2018 motor neuron disease muscular atrophy spinal. Medical search. Frequent questions

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Anatomy24

Motor Neurons Spinal Cord Neurons Anterior Horn Cells Axons Motor Cortex Neurons, Afferent Inclusion Bodies Spinal Nerve Roots Neuromuscular Junction Ulnar Nerve Muscle, Skeletal Brain Peripheral Nerves Muscles Cricoid Cartilage Cells, Cultured Spinal Nerves Coiled Bodies Ganglia, Spinal Chromosomes, Human, Pair 5 Synapses Interneurons Ganglia, Invertebrate

Organisms6

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

Diseases38

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

Chemicals and Drugs21

Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Nerve Tissue Proteins Superoxide Dismutase Neuronal Apoptosis-Inhibitory Protein DEAD Box Protein 20 Cyclic AMP Response Element-Binding Protein RNA-Binding Proteins Neurofilament Proteins beta-Hexosaminidase beta Chain RNA-Binding Protein FUS Riluzole Pyrrolidonecarboxylic Acid Ribonucleoproteins, Small Nuclear Receptors, Androgen Neuroprotective Agents snRNP Core Proteins Molecular Motor Proteins DNA-Binding Proteins Thyrotropin-Releasing Hormone

Analytical, Diagnostic and Therapeutic Techniques and Equipment13

Electromyography Disease Models, Animal Pharyngostomy Pedigree Neurologic Examination Electric Stimulation Immunohistochemistry Magnetic Resonance Imaging Injections, Spinal Gastrostomy Cell Count Anesthesia, Spinal Neuroimaging

Psychiatry and Psychology5

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

Phenomena and Processes18

Gagging Neural Conduction Motor Activity Evoked Potentials, Motor Mutation Action Potentials Phenotype Axonal Transport DNA Repeat Expansion Time Factors Recruitment, Neurophysiological Exons Chromosomes, Human, Pair 5 Mutation, Missense Cell Death Cell Count Synaptic Transmission Movement

Disciplines and Occupations2

Immunohistochemistry Electrophysiology

Information Science1

Molecular Sequence Data

Health Care1

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

Motor Neuron Disease Muscular Atrophy, Spinal Motor Neurons Neuromuscular Diseases Spinal Muscular Atrophies of Childhood Bulbar Palsy, Progressive Survival of Motor Neuron 1 Protein SMN Complex Proteins Spinal Cord Survival of Motor Neuron 2 Protein Amyotrophic Lateral Sclerosis Muscular Atrophy Atrophy Neurons Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Anterior Horn Cells Nerve Degeneration Nerve Tissue Proteins Spinal Cord Injuries Axons Spinal Cord Diseases Fasciculation Superoxide Dismutase Neuronal Apoptosis-Inhibitory Protein DEAD Box Protein 20 Cyclic AMP Response Element-Binding Protein Electromyography RNA-Binding Proteins Disease Models, Animal Motor Cortex Neurons, Afferent Neurofilament Proteins Gagging Neural Conduction Mice, Transgenic TDP-43 Proteinopathies Inclusion Bodies Frontotemporal Lobar Degeneration Frontotemporal Dementia Motor Activity Evoked Potentials, Motor Mutation Spinal Nerve Roots Toxascariasis beta-Hexosaminidase beta Chain Neuromuscular Junction RNA-Binding Protein FUS Riluzole Ulnar Nerve Muscle, Skeletal Pharyngostomy Pyrrolidonecarboxylic Acid Brain Electric Injuries Deglutition Disorders Pick Disease of the Brain Peripheral Nerves Brain Injury, Chronic Action Potentials Lathyrism Muscle Weakness Pedigree Ribonucleoproteins, Small Nuclear Neurologic Examination Phenotype Sandhoff Disease Rats, Transgenic Marchiafava-Bignami Disease Paralysis Receptors, Androgen Muscles Dementia Axonal Transport Age of Onset Electric Stimulation Cricoid Cartilage Optic Atrophy Immunohistochemistry DNA Repeat Expansion Cells, Cultured Time Factors Recruitment, Neurophysiological Animals, Genetically Modified Spinal Nerves Mice, Inbred C57BL Exons Coiled Bodies Magnetic Resonance Imaging Injections, Spinal Ganglia, Spinal Chromosomes, Human, Pair 5 Mutation, Missense Nervous System Diseases Spastic Paraplegia, Hereditary Synapses Mice, Knockout Disease Progression Neuroprotective Agents Gastrostomy

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