Symptoms muscular atrophy spinal. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy37

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

Organisms6

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

Diseases54

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

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment33

Disease Models, Animal Injections, Spinal Anesthesia, Spinal Pedigree Magnetic Resonance Imaging Spinal Fusion Electromyography Heterozygote Detection Severity of Illness Index Treatment Outcome Myelography Laminectomy Prenatal Diagnosis Symptom Assessment Genetic Testing Rotarod Performance Test Immunohistochemistry Muscle Denervation Retrospective Studies Genetic Therapy Muscle Strength Polymerase Chain Reaction Questionnaires Pain Measurement Follow-Up Studies DNA Mutational Analysis Chromosome Mapping Analysis of Variance Blotting, Western Muscle Strength Dynamometer Prospective Studies Hindlimb Suspension Reproducibility of Results

Psychiatry and Psychology5

Motor Activity Depression Pain Behavioral Symptoms Psychiatric Status Rating Scales

Phenomena and Processes29

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

Disciplines and Occupations3

Chemistry, Analytic Genetic Counseling Immunohistochemistry

Information Science3

Molecular Sequence Data Base Sequence Questionnaires

Named Groups1

Infant, Newborn

Health Care13

Severity of Illness Index Treatment Outcome Age of Onset Genetic Counseling Genetic Testing Retrospective Studies Questionnaires Follow-Up Studies Age Factors Analysis of Variance Prospective Studies Hindlimb Suspension Reproducibility of Results

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 DEAD Box Protein 20 Spinal Nerve Roots Chromosomes, Human, Pair 5 Disease Models, Animal Injections, Spinal Exons Spinal Nerves Multiple System Atrophy Coiled Bodies Anesthesia, Spinal Receptors, Androgen snRNP Core Proteins Spinal Cord Neoplasms Spinal Canal Spinal Cord Compression Spinal Diseases Muscle, Skeletal Spinal Neoplasms Pedigree Magnetic Resonance Imaging Mice, Transgenic Spinal Stenosis Bulbar Palsy, Progressive Spinal Fusion Electromyography Muscle Weakness Phenotype Nerve Degeneration Charcot-Marie-Tooth Disease Heterozygote Detection Neuromuscular Diseases Contracture Olivopontocerebellar Atrophies Neural Conduction Axons Glycine-tRNA Ligase Arthrogryposis Gene Deletion Vocal Cord Paralysis Mutation Spinal Injuries Homozygote Gyrate Atrophy Severity of Illness Index Trinucleotide Repeat Expansion Time Factors Neuromuscular Junction Amyotrophic Lateral Sclerosis Neuromuscular Junction Diseases RNA Splicing Ganglia, Spinal Spinal Cord Ischemia Genes, Recessive Sural Nerve Brain Genetic Linkage Motor Activity Trinucleotide Repeats Geographic Atrophy Gene Dosage Treatment Outcome Genes, Dominant Intranuclear Inclusion Bodies Myelography Paraplegia Inclusion Bodies Fasciculation Spine Myoclonic Epilepsies, Progressive Thoracic Vertebrae Disease Progression Chemistry, Analytic Ulnar Nerve Respiratory Paralysis Tuberculosis, Spinal Laminectomy Muscles Prenatal Diagnosis Age of Onset

No FAQ available that match "symptoms muscular atrophy spinal"