Development of a brief ataxia rating scale (BARS) based on a modified form of the ICARS. - Test2 - elhamkhani - TriplyDB

Development of a brief ataxia rating scale (BARS) based on a modified form of the ICARS.

Development of a brief ataxia rating scale (BARS) based on a modified form of the ICARS.

http://www.wikidata.org/entity/Q34989635

about

Niemann-Pick disease type C symptomatology: an expert-based clinical description Schmahmann's syndrome - identification of the third cornerstone of clinical ataxiology Evidence for topographic organization in the cerebellum of motor control versus cognitive and affective processing.Longitudinal tracking of gait and balance impairments in cerebellar disease Cerebellar theta burst stimulation in stroke patients with ataxia.The fragile X-associated tremor ataxia syndrome (FXTAS) in Indonesia."Apraxic dysgraphia" in a 15-year-old left-handed patient: disruption of the cerebello-cerebral network involved in the planning and execution of graphomotor movements.Langerhans cell histiocytosis (LCH): guidelines for diagnosis, clinical work-up, and treatment for patients till the age of 18 years Location of lesion determines motor vs. cognitive consequences in patients with cerebellar stroke.Korean version of the scale for the assessment and rating of ataxia in ataxic stroke patients.Robotic and clinical evaluation of upper limb motor performance in patients with Friedreich's Ataxia: an observational study.Longitudinal follow up of a boy affected by Pol III-related leukodystrophy: a detailed phenotype description.A comparison of linear and nonlinear stability parameters in different clinical forms of multiple sclerosis Spinocerebellar ataxia type 7: clinical course, phenotype-genotype correlations, and neuropathology The effects of prolonged wear of textured shoe insoles on gait, foot sensation and proprioception in people with multiple sclerosis: study protocol for a randomised controlled trial.Relationship between proprioception at the knee joint and gait ataxia in HSAN III.Spinocerebellar ataxia type 7: Report of an Indian family.Cerebellar stroke without motor deficit: clinical evidence for motor and non-motor domains within the human cerebellum.Cerebellar Contribution to Pattern Separation of Human Hippocampal Memory Circuits.Ataxia rating scales--psychometric profiles, natural history and their application in clinical trials.Consensus Paper: Revisiting the Symptoms and Signs of Cerebellar Syndrome.Age-related reference values for the pediatric Scale for Assessment and Rating of Ataxia: a multicentre study.An electrophysiological study of visual processing in spinocerebellar ataxia type 2 (SCA2).Increasing cutaneous afferent feedback improves proprioceptive accuracy at the knee in patients with sensory ataxia.Longitudinal changes in cerebellar and subcortical volumes in adult-onset Niemann-Pick disease type C patients treated with miglustat.Evaluation and treatment of Langerhans cell histiocytosis patients with central nervous system abnormalities: Current views and new vistas.A multidimensional physical therapy program for individuals with cerebellar ataxia secondary to traumatic brain injury: a case series.Clinical and genetic analysis of spinocerebellar ataxia type 7 (SCA7) in Zambian families.The cerebellar cognitive affective/Schmahmann syndrome scale.Ataxia rating scales are age-dependent in healthy children.Inter-rater reliability and validity of two ataxia rating scales in children with brain tumours.Mastication dyspraxia: a neurodevelopmental disorder reflecting disruption of the cerebellocerebral network involved in planned actions.Insights from ERPs into attention during recovery after cerebellar stroke: a case report.Monitoring disease progression in spinocerebellar ataxias: implications for treatment and clinical research.Reliability and discriminant validity of ataxia rating scales in early onset ataxia.Cortical dysfunction in cerebellar ataxia with antibodies to glutamic acid decarboxylase.Posterior fossa syndrome in an adult patient following surgical evacuation of an intracerebellar haematoma.Effects of structural and functional cerebellar lesions on sensorimotor adaptation of saccades.A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures.Neuroprotective effects of mesenchymal stem cell transplantation in animal model of cerebellar degeneration.

P2860

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P2860

Development of a brief ataxia rating scale (BARS) based on a modified form of the ICARS.

http://www.wikidata.org/entity/Q34989635

description

2009 nî lūn-bûn

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2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Development of a brief ataxia rating scale (BARS) based on a modified form of the ICARS.

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Development of a brief ataxia rating scale (BARS) based on a modified form of the ICARS.

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Development of a brief ataxia rating scale

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type

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Development of a brief ataxia rating scale (BARS) based on a modified form of the ICARS.

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Development of a brief ataxia rating scale (BARS) based on a modified form of the ICARS.

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Development of a brief ataxia rating scale

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Development of a brief ataxia rating scale (BARS) based on a modified form of the ICARS.

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Development of a brief ataxia rating scale (BARS) based on a modified form of the ICARS.

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Development of a brief ataxia rating scale

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Movement Disorders

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Development of a brief ataxia rating scale (BARS) based on a modified form of the ICARS.

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P2093

Jason MacMore

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

Mark G Vangel

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Raquel Gardner

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P2860

The human basis pontis: motor syndromes and topographic organization

Inter-rater reliability of the International Cooperative Ataxia Rating Scale (ICARS).

Reliability and validity of the International Cooperative Ataxia Rating Scale: a study in 156 spinocerebellar ataxia patients.

Scale for the assessment and rating of ataxia: development of a new clinical scale.

Reliability and validity of the scale for the assessment and rating of ataxia: a study in 64 ataxia patients.

Reliability and validity of ICARS in focal cerebellar lesions.

FUNCTIONAL ORGANIZATION OF THE SPINO- AND CUNEOCEREBELLAR TRACTS.

The cerebrocerebellar system.

Neurological, cardiological, and oculomotor progression in 104 patients with Friedreich ataxia during long-term follow-up.

Functional topography in the human cerebellum: a meta-analysis of neuroimaging studies.

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1820-1828

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scholarly article

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10.1002/MDS.22681

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12

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24

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Jeremy D. Schmahmann

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2009-09-01T00:00:00Z

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26326834

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19562773

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severity of illness index

neurological examination

disability evaluation

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3800087

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