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1 Parkinson disease (PD) is a devastating, largely nonfami
2 Parkinson disease (PD), the most common movement disorde
3 Parkinson disease is a heterogeneous disease with rapidl
4 Parkinson disease is characterized by motor and nonmotor
5 Parkinson's disease (PD) affects millions of patients wo
6 Parkinson's disease (PD) is a common neurodegenerative d
7 Parkinson's disease (PD) is a multifactorial malady and
8 Parkinson's disease (PD) is a progressive neurodegenerat
9 Parkinson's disease (PD) is characterized by dopaminergi
10 Parkinson's disease (PD) pathogenesis may involve the ep
11 Parkinson's disease is a synucleinopathy that is charact
12 Parkinson's disease is caused by a loss of dopaminergic
13 Parkinson's disease is characterized by the presence of
14 Parkinson's disease is the second most common neurodegen
15 Parkinson's disease protein 7 (PARK7/DJ-1) was successfu
16 probable dementia with Lewy bodies (n = 1), Parkinson disease with mild cognitive impairment (n = 2)
17 We studied 22 individuals [8 Stroke and 14 Parkinson Disease (PD) subjects aged between 41 and 75 y
18 es and 180 355 controls), we identified 1691 Parkinson's disease cases, 81 Lewy body dementia cases,
20 cohort of patients with early MSA (n = 38), Parkinson disease (PD, n = 16), and dementia with Lewy b
21 ls (22 757 Parkinson's disease cases, 13 431 Parkinson's disease proxy cases, 622 Lewy body dementia
22 asets, totalling 217 165 individuals (22 757 Parkinson's disease cases, 13 431 Parkinson's disease pr
23 k factor for neurologic disorders, such as a Parkinson's disease-like syndrome known as manganism.
24 rative disorders (ND) like Alzheimer's (AD), Parkinson's (PD), Huntington's or Prion diseases share s
25 nts with de novo Parkinson disease, advanced Parkinson disease, and healthy control participants.
28 mortem studies on two patients with advanced Parkinson's disease 8 and10 years following AAV2-neurtur
29 tion of microglial activation with advancing Parkinson's disease, we investigated whether CSF and/or
33 alleles that have been identified, although Parkinson's disease risk variants appear to be in close
34 alcohol-use disorder (34%, P = 0.00084) and Parkinson disease (34%, P = 0.0032) than in their corres
35 y or corticobasal syndrome (AUC=88.47%), and Parkinson's disease or multiple systems atrophy (AUC=81.
36 neuron-specific protein PGP9.5 (PGP9.5) and Parkinson disease 5 (PARK5), a DUB active in neurons tha
37 n the brains of Alzheimer's disease (AD) and Parkinson's disease (PD) with dementia (PDD) patients, w
39 is, mild cognitive impairment, dementia, and Parkinson's disease, supporting the relevance of brainst
42 e between idiopathic Parkinson's disease and Parkinson's disease linked to heterozygous PRKN/PINK1 mu
45 ssociation between the use of glitazones and Parkinson's disease [incidence rate ratio (IRR) 1.17; 95
51 ral sclerosis (ALS), multiple sclerosis, and Parkinson's disease, peripheral nervous system (PNS) dis
55 ifferences between synucleinopathies such as Parkinson's disease and multiple system atrophy have bee
56 eature of neurodegenerative diseases such as Parkinson's disease, Alzheimer's disease and multiple sc
57 f treatments for related conditions, such as Parkinson's disease, for the management of common sympto
58 trigger a series of human diseases, such as Parkinson's disease, multifactor disorder and Type-II di
59 d Yahr scale, Montreal Cognitive Assessment, Parkinson's Disease Questionnaire-39 and PD subtype asse
60 a dual pharmacological action of attenuating Parkinson's disease (PD) motor symptoms and development
62 ations in alpha-synuclein are linked to both Parkinson's disease and Lewy body dementia; in particula
63 10 (C10) were recently identified as causing Parkinson's disease and amyotrophic lateral sclerosis/fr
64 erformance (AUC=0.86) in separating clinical Parkinson's disease from controls across populations.
