Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?
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VGF Protein and Its C-Terminal Derived Peptides in Amyotrophic Lateral Sclerosis: Human and Animal Model StudiesMRI-based functional neuroimaging in ALS: an update.Characterization of thoracic motor and sensory neurons and spinal nerve roots in canine degenerative myelopathy, a potential disease model of amyotrophic lateral sclerosis.Selective pattern of motor system damage in gamma-synuclein transgenic mice mirrors the respective pathology in amyotrophic lateral sclerosis.Patterns of spontaneous brain activity in amyotrophic lateral sclerosis: a resting-state FMRI studyMotor neuron trophic factors: therapeutic use in ALS?An Autopsy Case of Amyotrophic Lateral Sclerosis with Waldenström Macroglobulinemia and Anti-MAG GammopathyVisualization of Sensory Neurons and Their Projections in an Upper Motor Neuron Reporter Line.Dusty: an assistive mobile manipulator that retrieves dropped objects for people with motor impairments.Prion-like propagation of mutant SOD1 misfolding and motor neuron disease spread along neuroanatomical pathwaysSensory involvement in the SOD1-G93A mouse model of amyotrophic lateral sclerosis.Clinical neurogenetics: amyotrophic lateral sclerosis.D90A-SOD1 mutation in ALS: The first report of heterozygous Italian patients and unusual findings.Pain and death: neurodegenerative disease mechanisms in the nociceptor.The phenotypic variability of amyotrophic lateral sclerosis.Trends in Research Literature Describing Dysphagia in Motor Neuron Diseases (MND): A Scoping Review.Extra-motor abnormalities in amyotrophic lateral sclerosis: another layer of heterogeneity.Corneal confocal microscopy reveals trigeminal small sensory fiber neuropathy in amyotrophic lateral sclerosis.Concomitant amyotrophic lateral sclerosis and paraclinical laboratory features of multiple sclerosis: coincidence or causal relationship?Vasculitis-like neuropathy in amyotrophic lateral sclerosis unresponsive to treatment.Sensory neuropathy in progressive motor neuronopathy (pmn) mice is associated with defects in microtubule polymerization and axonal transport.Clinical features and follow-up of four new cases of facial-onset sensory and motor neuronopathy.Optical coherence tomography does not support optic nerve involvement in amyotrophic lateral sclerosis.
P2860
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P2860
Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?
@en
Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?
@nl
type
label
Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?
@en
Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?
@nl
prefLabel
Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?
@en
Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?
@nl
P2093
P2860
P50
P356
P1476
Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?
@en
P2093
Andrew F Dean
Jeremy D Isaacs
Kerry R Mills
P2860
P304
P356
10.1136/JNNP.2006.098798
P407
P577
2007-07-01T00:00:00Z