice|October 27, 2018
Pain in Parkinson's Disease: Current Concepts and a New Diagnostic AlgorithmVeit Mylius, Daniel Ciampi de Andrade, Rubens Gisbert Cury, et al.The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|August 8, 2020
Frailty and Prodromal Parkinson's Disease: Results From the HELIAD StudyEva Ntanasi, Maria Maraki, Mary Yannakoulia, et al.Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2019
Circulating Brain-enriched MicroRNAs for detection and discrimination of idiopathic and genetic Parkinson's diseaseStylianos Ravanidis, Anastasia Bougea, Nikolaos Papagiannakis, et al.Journal of Parkinson'S Disease|March 17, 2020
Serum Uric Acid Level as a Biomarker in Idiopathic and Genetic (p.A53T Alpha-Synuclein Carriers) Parkinson's Disease: Data from the PPMI StudyChristos Koros, Athina-Maria Simitsi, Dimitra Papadimitriou, et al.Parkinsonism & Related Disorders|August 23, 2021
Apathy: An underestimated feature in GBA and LRRK2 non-manifesting mutation carriersIoanna Pachi, Christos Koros, Athina M Simitsi, et al.Journal of Parkinson'S Disease|March 8, 2021
Serum Uric Acid in LRRK2 Related Parkinson's Disease: Longitudinal Data from the PPMI StudyAnastasia Bougea, Christos Koros, Nikolaos Papagiannakis, et al.Alzheimer'S & Dementia (Amsterdam, Netherlands)|July 18, 2022
Hepatic and renal function impact concentrations of plasma biomarkers of neuropathologyKacey Berry, Breton M Asken, Joshua D Grab, et al.Parkinsonism & Related Disorders|January 28, 2021
Serum uric acid level as a putative biomarker in Parkinson's disease patients carrying GBA1 mutations: 2-Year data from the PPMI studyChristos Koros, Athina-Maria Simitsi, Nikolaos Papagiannakis, et al.Plos Genetics|March 8, 2014
An epigenetic signature in peripheral blood associated with the haplotype on 17q21.31, a risk factor for neurodegenerative tauopathyYun Li, Jason A Chen, Renee L Sears, et al.Acta Neuropathologica|July 10, 2013
Modeling key pathological features of frontotemporal dementia with C9ORF72 repeat expansion in iPSC-derived human neuronsSandra Almeida, Eduardo Gascon, Hélène Tran, et al.Pageof 43