Brainstem conditions muscular atrophy spinal. Medical search. Frequent questions

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Anatomy52

Spinal Cord Brain Stem Motor Neurons Anterior Horn Cells Spinal Nerve Roots Chromosomes, Human, Pair 5 Spinal Nerves Coiled Bodies Spinal Canal Muscle, Skeletal Axons Neurons Brain Pons Neuromuscular Junction Ganglia, Spinal Sural Nerve Auditory Pathways Medulla Oblongata Inclusion Bodies Intranuclear Inclusion Bodies Spine Thoracic Vertebrae Afferent Pathways Ulnar Nerve Muscles Trigeminal Nucleus, Spinal Peripheral Nerves Spliceosomes Cervical Vertebrae Trigeminal Nuclei Acanthocytes Central Nervous System Posterior Horn Cells Sciatic Nerve Lumbosacral Region Reticular Formation Muscle Fibers, Skeletal Fibroblasts Solitary Nucleus Lumbar Vertebrae Cochlear Nucleus Cells, Cultured Neural Pathways Efferent Pathways Synapses Respiratory Center Cerebellum HeLa Cells Growth Cones Cell Line Neurons, Afferent

Organisms8

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

Diseases59

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 Multiple System Atrophy Brain Stem Neoplasms Spinal Cord Neoplasms Spinal Diseases Spinal Cord Compression Spinal Neoplasms Bulbar Palsy, Progressive Spinal Stenosis Nerve Degeneration Olivopontocerebellar Atrophies Charcot-Marie-Tooth Disease Muscle Weakness Contracture Neuromuscular Diseases Arthrogryposis Vocal Cord Paralysis Spinal Injuries Gyrate Atrophy Amyotrophic Lateral Sclerosis Neuromuscular Junction Diseases Spinal Cord Ischemia Geographic Atrophy Paraplegia Fasciculation Myoclonic Epilepsies, Progressive Brain Stem Infarctions Respiratory Paralysis Tuberculosis, Spinal Ophthalmoplegia Scoliosis Disease Progression Spinal Curvatures Postpoliomyelitis Syndrome Muscular Dystrophies Hematoma, Epidural, Spinal Hereditary Sensory and Motor Neuropathy Optic Atrophy, Autosomal Dominant Neurodegenerative Diseases Cerebellar Ataxia Quadriplegia Muscular Diseases Syndrome Nervous System Diseases Reflex, Abnormal Pain Tremor Spinal Fractures Hyperalgesia

Chemicals and Drugs19

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 Glycine-tRNA Ligase RNA, Messenger Valproic Acid Furylfuramide Neurofilament Proteins Aclarubicin Peptides Heterogeneous-Nuclear Ribonucleoprotein Group A-B

Analytical, Diagnostic and Therapeutic Techniques and Equipment30

Disease Models, Animal Injections, Spinal Anesthesia, Spinal Magnetic Resonance Imaging Electromyography Pedigree Spinal Fusion Heterozygote Detection Immunohistochemistry Myelography Prenatal Diagnosis Rotarod Performance Test Laminectomy Genetic Testing Muscle Denervation Electric Stimulation Genetic Therapy Muscle Strength Polymerase Chain Reaction Blotting, Western Reflex, Abnormal Audiometry, Evoked Response DNA Mutational Analysis Chromosome Mapping Muscle Strength Dynamometer Analysis of Variance Severity of Illness Index Hindlimb Suspension Acoustic Stimulation Reflex

Psychiatry and Psychology3

Motor Activity Pain Reflex

Phenomena and Processes32

Evoked Potentials, Auditory, Brain Stem Chromosomes, Human, Pair 5 Exons Phenotype Neural Conduction Gene Deletion Mutation Homozygote Trinucleotide Repeat Expansion RNA Splicing Genes, Recessive Motor Activity Genetic Linkage Gene Dosage Trinucleotide Repeats Time Factors Genes, Dominant Alternative Splicing Mutation, Missense Base Sequence Gene Expression Regulation Action Potentials Muscle Strength Reflex, Abnormal Founder Effect Locomotion Heterozygote Pain Gene Expression Spinal Cord Regeneration Recovery of Function Reflex

Disciplines and Occupations3

Immunohistochemistry Chemistry, Analytic Genetic Counseling

Information Science2

Molecular Sequence Data Base Sequence

Health Care6

Genetic Counseling Genetic Testing Age of Onset Analysis of Variance Severity of Illness Index 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 Spinal Cord Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Brain Stem Spinal Cord Injuries Neuronal Apoptosis-Inhibitory Protein Motor Neurons Cyclic AMP Response Element-Binding Protein Anterior Horn Cells RNA-Binding Proteins Nerve Tissue Proteins Spinal Cord Diseases Evoked Potentials, Auditory, Brain Stem Optic Atrophy Motor Neuron Disease Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 Disease Models, Animal Spinal Nerve Roots Chromosomes, Human, Pair 5 Injections, Spinal Exons Spinal Nerves Multiple System Atrophy Coiled Bodies Anesthesia, Spinal Brain Stem Neoplasms Receptors, Androgen snRNP Core Proteins Spinal Cord Neoplasms Spinal Canal Magnetic Resonance Imaging Muscle, Skeletal Spinal Diseases Spinal Cord Compression Electromyography Mice, Transgenic Spinal Neoplasms Pedigree Bulbar Palsy, Progressive Spinal Stenosis Nerve Degeneration Axons Spinal Fusion Olivopontocerebellar Atrophies Phenotype Neurons Charcot-Marie-Tooth Disease Brain Muscle Weakness Heterozygote Detection Neural Conduction Contracture Pons Neuromuscular Diseases Glycine-tRNA Ligase Arthrogryposis Gene Deletion Vocal Cord Paralysis Mutation Homozygote Spinal Injuries Gyrate Atrophy Amyotrophic Lateral Sclerosis Rats, Sprague-Dawley Neuromuscular Junction Trinucleotide Repeat Expansion Neuromuscular Junction Diseases RNA Splicing Ganglia, Spinal Spinal Cord Ischemia Genes, Recessive Motor Activity Sural Nerve Geographic Atrophy Genetic Linkage Gene Dosage Trinucleotide Repeats Auditory Pathways Medulla Oblongata Time Factors Animals, Newborn Immunohistochemistry Inclusion Bodies Intranuclear Inclusion Bodies Genes, Dominant Myelography Paraplegia Fasciculation Myoclonic Epilepsies, Progressive Chemistry, Analytic Spine Brain Stem Infarctions

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