A multidisciplinary study of patients with early-onset PD with and without parkin mutations.
about
Psychosis in Parkinson's Disease: Epidemiology, Pathophysiology, and Management.The Monoamine Brainstem Reticular Formation as a Paradigm for Re-Defining Various Phenotypes of Parkinson's Disease Owing Genetic and Anatomical Specificity.Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell linesA meta-analysis of the relationship of the Parkin p.Val380Leu polymorphism to Parkinson's disease.The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD studyAltered hippocampal synaptic physiology in aged parkin-deficient mice.The relation between depression and parkin genotype: the CORE-PD study.A Peruvian family with a novel PARK2 mutation: Clinical and pathological characteristicsNeuropsychological Profile of Parkin Mutation Carriers with and without Parkinson Disease: The CORE-PD Study.CSF Biomarkers and Its Associations with 18F-AV133 Cerebral VMAT2 Binding in Parkinson's Disease-A Preliminary Report.Brain Connectivity Changes in Autosomal Recessive Parkinson Disease: A Model for the Sporadic FormUnderstanding the susceptibility of dopamine neurons to mitochondrial stressors in Parkinson's disease.Cognitive and motor function in long-duration PARKIN-associated Parkinson disease.Lysosome-dependent pathways as a unifying theme in Parkinson's disease.Parkinson's disease: chameleons and mimics.Neuromelanin MRI is useful for monitoring motor complications in Parkinson's and PARK2 disease.Self-report of cognitive impairment and mini-mental state examination performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson's disease.Parkin and PINK1 parkinsonism may represent nigral mitochondrial cytopathies distinct from Lewy body Parkinson's disease.Phenotype analysis in patients with early onset Parkinson's disease with and without parkin mutations.Nonmotor symptoms in Parkin gene-related parkinsonism.Cognitive changes in prodromal Parkinson's disease: A review.Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array.Parkinson Disease from Mendelian Forms to Genetic Susceptibility: New Molecular Insights into the Neurodegeneration Process.Lack of association between p.Ser167Asn variant of Parkin and Parkinson's disease: a meta-analysis of 15 studies involving 2,280 cases and 2,459 controls.A Case of Parkinson's Disease with No Lewy Body Pathology due to a Homozygous Exon Deletion in
P2860
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P2860
A multidisciplinary study of patients with early-onset PD with and without parkin mutations.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
A multidisciplinary study of p ...... and without parkin mutations.
@en
A multidisciplinary study of p ...... and without parkin mutations.
@nl
type
label
A multidisciplinary study of p ...... and without parkin mutations.
@en
A multidisciplinary study of p ...... and without parkin mutations.
@nl
prefLabel
A multidisciplinary study of p ...... and without parkin mutations.
@en
A multidisciplinary study of p ...... and without parkin mutations.
@nl
P2093
P2860
P50
P1433
P1476
A multidisciplinary study of p ...... and without parkin mutations.
@en
P2093
A Pelissolo
E Broussolle
M-J Ribeiro
S Tezenas du Montcel
P2860
P304
P356
10.1212/01.WNL.0000327098.86861.D4
P407
P577
2008-11-05T00:00:00Z