Area spinal muscular atrophies of childhood. Medical search. Frequent questions

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Anatomy16

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

Organisms2

Mice, Transgenic Mice, Knockout

Diseases30

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

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment14

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

Psychiatry and Psychology1

Phenomena and Processes17

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

Disciplines and Occupations2

Chemistry, Analytic Genetic Counseling

Information Science2

Molecular Sequence Data Base Sequence

Named Groups1

Infant, Newborn

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

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