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

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Anatomy17

Spinal Cord Motor Neurons Anterior Horn Cells Chromosomes, Human, Pair 5 Coiled Bodies Muscle, Skeletal Spinal Nerve Roots Spinal Nerves Axons Neuromuscular Junction Spinal Canal Spliceosomes Fibroblasts HeLa Cells Muscles Growth Cones Ganglia, Spinal

Organisms2

Mice, Transgenic Mice, Knockout

Diseases35

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 Motor Neuron Disease Disease Models, Animal Optic Atrophy Neuromuscular Junction Diseases Arthrogryposis Multiple System Atrophy Contracture Nerve Degeneration Neuromuscular Diseases Charcot-Marie-Tooth Disease Muscle Weakness Spinal Cord Neoplasms Vocal Cord Paralysis Spinal Diseases Spinal Cord Compression Spinal Neoplasms Fasciculation Amyotrophic Lateral Sclerosis Respiratory Paralysis Spinal Stenosis Bulbar Palsy, Progressive Muscular Dystrophies Olivopontocerebellar Atrophies Hereditary Sensory and Motor Neuropathy Spinal Injuries Gyrate Atrophy Scoliosis

Chemicals and Drugs17

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 Glycine-tRNA Ligase Receptors, Androgen Valproic Acid Aclarubicin Heterogeneous-Nuclear Ribonucleoprotein Group A-B RNA, Messenger Oligonucleotides, Antisense

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

Disease Models, Animal Pedigree Heterozygote Detection Injections, Spinal Anesthesia, Spinal Electromyography Prenatal Diagnosis Magnetic Resonance Imaging Spinal Fusion Genetic Testing Genetic Therapy Muscle Strength Dynamometer Chromosome Mapping Polymerase Chain Reaction Muscle Strength

Psychiatry and Psychology1

Phenomena and Processes20

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

Disciplines and Occupations2

Chemistry, Analytic Genetic Counseling

Information Science2

Molecular Sequence Data Base Sequence

Health Care2

Genetic Counseling Genetic Testing

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 SMN Complex Proteins Survival of Motor Neuron 2 Protein Atrophy Muscular Atrophy Spinal Cord Neuronal Apoptosis-Inhibitory Protein Cyclic AMP Response Element-Binding Protein Motor Neurons RNA-Binding Proteins Anterior Horn Cells Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Nerve Tissue Proteins Spinal Cord Injuries Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 Chromosomes, Human, Pair 5 Exons Spinal Cord Diseases Coiled Bodies Motor Neuron Disease snRNP Core Proteins Disease Models, Animal Optic Atrophy Pedigree Heterozygote Detection Muscle, Skeletal Glycine-tRNA Ligase Spinal Nerve Roots Mice, Transgenic Injections, Spinal Phenotype Gene Deletion Neuromuscular Junction Diseases Spinal Nerves RNA Splicing Homozygote Arthrogryposis Multiple System Atrophy Motor Activity Anesthesia, Spinal Electromyography Axons Neuromuscular Junction Contracture Nerve Degeneration Neuromuscular Diseases Receptors, Androgen Charcot-Marie-Tooth Disease Gene Dosage Mutation Muscle Weakness Spinal Cord Neoplasms Spinal Canal Vocal Cord Paralysis Spinal Diseases Spinal Cord Compression Genes, Recessive Neural Conduction Genetic Linkage Chemistry, Analytic Spinal Neoplasms Genes, Dominant Fasciculation Prenatal Diagnosis Spliceosomes Genetic Counseling Alternative Splicing Amyotrophic Lateral Sclerosis Respiratory Paralysis Spinal Stenosis Bulbar Palsy, Progressive Magnetic Resonance Imaging Spinal Fusion Valproic Acid Molecular Sequence Data Genetic Testing Fibroblasts Aclarubicin Base Sequence Muscular Dystrophies Olivopontocerebellar Atrophies Mutation, Missense Hereditary Sensory and Motor Neuropathy Genetic Therapy HeLa Cells Muscles Heterogeneous-Nuclear Ribonucleoprotein Group A-B Muscle Strength Dynamometer Spinal Injuries RNA, Messenger Chromosome Mapping Gyrate Atrophy Scoliosis Mice, Knockout Polymerase Chain Reaction Muscle Strength

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