Neuromuscular muscular atrophy. Medical search. Frequent questions

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Anatomy19

Anterior Horn Cells Motor Neurons Chromosomes, Human, Pair 5 Coiled Bodies Spinal Cord Muscle, Skeletal Neuromuscular Junction Intranuclear Inclusion Bodies Sural Nerve Inclusion Bodies Axons Ulnar Nerve Spliceosomes Acanthocytes Muscles Brain Fibroblasts Muscle Fibers, Skeletal HeLa Cells

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

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment16

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

Psychiatry and Psychology1

Phenomena and Processes22

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

Disciplines and Occupations2

Chemistry, Analytic Genetic Counseling

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

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