Articles with public access mandates - Jeon AnaLearn more
OverallNIHMichael J Fox FoundationNSFGenome CanadaNMRCNHMRCFWOCIHRNSERCASAPNSFCDFGINSERMNIHRParkinson's UKTelethonSwedish Research CouncilEuropean CommissionParkinson's Foundation, USANational Research Foundation, SingaporeSNSFVADBTDSTNWOA*StarAlzheimers's UKMotor Neurone Disease Association, UKMRCZonMwANRBMBFGovernment of ItalyUK Research & InnovationAASGovernment of Argentina
Not available anywhere: 19
Parkinson's disease in the Western Pacific Region
SY Lim, AH Tan, A Ahmad-Annuar, C Klein, LCS Tan, RL Rosales, ...
The Lancet Neurology 18 (9), 865-879, 2019
Mandates: Canadian Institutes of Health Research, National Medical Research Council …
Survival of Korean patients with multiple system atrophy
HJ Kim, BS Jeon, JY Lee, JY Yun
Movement disorders 26 (5), 909-912, 2011
Mandates: US National Institutes of Health
Retina thickness as a marker of neurodegeneration in prodromal lewy body disease
JY Lee, J Ahn, S Oh, JY Shin, YK Kim, H Nam, B Jeon
Movement Disorders 35 (2), 349-354, 2020
Mandates: US National Institutes of Health
DCTN1 p. K56R in progressive supranuclear palsy
EK Gustavsson, J Trinh, I Guella, C Szu-Tu, J Khinda, CH Lin, RM Wu, ...
Parkinsonism & Related Disorders 28, 56-61, 2016
Mandates: Canadian Institutes of Health Research, Genome Canada, Natural Sciences and …
Vestibular performance during high-acceleration stimuli correlates with clinical decline in SCA6
YE Huh, JS Kim, HJ Kim, SH Park, BS Jeon, JM Kim, JW Cho, DS Zee
The Cerebellum 14, 284-291, 2015
Mandates: US National Institutes of Health
Genetic variability of the retromer cargo recognition complex in parkinsonism
EK Gustavsson, I Guella, J Trinh, C Szu‐Tu, A Rajput, AH Rajput, ...
Movement Disorders 30 (4), 580-584, 2015
Mandates: US National Institutes of Health, Genome Canada
Two Parkinson's disease patients with α‐synuclein gene duplication and rapid cognitive decline
CW Shin, HJ Kim, SS Park, SY Kim, JY Kim, BS Jeon
Movement Disorders 25 (7), 957-959, 2010
Mandates: Swiss National Science Foundation
Role of ANO3 mutations in dystonia: a large-scale mutational screening study
L Olschewski, S Jesús, HJ Kim, S Tunc, S Löns, J Junker, KE Zeuner, ...
Parkinsonism & related disorders 62, 196-200, 2019
Mandates: US National Institutes of Health, Federal Ministry of Education and Research …
Serum inflammatory markers and progression of nonmotor symptoms in early Parkinson's disease
R Kim, HJ Kim, JH Shin, CY Lee, SH Jeon, B Jeon
Movement Disorders 37 (7), 1535-1541, 2022
Mandates: National Natural Science Foundation of China
Association of Physical Activity and APOE Genotype With Longitudinal Cognitive Change in Early Parkinson Disease
R Kim, S Park, D Yoo, JS Jun, B Jeon
Neurology 96 (19), e2429-e2437, 2021
Mandates: Michael J Fox Foundation
Apolipoprotein E ε4 genotype and risk of freezing of gait in Parkinson's disease
R Kim, JH Shin, S Park, HJ Kim, B Jeon
Parkinsonism & Related Disorders 81, 173-178, 2020
Mandates: Michael J Fox Foundation
SCA2 family presenting as typical Parkinson's disease: 34 year follow up
YE Kim, B Jeon, MJ Farrer, E Scott, I Guella, SS Park, JM Kim, HY Park, ...
Parkinsonism & Related Disorders 40, 69-72, 2017
Mandates: Genome Canada, Natural Sciences and Engineering Research Council of Canada
SCA6 presenting with young‐onset parkinsonism without ataxia
JY Yun, JM Kim, HJ Kim, YE Kim, BS Jeon
Movement disorders 27 (8), 1067-1068, 2012
Mandates: US National Institutes of Health, Motor Neurone Disease Association, UK
Longitudinal evolution of non-motor symptoms according to age at onset in early Parkinson's disease
R Kim, JH Shin, S Park, HJ Kim, B Jeon
Journal of the Neurological Sciences 418, 117157, 2020
Mandates: Michael J Fox Foundation
GBA mutations and Parkinson disease: When genotype meets phenotype
SW Scholz, BS Jeon
Neurology 84 (9), 866-867, 2015
Mandates: US National Institutes of Health
Impact of the apolipoprotein E ε4 allele on early Parkinson's disease progression
R Kim, S Park, D Yoo, JS Jun, B Jeon
Parkinsonism & Related Disorders 83, 66-70, 2021
Mandates: Michael J Fox Foundation
Novel LRRK2 mutations in Parkinsonism
J Trinh, I Guella, M McKenzie, EK Gustavsson, C Szu-Tu, MS Petersen, ...
Parkinsonism & Related Disorders 21 (9), 1119-1121, 2015
Mandates: Canadian Institutes of Health Research, Genome Canada, Natural Sciences and …
Potential sex-specific effects of apolipoprotein E ɛ4 on cognitive decline in early Parkinson’s disease
R Kim, S Park, D Yoo, Y Ju Suh, JS Jun, B Jeon
Journal of Parkinson's Disease 11 (2), 497-505, 2021
Mandates: Michael J Fox Foundation
Uncovering User Affect Towards AI in Cancer Diagnostics
ST Tong, P Sopory
Digital Human Modeling and Applications in Health, Safety, Ergonomics and …, 2019
Mandates: US National Science Foundation
Available somewhere: 36
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study
OA Ross, AI Soto-Ortolaza, MG Heckman, JO Aasly, N Abahuni, G Annesi, ...
The Lancet Neurology 10 (10), 898-908, 2011
Mandates: US National Institutes of Health, Research Foundation (Flanders), Genome …
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