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

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Anatomy16

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

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 Charcot-Marie-Tooth Disease Neuromuscular Diseases Spinal Cord Neoplasms Muscle Weakness Vocal Cord Paralysis Spinal Diseases Spinal Cord Compression Spinal Neoplasms Fasciculation Respiratory Paralysis Amyotrophic Lateral Sclerosis Bulbar Palsy, Progressive Spinal Stenosis Olivopontocerebellar Atrophies Muscular Dystrophies 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 Equipment14

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

Psychiatry and Psychology1

Phenomena and Processes18

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

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 Glycine-tRNA Ligase Muscle, Skeletal Spinal Nerve Roots Mice, Transgenic Injections, Spinal Phenotype Gene Deletion Neuromuscular Junction Diseases Spinal Nerves RNA Splicing Homozygote Arthrogryposis Multiple System Atrophy Anesthesia, Spinal Electromyography Axons Neuromuscular Junction Contracture Nerve Degeneration Receptors, Androgen Charcot-Marie-Tooth Disease Neuromuscular Diseases Gene Dosage Spinal Cord Neoplasms Spinal Canal Mutation Muscle Weakness Vocal Cord Paralysis Spinal Diseases Spinal Cord Compression Genes, Recessive Neural Conduction Chemistry, Analytic Spinal Neoplasms Fasciculation Genetic Linkage Genes, Dominant Prenatal Diagnosis Spliceosomes Genetic Counseling Respiratory Paralysis Alternative Splicing Amyotrophic Lateral Sclerosis Bulbar Palsy, Progressive Spinal Stenosis Spinal Fusion Magnetic Resonance Imaging Valproic Acid Genetic Testing Motor Activity Aclarubicin Molecular Sequence Data Fibroblasts Olivopontocerebellar Atrophies Muscular Dystrophies Mutation, Missense Hereditary Sensory and Motor Neuropathy Base Sequence Genetic Therapy Heterogeneous-Nuclear Ribonucleoprotein Group A-B HeLa Cells Muscles Spinal Injuries Muscle Strength Dynamometer Gyrate Atrophy RNA, Messenger Scoliosis Mice, Knockout Trinucleotide Repeat Expansion Polymerase Chain Reaction Heterozygote

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