66 esent study profiled two EMVs from different Parkinson's disease (PD) tissue sources: (a) neural prog
67 d multiple protein ratios that differentiate Parkinson's disease from healthy controls and validated
69 e system atrophy (MSA), Parkinson's disease, Parkinson's disease with dementia and dementia with Lewy
71 brain maladies such as Alzheimer's disease, Parkinson's disease, brain lymphomas, and other ailments
72 tween LNB and dementia, Alzheimer's disease, Parkinson's disease, motor neuron disease, epilepsy, and
73 term risks of dementia, Alzheimer's disease, Parkinson's disease, motor neuron diseases, epilepsy, or
74 ased risks of dementia, Alzheimer's disease, Parkinson's disease, motor neuron diseases, or epilepsy.
75 implicated in the neurodegenerative disorder Parkinson's disease (PD); however, it is unclear how mit
76 pid eye movement sleep behavioural disorder, Parkinson's disease, dementia with Lewy bodies, multiple
78 192, 33.85%) than in the autosomal-dominant Parkinson's disease cohort (10 of 242, 4.13%) and the sE
80 ibrillar alpha-Syn polymorphs trigger either Parkinson's disease or multiple system atrophy hallmarks
83 s the most commonly mutated gene in familial Parkinson's disease(1) and is also linked to its idiopat
87 ary refers to 'Brain-first versus body-first Parkinson's disease: a multi-modal imaging case-control
88 ired, now that gene-targeting approaches for Parkinson's disease have reached the clinical trial stag
97 We show that the common genetic risk for Parkinson's disease (PD) is associated with dopaminergic
101 mpairment) on the phenotype of LRRK2 and GBA Parkinson's disease (PD), and on the prevalence of prodr
104 potential to discriminate between idiopathic Parkinson's disease and Parkinson's disease linked to he
107 We also analyzed six cases of idiopathic Parkinson's disease (PD), one case of familial PD, and s
108 PRKN/PINK1 mutations compared to idiopathic Parkinson's disease, which is in line with previous find
110 mography (PET) imaging that is used to image Parkinson's disease, brain tumors, and focal hyperinsuli
116 a-synuclein, a protein known to aggregate in Parkinson's disease, dementia with Lewy bodies, and mult
117 m human studies on microbiome alterations in Parkinson's disease, Alzheimer's disease, amyotrophic la
119 identifies several novel protein changes in Parkinson's disease cerebrospinal fluid that may be expl
123 nucleus deep brain stimulation (STN-DBS) in Parkinson's disease (PD) not only stimulates focal targe
125 transplantation can rescue motor defects in Parkinson's disease (PD) models, whether and how grafts
130 tiple brain disorders and injuries, e.g., in Parkinson's disease or traumatic brain injury (TBI), and
131 nges that accompany visual hallucinations in Parkinson's disease and the organizational and gene expr
132 of alpha-synuclein, a protein implicated in Parkinson's disease that predominately nucleates on memb
135 n brain and drives symptom lateralization in Parkinson's disease (PD), but its molecular determinants
137 he potential of IL6 as progression marker in Parkinson's disease due to PRKN/PINK1 mutations; (iii) i
141 proteolytic truncations of alphasyn occur in Parkinson's disease, Lewy body dementia, and multiple sy
144 s now known that the pathological process in Parkinson disease may begin decades before the clinical
145 re, we demonstrate that Netrin1 reduction in Parkinson's disease (PD) activates MST1, which selective
146 he demonstrated implication of the retina in Parkinson disease (PD) pathology and the importance of d
148 ta activity is linked to symptom severity in Parkinson's disease (PD), but few studies have character
149 the substantia nigra pars compacta (SNpc) in Parkinson disease (PD) is not uniform, as dopamine neuro
151 m is one of most common nonmotor symptoms in Parkinson's disease (PD), but the molecular role of the
154 tau in Alzheimer disease, alpha-synuclein in Parkinson disease, and TAR DNA-binding protein 43 in amy
155 ghlight the importance of genetic testing in Parkinson's disease patients with age at onset < 40 year
156 Data mining of the brain transcriptome in Parkinson disease patients supported CR4 as an active al
158 ting neurodegenerative conditions, including Parkinson's disease (PD), dementia with Lewy bodies (DLB
160 ons in neurodegenerative diseases, including Parkinson's disease, Lewy body dementia, and multiple sy
161 ed neurological movement disorders including Parkinson's Disease (PD) and Essential Tremor (ET).
