Muscular atrophy mainly affects conditions muscular atrophy spinal. Medical search. Frequent questions

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Anatomy27

Spinal Cord Anterior Horn Cells Motor Neurons Chromosomes, Human, Pair 5 Coiled Bodies Muscle, Skeletal Spinal Nerve Roots Neuromuscular Junction Axons Spinal Nerves Sural Nerve Intranuclear Inclusion Bodies Spinal Canal Inclusion Bodies Ulnar Nerve Spliceosomes Acanthocytes Brain Muscles Fibroblasts Muscle Fibers, Skeletal HeLa Cells Peripheral Nerves Neurons Sciatic Nerve Cells, Cultured Growth Cones

Organisms3

Mice, Transgenic Mice, Knockout Mice, Neurologic Mutants

Diseases43

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

Chemicals and Drugs19

Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Neuronal Apoptosis-Inhibitory Protein Cyclic AMP Response Element-Binding Protein RNA-Binding Proteins Nerve Tissue Proteins Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 snRNP Core Proteins Receptors, Androgen Glycine-tRNA Ligase Valproic Acid Furylfuramide Aclarubicin RNA, Messenger Heterogeneous-Nuclear Ribonucleoprotein Group A-B Neurofilament Proteins Peptides

Analytical, Diagnostic and Therapeutic Techniques and Equipment21

Disease Models, Animal Pedigree Heterozygote Detection Electromyography Injections, Spinal Magnetic Resonance Imaging Anesthesia, Spinal Prenatal Diagnosis Genetic Testing Rotarod Performance Test Spinal Fusion Muscle Denervation Myelography Genetic Therapy Muscle Strength Polymerase Chain Reaction Chromosome Mapping DNA Mutational Analysis Muscle Strength Dynamometer Hindlimb Suspension Immunohistochemistry

Psychiatry and Psychology1

Phenomena and Processes23

Chromosomes, Human, Pair 5 Exons Phenotype Gene Deletion Neural Conduction Homozygote Mutation Trinucleotide Repeat Expansion RNA Splicing Genes, Recessive Genetic Linkage Trinucleotide Repeats Gene Dosage Genes, Dominant Alternative Splicing Motor Activity Mutation, Missense Base Sequence Muscle Strength Founder Effect Gene Expression Regulation Heterozygote Time Factors

Disciplines and Occupations3

Chemistry, Analytic Genetic Counseling Immunohistochemistry

Information Science2

Molecular Sequence Data Base Sequence

Health Care4

Genetic Counseling Genetic Testing Age of Onset Hindlimb Suspension

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 Atrophy SMN Complex Proteins Muscular Atrophy Survival of Motor Neuron 2 Protein Spinal Cord Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Neuronal Apoptosis-Inhibitory Protein Cyclic AMP Response Element-Binding Protein Anterior Horn Cells Motor Neurons RNA-Binding Proteins Nerve Tissue Proteins Spinal Cord Injuries Optic Atrophy Motor Neuron Disease Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 Chromosomes, Human, Pair 5 Exons Spinal Cord Diseases Disease Models, Animal Multiple System Atrophy Coiled Bodies snRNP Core Proteins Receptors, Androgen Muscle, Skeletal Pedigree Bulbar Palsy, Progressive Mice, Transgenic Spinal Nerve Roots Charcot-Marie-Tooth Disease Heterozygote Detection Muscle Weakness Phenotype Olivopontocerebellar Atrophies Contracture Nerve Degeneration Glycine-tRNA Ligase Arthrogryposis Neuromuscular Diseases Electromyography Vocal Cord Paralysis Gene Deletion Gyrate Atrophy Neural Conduction Injections, Spinal Magnetic Resonance Imaging Homozygote Mutation Trinucleotide Repeat Expansion Neuromuscular Junction Diseases RNA Splicing Neuromuscular Junction Axons Spinal Nerves Genes, Recessive Anesthesia, Spinal Amyotrophic Lateral Sclerosis Geographic Atrophy Genetic Linkage Trinucleotide Repeats Gene Dosage Sural Nerve Intranuclear Inclusion Bodies Spinal Cord Neoplasms Genes, Dominant Spinal Canal Spinal Diseases Spinal Cord Compression Myoclonic Epilepsies, Progressive Inclusion Bodies Fasciculation Chemistry, Analytic Prenatal Diagnosis Spinal Neoplasms Ulnar Nerve Spliceosomes Genetic Counseling Acanthocytes Brain Alternative Splicing Respiratory Paralysis Muscles Motor Activity Genetic Testing Valproic Acid Postpoliomyelitis Syndrome Furylfuramide Mutation, Missense Spinal Stenosis Rotarod Performance Test Muscular Dystrophies Molecular Sequence Data Spinal Fusion Optic Atrophy, Autosomal Dominant Hereditary Sensory and Motor Neuropathy

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