Amyotrophic lateral s conditions muscular atrophy spinal. Medical search. Frequent questions

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Anatomy53

Spinal Cord Motor Neurons Anterior Horn Cells Inclusion Bodies Spinal Nerve Roots Muscle, Skeletal Axons Brain Neurons Chromosomes, Human, Pair 5 Spinal Nerves Neuromuscular Junction Coiled Bodies Spinal Canal Astrocytes Pyramidal Tracts Intranuclear Inclusion Bodies Microglia Central Nervous System Peripheral Nerves Cells, Cultured Neuroglia Cell Line Muscles Mitochondria Lateral Line System Brain Stem Ganglia, Spinal Muscle Fibers, Skeletal Sural Nerve Motor Cortex Spine HeLa Cells Thoracic Vertebrae Cytoplasm Cerebral Cortex Cell Nucleus HEK293 Cells Ulnar Nerve Chromosomes, Human, Pair 9 Synapses Fibroblasts Hindlimb Lateral Ventricles Nerve Fibers, Myelinated Tongue Lumbar Vertebrae Spliceosomes Neurites Lumbosacral Region Acanthocytes Hypothalamic Area, Lateral Posterior Horn Cells

Organisms12

Mice, Transgenic Rats, Transgenic Cycas Animals, Genetically Modified Mice, Inbred C57BL Rats, Sprague-Dawley Mice, Neurologic Mutants Mice, Knockout Animals, Newborn Dependovirus Mice, Mutant Strains Zebrafish

Diseases56

Amyotrophic Lateral Sclerosis Muscular Atrophy, Spinal Spinal Muscular Atrophies of Childhood Atrophy Muscular Atrophy Motor Neuron Disease Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Disease Models, Animal Nerve Degeneration Frontotemporal Dementia Frontotemporal Lobar Degeneration Bulbar Palsy, Progressive Fasciculation Neurodegenerative Diseases Spinal Cord Diseases Optic Atrophy TDP-43 Proteinopathies Disease Progression Muscle Weakness Neuromuscular Diseases Multiple System Atrophy Spinal Cord Neoplasms Spinal Cord Compression Spinal Diseases Spinal Neoplasms Spinal Stenosis Paralysis Charcot-Marie-Tooth Disease Contracture Pseudobulbar Palsy Olivopontocerebellar Atrophies Sialorrhea Arthrogryposis Nervous System Diseases Dementia Vocal Cord Paralysis Spinal Injuries Gyrate Atrophy Neuromuscular Junction Diseases Parkinson Disease Gliosis Spinal Cord Ischemia Genetic Predisposition to Disease Geographic Atrophy Alzheimer Disease Syndrome Paraplegia Respiratory Insufficiency Myoclonic Epilepsies, Progressive Scoliosis Respiratory Paralysis Tuberculosis, Spinal Pick Disease of the Brain Spinal Curvatures

Chemicals and Drugs38

Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Superoxide Dismutase RNA-Binding Protein FUS Neuronal Apoptosis-Inhibitory Protein Cyclic AMP Response Element-Binding Protein RNA-Binding Proteins Nerve Tissue Proteins Riluzole Ribonucleoproteins, Small Nuclear Neurofilament Proteins DEAD Box Protein 20 Neuroprotective Agents Receptors, Androgen snRNP Core Proteins Mutant Proteins DNA-Binding Proteins Lithium Carbonate Excitatory Amino Acid Transporter 2 Glycine-tRNA Ligase Ribonuclease, Pancreatic RNA, Messenger Amino Acids, Diamino Peripherins Glial Fibrillary Acidic Protein Glutamic Acid Copper Glycine Ubiquitin Peptides Genetic Markers Proteins Pyrazolones Green Fluorescent Proteins DNA Primers Choline O-Acetyltransferase Valproic Acid

Analytical, Diagnostic and Therapeutic Techniques and Equipment40

Disease Models, Animal Injections, Spinal Pedigree Electromyography Magnetic Resonance Imaging Rotarod Performance Test Anesthesia, Spinal Immunohistochemistry Spinal Fusion Heterozygote Detection Amino Acid Substitution Noninvasive Ventilation Case-Control Studies Models, Biological Muscle Denervation DNA Mutational Analysis Blotting, Western Genetic Testing Autopsy Genetic Therapy Analysis of Variance Polymerase Chain Reaction Chromosome Mapping Muscle Strength Severity of Illness Index Myelography Tracheostomy Neuroimaging Stem Cell Transplantation Communication Aids for Disabled Reproducibility of Results Electric Stimulation Neurologic Examination Laminectomy Treatment Outcome Prenatal Diagnosis Cohort Studies Reverse Transcriptase Polymerase Chain Reaction Transfection Retrospective Studies

