Genetic conditions conditions muscular atrophy spinal. Medical search. Frequent questions

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Anatomy35

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 Intranuclear Inclusion Bodies Inclusion Bodies Brain Spine Thoracic Vertebrae Ulnar Nerve Muscles Spliceosomes Acanthocytes Neurons Cervical Vertebrae Posterior Horn Cells Peripheral Nerves Sciatic Nerve Muscle Fibers, Skeletal Fibroblasts Lumbosacral Region Lumbar Vertebrae HeLa Cells Cells, Cultured Growth Cones Central Nervous System

Organisms6

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

Diseases53

Muscular Atrophy, Spinal Genetic Diseases, Inborn Spinal Muscular Atrophies of Childhood Atrophy Muscular Atrophy Williams Syndrome Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Genetic Predisposition to Disease 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 Syndrome

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 Equipment23

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

Psychiatry and Psychology1

Phenomena and Processes25

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

Disciplines and Occupations3

Genetic Counseling Chemistry, Analytic Immunohistochemistry

Information Science2

Molecular Sequence Data Base Sequence

Health Care4

Genetic Counseling Genetic Testing Age of Onset 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 Genetic Diseases, Inborn Spinal Muscular Atrophies of Childhood Genetic Counseling Survival of Motor Neuron 1 Protein Atrophy SMN Complex Proteins Genetic Testing Muscular Atrophy Survival of Motor Neuron 2 Protein Williams Syndrome Spinal Cord Muscular Disorders, Atrophic Mutation Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Neuronal Apoptosis-Inhibitory Protein Heterozygote Phenotype Cyclic AMP Response Element-Binding Protein Motor Neurons Anterior Horn Cells RNA-Binding Proteins Genetic Predisposition to Disease 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 Exons Disease Models, Animal Spinal Nerves Coiled Bodies Multiple System Atrophy Anesthesia, Spinal Receptors, Androgen snRNP Core Proteins Spinal Cord Neoplasms Spinal Canal Spinal Diseases Spinal Cord Compression Muscle, Skeletal Spinal Neoplasms Pedigree Mice, Transgenic Bulbar Palsy, Progressive Spinal Stenosis Spinal Fusion Electromyography Nerve Degeneration Charcot-Marie-Tooth Disease Muscle Weakness Heterozygote Detection Magnetic Resonance Imaging Contracture Olivopontocerebellar Atrophies Neuromuscular Diseases Axons Glycine-tRNA Ligase Arthrogryposis Neural Conduction Gene Deletion Vocal Cord Paralysis Spinal Injuries Gyrate Atrophy Homozygote Neuromuscular Junction Trinucleotide Repeat Expansion Neuromuscular Junction Diseases RNA Splicing Amyotrophic Lateral Sclerosis Spinal Cord Ischemia Ganglia, Spinal Genes, Recessive Sural Nerve Geographic Atrophy Genetic Linkage Gene Dosage Trinucleotide Repeats Intranuclear Inclusion Bodies Genes, Dominant Myelography Motor Activity Inclusion Bodies Paraplegia Brain Fasciculation Myoclonic Epilepsies, Progressive Chemistry, Analytic Spine Thoracic Vertebrae Ulnar Nerve Respiratory Paralysis Muscles Tuberculosis, Spinal Prenatal Diagnosis

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