Spinal muscle atrophy muscular atrophy spinal. Medical search. Frequent questions

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Anatomy67

Spinal Cord Muscle, Skeletal Muscles Muscle Fibers, Skeletal Motor Neurons Anterior Horn Cells Spinal Nerve Roots Spinal Nerves Muscle, Smooth Spinal Canal Muscle, Smooth, Vascular Muscle Fibers, Slow-Twitch Muscle Fibers, Fast-Twitch Mitochondria, Muscle Hindlimb Satellite Cells, Skeletal Muscle Chromosomes, Human, Pair 5 Axons Neuromuscular Junction Coiled Bodies Quadriceps Muscle Ganglia, Spinal Cells, Cultured Muscle Cells Myoblasts Spine Myofibrils Myocytes, Smooth Muscle Sciatic Nerve Thoracic Vertebrae Neck Muscles Brain Oculomotor Muscles Muscle, Striated Muscle Spindles Lumbosacral Region Diaphragm Cervical Vertebrae Respiratory Muscles Leg Posterior Horn Cells Myoblasts, Skeletal Lumbar Vertebrae Velopharyngeal Sphincter Cell Line Papillary Muscles Neurons Abdominal Muscles Sural Nerve Facial Muscles Masseter Muscle Intercostal Muscles Masticatory Muscles Peripheral Nerves Inclusion Bodies Trigeminal Nucleus, Spinal Ulnar Nerve Intranuclear Inclusion Bodies Pectoralis Muscles Neurons, Afferent Afferent Pathways Central Nervous System Arm Thigh Fibroblasts Epidural Space Cell Nucleus

Organisms8

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

Diseases61

Muscular Atrophy, Spinal Muscular Atrophy Spinal Muscular Atrophies of Childhood Atrophy Muscular Disorders, Atrophic Spinal Cord Injuries Bulbo-Spinal Atrophy, X-Linked Optic Atrophy Spinal Cord Diseases Muscle Weakness Multiple System Atrophy Disease Models, Animal Motor Neuron Disease Spinal Cord Neoplasms Spinal Diseases Spinal Cord Compression Spinal Neoplasms Spinal Stenosis Neuromuscular Diseases Olivopontocerebellar Atrophies Muscular Diseases Cachexia Spinal Injuries Gyrate Atrophy Spinal Cord Ischemia Nerve Degeneration Geographic Atrophy Amyotrophic Lateral Sclerosis Paraplegia Sarcopenia Paralysis Tuberculosis, Spinal Bulbar Palsy, Progressive Hypertrophy Contracture Spinal Curvatures Charcot-Marie-Tooth Disease Hematoma, Epidural, Spinal Optic Atrophy, Autosomal Dominant Arthrogryposis Wasting Syndrome Vocal Cord Paralysis Scoliosis Spinal Fractures Muscular Dystrophies Quadriplegia Pain Neuromuscular Junction Diseases Myoclonic Epilepsies, Progressive Hyperalgesia Body Weight Disease Progression Respiratory Paralysis Fasciculation Lameness, Animal Muscle Spasticity Gastritis, Atrophic Ophthalmoplegia Neuralgia Hammer Toe Syndrome Neurodegenerative Diseases

Chemicals and Drugs31

Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Muscle Proteins SKP Cullin F-Box Protein Ligases Neuronal Apoptosis-Inhibitory Protein Cyclic AMP Response Element-Binding Protein RNA-Binding Proteins Myostatin Nerve Tissue Proteins Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 Ubiquitin-Protein Ligases RNA, Messenger Receptors, Androgen Myosin Heavy Chains snRNP Core Proteins Proteasome Endopeptidase Complex Myogenin Glycine-tRNA Ligase Insulin-Like Growth Factor I Forkhead Transcription Factors MyoD Protein Ubiquitin Superoxide Dismutase Proto-Oncogene Proteins c-akt Skeletal Muscle Myosins Glucocorticoids Actins Transcription Factors Protein Isoforms

