Less common diseases disease that affects muscular atrophy spinal. Medical search. Frequent questions

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Anatomy35

Spinal Cord Motor Neurons Anterior Horn Cells Chromosomes, Human, Pair 5 Spinal Nerve Roots Spinal Nerves Coiled Bodies Spinal Canal Muscle, Skeletal Axons Neuromuscular Junction Ganglia, Spinal Sural Nerve Intranuclear Inclusion Bodies Inclusion Bodies Brain Spine Thoracic Vertebrae Ulnar Nerve Muscles Spliceosomes Acanthocytes Neurons Cervical Vertebrae Posterior Horn Cells Peripheral Nerves Sciatic Nerve Muscle Fibers, Skeletal Fibroblasts Lumbosacral Region Lumbar Vertebrae HeLa Cells Cells, Cultured Growth Cones Central Nervous System

Organisms6

Mice, Transgenic Mice, Knockout Mice, Inbred C57BL Rats, Sprague-Dawley Animals, Newborn Mice, Neurologic Mutants

Diseases55

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 Optic Atrophy Motor Neuron Disease Disease Models, Animal Genetic Predisposition to Disease Disease Genetic Diseases, Inborn Multiple System Atrophy Spinal Cord Neoplasms Spinal Diseases Spinal Cord Compression Spinal Neoplasms Bulbar Palsy, Progressive Spinal Stenosis Nerve Degeneration Charcot-Marie-Tooth Disease Muscle Weakness Contracture Olivopontocerebellar Atrophies Neuromuscular Diseases Arthrogryposis Vocal Cord Paralysis Rare Diseases Spinal Injuries Gyrate Atrophy Neuromuscular Junction Diseases Amyotrophic Lateral Sclerosis Spinal Cord Ischemia Geographic Atrophy Paraplegia Fasciculation Myoclonic Epilepsies, Progressive Respiratory Paralysis Tuberculosis, Spinal Scoliosis Spinal Curvatures Diverticulitis, Colonic Postpoliomyelitis Syndrome Muscular Dystrophies Hematoma, Epidural, Spinal Hereditary Sensory and Motor Neuropathy Optic Atrophy, Autosomal Dominant Disease Progression Ophthalmoplegia Muscular Diseases Neurodegenerative Diseases Spinal Fractures Syndrome

Chemicals and Drugs20

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 Receptors, Androgen snRNP Core Proteins Genetic Markers Glycine-tRNA Ligase Valproic Acid Furylfuramide RNA, Messenger Aclarubicin Neurofilament Proteins Heterogeneous-Nuclear Ribonucleoprotein Group A-B Peptides

Analytical, Diagnostic and Therapeutic Techniques and Equipment36

Disease Models, Animal Genome-Wide Association Study Injections, Spinal Pedigree Anesthesia, Spinal Genetic Testing Magnetic Resonance Imaging Chromosome Mapping Models, Genetic Spinal Fusion Electromyography Heterozygote Detection Polymerase Chain Reaction Case-Control Studies Myelography DNA Mutational Analysis Prenatal Diagnosis Risk Factors Treatment Outcome Laminectomy Sequence Analysis, DNA Severity of Illness Index Rotarod Performance Test Muscle Denervation Individualized Medicine Cohort Studies Immunohistochemistry Retrospective Studies Genetic Therapy Muscle Strength Reproducibility of Results Muscle Strength Dynamometer Blotting, Western Tomography, X-Ray Computed Genetic Techniques Hindlimb Suspension

Psychiatry and Psychology1

Phenomena and Processes44

Genetic Predisposition to Disease Exons Chromosomes, Human, Pair 5 Genetic Linkage Phenotype Polymorphism, Single Nucleotide Genome, Human Genotype Genetic Variation Haplotypes Founder Effect Mutation Alleles Multifactorial Inheritance Genetic Markers Linkage Disequilibrium Gene Dosage Neural Conduction Gene Deletion Homozygote Gene Frequency Trinucleotide Repeat Expansion RNA Splicing Mutation, Missense Genes, Recessive Base Sequence Trinucleotide Repeats Genetic Loci Time Factors Gene Expression Regulation Genes, Dominant Heterozygote Motor Activity Alternative Splicing Polymorphism, Genetic Gene Expression Epistasis, Genetic Genetic Heterogeneity Muscle Strength Lod Score Algorithms Spinal Cord Regeneration Quantitative Trait, Heritable Signal Transduction

Disciplines and Occupations8

Genetics, Medical Genetics, Population Chemistry, Analytic Genetic Counseling Human Genome Project Individualized Medicine Immunohistochemistry Genomics

Information Science4

Molecular Sequence Data Base Sequence Human Genome Project Algorithms

Named Groups1

Infant, Newborn

Health Care14

Genome-Wide Association Study Genetic Testing Case-Control Studies Family Health Genetic Counseling Risk Factors Treatment Outcome Severity of Illness Index Cohort Studies Retrospective Studies Age of Onset Age Factors Reproducibility of Results 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 Named Groups 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 Spinal Cord Injuries Neuronal Apoptosis-Inhibitory Protein Cyclic AMP Response Element-Binding Protein Motor Neurons Anterior Horn Cells RNA-Binding Proteins Nerve Tissue Proteins Spinal Cord Diseases Optic Atrophy Motor Neuron Disease Ribonucleoproteins, Small Nuclear Disease Models, Animal DEAD Box Protein 20 Genetic Predisposition to Disease Disease Exons Genetic Diseases, Inborn Genome-Wide Association Study Chromosomes, Human, Pair 5 Spinal Nerve Roots Injections, Spinal Spinal Nerves Genetic Linkage Pedigree Coiled Bodies Phenotype Multiple System Atrophy Anesthesia, Spinal Polymorphism, Single Nucleotide Genome, Human Receptors, Androgen snRNP Core Proteins Genetic Testing Spinal Cord Neoplasms Spinal Canal Genotype Spinal Diseases Spinal Cord Compression Muscle, Skeletal Genetic Variation Spinal Neoplasms Haplotypes Founder Effect Mutation Alleles Magnetic Resonance Imaging Mice, Transgenic Bulbar Palsy, Progressive Genetics, Medical Spinal Stenosis Chromosome Mapping Models, Genetic Multifactorial Inheritance Spinal Fusion Electromyography Nerve Degeneration Charcot-Marie-Tooth Disease Muscle Weakness Heterozygote Detection Genetic Markers Linkage Disequilibrium Contracture Olivopontocerebellar Atrophies Gene Dosage Neuromuscular Diseases Axons Glycine-tRNA Ligase Arthrogryposis Neural Conduction Gene Deletion Vocal Cord Paralysis Rare Diseases Spinal Injuries Gyrate Atrophy Homozygote Gene Frequency Neuromuscular Junction Trinucleotide Repeat Expansion Neuromuscular Junction Diseases RNA Splicing Mutation, Missense Amyotrophic Lateral Sclerosis Spinal Cord Ischemia Ganglia, Spinal Genes, Recessive Molecular Sequence Data Polymerase Chain Reaction Sural Nerve Case-Control Studies Geographic Atrophy

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