Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
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Patterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit.Clinical and neuroradiological features of spinocerebellar ataxia 38 (SCA38)Genetic analysis of age at onset variation in spinocerebellar ataxia type 2.Ataxin-2: From RNA Control to Human Health and DiseaseTwo novel SNPs in ATXN3 3' UTR may decrease age at onset of SCA3/MJD in Chinese patients.Analysis of the GGGGCC Repeat Expansions of the C9orf72 Gene in SCA3/MJD Patients from China.Depression and clinical progression in spinocerebellar ataxias.DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseasesATXN2 trinucleotide repeat length correlates with risk of ALS.Chaperones in Polyglutamine Aggregation: Beyond the Q-Stretch.Genetic landscape remodelling in spinocerebellar ataxias: the influence of next-generation sequencing.Rare neurological channelopathies--networks to study patients, pathogenesis and treatment.Individual changes in preclinical spinocerebellar ataxia identified via increased motor complexity.Spinocerebellar ataxia type 3 in Israel: phenotype and genotype of a Jew Yemenite subpopulation.Normal ATXN2 alleles influences on the age at onset in spinocerebellar ataxia type 2.Treatment with Caffeic Acid and Resveratrol Alleviates Oxidative Stress Induced Neurotoxicity in Cell and Drosophila Models of Spinocerebellar Ataxia Type3.Wild type huntingtin toxicity in yeast: Implications for the role of amyloid cross-seeding in polyQ diseases.Dystonia and ataxia progression in spinocerebellar ataxias.Postural Tremor and Ataxia Progression in Spinocerebellar Ataxias.Co-expression Patterns between ATN1 and ATXN2 Coincide with Brain Regions Affected in Huntington's Disease.Identification and functional characterization of two missense mutations in NDRG1 associated with Charcot-Marie-Tooth disease type 4D.Spinocerebellar ataxia type 3/Machado-Joseph disease starting before adolescence.Monitoring disease progression in spinocerebellar ataxias: implications for treatment and clinical research.ATXN2 polymorphism modulates age at onset in Machado-Joseph disease.(CAG)n loci as genetic modifiers of age-at-onset in patients with Machado-Joseph disease from mainland China.Reply: Replicating studies of genetic modifiers in spinocerebellar ataxia type 3: can homogeneous cohorts aid?Replicating studies of genetic modifiers in spinocerebellar ataxia type 3: can homogeneous cohorts aid?Analysis of (CAG)n expansion in ATXN1, ATXN2 and ATXN3 in Chinese patients with multiple system atrophy.
P2860
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P2860
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
description
2014 nî lūn-bûn
@nan
2014 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
@ast
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
@en
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
@nl
type
label
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
@ast
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
@en
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
@nl
prefLabel
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
@ast
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
@en
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
@nl
P2093
P2860
P50
P356
P1433
P1476
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
@en
P2093
Agnès Camuzat
Alessandro Brussino
Alessandro Filla
Bart P C van de Warrenburg
Bela Melegh
Caterina Mariotti
Clinical Research Consortium for Spinocerebellar Ataxia (CRC-SCA)
Cécile Cazeneuve
EUROSCA network
P2860
P304
P356
10.1093/BRAIN/AWU174
P407
P50
P577
2014-06-26T00:00:00Z