Congenital physical muscular atrophy spinal. Medical search. Frequent questions

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Anatomy38

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

Organisms6

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

Diseases53

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 Diseases Spinal Cord Compression Spinal Neoplasms Spinal Stenosis Bulbar Palsy, Progressive Muscle Weakness Charcot-Marie-Tooth Disease Nerve Degeneration Neuromuscular Diseases Contracture Olivopontocerebellar Atrophies 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 Postpoliomyelitis Syndrome Spinal Curvatures Muscular Dystrophies Disease Progression Hematoma, Epidural, Spinal Pain Hereditary Sensory and Motor Neuropathy Optic Atrophy, Autosomal Dominant Muscular Diseases Ophthalmoplegia Neurodegenerative Diseases Spinal Fractures Syndrome Quadriplegia Nervous System Diseases

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment33

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

Psychiatry and Psychology2

Motor Activity Pain

Phenomena and Processes37

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

Disciplines and Occupations4

Chemistry, Analytic Physical Therapy Specialty Genetic Counseling Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena3

Physical Fitness Exercise Physical Education and Training

Information Science4

Molecular Sequence Data Base Sequence Questionnaires Amino Acid Sequence

Health Care11

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

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