166 genic/likely pathogenic variants in 23 known Parkinson's disease-associated genes occurred more frequ
168 nts appear to be in close proximity to known Parkinson's disease genes and lysosomal-related genes.
173 ifferentiate, using a physiological measure, Parkinson's disease patients with impulse control disord
175 which include multiple system atrophy (MSA), Parkinson's disease, Parkinson's disease with dementia a
177 11; 11 women), 29 participants with de novo Parkinson disease (64 years +/- 10; 19 men), and 31 part
178 d October 2015 for participants with de novo Parkinson disease, advanced Parkinson disease, and healt
180 gh our understanding of the genetic basis of Parkinson's disease has advanced considerably, much rema
181 repeat kinase 2 (LRRK2) is a common cause of Parkinson's disease (PD) and results in age-related dopa
182 les, representing 40 patients) consisting of Parkinson's disease and healthy control samples from thr
183 potential to influence the disease course of Parkinson's disease, at least in this subset of patients
184 ia/macrophage derived exosomes in the CSF of Parkinson's disease patients, we confirmed the presence
190 SNCA has been implicated in the etiology of Parkinson's disease (PD); however, the normal function o
191 st genetic and environmental risk factors of Parkinson's disease, whereas loss of ATP13A2 compromises
194 in one hemisphere improved motor features of Parkinson's disease in selected patients with asymmetric
195 of dopaminergic neurons in familial forms of Parkinson's disease but the precise pathogenic mechanism
198 ignificant enrichment of the heritability of Parkinson's disease within the substantia nigra module.
200 etic spectrum and clinical manifestations of Parkinson's disease in mainland China and expand the exi
201 bumin-expressing neurons in a mouse model of Parkinson's disease, we discovered evidence for an upreg
202 eficits of dopamine-depleted mouse models of Parkinson's disease, where cell type-specific optogeneti
204 hibitors and GLP-1 mimetics and the onset of Parkinson's disease (IRR 0.64; 95% CI 0.43-0.88; P < 0.0
207 ual hit hypothesis about the pathogenesis of Parkinson disease (PD) suggests that the brainstem is a
209 osomes predates the clinical presentation of Parkinson's disease (PD), offering a means of developing
211 changes that occur during the progression of Parkinson's disease pathology will aid the development o
213 current limitations and the broader range of Parkinson disease features that dopamine cell replacemen
214 mimetics is associated with a lower rate of Parkinson's disease compared to the use of other oral an
215 A recent study found a decreased risk of Parkinson disease (PD) associated with the beta2 adrener
216 served to be associated with a lower risk of Parkinson disease (PD) in previous epidemiologic studies
217 have examined the modulation of the risk of Parkinson's disease as a result of the use of beta-adren
218 indings suggest that the increase in risk of Parkinson's disease associated with beta-adrenoceptor an
221 tidase 4 (DPP4) inhibitors, with the risk of Parkinson's disease of users of any other oral glucose l
222 by a dose-dependent decrease in the risk of Parkinson's disease with chronic beta-adrenoceptor agoni
223 beta-adrenoceptor antagonists on the risk of Parkinson's disease would be small compared with other P
224 have been shown to contribute to the risk of Parkinson's disease, and currently 90 independent risk v
225 agonist propranolol and an increased risk of Parkinson's disease, while the chronic use of the beta-a
226 hibitors that specifically target seeding of Parkinson's disease (PD)-associated alpha-synuclein (alp
227 xosomes as biomarkers across the spectrum of Parkinson's disease, multiple system atrophy and other p
233 alamic nucleus is a symptomatic treatment of Parkinson's disease but benefits only to a minority of p
244 degenerative diseases such as Alzheimer's or Parkinson's are associated with the prion-like propagati
245 s disease would be small compared with other Parkinson's disease risk factors and would be similar to
246 (n = 102) and from a comparative population (Parkinson's disease or healthy participants, n = 61).
