Motor Neuron Disorders
Pamela J. Shaw, Michael J. Strong
Butterworth-Heinemann, 2003 - Medical - 569 pages
Clinical and scientific text on the current knowledge about motor neuron disorders, most especially amyotrophic lateral sclerosis.
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Key Principles in the Clinical Diagnosis Pathology
Pathology of Motor Neuron Disorders
Neurophysiological Investigation of Motor Neuron Disorders
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abnormalities Acad Sci USA activity age at onset ALS/MND AMPA receptor amyotrophic lateral sclerosis Ann Neurol apoptosis Arch Neurol associated autosomal dominant axonal Biol Brain bulbar cell death chromosome cognitive cortical corticospinal tract dementia diagnosis distal dysfunction EAAT2 effect evidence excitotoxicity Exp Neurol expression FALS familial amyotrophic lateral fasciculations frontotemporal function gene glutamate transporter hereditary spastic paraplegia increased involvement limb microglia microglial mitochondrial molecular motor neuron disease Motor Neuron Disord motor units mouse model mutant SOD1 mutations Natl Acad Sci neurodegenerative neurofilament Neurol Neurosurg Psychiatry Neurol Sci Neurology neuron death neuropathy Neurosci NF-H NF-L normal overexpression oxidative stress pathogenesis pathology patients with amyotrophic percent peripherin phenotype Proc Natl Acad progressive protein reported riluzole risk factor role sensory SOD1 mutations SOD1 transgenic spastic paraplegia spinal cord spinal muscular atrophy subunit superoxide dismutase survival symptoms syndrome tion toxicity transgenic transgenic mice X-linked