Abstract clinical muscular atrophy spinal. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy37

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

Organisms6

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

Diseases52

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 Bulbar Palsy, Progressive Spinal Stenosis Nerve Degeneration 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 Neurodegenerative Diseases Spinal Fractures Nervous System Diseases Syndrome 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 RNA, Messenger Valproic Acid Furylfuramide Aclarubicin Neurofilament Proteins Peptides Heterogeneous-Nuclear Ribonucleoprotein Group A-B

Analytical, Diagnostic and Therapeutic Techniques and Equipment24

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

Psychiatry and Psychology1

Phenomena and Processes27

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

Disciplines and Occupations3

Chemistry, Analytic Genetic Counseling Immunohistochemistry

Information Science4

Molecular Sequence Data Abstracting and Indexing as Topic Base Sequence Amino Acid Sequence

Health Care5

Genetic Counseling Genetic Testing Age of Onset Hindlimb Suspension Severity of Illness Index

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 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 Spinal Nerves Coiled Bodies Multiple System Atrophy Anesthesia, Spinal Receptors, Androgen snRNP Core Proteins Spinal Cord Neoplasms Spinal Canal Muscle, Skeletal Spinal Diseases Spinal Cord Compression Spinal Neoplasms Pedigree Mice, Transgenic Bulbar Palsy, Progressive Spinal Stenosis Electromyography Spinal Fusion Magnetic Resonance Imaging Phenotype Nerve Degeneration Heterozygote Detection Charcot-Marie-Tooth Disease Muscle Weakness Axons Contracture Olivopontocerebellar Atrophies Neuromuscular Diseases Neural Conduction Glycine-tRNA Ligase Arthrogryposis Gene Deletion Vocal Cord Paralysis Mutation Spinal Injuries Homozygote Gyrate Atrophy Neuromuscular Junction Trinucleotide Repeat Expansion Neuromuscular Junction Diseases RNA Splicing Amyotrophic Lateral Sclerosis Spinal Cord Ischemia Ganglia, Spinal Genes, Recessive Sural Nerve Genetic Linkage Geographic Atrophy Gene Dosage Trinucleotide Repeats Brain Muscles Time Factors Intranuclear Inclusion Bodies Motor Activity Genes, Dominant Myelography Paraplegia Inclusion Bodies Molecular Sequence Data Neurons Fasciculation Myoclonic Epilepsies, Progressive Abstracting and Indexing as Topic Chemistry, Analytic Spine Thoracic Vertebrae Ulnar Nerve Respiratory Paralysis Tuberculosis, Spinal Prenatal Diagnosis Base Sequence Spliceosomes

No FAQ available that match "abstract clinical muscular atrophy spinal"