Cure muscular dystrophy association muscular atrophy spinal. Medical search. Frequent questions

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Anatomy42

Spinal Cord Muscle, Skeletal Motor Neurons Anterior Horn Cells Muscles Muscle Fibers, Skeletal Chromosomes, Human, Pair 5 Sarcolemma Myoblasts Spinal Nerve Roots X Chromosome Chromosomes, Human, Pair 4 Spinal Nerves Coiled Bodies Spinal Canal Neuromuscular Junction Diaphragm Axons Cells, Cultured Brain Fibroblasts Intranuclear Inclusion Bodies Spine Satellite Cells, Skeletal Muscle Cell Line Inclusion Bodies Sural Nerve Ganglia, Spinal Myoblasts, Skeletal Muscle Cells Cell Nucleus Neurons Fundus Oculi Thoracic Vertebrae Ulnar Nerve HeLa Cells Hindlimb Spliceosomes Acanthocytes Nuclear Envelope Sciatic Nerve Arm

Organisms9

Mice, Inbred mdx Mice, Transgenic Mice, Inbred C57BL Mice, Knockout Dependovirus Mice, Mutant Strains Zebrafish Animals, Newborn Dogs

Diseases70

Muscular Dystrophies Muscular Atrophy, Spinal Muscular Dystrophy, Duchenne Spinal Muscular Atrophies of Childhood Muscular Dystrophy, Animal Atrophy Muscular Atrophy Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Corneal Dystrophies, Hereditary Spinal Cord Injuries Muscular Dystrophy, Oculopharyngeal Disease Models, Animal Fuchs' Endothelial Dystrophy Spinal Cord Diseases Retinal Dystrophies Neuromuscular Diseases Optic Atrophy Motor Neuron Disease Muscle Weakness Muscular Diseases Multiple System Atrophy Contracture Spinal Cord Neoplasms Neuroaxonal Dystrophies Spinal Diseases Spinal Cord Compression Spinal Neoplasms Sarcoglycanopathies Walker-Warburg Syndrome Cardiomyopathies Bulbar Palsy, Progressive Spinal Stenosis Syndrome Nerve Degeneration Charcot-Marie-Tooth Disease Scoliosis Disease Progression Olivopontocerebellar Atrophies Reflex Sympathetic Dystrophy Arthrogryposis Vocal Cord Paralysis Myositis Spinal Injuries Vitelliform Macular Dystrophy Gyrate Atrophy Amyotrophic Lateral Sclerosis Neuromuscular Junction Diseases Spinal Cord Ischemia Spinal Curvatures Retinal Degeneration Geographic Atrophy Cardiomyopathy, Dilated Myotonic Disorders Paraplegia Fasciculation Myoclonic Epilepsies, Progressive Distal Myopathies Retinitis Pigmentosa Respiratory Paralysis Tuberculosis, Spinal Intellectual Disability Ophthalmoplegia Fibrosis Macular Degeneration Hereditary Sensory and Motor Neuropathy

Chemicals and Drugs52

Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Dystrophin Sarcoglycans Dystroglycans Neuronal Apoptosis-Inhibitory Protein Utrophin Cyclic AMP Response Element-Binding Protein RNA-Binding Proteins Nerve Tissue Proteins Thymopoietins Collagen Type VI Ribonucleoproteins, Small Nuclear Muscle Proteins DEAD Box Protein 20 Dystrophin-Associated Proteins Creatine Kinase Lamin Type A Laminin Dystrophin-Associated Protein Complex Caveolin 3 Poly(A)-Binding Protein II Receptors, Androgen snRNP Core Proteins Cytoskeletal Proteins Calpain Plectin RNA, Messenger Membrane Proteins Connectin Myostatin Genetic Markers Glycine-tRNA Ligase Oligonucleotides, Antisense Lamins DNA Primers DNA Creatine Kinase, MM Form Morpholinos Membrane Glycoproteins Nuclear Proteins Mannosyltransferases N-Acetylglucosaminyltransferases Codon, Nonsense Poly(A)-Binding Protein I Peptides Oxepins Evans Blue Integrin alpha Chains Pregnenediones Valproic Acid

