Upper motor neuron and extra-motor neuron involvement in amyotrophic lateral sclerosis: a clinical and brain imaging review.
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Lessons of ALS imaging: Pitfalls and future directions - A critical reviewG-CSF prevents the progression of structural disintegration of white matter tracts in amyotrophic lateral sclerosis: a pilot trialA pilot study of the prevalence of psychiatric disorders in PLS and ALSMoving toward a predictive and personalized clinical approach in amyotrophic lateral sclerosis: novel developments and future directions in diagnosis, genetics, pathogenesis and therapiesHigh and Low Contrast Visual Acuity Are Not Affected in Amyotrophic Lateral Sclerosis.F Wave Study in Amyotrophic Lateral Sclerosis: Assessment of Segmental Motoneuronal DysfunctionDeciphering amyotrophic lateral sclerosis: what phenotype, neuropathology and genetics are telling us about pathogenesis.Motoneuron firing in amyotrophic lateral sclerosis (ALS)Overexpression of Human SOD1 Leads to Discrete Defects in the Cerebellar Architecture in the Mouse.Amyotrophic lateral sclerosis: a dying motor unit?Severe brain atrophy after long-term survival seen in siblings with familial amyotrophic lateral sclerosis and a mutation in the optineurin gene: a case series.Non-Motor Symptoms in Patients Suffering from Motor Neuron Diseases.Reduced Interhemispheric Functional Connectivity in the Motor Cortex during Rest in Limb-Onset Amyotrophic Lateral Sclerosis.Focal thinning of the motor cortex mirrors clinical features of amyotrophic lateral sclerosis and their phenotypes: a neuroimaging study.Frequency-Specific Abnormalities of Intrinsic Functional Connectivity Strength among Patients with Amyotrophic Lateral Sclerosis: A Resting-State fMRI Study.Clinical Spectrum of Amyotrophic Lateral Sclerosis (ALS).SPG3A-linked hereditary spastic paraplegia associated with cerebral glucose hypometabolism.An antibody-based affinity chromatography tool to assess Cu, Zn superoxide dismutase (SOD) G93A structural complexity in vivo.Sensory neuropathy in progressive motor neuronopathy (pmn) mice is associated with defects in microtubule polymerization and axonal transport.Reduced structural connectivity within a prefrontal-motor-subcortical network in amyotrophic lateral sclerosis.Value of quantitative analysis of routine clinical MRI sequences in ALS.Sympathetic vascular response to facial cooling is increased in flail phenotypes of amyotrophic lateral sclerosis.Urodynamic findings in amyotrophic lateral sclerosis patients with lower urinary tract symptoms: Results from a pilot study.Increased prevalence of bladder and intestinal dysfunction in amyotrophic lateral sclerosis.Genome-wide association study of motor coordination problems in ADHD identifies genes for brain and muscle function.Grey matter volume changes over the whole brain in amyotrophic lateral sclerosis: A voxel-wise meta-analysis of voxel based morphometry studiesParkinson-like features in ALS with predominant upper motor neuron involvement
P2860
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P2860
Upper motor neuron and extra-motor neuron involvement in amyotrophic lateral sclerosis: a clinical and brain imaging review.
description
2008 nî lūn-bûn
@nan
2008 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
name
Upper motor neuron and extra-m ...... ical and brain imaging review.
@ast
Upper motor neuron and extra-m ...... ical and brain imaging review.
@en
type
label
Upper motor neuron and extra-m ...... ical and brain imaging review.
@ast
Upper motor neuron and extra-m ...... ical and brain imaging review.
@en
prefLabel
Upper motor neuron and extra-m ...... ical and brain imaging review.
@ast
Upper motor neuron and extra-m ...... ical and brain imaging review.
@en
P2093
P1476
Upper motor neuron and extra-m ...... ical and brain imaging review.
@en
P2093
J M B V de Jong
M M van der Graaff
M de Visser
P356
10.1016/J.NMD.2008.10.002
P50
P577
2008-12-12T00:00:00Z