Rare disease disease that affects muscular atrophy spinal. Medical search. Frequent questions

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Anatomy28

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

Organisms4

Mice, Transgenic Tropheryma Rats, Sprague-Dawley Mice, Knockout

Diseases64

Rare Diseases 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 Lymphangioleiomyomatosis Spinal Neoplasms Lithiasis Bulbar Palsy, Progressive Spinal Stenosis Nerve Degeneration Charcot-Marie-Tooth Disease Muscle Weakness Contracture Syndrome Olivopontocerebellar Atrophies Neuromuscular Diseases Actinomycosis Arthrogryposis Pulmonary Alveolar Proteinosis Neuroaxonal Dystrophies Vocal Cord Paralysis Spinal Injuries Gyrate Atrophy Histiocytosis, Langerhans-Cell Birt-Hogg-Dube Syndrome Neuromuscular Junction Diseases Amyotrophic Lateral Sclerosis Retroperitoneal Fibrosis Spinal Cord Ischemia Histiocytoma Disease Progression Geographic Atrophy Urea Cycle Disorders, Inborn Erdheim-Chester Disease Paraplegia Fasciculation Myoclonic Epilepsies, Progressive Eosinophilic Granuloma Angioedemas, Hereditary Respiratory Paralysis Tuberculosis, Spinal Iron Metabolism Disorders Epidermolysis Bullosa Scoliosis Breast Neoplasms, Male Lipomatosis Spinal Curvatures Postpoliomyelitis Syndrome Muscular Dystrophies Hematoma, Epidural, Spinal Hereditary Sensory and Motor Neuropathy Optic Atrophy, Autosomal Dominant

Chemicals and Drugs15

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment24

Injections, Spinal Disease Models, Animal Pedigree Anesthesia, Spinal Magnetic Resonance Imaging Tomography, X-Ray Computed Spinal Fusion Electromyography Heterozygote Detection Fatal Outcome Treatment Outcome Laminectomy Drug Approval Immunohistochemistry Retrospective Studies Myelography DNA Mutational Analysis Severity of Illness Index Prenatal Diagnosis Polymerase Chain Reaction Genetic Testing Biopsy Rotarod Performance Test Muscle Denervation

Psychiatry and Psychology1

Phenomena and Processes22

Chromosomes, Human, Pair 5 Exons Phenotype Mutation Neural Conduction Gene Deletion Homozygote Trinucleotide Repeat Expansion RNA Splicing Genes, Recessive Time Factors Genetic Linkage Gene Dosage Trinucleotide Repeats Heterozygote Genes, Dominant Motor Activity Genotype Alternative Splicing Mutation, Missense Alleles Base Sequence

Disciplines and Occupations4

Immunohistochemistry Chemistry, Analytic Genetic Counseling Biomedical Research

Anthropology, Education, Sociology and Social Phenomena7

Patient Advocacy Legislation, Drug Drug Approval National Institutes of Health (U.S.)Patient Rights European Union United States Food and Drug Administration

Technology, Industry, Agriculture2

Orphan Drug Production Drug Industry

Information Science4

Fatal Outcome Biological Ontologies Molecular Sequence Data Base Sequence

Named Groups2

Infant, Newborn Medical Laboratory Personnel

Health Care15

Patient Advocacy Fatal Outcome Legislation, Drug Treatment Outcome National Institutes of Health (U.S.)Health Level Seven Patient Rights Age of Onset Retrospective Studies United States Food and Drug Administration Severity of Illness Index Medical Laboratory Personnel Genetic Counseling Academies and Institutes Genetic Testing

Geographicals1

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 Technology, Industry, Agriculture Information Science Named Groups Health Care Geographicals

Rare Diseases 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 Orphan Drug Production 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 Exons Disease Models, Animal Pedigree Spinal Nerves Coiled Bodies Multiple System Atrophy Anesthesia, Spinal Magnetic Resonance Imaging Receptors, Androgen snRNP Core Proteins Spinal Cord Neoplasms Spinal Canal Phenotype Spinal Diseases Spinal Cord Compression Muscle, Skeletal Mutation Lymphangioleiomyomatosis Spinal Neoplasms Lithiasis Mice, Transgenic Tomography, X-Ray Computed Bulbar Palsy, Progressive Spinal Stenosis Spinal Fusion Electromyography Nerve Degeneration Charcot-Marie-Tooth Disease Patient Advocacy Muscle Weakness Heterozygote Detection Contracture Syndrome Olivopontocerebellar Atrophies Fatal Outcome Neuromuscular Diseases Axons Actinomycosis Legislation, Drug Glycine-tRNA Ligase Arthrogryposis Neural Conduction Pulmonary Alveolar Proteinosis Neuroaxonal Dystrophies Treatment Outcome Gene Deletion Vocal Cord Paralysis Laminectomy Drug Approval Spinal Injuries Gyrate Atrophy National Institutes of Health (U.S.)Homozygote Histiocytosis, Langerhans-Cell Birt-Hogg-Dube Syndrome Neuromuscular Junction Trinucleotide Repeat Expansion Neuromuscular Junction Diseases RNA Splicing Health Level Seven Patient Rights Amyotrophic Lateral Sclerosis Biological Ontologies Retroperitoneal Fibrosis Spinal Cord Ischemia Ganglia, Spinal Genes, Recessive Histiocytoma Time Factors Immunohistochemistry Sural Nerve European Union Disease Progression

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