Analytical, Diagnostic and Therapeutic Techniques and Equipment38

Hindlimb Suspension Muscle Denervation Injections, Spinal Disease Models, Animal Anesthesia, Spinal Immobilization Electromyography Magnetic Resonance Imaging Spinal Fusion Organ Size Bed Rest Pedigree Electric Stimulation Immunohistochemistry Muscle Strength Laminectomy Electric Stimulation Therapy Heterozygote Detection Blotting, Western Myelography Reverse Transcriptase Polymerase Chain Reaction Analysis of Variance Models, Biological Reflex Body Weight Weightlessness Countermeasures Manipulation, Spinal Muscle Strength Dynamometer Polymerase Chain Reaction Treatment Outcome Weightlessness Simulation Pain Measurement Biopsy Cordotomy Physical Stimulation Spinal Puncture Genetic Therapy Prenatal Diagnosis

Psychiatry and Psychology3

Motor Activity Pain Reflex

Phenomena and Processes51

Muscle Contraction Muscle Development Muscle Fatigue Exons Chromosomes, Human, Pair 5 Organ Size Time Factors Phenotype Neural Conduction Gene Expression Regulation Signal Transduction Isometric Contraction Mutation Motor Activity Muscle Strength Aging Recovery of Function Muscle Relaxation Gene Expression Proteolysis Gene Deletion Locomotion Homozygote Biomechanical Phenomena Base Sequence Weight-Bearing Trinucleotide Repeat Expansion RNA Splicing Genes, Recessive Estivation Spinal Cord Regeneration Pain Weightlessness Genetic Linkage Genes, Dominant Regeneration Reflex Nerve Regeneration Trinucleotide Repeats Action Potentials Cell Differentiation Body Weight Gene Dosage Amino Acid Sequence Dose-Response Relationship, Drug Oxidative Stress Alternative Splicing Apoptosis Mutation, Missense Phosphorylation Physical Conditioning, Animal

Disciplines and Occupations2

Immunohistochemistry Chemistry, Analytic

Technology, Industry, Agriculture1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care4

Hindlimb Suspension Analysis of Variance Treatment Outcome Weightlessness Simulation

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

Muscular Atrophy, Spinal Muscular Atrophy Spinal Muscular Atrophies of Childhood Atrophy Spinal Cord Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Muscular Disorders, Atrophic Spinal Cord Injuries Muscle, Skeletal Muscle Proteins Hindlimb Suspension Muscles SKP Cullin F-Box Protein Ligases Muscle Fibers, Skeletal Bulbo-Spinal Atrophy, X-Linked Motor Neurons Neuronal Apoptosis-Inhibitory Protein Optic Atrophy Muscle Denervation Anterior Horn Cells Cyclic AMP Response Element-Binding Protein Spinal Cord Diseases Injections, Spinal RNA-Binding Proteins Spinal Nerve Roots Myostatin Spinal Nerves Muscle Weakness Muscle, Smooth Muscle Contraction Multiple System Atrophy Nerve Tissue Proteins Disease Models, Animal Anesthesia, Spinal Muscle Development Motor Neuron Disease Spinal Cord Neoplasms Spinal Canal Muscle, Smooth, Vascular Spinal Diseases Muscle Fibers, Slow-Twitch Spinal Cord Compression Muscle Fibers, Fast-Twitch Immobilization Electromyography Spinal Neoplasms Spinal Stenosis Magnetic Resonance Imaging Ribonucleoproteins, Small Nuclear Mice, Transgenic Spinal Fusion Muscle Fatigue DEAD Box Protein 20 Rats, Sprague-Dawley Neuromuscular Diseases Olivopontocerebellar Atrophies Mitochondria, Muscle Muscular Diseases Hindlimb Exons Satellite Cells, Skeletal Muscle Chromosomes, Human, Pair 5 Organ Size Ubiquitin-Protein Ligases Cachexia Spinal Injuries Gyrate Atrophy Time Factors Axons Neuromuscular Junction Coiled Bodies Quadriceps Muscle RNA, Messenger Phenotype Ganglia, Spinal Neural Conduction Receptors, Androgen Spinal Cord Ischemia Gene Expression Regulation Myosin Heavy Chains Mice, Inbred C57BL Nerve Degeneration snRNP Core Proteins Geographic Atrophy Mice, Knockout Amyotrophic Lateral Sclerosis Bed Rest Signal Transduction Pedigree Isometric Contraction Cells, Cultured Rats, Wistar Paraplegia Muscle Cells Sarcopenia Myoblasts Electric Stimulation Spine

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