Muscular dystrophy association physical muscular atrophy spinal. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy39

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 Spine Intranuclear Inclusion Bodies Cell Line Satellite Cells, Skeletal Muscle Inclusion Bodies Sural Nerve Ganglia, Spinal Myoblasts, Skeletal Cell Nucleus Muscle Cells Neurons HeLa Cells Thoracic Vertebrae Fundus Oculi Ulnar Nerve Hindlimb Spliceosomes Arm

Organisms8

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

Diseases66

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 Spinal Diseases Neuroaxonal Dystrophies Spinal Cord Compression Spinal Neoplasms Sarcoglycanopathies Walker-Warburg Syndrome Cardiomyopathies Spinal Stenosis Syndrome Bulbar Palsy, Progressive Nerve Degeneration Scoliosis Charcot-Marie-Tooth Disease Disease Progression Reflex Sympathetic Dystrophy Olivopontocerebellar Atrophies Arthrogryposis Vocal Cord Paralysis Myositis Spinal Injuries Vitelliform Macular Dystrophy Gyrate Atrophy Neuromuscular Junction Diseases Amyotrophic Lateral Sclerosis Spinal Cord Ischemia Spinal Curvatures Retinal Degeneration Geographic Atrophy Cardiomyopathy, Dilated Paraplegia Myotonic Disorders Fasciculation Myoclonic Epilepsies, Progressive Intellectual Disability Distal Myopathies Retinitis Pigmentosa Respiratory Paralysis Tuberculosis, Spinal

Chemicals and Drugs50

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 Membrane Proteins RNA, Messenger Genetic Markers Myostatin Connectin Glycine-tRNA Ligase Oligonucleotides, Antisense DNA Lamins DNA Primers Creatine Kinase, MM Form Nuclear Proteins Morpholinos Membrane Glycoproteins Mannosyltransferases Codon, Nonsense N-Acetylglucosaminyltransferases Peptides Poly(A)-Binding Protein I Oxepins Evans Blue Integrin alpha Chains

Analytical, Diagnostic and Therapeutic Techniques and Equipment34

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

Psychiatry and Psychology2

Motor Activity Intellectual Disability

Phenomena and Processes52

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

Disciplines and Occupations4

Immunohistochemistry Genetic Counseling Chemistry, Analytic Physical Therapy Specialty

Anthropology, Education, Sociology and Social Phenomena3

Physical Fitness Exercise Physical Education and Training

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Questionnaires

Named Groups1

Infant, Newborn

Health Care11

Physical Fitness Genetic Counseling Genetic Testing Age of Onset Severity of Illness Index Family Health Age Factors Treatment Outcome Analysis of Variance Reproducibility of Results Questionnaires

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 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 Muscle, Skeletal Bulbo-Spinal Atrophy, X-Linked 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 Mutation Retinal Dystrophies Phenotype Muscles Collagen Type VI Neuromuscular Diseases Muscle Fibers, Skeletal Optic Atrophy Motor Neuron Disease Ribonucleoproteins, Small Nuclear Muscle Proteins Chromosomes, Human, Pair 5 Muscle Weakness Genetic Linkage Muscular Diseases DEAD Box Protein 20 Sarcolemma Dystrophin-Associated Proteins Creatine Kinase Genes, Recessive Motor Activity Mice, Transgenic Myoblasts Spinal Nerve Roots Injections, Spinal X Chromosome Chromosomes, Human, Pair 4 Lamin Type A Spinal Nerves Muscle Strength Laminin Dystrophin-Associated Protein Complex Caveolin 3 Homozygote Molecular Sequence Data Genetic Therapy Coiled Bodies Trinucleotide Repeat Expansion Multiple System Atrophy Genes, Dominant Poly(A)-Binding Protein II Anesthesia, Spinal Contracture Electromyography Gene Deletion Chromosome Mapping Receptors, Androgen snRNP Core Proteins Physical Fitness DNA Mutational Analysis Magnetic Resonance Imaging Spinal Cord Neoplasms Base Sequence Spinal Canal Heterozygote Spinal Diseases Neuroaxonal Dystrophies Mice, Inbred C57BL Spinal Fusion Neuromuscular Junction Cytoskeletal Proteins

No FAQ available that match "muscular dystrophy association physical muscular atrophy spinal"