Affects muscle muscular atrophy spinal. Medical search. Frequent questions

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Anatomy70

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

Organisms10

Mice, Transgenic Rats, Sprague-Dawley Mice, Knockout Mice, Inbred C57BL Animals, Newborn Rats, Wistar Rabbits Cats Mice, Neurologic Mutants Mice, Mutant Strains

Diseases58

Muscular Atrophy, Spinal Spinal Muscular Atrophies of Childhood Atrophy Muscular Atrophy Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Spinal Cord Diseases Optic Atrophy Motor Neuron Disease Muscle Weakness Disease Models, Animal Multiple System Atrophy Spinal Cord Neoplasms Spinal Diseases Spinal Cord Compression Spinal Neoplasms Neuromuscular Diseases Muscular Diseases Bulbar Palsy, Progressive Spinal Stenosis Contracture Charcot-Marie-Tooth Disease Nerve Degeneration Arthrogryposis Olivopontocerebellar Atrophies Vocal Cord Paralysis Spinal Injuries Gyrate Atrophy Amyotrophic Lateral Sclerosis Muscular Dystrophies Neuromuscular Junction Diseases Spinal Cord Ischemia Geographic Atrophy Paraplegia Fasciculation Respiratory Paralysis Myoclonic Epilepsies, Progressive Scoliosis Tuberculosis, Spinal Ophthalmoplegia Postpoliomyelitis Syndrome Spinal Curvatures Hereditary Sensory and Motor Neuropathy Disease Progression Hematoma, Epidural, Spinal Optic Atrophy, Autosomal Dominant Paralysis Muscle Spasticity Neurodegenerative Diseases Syndrome Quadriplegia Pain Tremor Spinal Fractures Muscular Dystrophy, Animal Hypertrophy Nervous System Diseases

Chemicals and Drugs30

Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Muscle Proteins Neuronal Apoptosis-Inhibitory Protein Cyclic AMP Response Element-Binding Protein Phosphocreatine RNA-Binding Proteins Nerve Tissue Proteins Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 Receptors, Androgen snRNP Core Proteins Glycine-tRNA Ligase RNA, Messenger Myosin Heavy Chains Actins Valproic Acid Calcium Furylfuramide Myostatin Peptides Neurofilament Proteins Aclarubicin DNA Primers SKP Cullin F-Box Protein Ligases Oligonucleotides, Antisense Heterogeneous-Nuclear Ribonucleoprotein Group A-B Glycogen Protein Isoforms

Analytical, Diagnostic and Therapeutic Techniques and Equipment32

Muscle Strength Muscle Denervation Disease Models, Animal Electromyography Injections, Spinal Anesthesia, Spinal Pedigree Magnetic Resonance Imaging Spinal Fusion Heterozygote Detection Electric Stimulation Immunohistochemistry Hindlimb Suspension Muscle Strength Dynamometer Myelography Blotting, Western Prenatal Diagnosis Laminectomy Models, Biological Genetic Therapy Polymerase Chain Reaction Genetic Testing Reverse Transcriptase Polymerase Chain Reaction Rotarod Performance Test Organ Size Analysis of Variance Reflex Chromosome Mapping DNA Mutational Analysis Severity of Illness Index Immobilization Hand Strength

Psychiatry and Psychology3

Motor Activity Reflex Pain

Phenomena and Processes49

Muscle Fatigue Muscle Contraction Muscle Development Muscle Strength Time Factors Energy Metabolism Exons Chromosomes, Human, Pair 5 Phenotype Neural Conduction Muscle Relaxation Mutation Gene Deletion Homozygote RNA Splicing Trinucleotide Repeat Expansion Motor Activity Isometric Contraction Gene Expression Regulation Genes, Recessive Base Sequence Genetic Linkage Gene Dosage Trinucleotide Repeats Genes, Dominant Alternative Splicing Gene Expression Biomechanical Phenomena Locomotion Action Potentials Amino Acid Sequence Mutation, Missense Signal Transduction Dose-Response Relationship, Drug Cell Differentiation Aging Organ Size Reflex Heterozygote Founder Effect Nerve Regeneration Pain Protein Binding Regeneration Spinal Cord Regeneration Genotype Alleles Hand Strength Movement

Disciplines and Occupations3

Immunohistochemistry Chemistry, Analytic Genetic Counseling

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care6

Hindlimb Suspension Genetic Counseling Genetic Testing Age of Onset Analysis of Variance Severity of Illness Index

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

Muscular Atrophy, Spinal Spinal Muscular Atrophies of Childhood Survival of Motor Neuron 1 Protein Muscle, Skeletal Atrophy SMN Complex Proteins Muscular Atrophy Survival of Motor Neuron 2 Protein Spinal Cord Muscles Muscle Fibers, Skeletal Muscle Proteins Muscular Disorders, Atrophic Muscle Fatigue Muscle Contraction Muscle Development Muscle Fibers, Fast-Twitch Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Neuronal Apoptosis-Inhibitory Protein Motor Neurons Cyclic AMP Response Element-Binding Protein Anterior Horn Cells Phosphocreatine Muscle Strength Muscle, Smooth RNA-Binding Proteins Nerve Tissue Proteins Muscle, Smooth, Vascular Spinal Cord Diseases Optic Atrophy Time Factors Energy Metabolism Motor Neuron Disease Ribonucleoproteins, Small Nuclear Muscle Denervation Muscle Weakness DEAD Box Protein 20 Disease Models, Animal Electromyography Spinal Nerve Roots Exons Chromosomes, Human, Pair 5 Injections, Spinal Spinal Nerves Muscle Fibers, Slow-Twitch Coiled Bodies Multiple System Atrophy Anesthesia, Spinal Receptors, Androgen snRNP Core Proteins Spinal Cord Neoplasms Mice, Transgenic Spinal Canal Mitochondria, Muscle Spinal Diseases Myocytes, Smooth Muscle Spinal Cord Compression Neuromuscular Junction Spinal Neoplasms Neck Muscles Pedigree Phenotype Oculomotor Muscles Neuromuscular Diseases Muscle, Striated Muscular Diseases Muscle Spindles Bulbar Palsy, Progressive Neural Conduction Magnetic Resonance Imaging Spinal Stenosis Axons Respiratory Muscles Spinal Fusion Muscle Relaxation Contracture Charcot-Marie-Tooth Disease Nerve Degeneration Papillary Muscles Mutation Heterozygote Detection Quadriceps Muscle Cells, Cultured Arthrogryposis Olivopontocerebellar Atrophies Gene Deletion Abdominal Muscles Glycine-tRNA Ligase Rats, Sprague-Dawley RNA, Messenger Muscle Cells Vocal Cord Paralysis Homozygote Hindlimb Masseter Muscle Spinal Injuries Facial Muscles Gyrate Atrophy RNA Splicing

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