Scale for the assessment and rating of ataxia: development of a new clinical scale.
about
Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohortsX-linked Charcot-Marie-Tooth disease, Arts syndrome, and prelingual non-syndromic deafness form a disease continuum: evidence from a family with a novel PRPS1 mutationExome sequencing reveals a homozygous SYT14 mutation in adult-onset, autosomal-recessive spinocerebellar ataxia with psychomotor retardationDiagnostic workup and management of patients with suspected Niemann-Pick type C diseaseErythropoietin in Friedreich ataxiaMotor training in degenerative spinocerebellar disease: ataxia-specific improvements by intensive physiotherapy and exergamesPatterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit.Benign hereditary chorea, not only chorea: a family case presentationFunctional and Gait Assessment in Children and Adolescents Affected by Friedreich's Ataxia: A One-Year Longitudinal StudySchmahmann's syndrome - identification of the third cornerstone of clinical ataxiologyIn vivo neurometabolic profiling in patients with spinocerebellar ataxia types 1, 2, 3, and 7Spinocerebellar ataxia type 36 in the Han ChineseTherapeutic prospects for spinocerebellar ataxia type 2 and 3.Cerebellar pathology in Friedreich's ataxia: atrophied dentate nuclei with normal iron content.Spinocerebellar ataxia: patient and health professional perspectives on whether and how patents affect access to clinical genetic testing.Friedreich ataxia: dysarthria profile and clinical data.Dyclonine rescues frataxin deficiency in animal models and buccal cells of patients with Friedreich's ataxia.Social and Cultural Elements Associated with Neurocognitive Dysfunctions in Spinocerebellar Ataxia Type 2 Patients.Neurochondrin is a neuronal target antigen in autoimmune cerebellar degeneration.A generic solution for web-based management of pseudonymized data.Expanded phenotypic spectrum of the m.8344A>G "MERRF" mutation: data from the German mitoNET registry.Motor decline in clinically presymptomatic spinocerebellar ataxia type 2 gene carriers.Principal component analysis for ataxic gait using a triaxial accelerometer.Visuomotor adaptive improvement and aftereffects are impaired differentially following cerebellar lesions in SCA and PICA territory.Noninvasive detection of presymptomatic and progressive neurodegeneration in a mouse model of spinocerebellar ataxia type 1.Neural correlates of ataxia severity in spinocerebellar ataxia type 3/Machado-Joseph disease.Spinocerebellar Ataxia Type 2 Is Associated with the Extracellular Loss of Superoxide Dismutase but Not Catalase Activity.Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6.Mutations in KCND3 cause spinocerebellar ataxia type 22.Stratification of disease progression in a broad spectrum of degenerative cerebellar ataxias with a clustering method using MRI-based atrophy rates of brain structures.Linear path integration deficits in patients with abnormal vestibular afference.Validity and reliability of a pilot scale for assessment of multiple system atrophy symptoms.PhenX measures for phenotyping rare genetic conditions.Circulating miR-323-3p is a biomarker for cardiomyopathy and an indicator of phenotypic variability in Friedreich's ataxia patients.An investigation of diffusion imaging techniques in the evaluation of spinocerebellar ataxia and multisystem atrophy.Temporal retinal nerve fiber loss in patients with spinocerebellar ataxia type 1Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.Neurochemical alterations in spinocerebellar ataxia type 1 and their correlations with clinical status.Hepatic mitochondrial dysfunction in Friedreich ataxia.Longitudinal tracking of gait and balance impairments in cerebellar disease
P2860
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P2860
Scale for the assessment and rating of ataxia: development of a new clinical scale.
description
2006 nî lūn-bûn
@nan
2006 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Scale for the assessment and rating of ataxia: development of a new clinical scale.
@ast
Scale for the assessment and rating of ataxia: development of a new clinical scale.
@en
Scale for the assessment and rating of ataxia: development of a new clinical scale.
@nl
type
label
Scale for the assessment and rating of ataxia: development of a new clinical scale.
@ast
Scale for the assessment and rating of ataxia: development of a new clinical scale.
@en
Scale for the assessment and rating of ataxia: development of a new clinical scale.
@nl
prefLabel
Scale for the assessment and rating of ataxia: development of a new clinical scale.
@ast
Scale for the assessment and rating of ataxia: development of a new clinical scale.
@en
Scale for the assessment and rating of ataxia: development of a new clinical scale.
@nl
P2093
P1433
P1476
Scale for the assessment and rating of ataxia: development of a new clinical scale.
@en
P2093
B P van de Warrenburg
C Mariotti
J Berciano
P304
P356
10.1212/01.WNL.0000219042.60538.92
P407
P577
2006-06-01T00:00:00Z