about
Huntington's disease: a clinical review.C9orf72 expansions are the most common genetic cause of Huntington disease phenocopiesA novel manganese-dependent ATM-p53 signaling pathway is selectively impaired in patient-based neuroprogenitor and murine striatal models of Huntington's diseaseThe gene coding for PGC-1alpha modifies age at onset in Huntington's DiseaseSymptomatic treatment of Huntington diseaseClinical and genetic investigation of a Brazilian family with Huntington's disease.MicroRNA implications across neurodevelopment and neuropathology.Genetic variants in diseases of the extrapyramidal system.The clinical and genetic features of Huntington disease.Exploring the correlates of intermediate CAG repeats in Huntington disease.Genetic diagnosis of hyperkinetic movement disorders.Genes and functional GI disorders: from casual to causal relationship.Diagnosis and treatment of chorea syndromes.The global prevalence of Huntington's disease: a systematic review and discussion.Quantitative Proteomic Analysis Reveals Similarities between Huntington's Disease (HD) and Huntington's Disease-Like 2 (HDL2) Human Brains.Recent advances in the management of choreas.EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias.Differential diagnosis of Huntington's disease: what the clinician should know.C9orf72 expansion as a possible genetic cause of Huntington disease phenocopy syndrome.Huntington's disease: a field on the move. Introduction.Genetic screening of Greek patients with Huntington’s disease phenocopies identifies an SCA8 expansion.Xeroderma pigmentosum is a definite cause of Huntington's disease-like syndrome.
P2860
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P2860
description
2007 nî lūn-bûn
@nan
2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Huntington's disease phenocopy syndromes.
@ast
Huntington's disease phenocopy syndromes.
@en
Huntington's disease phenocopy syndromes.
@nl
type
label
Huntington's disease phenocopy syndromes.
@ast
Huntington's disease phenocopy syndromes.
@en
Huntington's disease phenocopy syndromes.
@nl
prefLabel
Huntington's disease phenocopy syndromes.
@ast
Huntington's disease phenocopy syndromes.
@en
Huntington's disease phenocopy syndromes.
@nl
P1476
Huntington's disease phenocopy syndromes.
@en
P304
P356
10.1097/WCO.0B013E3282F12074
P577
2007-12-01T00:00:00Z