Psychiatry and Psychology9

Frontotemporal Dementia Frontotemporal Lobar Degeneration Motor Activity Dementia Alzheimer Disease Laughter Pick Disease of the Brain Cognition Disorders Behavior, Animal

Phenomena and Processes47

DNA Repeat Expansion Mutation Exons Phenotype Chromosomes, Human, Pair 5 Mutation, Missense Neural Conduction Motor Activity Time Factors Homozygote Genes, Dominant Axonal Transport Gene Deletion Trinucleotide Repeat Expansion RNA Splicing Amino Acid Substitution Genetic Linkage Genes, Recessive Gene Expression Regulation Gene Dosage Cell Death Base Sequence Cell Survival Protein Folding Amino Acid Sequence Genotype Genetic Predisposition to Disease Protein Binding Alternative Splicing Trinucleotide Repeats Gene Expression Muscle Strength Protein Transport Heterozygote Transgenes Oxidative Stress Longevity Alleles Action Potentials Signal Transduction Genetic Markers Chromosomes, Human, Pair 9 Point Mutation Protein Structure, Tertiary Transfection Evoked Potentials, Motor Apoptosis

Disciplines and Occupations3

Immunohistochemistry Chemistry, Analytic Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Image Processing, Computer-Assisted

Health Care12

Age of Onset Case-Control Studies Genetic Testing Family Health Analysis of Variance Severity of Illness Index Age Factors Reproducibility of Results Treatment Outcome Cohort Studies Genetic Counseling Retrospective Studies

Geographicals2

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 Geographicals

Amyotrophic Lateral Sclerosis Muscular Atrophy, Spinal Spinal Muscular Atrophies of Childhood Survival of Motor Neuron 1 Protein Atrophy Spinal Cord SMN Complex Proteins Muscular Atrophy Survival of Motor Neuron 2 Protein Motor Neurons Motor Neuron Disease Superoxide Dismutase Anterior Horn Cells Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries RNA-Binding Protein FUS Neuronal Apoptosis-Inhibitory Protein Cyclic AMP Response Element-Binding Protein Disease Models, Animal Mice, Transgenic DNA Repeat Expansion Inclusion Bodies RNA-Binding Proteins Nerve Tissue Proteins Nerve Degeneration Frontotemporal Dementia Mutation Riluzole Guam Frontotemporal Lobar Degeneration Bulbar Palsy, Progressive Fasciculation Neurodegenerative Diseases Spinal Cord Diseases Optic Atrophy Ribonucleoproteins, Small Nuclear Neurofilament Proteins Exons Spinal Nerve Roots Muscle, Skeletal Injections, Spinal Axons DEAD Box Protein 20 TDP-43 Proteinopathies Disease Progression Pedigree Brain Muscle Weakness Neuromuscular Diseases Multiple System Atrophy Neurons Electromyography Phenotype Chromosomes, Human, Pair 5 Mutation, Missense Magnetic Resonance Imaging Age of Onset Spinal Nerves Neuromuscular Junction Rotarod Performance Test Coiled Bodies Anesthesia, Spinal Neuroprotective Agents Receptors, Androgen snRNP Core Proteins Neural Conduction Spinal Canal Rats, Transgenic Spinal Cord Neoplasms Mutant Proteins Spinal Cord Compression Spinal Diseases DNA-Binding Proteins Astrocytes Spinal Neoplasms Pyramidal Tracts Cycas Intranuclear Inclusion Bodies Motor Activity Animals, Genetically Modified Microglia Immunohistochemistry Spinal Fusion Time Factors Lithium Carbonate Spinal Stenosis Homozygote Excitatory Amino Acid Transporter 2 Mice, Inbred C57BL Central Nervous System Genes, Dominant Axonal Transport Molecular Sequence Data Gene Deletion Trinucleotide Repeat Expansion Paralysis Charcot-Marie-Tooth Disease Heterozygote Detection Contracture

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