Analytical, Diagnostic and Therapeutic Techniques and Equipment30

Pedigree Disease Models, Animal Heterozygote Detection Injections, Spinal Genetic Therapy Anesthesia, Spinal Electromyography Muscle Strength DNA Mutational Analysis Magnetic Resonance Imaging Chromosome Mapping Spinal Fusion Prenatal Diagnosis Immunohistochemistry Genetic Testing Polymerase Chain Reaction Blotting, Western Biopsy Reverse Transcriptase Polymerase Chain Reaction Electroretinography Fluorescent Antibody Technique Treatment Outcome Muscle Denervation Stem Cell Transplantation Myelography Severity of Illness Index Gene Transfer Techniques Models, Biological Laminectomy Retrospective Studies

Psychiatry and Psychology2

Motor Activity Intellectual Disability

Phenomena and Processes48

Exons Mutation Phenotype Chromosomes, Human, Pair 5 Genetic Linkage Genes, Recessive X Chromosome Chromosomes, Human, Pair 4 Homozygote Trinucleotide Repeat Expansion Genes, Dominant Gene Deletion Muscle Strength Heterozygote Base Sequence Mutation, Missense RNA Splicing Regeneration Consanguinity Muscle Development Gene Expression Regulation Alternative Splicing Time Factors Neural Conduction Genetic Markers Amino Acid Sequence Founder Effect Genotype Motor Activity Sequence Deletion Gene Dosage Alleles Gene Expression Transgenes Polymorphism, Single-Stranded Conformational Trinucleotide Repeats Point Mutation Introns Haplotypes Genetic Vectors Lod Score Glycosylation Frameshift Mutation Codon, Nonsense Protein Binding Cell Differentiation Muscle Contraction Polymorphism, Restriction Fragment Length

Disciplines and Occupations3

Immunohistochemistry Genetic Counseling Chemistry, Analytic

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups1

Infant, Newborn

Health Care8

Genetic Counseling Genetic Testing Age of Onset Family Health Treatment Outcome Severity of Illness Index Age Factors Retrospective Studies

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 Dystrophies Muscular Atrophy, Spinal Muscular Dystrophy, Duchenne Spinal Muscular Atrophies of Childhood Muscular Dystrophy, Animal Survival of Motor Neuron 1 Protein Atrophy SMN Complex Proteins Muscular Atrophy Survival of Motor Neuron 2 Protein Dystrophin Spinal Cord Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Mice, Inbred mdx Muscular Dystrophy, Emery-Dreifuss Sarcoglycans Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Muscle, Skeletal Corneal Dystrophies, Hereditary Spinal Cord Injuries Dystroglycans Muscular Dystrophy, Oculopharyngeal Neuronal Apoptosis-Inhibitory Protein Utrophin Cyclic AMP Response Element-Binding Protein Motor Neurons Anterior Horn Cells RNA-Binding Proteins Pedigree Exons Disease Models, Animal Heterozygote Detection Nerve Tissue Proteins Fuchs' Endothelial Dystrophy Spinal Cord Diseases Thymopoietins Retinal Dystrophies Mutation Collagen Type VI Phenotype Muscles Neuromuscular Diseases Muscle Fibers, Skeletal Optic Atrophy Motor Neuron Disease Ribonucleoproteins, Small Nuclear Muscle Proteins Chromosomes, Human, Pair 5 Muscle Weakness Muscular Diseases Genetic Linkage DEAD Box Protein 20 Sarcolemma Dystrophin-Associated Proteins Creatine Kinase Genes, Recessive Mice, Transgenic Myoblasts Injections, Spinal Spinal Nerve Roots X Chromosome Chromosomes, Human, Pair 4 Spinal Nerves Lamin Type A Genetic Therapy Laminin Dystrophin-Associated Protein Complex Caveolin 3 Homozygote Coiled Bodies Trinucleotide Repeat Expansion Multiple System Atrophy Poly(A)-Binding Protein II Anesthesia, Spinal Genes, Dominant Contracture Gene Deletion Electromyography Molecular Sequence Data Receptors, Androgen snRNP Core Proteins Muscle Strength DNA Mutational Analysis Spinal Cord Neoplasms Spinal Canal Magnetic Resonance Imaging Heterozygote Neuroaxonal Dystrophies Mice, Inbred C57BL Chromosome Mapping Spinal Diseases Spinal Fusion Neuromuscular Junction Spinal Cord Compression Cytoskeletal Proteins Base Sequence Prenatal Diagnosis

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