Substantia nigra hyperechogenicity with LRRK2 G2019S mutations - Wikidata - wikimedia - TriplyDB

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations

http://www.wikidata.org/entity/Q34861140

about

Neuroimaging in pre-motor Parkinson's disease Neuroimaging: current role in detecting pre-motor Parkinson's disease.Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson disease Biological metals and metal-targeting compounds in major neurodegenerative diseases.Biomarkers in Prodromal Parkinson Disease: a Qualitative Review.Nigral iron elevation is an invariable feature of Parkinson's disease and is a sufficient cause of neurodegeneration.Clinical and brain imaging characteristics in leucine-rich repeat kinase 2-associated PD and asymptomatic mutation carriers.Echogenicity of basal ganglia structures in different Huntington's disease phenotypes.Iron deposition in substantia nigra: abnormal iron metabolism, neuroinflammatory mechanism and clinical relevance.High nigral iron deposition in LRRK2 and Parkin mutation carriers using R2* relaxometry.Cerebral pathological and compensatory mechanisms in the premotor phase of leucine-rich repeat kinase 2 parkinsonism.

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P2860

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations

http://www.wikidata.org/entity/Q34861140

description

2011 nî lūn-bûn

@nan

2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2011年の論文

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2011年論文

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2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

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2011年论文

@wuu

name

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations

@ast

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations

@en

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations

@nl

type

label

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations

@ast

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations

@en

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations

@nl

prefLabel

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations

@ast

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations

@en

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations

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P1433

Movement Disorders

P1476

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations

@en

P2093

Cuiling Wang

http://www.w3.org/2001/XMLSchema#string

Deborah Raymond

http://www.w3.org/2001/XMLSchema#string

Johann Hagenah

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Kaili Stanley

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Laurie Ozelius

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Norbert Brüggemann

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Susan Bressman

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P2860

Random-effects models for longitudinal data

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

Transcranial brain parenchyma sonography in movement disorders: state of the art.

Echogenicity of the substantia nigra: association with increased iron content and marker for susceptibility to nigrostriatal injury.

The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease

Leucine-rich repeat kinase 2 gene-associated disease: redefining genotype-phenotype correlation

Gaucher disease ascertained through a Parkinson's center: imaging and clinical characterization.

Clinical expression of LRRK2 G2019S mutations in the elderly.

Detection of presymptomatic Parkinson's disease: combining smell tests, transcranial sonography, and SPECT.

Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype.

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885-888

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10.1002/MDS.23644

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5

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26

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Christine Klein

Rachel Saunders-Pullman

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2011-02-10T00:00:00Z

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49827769

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21312285

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P921

substantia nigra

P932

3082617

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