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

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Anatomy37

Motor Neurons Spinal Cord Muscle, Skeletal Neurons Anterior Horn Cells Muscles Muscle Fibers, Skeletal Axons Motor Cortex Neurons, Afferent Neuromuscular Junction Inclusion Bodies Brain Spinal Nerve Roots Ulnar Nerve Muscle, Smooth Peripheral Nerves Cells, Cultured Muscle, Smooth, Vascular Muscle Fibers, Slow-Twitch Muscle Fibers, Fast-Twitch Cricoid Cartilage Hindlimb Spinal Nerves Mitochondria, Muscle Coiled Bodies Chromosomes, Human, Pair 5 Ganglia, Spinal Synapses Satellite Cells, Skeletal Muscle Sciatic Nerve Quadriceps Muscle Interneurons Ganglia, Invertebrate Muscle Spindles Oculomotor Muscles Neck Muscles

Organisms9

Mice, Transgenic Mice, Inbred C57BL Mice, Knockout Rats, Transgenic Rats, Sprague-Dawley Animals, Genetically Modified Rats, Wistar Animals, Newborn Cats

Diseases45

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

Chemicals and Drugs28

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment21

Hindlimb Suspension Electromyography Disease Models, Animal Muscle Denervation Pharyngostomy Electric Stimulation Pedigree Magnetic Resonance Imaging Immunohistochemistry Neurologic Examination Immobilization Organ Size Injections, Spinal Blotting, Western Cell Count Gastrostomy Neuroimaging Analysis of Variance Anesthesia, Spinal Bed Rest Models, Biological

Psychiatry and Psychology5

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

Phenomena and Processes31

Neural Conduction Gagging Motor Activity Mutation Muscle Contraction Evoked Potentials, Motor Muscle Development Action Potentials Time Factors Phenotype Axonal Transport Recruitment, Neurophysiological DNA Repeat Expansion Muscle Fatigue Exons Signal Transduction Gene Expression Regulation Chromosomes, Human, Pair 5 Mutation, Missense Organ Size Cell Count Cell Death Movement Isometric Contraction Synaptic Transmission Amino Acid Sequence Locomotion Cell Differentiation Cell Survival Aging Gene Expression

Disciplines and Occupations2

Immunohistochemistry Electrophysiology

Information Science2

Molecular Sequence Data Amino Acid Sequence

Health Care4

Hindlimb Suspension Age of Onset Analysis of Variance Age Factors

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 Muscular Atrophy Neuromuscular Diseases Spinal Muscular Atrophies of Childhood Atrophy Bulbar Palsy, Progressive Survival of Motor Neuron 1 Protein SMN Complex Proteins Spinal Cord Survival of Motor Neuron 2 Protein Amyotrophic Lateral Sclerosis Muscular Disorders, Atrophic Muscle, Skeletal Neurons Bulbo-Spinal Atrophy, X-Linked Anterior Horn Cells Muscles Muscle Proteins Hindlimb Suspension Nerve Degeneration SKP Cullin F-Box Protein Ligases Electromyography Muscle Fibers, Skeletal Spinal Cord Injuries Nerve Tissue Proteins Disease Models, Animal Superoxide Dismutase Axons Spinal Cord Diseases Fasciculation Neuronal Apoptosis-Inhibitory Protein Mice, Transgenic Muscle Weakness Cyclic AMP Response Element-Binding Protein DEAD Box Protein 20 Muscle Denervation RNA-Binding Proteins Neural Conduction Optic Atrophy Motor Cortex Neurons, Afferent Neurofilament Proteins Gagging Neuromuscular Junction Inclusion Bodies Motor Activity TDP-43 Proteinopathies Frontotemporal Lobar Degeneration Frontotemporal Dementia Mutation Muscle Contraction Brain Evoked Potentials, Motor Spinal Nerve Roots Ulnar Nerve RNA-Binding Protein FUS Muscle, Smooth Toxascariasis beta-Hexosaminidase beta Chain Riluzole Myostatin Pyrrolidonecarboxylic Acid Pharyngostomy Peripheral Nerves Deglutition Disorders Electric Injuries Pick Disease of the Brain Muscle Development Multiple System Atrophy Action Potentials Electric Stimulation Paralysis Time Factors Phenotype Cells, Cultured Mice, Inbred C57BL Pedigree Brain Injury, Chronic Magnetic Resonance Imaging Immunohistochemistry Lathyrism Muscle, Smooth, Vascular Neurologic Examination Muscle Fibers, Slow-Twitch Ribonucleoproteins, Small Nuclear Muscle Fibers, Fast-Twitch Mice, Knockout Dementia Immobilization Receptors, Androgen Rats, Transgenic Age of Onset Sandhoff Disease Marchiafava-Bignami Disease Axonal Transport Rats, Sprague-Dawley Cricoid Cartilage Recruitment, Neurophysiological

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