Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype.
about
Brain region specific mitophagy capacity could contribute to selective neuronal vulnerability in Parkinson's diseasePreservation of function in Parkinson's disease: what's learning got to do with it?Neuroimaging in pre-motor Parkinson's disease[The presymptomatic stage of neurodegenerative disorders].Preclinical and clinical neural network changes in SCA2 parkinsonism.Altered hippocampal synaptic physiology in aged parkin-deficient mice.Deletion of a single allele of the Pex11β gene is sufficient to cause oxidative stress, delayed differentiation and neuronal death in mouse brainCompensatory premotor activity during affective face processing in subclinical carriers of a single mutant Parkin allele.Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease study.Neuropsychological Profile of Parkin Mutation Carriers with and without Parkinson Disease: The CORE-PD Study.Brain Connectivity Changes in Autosomal Recessive Parkinson Disease: A Model for the Sporadic FormBDNF Val66Met Polymorphism Is Related to Motor System Function After Stroke.Functional compensation of motor function in pre-symptomatic Huntington's disease.How might physical activity benefit patients with Parkinson disease?Motor signs in the prodromal phase of Parkinson's disease.Is there a need to redefine Parkinson's disease?Annual research review: Rare genotypes and childhood psychopathology--uncovering diverse developmental mechanisms of ADHD risk.Ultrasound-based motion analysis demonstrates bilateral arm hypokinesia during gait in heterozygous PINK1 mutation carriers.PINK1 heterozygous mutations induce subtle alterations in dopamine-dependent synaptic plasticity.Clinical phenotype and risk of levodopa-induced dyskinesia in Parkinson's disease.Neuroimaging in the early diagnosis of neurodegenerative disease.Cognitive changes in prodromal Parkinson's disease: A review.Phenotypic variability of PINK1 expression: 12 Years' clinical follow-up of two Italian families.Clinical features and [11C]-CFT PET analysis of PARK2, PARK6, PARK7-linked autosomal recessive early onset Parkinsonism.Cerebral pathological and compensatory mechanisms in the premotor phase of leucine-rich repeat kinase 2 parkinsonism.Effects of dopaminergic treatment on functional cortico-cortical connectivity in Parkinson's disease."Lazy" nigrostriatal synapses in the heterozygous PINK1 mouse model of familial Parkinson's disease.Gait alterations in healthy carriers of the LRRK2 G2019S mutation.
P2860
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P2860
Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype.
description
2008 nî lūn-bûn
@nan
2008 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Heterozygous carriers of a Par ...... mmon functional endophenotype.
@ast
Heterozygous carriers of a Par ...... mmon functional endophenotype.
@en
type
label
Heterozygous carriers of a Par ...... mmon functional endophenotype.
@ast
Heterozygous carriers of a Par ...... mmon functional endophenotype.
@en
prefLabel
Heterozygous carriers of a Par ...... mmon functional endophenotype.
@ast
Heterozygous carriers of a Par ...... mmon functional endophenotype.
@en
P2093
P2860
P1433
P1476
Heterozygous carriers of a Par ...... mmon functional endophenotype.
@en
P2093
B F L van Nuenen
F Binkofski
P P Pramstaller
T van Eimeren
P2860
P304
P356
10.1212/01.WNL.0000338699.56379.11
P407
P577
2008-11-26T00:00:00Z