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Epidemiology of Parkinson’s disease

Journal of Neural Transmission, 2017-08, Vol.124 (8), p.901-905

2017

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GBA and APOE Impact Cognitive Decline in Parkinson's Disease: A 10‐Year Population‐Based Study

Movement disorders, 2022-05, Vol.37 (5), p.1016-1027

2022

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Defective mitochondrial DNA homeostasis in the substantia nigra in Parkinson disease

Nature communications, 2016-11, Vol.7 (1), p.13548-11, Article 13548

2016

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Orthostatic hypotension in Parkinson disease: A 7-year prospective population-based study

Neurology, 2019-10, Vol.93 (16), p.e1526

2019

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The NADPARK study: A randomized phase I trial of nicotinamide riboside supplementation in Parkinson’s disease

Cell metabolism, 2022-03, Vol.34 (3), p.396-407.e6

2022

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Fatigue in Parkinson's Disease: A Proteomic Study of Cerebrospinal Fluid

Movement disorders, 2024-04, Vol.39 (4), p.749-751

2024

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Neuronal complex I deficiency occurs throughout the Parkinson’s disease brain, but is not associated with neurodegeneration or mitochondrial DNA damage

Acta neuropathologica, 2018-03, Vol.135 (3), p.409-425

2018

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NSAID use is not associated with Parkinson’s disease incidence: A Norwegian Prescription Database study

PloS one, 2021-09, Vol.16 (9), p.e0256602

2021

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European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERN EURO‐NMD)

European journal of neurology, 2024-06, Vol.31 (6), p.e16264-n/a

2024

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Association of CSF Glucocerebrosidase Activity With the Risk of Incident Dementia in Patients With Parkinson Disease

Neurology, 2023-01, Vol.100 (4), p.e388

2023

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Does vagotomy reduce the risk of Parkinson's disease?

Annals of neurology, 2015-12, Vol.78 (6), p.1011-1012

2015

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Laryngeal response patterns influence the efficacy of mechanical assisted cough in amyotrophic lateral sclerosis

Thorax, 2017-03, Vol.72 (3), p.221-229

2017

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Importance of motor vs. non-motor symptoms for health-related quality of life in early Parkinson's disease

Parkinsonism & related disorders, 2013-11, Vol.19 (11), p.1027-1032

2013

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Genome-wide histone acetylation analysis reveals altered transcriptional regulation in the Parkinson's disease brain

Molecular neurodegeneration, 2021-05, Vol.16 (1), p.31-20, Article 31

2021

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Identification of diagnostic and prognostic biomarkers of PD using a multiplex proteomics approach

Neurobiology of disease, 2023-10, Vol.186, p.106281-106281, Article 106281

2023

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Development of excessive daytime sleepiness in early Parkinson disease

Neurology, 2015-07, Vol.85 (2), p.162-168

2015

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Severe Hyperhomocysteinemia in a Patient with Parkinson Disease

Clinical chemistry (Baltimore, Md.), 2022-03, Vol.68 (3), p.396-401

2022

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Hyposmia in a simple smell test is associated with accelerated cognitive decline in early Parkinson's disease

Acta neurologica Scandinavica, 2018-12, Vol.138 (6), p.508-514

2018

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Development and validation of prognostic survival models in newly diagnosed Parkinson's disease

Movement disorders, 2018-01, Vol.33 (1), p.108-116

2018

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Association of GBA Genotype With Motor and Functional Decline in Patients With Newly Diagnosed Parkinson Disease

Neurology, 2021-02, Vol.96 (7), p.e1036

2021

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Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease

Movement disorders, 2018-10, Vol.33 (10), p.1591-1600

2018

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The GBA variant E326K is associated with Parkinson's disease and explains a genome-wide association signal

Neuroscience letters, 2017-09, Vol.658, p.48-52

2017

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Risk and course of motor complications in a population-based incident Parkinson's disease cohort

Parkinsonism & related disorders, 2016-01, Vol.22, p.48-53

2016

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Mitochondrial complex I deficiency stratifies idiopathic Parkinson’s disease

Nature communications, 2024-04, Vol.15 (1), p.3631-3631, Article 3631

2024

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The natural history of depressive symptoms in patients with incident Parkinson’s disease: a prospective cohort study

Journal of neurology, 2017-12, Vol.264 (12), p.2401-2408

2017

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Epidemiology of Parkinson’s disease

GBA and APOE Impact Cognitive Decline in Parkinson's Disease: A 10‐Year Population‐Based Study

Defective mitochondrial DNA homeostasis in the substantia nigra in Parkinson disease

Orthostatic hypotension in Parkinson disease: A 7-year prospective population-based study

The NADPARK study: A randomized phase I trial of nicotinamide riboside supplementation in Parkinson’s disease

Fatigue in Parkinson's Disease: A Proteomic Study of Cerebrospinal Fluid

Neuronal complex I deficiency occurs throughout the Parkinson’s disease brain, but is not associated with neurodegeneration or mitochondrial DNA damage

NSAID use is not associated with Parkinson’s disease incidence: A Norwegian Prescription Database study

European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERN EURO‐NMD)

Association of CSF Glucocerebrosidase Activity With the Risk of Incident Dementia in Patients With Parkinson Disease

Does vagotomy reduce the risk of Parkinson's disease?

Laryngeal response patterns influence the efficacy of mechanical assisted cough in amyotrophic lateral sclerosis

Importance of motor vs. non-motor symptoms for health-related quality of life in early Parkinson's disease

Genome-wide histone acetylation analysis reveals altered transcriptional regulation in the Parkinson's disease brain

Identification of diagnostic and prognostic biomarkers of PD using a multiplex proteomics approach

Development of excessive daytime sleepiness in early Parkinson disease

Severe Hyperhomocysteinemia in a Patient with Parkinson Disease

Hyposmia in a simple smell test is associated with accelerated cognitive decline in early Parkinson's disease

Development and validation of prognostic survival models in newly diagnosed Parkinson's disease

Association of GBA Genotype With Motor and Functional Decline in Patients With Newly Diagnosed Parkinson Disease

Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease

The GBA variant E326K is associated with Parkinson's disease and explains a genome-wide association signal

Risk and course of motor complications in a population-based incident Parkinson's disease cohort

Mitochondrial complex I deficiency stratifies idiopathic Parkinson’s disease

The natural history of depressive symptoms in patients with incident Parkinson’s disease: a prospective cohort study

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