Occurs with motor neuron disease. Medical search. Frequent questions

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Anatomy19

Motor Neurons Neurons Spinal Cord Anterior Horn Cells Motor Cortex Axons Neurons, Afferent Inclusion Bodies Ulnar Nerve Brain Peripheral Nerves Neuromuscular Junction Cricoid Cartilage Muscle, Skeletal Muscles Spinal Nerve Roots Cells, Cultured Synapses Ganglia, Invertebrate

Organisms4

Mice, Transgenic Rats, Transgenic Animals, Genetically Modified Mice, Inbred C57BL

Diseases31

Motor Neuron Disease Neuromuscular Diseases Bulbar Palsy, Progressive Amyotrophic Lateral Sclerosis Muscular Atrophy, Spinal Nerve Degeneration Muscular Disorders, Atrophic Fasciculation Bulbo-Spinal Atrophy, X-Linked Gagging Muscular Atrophy TDP-43 Proteinopathies Frontotemporal Lobar Degeneration Frontotemporal Dementia Toxascariasis Electric Injuries Deglutition Disorders Pick Disease of the Brain Brain Injury, Chronic Lathyrism Disease Models, Animal Spinal Cord Diseases Sandhoff Disease Marchiafava-Bignami Disease Dementia Paralysis Spinal Muscular Atrophies of Childhood Spastic Paraplegia, Hereditary Muscle Weakness Nervous System Diseases Atrophy

Chemicals and Drugs14

Survival of Motor Neuron 1 Protein Survival of Motor Neuron 2 Protein SMN Complex Proteins Superoxide Dismutase Neurofilament Proteins beta-Hexosaminidase beta Chain RNA-Binding Protein FUS Riluzole Pyrrolidonecarboxylic Acid DEAD Box Protein 20 Nerve Tissue Proteins Molecular Motor Proteins Thyrotropin-Releasing Hormone Neuroprotective Agents

Analytical, Diagnostic and Therapeutic Techniques and Equipment10

Electromyography Pharyngostomy Disease Models, Animal Neurologic Examination Electric Stimulation Gastrostomy Immunohistochemistry Pedigree Cell Count Neuroimaging

Psychiatry and Psychology5

Frontotemporal Lobar Degeneration Frontotemporal Dementia Pick Disease of the Brain Motor Activity Dementia

Phenomena and Processes13

Gagging Evoked Potentials, Motor Neural Conduction Motor Activity Mutation Action Potentials Axonal Transport DNA Repeat Expansion Recruitment, Neurophysiological Cell Death Time Factors Cell Count Phenotype

Disciplines and Occupations1

Immunohistochemistry

Health Care1

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Health Care

Motor Neuron Disease Motor Neurons Neuromuscular Diseases Bulbar Palsy, Progressive Amyotrophic Lateral Sclerosis Muscular Atrophy, Spinal Neurons Survival of Motor Neuron 1 Protein Spinal Cord Survival of Motor Neuron 2 Protein Anterior Horn Cells Nerve Degeneration SMN Complex Proteins Superoxide Dismutase Muscular Disorders, Atrophic Motor Cortex Fasciculation Bulbo-Spinal Atrophy, X-Linked Gagging Muscular Atrophy Axons Neurons, Afferent TDP-43 Proteinopathies Frontotemporal Lobar Degeneration Neurofilament Proteins Frontotemporal Dementia Electromyography Toxascariasis beta-Hexosaminidase beta Chain Evoked Potentials, Motor RNA-Binding Protein FUS Pharyngostomy Riluzole Pyrrolidonecarboxylic Acid Inclusion Bodies Neural Conduction Electric Injuries Deglutition Disorders Pick Disease of the Brain Motor Activity Mice, Transgenic Brain Injury, Chronic Lathyrism DEAD Box Protein 20 Disease Models, Animal Ulnar Nerve Mutation Nerve Tissue Proteins Spinal Cord Diseases Brain Peripheral Nerves Neuromuscular Junction Action Potentials Sandhoff Disease Marchiafava-Bignami Disease Rats, Transgenic Neurologic Examination Cricoid Cartilage Axonal Transport Dementia DNA Repeat Expansion Paralysis Spinal Muscular Atrophies of Childhood Recruitment, Neurophysiological Electric Stimulation Muscle, Skeletal Age of Onset Animals, Genetically Modified Spastic Paraplegia, Hereditary Muscles Gastrostomy Muscle Weakness Immunohistochemistry Spinal Nerve Roots Cells, Cultured Cell Death Time Factors Molecular Motor Proteins Mice, Inbred C57BL Pedigree Cell Count Synapses Thyrotropin-Releasing Hormone Phenotype Ganglia, Invertebrate Nervous System Diseases Atrophy Neuroprotective Agents Neuroimaging

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