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Journal of Clinical & Experimental Neuroimmunology

Amyotrophic lateral sclerosis

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Amyotrophic lateral sclerosis

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ALS and other motor neuron diseases are specified by steady, unabated, escalating degeneration of corticospinal tracts, anterior horn cells and bulbar motor nuclei. Symptoms vary in extremity and may include muscle weakness and atrophy, fasciculations, emotional lability and respiratory muscle weakness.

Related Journals for Amyotrophic lateral sclerosis

Journal of Clinical & Experimental Neuroimmunology, Journal of Neurology & Neurophysiology, Journal of Neurological Disorders, Journal of Neuroinfectious Diseases, Rheumatology: Current Research, Advances in Neuroimmunology, Clinical and Experimental Neuroimmunology, NeuroImmune Biology, Advances in Neuroimmune Biology, Journal of Neuroimmunology, NeuroImmunoModulation, Journal of NeuroImmune Pharmacology

Amyotrophic lateral sclerosis

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