Search Results - "Alcalay, Roy N"
-
1
Precision medicine in Parkinson’s disease: emerging treatments for genetic Parkinson’s disease
Published in Journal of neurology (01-03-2020)“…In recent years, numerous clinical trials for disease modification in Parkinson’s disease (PD) have failed, possibly because of a “one-size-fits all” approach…”
Get full text
Journal Article -
2
Impact of the COVID‐19 Pandemic on Parkinson's Disease and Movement Disorders
Published in Movement disorders (01-05-2020)Get full text
Journal Article -
3
Ser(P)-1292 LRRK2 in urinary exosomes is elevated in idiopathic Parkinson's disease
Published in Movement disorders (01-10-2016)“…ABSTRACT Background Mutations in Leucine‐rich repeat kinase 2 (LRRK2) enhance levels of the autophosphorylated LRRK2 protein and are the most common known…”
Get full text
Journal Article -
4
The neuropathology of genetic Parkinson's disease
Published in Movement disorders (01-06-2012)“…Pathological data from autopsies genotyped for Parkinson's disease (PD)‐related mutations in alpha‐synuclein, Parkin, PINK1, DJ1, LRRK2, and glucocerebrosidase…”
Get full text
Journal Article -
5
Urinary proteome profiling for stratifying patients with familial Parkinson’s disease
Published in EMBO molecular medicine (05-03-2021)“…The prevalence of Parkinson's disease (PD) is increasing but the development of novel treatment strategies and therapeutics altering the course of the disease…”
Get full text
Journal Article -
6
Cerebrospinal fluid, plasma, and saliva in the BioFIND study: Relationships among biomarkers and Parkinson's disease Features
Published in Movement disorders (01-02-2018)“…ABSTRACT Objective: Examine relationships among neurodegenerative biomarkers and PD motor and nonmotor symptoms. Background: CSF alpha‐synuclein is decreased…”
Get full text
Journal Article -
7
Higher Urine bis(Monoacylglycerol)Phosphate Levels in LRRK2 G2019S Mutation Carriers: Implications for Therapeutic Development
Published in Movement disorders (01-01-2020)“…Background LRRK2 mutations are a common cause of dominantly inherited PD. Previous studies showed decreases in urine levels of didocohexaenoyl (22:6)…”
Get full text
Journal Article -
8
Elevated GM3 plasma concentration in idiopathic Parkinson's disease: A lipidomic analysis
Published in PloS one (17-02-2017)“…Parkinson's disease (PD) is a common neurodegenerative disease whose pathological hallmark is the accumulation of intracellular α-synuclein aggregates in Lewy…”
Get full text
Journal Article -
9
Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non‐Ashkenazi Jewish ancestry
Published in Movement disorders (01-10-2017)“…ABSTRACT Background Penetrance estimates of the leucine‐rich repeat kinase 2 (LRRK2) p.G2019S mutation for PD vary widely (24%‐100%). The p.G2019S penetrance…”
Get full text
Journal Article -
10
Targeted sequencing of Parkinson's disease loci genes highlights SYT11, FGF20 and other associations
Published in Brain (London, England : 1878) (03-03-2021)“…Genome-wide association studies (GWAS) have identified numerous loci associated with Parkinson's disease. The specific genes and variants that drive the…”
Get full text
Journal Article -
11
Cerebrospinal fluid proteomics implicates the granin family in Parkinson’s disease
Published in Scientific reports (12-02-2020)“…Parkinson’s disease, the most common age-related movement disorder, is a progressive neurodegenerative disease with unclear etiology. Better understanding of…”
Get full text
Journal Article -
12
The association between Mediterranean diet adherence and Parkinson's disease
Published in Movement disorders (01-05-2012)“…Background: Recent studies have demonstrated an association between a Mediterranean‐type diet and Alzheimer's risk. We assessed the association between…”
Get full text
Journal Article -
13
Arm swing as a potential new prodromal marker of Parkinson's disease
Published in Movement disorders (01-10-2016)“…ABSTRACT Background Reduced arm swing is a well‐known clinical feature of Parkinson's disease (PD), often observed early in the course of the disease. We…”
Get full text
Journal Article -
14
Patterns of TDP‐43 Deposition in Brains with LRRK2 G2019S Mutations
Published in Movement disorders (01-08-2023)“…Objective To assess for TDP‐43 deposits in brains with and without a LRRK2 G2019S mutation. Background LRRK2 G2019S mutations have been associated with…”
Get full text
Journal Article -
15
Subnormal GM1 in PBMCs: Promise for Early Diagnosis of Parkinson's Disease?
Published in International journal of molecular sciences (26-10-2021)“…The fact that Parkinson's disease (PD) pathologies are well advanced in most PD patients by the time of clinical elucidation attests to the importance of early…”
Get full text
Journal Article -
16
Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease
Published in Movement disorders (01-01-2021)“…ABSTRACT Background Biallelic PRKN mutation carriers with Parkinson's disease (PD) typically have an earlier disease onset, slow disease progression, and,…”
Get full text
Journal Article -
17
The impact of COVID-19 and social distancing on people with Parkinson’s disease: a survey study
Published in NPJ Parkinson's Disease (21-01-2021)“…As the COVID-19 pandemic continues to affect the international community, very little is known about its impact on the health and day-to-day activities of…”
Get full text
Journal Article -
18
Sequencing of the GBA coactivator, Saposin C, in Parkinson disease
Published in Neurobiology of aging (01-12-2018)“…Saposin C (SapC), encoded by PSAP, is required for the activity of glucocerebrosidase, encoded by GBA. Although GBA mutations have been studied thoroughly in…”
Get full text
Journal Article -
19
Clinical and neuropathological features of progressive supranuclear palsy in Leucine rich repeat kinase (LRRK2) G2019S mutation carriers
Published in Movement disorders (01-02-2018)Get full text
Journal Article -
20
Toward a biomarker panel measured in CNS-originating extracellular vesicles for improved differential diagnosis of Parkinson's disease and multiple system atrophy
Published in Translational neurodegeneration (20-03-2023)“…[...]the oEV concentrations of pS129-α-syn increased in the same order, HC < PD < MSA, and were significantly higher in both disease groups (Fig. 1a)…”
Get full text
Journal Article