Body disease that affects muscular atrophy spinal. Medical search. Frequent questions

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Anatomy41

Spinal Cord Lewy Bodies Inclusion Bodies Motor Neurons Anterior Horn Cells Neurofibrils Brain Inclusion Bodies, Viral Brain Stem Chromosomes, Human, Pair 5 Spinal Nerve Roots Spinal Nerves Neurons Coiled Bodies Substantia Nigra Spinal Canal Muscle, Skeletal Basal Ganglia Frontal Lobe Cerebral Cortex Axons Neuromuscular Junction Ganglia, Spinal Sural Nerve Intranuclear Inclusion Bodies Spine Thoracic Vertebrae Ulnar Nerve Muscles Spliceosomes Acanthocytes Cervical Vertebrae Posterior Horn Cells Peripheral Nerves Sciatic Nerve Muscle Fibers, Skeletal Fibroblasts Lumbosacral Region Lumbar Vertebrae HeLa Cells Cells, Cultured

Organisms6

Boidae Arenavirus Mice, Transgenic Rats, Sprague-Dawley Mice, Knockout Animals, Newborn

Diseases55

Lewy Body Disease Muscular Atrophy, Spinal Spinal Muscular Atrophies of Childhood Atrophy Muscular Atrophy Muscular Disorders, Atrophic Parkinson Disease Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Multiple System Atrophy Myoclonus Dementia Spinal Cord Diseases Supranuclear Palsy, Progressive Nerve Degeneration Optic Atrophy Alzheimer Disease Hallucinations Motor Neuron Disease Neurodegenerative Diseases Disease Models, Animal Spinal Cord Neoplasms Spinal Diseases Spinal Cord Compression Spinal Neoplasms Bulbar Palsy, Progressive Spinal Stenosis Charcot-Marie-Tooth Disease Muscle Weakness Contracture Olivopontocerebellar Atrophies Neuromuscular Diseases Arthrogryposis Vocal Cord Paralysis 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 Postpoliomyelitis Syndrome Muscular Dystrophies Hematoma, Epidural, Spinal Hereditary Sensory and Motor Neuropathy Optic Atrophy, Autosomal Dominant Disease Progression Ophthalmoplegia Muscular Diseases

Chemicals and Drugs21

Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein alpha-Synuclein Neuronal Apoptosis-Inhibitory Protein Cyclic AMP Response Element-Binding Protein Synucleins Nerve Tissue Proteins RNA-Binding Proteins Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 Synaptophysin Enkephalin, Leucine Receptors, Androgen snRNP Core Proteins Glycine-tRNA Ligase Valproic Acid Furylfuramide RNA, Messenger Aclarubicin Neurofilament Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment20

Autopsy Injections, Spinal Disease Models, Animal Anesthesia, Spinal Fatal Outcome Pedigree Immunohistochemistry Spinal Fusion Electromyography Heterozygote Detection Magnetic Resonance Imaging Myelography Prenatal Diagnosis Laminectomy Genetic Testing Rotarod Performance Test Muscle Denervation Genetic Therapy Muscle Strength Polymerase Chain Reaction

Psychiatry and Psychology7

Lewy Body Disease Dementia Alzheimer Disease Hallucinations Cognition Disorders Neuropsychological Tests Motor Activity

Phenomena and Processes23

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

Disciplines and Occupations3

Immunohistochemistry Chemistry, Analytic Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science3

Fatal Outcome Molecular Sequence Data Base Sequence

Health Care4

Fatal Outcome Genetic Counseling Genetic Testing Age of Onset

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Information Science Health Care

Lewy Body Disease 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 Lewy Bodies Inclusion Bodies Boidae alpha-Synuclein Muscular Disorders, Atrophic Parkinson Disease Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Neuronal Apoptosis-Inhibitory Protein Multiple System Atrophy Cyclic AMP Response Element-Binding Protein Motor Neurons Anterior Horn Cells Synucleins Arenavirus Nerve Tissue Proteins Neurofibrils RNA-Binding Proteins Brain Myoclonus Dementia Spinal Cord Diseases Supranuclear Palsy, Progressive Nerve Degeneration Optic Atrophy Alzheimer Disease Hallucinations Motor Neuron Disease Autopsy Ribonucleoproteins, Small Nuclear Neurodegenerative Diseases Inclusion Bodies, Viral DEAD Box Protein 20 Brain Stem Synaptophysin Chromosomes, Human, Pair 5 Spinal Nerve Roots Injections, Spinal Exons Enkephalin, Leucine Disease Models, Animal Spinal Nerves Neurons Coiled Bodies Anesthesia, Spinal Substantia Nigra Receptors, Androgen snRNP Core Proteins Fatal Outcome Spinal Cord Neoplasms Mutation Spinal Canal Spinal Diseases Spinal Cord Compression Muscle, Skeletal Spinal Neoplasms Pedigree Basal Ganglia Mice, Transgenic Bulbar Palsy, Progressive Spinal Stenosis Immunohistochemistry Spinal Fusion Electromyography Charcot-Marie-Tooth Disease Muscle Weakness Heterozygote Detection Phenotype Magnetic Resonance Imaging Frontal Lobe Cognition Disorders Contracture Olivopontocerebellar Atrophies Cerebral Cortex Neuromuscular Diseases Axons Glycine-tRNA Ligase Arthrogryposis Neural Conduction Gene Deletion Vocal Cord Paralysis Spinal Injuries Gyrate Atrophy Homozygote Neuropsychological Tests Neuromuscular Junction Trinucleotide Repeat Expansion Neuromuscular Junction Diseases RNA Splicing Amyotrophic Lateral Sclerosis Spinal Cord Ischemia

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