Primary lateral sclerosis: clinical, neurophysiological, and magnetic resonance findings
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Myelin imaging in amyotrophic and primary lateral sclerosis.Eye-tracking in amyotrophic lateral sclerosis: A longitudinal study of saccadic and cognitive tasksGray matter perfusion correlates with disease severity in ALS.Cortical processing of swallowing in ALS patients with progressive dysphagia--a magnetoencephalographic study.Extramotor damage is associated with cognition in primary lateral sclerosis patientsA pilot study of the prevalence of psychiatric disorders in PLS and ALSAmyotrophic lateral sclerosis: contemporary concepts in etiopathogenesis and pharmacotherapy.Primary lateral sclerosis, hereditary spastic paraplegia and amyotrophic lateral sclerosis: discrete entities or spectrum?Primary lateral sclerosis, hereditary spastic paraplegia, and mutations in the alsin gene: historical background for the first International Conference.Primary Lateral SclerosisVoxel-based diffusion tensor imaging detects pyramidal tract degeneration in primary lateral sclerosisAltered cortical beta-band oscillations reflect motor system degeneration in amyotrophic lateral sclerosis.Clinical and imaging characterization of progressive spastic dysarthria.The concept and diagnostic criteria of primary lateral sclerosis.Intrahemispheric and interhemispheric structural network abnormalities in PLS and ALS.Upper and extra-motoneuron involvement in early motoneuron disease: a diffusion tensor imaging study.Muscle histopathology in upper motor neuron-dominant amyotrophic lateral sclerosis.Degeneration of serotonergic neurons in amyotrophic lateral sclerosis: a link to spasticity.Use of intrathecal baclofen for treatment of severe spasticity in selected patients with motor neuron disease.Investigation of white matter pathology in ALS and PLS using tract-based spatial statistics.Demographics and clinical characteristics of primary lateral sclerosis: case series and a review of literature.Primary lateral sclerosis presenting with isolated progressive pseudobulbar syndrome.High T2 signal in primary lateral sclerosis supports the topographic distribution of fibers in the corpus callosum: assessing disease in the primary motor segment.Cortical excitability changes distinguish the motor neuron disease phenotypes from hereditary spastic paraplegia.Evidence for central abnormality in respiratory control in primary lateral sclerosis.Natural history of upper motor neuron-dominant ALS
P2860
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P2860
Primary lateral sclerosis: clinical, neurophysiological, and magnetic resonance findings
description
2001 nî lūn-bûn
@nan
2001 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
name
Primary lateral sclerosis: clinical, neurophysiological, and magnetic resonance findings
@ast
Primary lateral sclerosis: clinical, neurophysiological, and magnetic resonance findings
@en
Primary lateral sclerosis: clinical, neurophysiological, and magnetic resonance findings
@nl
type
label
Primary lateral sclerosis: clinical, neurophysiological, and magnetic resonance findings
@ast
Primary lateral sclerosis: clinical, neurophysiological, and magnetic resonance findings
@en
Primary lateral sclerosis: clinical, neurophysiological, and magnetic resonance findings
@nl
prefLabel
Primary lateral sclerosis: clinical, neurophysiological, and magnetic resonance findings
@ast
Primary lateral sclerosis: clinical, neurophysiological, and magnetic resonance findings
@en
Primary lateral sclerosis: clinical, neurophysiological, and magnetic resonance findings
@nl
P2093
P2860
P356
P1476
Primary lateral sclerosis: clinical, neurophysiological, and magnetic resonance findings
@en
P2093
A E de Jager
J Kuipers-Upmeijer
T W van Weerden
P2860
P304
P356
10.1136/JNNP.71.5.615
P407
P577
2001-11-01T00:00:00Z