Clinical characterization of dystonia in adult patients with Huntington's disease.

about

Genetics Modulate Gray Matter Variation Beyond Disease Burden in Prodromal Huntington's Disease.

P2860

Q52590778-FEAD875D-41D9-40CE-A2F8-304287A0D88D

P2860

Clinical characterization of dystonia in adult patients with Huntington's disease.

Item

http://www.wikidata.org/entity/Q45302935

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

Clinical characterization of dystonia in adult patients with Huntington's disease.

@en

Clinical characterization of dystonia in adult patients with Huntington's disease.

@nl

type

Item

label

Clinical characterization of dystonia in adult patients with Huntington's disease.

@en

Clinical characterization of dystonia in adult patients with Huntington's disease.

@nl

prefLabel

Clinical characterization of dystonia in adult patients with Huntington's disease.

@en

Clinical characterization of dystonia in adult patients with Huntington's disease.

@nl

P1476

Clinical characterization of dystonia in adult patients with Huntington's disease

@en

P2093

A E Rosser

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

A Pryce Roberts

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

C Clenaghan

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

D McLauchlan

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

G C Payne

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

K J Peall

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

M A J Tijssen

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

M Wardle

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

N A van de Zande

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

R Zutt

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

P2860

Huntington's disease: a clinical review.

Dynamic mutations: a decade of unstable expanded repeats in human genetic disease

Treatment strategies for dystonia.

Phenomenology and classification of dystonia: a consensus update.

Systematic review: efficacy and safety of medical marijuana in selected neurologic disorders: report of the Guideline Development Subcommittee of the American Academy of Neurology.

Dystonia in Huntington's disease: prevalence and clinical characteristics.

Hereditary dystonia as a neurodevelopmental circuit disorder: Evidence from neuroimaging.

Differences in duration of Huntington's disease based on age at onset.

Striatal parvalbuminergic neurons are lost in Huntington's disease: implications for dystonia

EFNS guidelines on diagnosis and treatment of primary dystonias.

P304

1140-1147

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

P31

scholarly article

P356

10.1111/ENE.13349

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

P433

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

P478

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

P50

Thomas H Massey

P577

2017-06-29T00:00:00Z

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

P698

28661018

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

P921

Huntington disease

Clinical characterization of dystonia in adult patients with Huntington's disease.

about

P2860

P2860

Clinical characterization of dystonia in adult patients with Huntington's disease.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921