Gaucher disease ascertained through a Parkinson's center: imaging and clinical characterization.
about
Olfactory deficits in Niemann-Pick type C1 (NPC1) diseaseNeuropsychiatric characteristics of GBA-associated Parkinson disease.Cognitive and Antipsychotic Medication Use in Monoallelic GBA-Related Parkinson Disease.Parkinson disease in Gaucher disease.The link between the GBA gene and parkinsonismHyposmia and cognitive impairment in Gaucher disease patients and carriersOlfactory identification in LRRK2 G2019S mutation carriers: a relevant marker?Substantia nigra hyperechogenicity with LRRK2 G2019S mutationsEvolution of prodromal clinical markers of Parkinson disease in a GBA mutation-positive cohort.Olfactory dysfunction in LRRK2 G2019S mutation carriersExploring the link between glucocerebrosidase mutations and parkinsonismThe neurobiology of glucocerebrosidase-associated parkinsonism: a positron emission tomography study of dopamine synthesis and regional cerebral blood flowOlfaction in Parkinson's disease and related disorders.Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson diseaseClinical course and prognosis in patients with Gaucher disease and parkinsonismA Personalized Approach to Parkinson's Disease Patients Based on Founder Mutation AnalysisA New Glucocerebrosidase Chaperone Reduces α-Synuclein and Glycolipid Levels in iPSC-Derived Dopaminergic Neurons from Patients with Gaucher Disease and Parkinsonism.Autosomal recessive mutations in the development of Parkinson's disease.Lysosomal storage disorders and Parkinson's disease: Gaucher disease and beyond.Parkinson's disease, proteins, and prions: milestones.Identifying prodromal Parkinson's disease: pre-motor disorders in Parkinson's disease.The association between ß-glucocerebrosidase mutations and parkinsonismGlucocerebrosidase mutations and the pathogenesis of Parkinson disease.Parkinson's disease: acid-glucocerebrosidase activity and alpha-synuclein clearance.New Directions in Gaucher Disease.The olfactory bulb as the entry site for prion-like propagation in neurodegenerative diseases.Cognitive and motor functioning in elderly glucocerebrosidase mutation carriers.Glucocerebrosidase enzyme activity in GBA mutation Parkinson's diseaseDual-Task Performance in GBA Parkinson's Disease.Clinical, genetic, and brain sonographic features related to Parkinson's disease in Gaucher disease.Cerebral pathological and compensatory mechanisms in the premotor phase of leucine-rich repeat kinase 2 parkinsonism.
P2860
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P2860
Gaucher disease ascertained through a Parkinson's center: imaging and clinical characterization.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Gaucher disease ascertained th ...... and clinical characterization.
@ast
Gaucher disease ascertained th ...... and clinical characterization.
@en
Gaucher disease ascertained th ...... and clinical characterization.
@nl
type
label
Gaucher disease ascertained th ...... and clinical characterization.
@ast
Gaucher disease ascertained th ...... and clinical characterization.
@en
Gaucher disease ascertained th ...... and clinical characterization.
@nl
prefLabel
Gaucher disease ascertained th ...... and clinical characterization.
@ast
Gaucher disease ascertained th ...... and clinical characterization.
@en
Gaucher disease ascertained th ...... and clinical characterization.
@nl
P2093
P2860
P356
P1433
P1476
Gaucher disease ascertained th ...... and clinical characterization.
@en
P2093
Christina Palmese
Gregory Pastores
Johann Hagenah
Kaili Stanley
Kelly Condefer
Laurie Ozelius
Michele Tagliati
Norbert Brüggemann
Ruth Kornreich
P2860
P304
P356
10.1002/MDS.23046
P407
P577
2010-07-01T00:00:00Z