247 ynuclein and clusterin measurement predicted Parkinson's disease from other proteinopathies with AUC=
248 ained by reverse causation because prodromal Parkinson's disease is often associated with non-specifi
249 verity in patients with early or progressing Parkinson's disease and patients with idiopathic rapid e
250 sociation study and analysed the most recent Parkinson's disease-associated genetic risk score to det
251 d more frequently in the autosomal-recessive Parkinson's disease cohort (65 of 192, 33.85%) than in t
252 f CNS diseases including multiple sclerosis, Parkinson's disease and amyotrophic lateral sclerosis re
253 domain (rs4747203 and rs885828) in sporadic Parkinson's disease had significantly higher allele freq
254 rapeutic intervention.SIGNIFICANCE STATEMENT Parkinson's disease (PD) prevalence is projected to rise
255 ns such as Alzheimer's disease (AD), stroke, Parkinson's disease, Amyotrophic lateral sclerosis (ALS)
256 nverted haplotype of the MAPT (encoding tau) Parkinson's disease risk locus, identifying putative ect
257 ss influence over other brain regions), than Parkinson's disease patients without hallucinations and
258 Parkin has functions in the nucleus and that Parkinson's disease-associated Parkin mutants, ParkinR42
261 its interaction and colocalisation with the Parkinson's disease-associated E3 ubiquitin ligase Parki
264 dividuals with freezing of gait (FoG) due to Parkinson's disease (PD) have small and long anticipator
266 aling of the VGLUT3-mGluR5 axis is linked to Parkinson disease, anxiety disorders, and drug addiction
268 rstood factor in human conditions related to Parkinson's disease and complex behaviors.SIGNIFICANCE S
269 LRRK2 associates with the susceptibility to Parkinson's disease, Crohn's disease, and mycobacteria i
270 pamine neurons are especially susceptible to Parkinson's disease and prematurely degenerate in the co
271 r of neurons expressing dopamine could treat Parkinson's disease, or one affecting the number express
274 d Montreal Cognitive Assessment, and Unified Parkinson's Disease Rating Scale score was obtained in p
275 ement Disorder Society [MDS]-revised Unified Parkinson Disease Rating Scale [UPDRS] [I-III] total sco
277 es on the Movement Disorders Society Unified Parkinson's Disease Rating Scale (total score 4.6 [SD 4.
278 ion of the Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS-III), and el
279 he primary outcome was change in the Unified Parkinson's Disease Rating Scale (UPDRS) parts I to III
280 D scored significantly higher on the Unified Parkinson's Disease Rating Scale motor subscale than oth
281 STN is modulated in a rhythmic pattern when Parkinson's patients perform stepping movements, raising
282 ynuclein aggregates that are associated with Parkinson's disease and multiple system atrophy correspo
284 brospinal fluid from patients diagnosed with Parkinson's disease and samples from patients with multi
286 derived cell transplants in individuals with Parkinson disease have been variable, in part owing to t
287 e wrist worn sensors in 35 participants with Parkinson's disease in-clinic and 25 participants monito
289 in a naturalistic fashion, 55 patients with Parkinson's disease (19 females, mean age 62, mean Hoehn
290 regulated in the cerebellum of patients with Parkinson's disease (PD) and Essential Tremor (ET).
291 tivity in the basal ganglia of patients with Parkinson's disease (PD) are associated with impaired mo
292 arameters in a large cohort of patients with Parkinson's disease (PD) compared to controls using a fu
293 eanwhile, studies of memory in patients with Parkinson's disease have focused on overall memory capac
295 motor symptoms, a majority of patients with Parkinson's disease subsequently develop cognitive impai
297 ly normal elderly subjects, 45 patients with Parkinson's disease with no cognitive impairment, 86 wit
300 in PD.SIGNIFICANCE STATEMENT In persons with Parkinson's disease, gait dysfunction and the associated