Symptoms of duchenne muscular dystrophy. Medical search. Frequent questions

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Anatomy17

Muscle, Skeletal Sarcolemma Muscle Fibers, Skeletal X Chromosome Muscles Myoblasts Diaphragm Satellite Cells, Skeletal Muscle Myoblasts, Skeletal Muscle Cells Chromosomes, Human, Pair 4 Respiratory Muscles Chromosomes, Human, 4-5 Myocardium Cells, Cultured Hyalin Spine

Organisms6

Mice, Inbred mdx Mice, Inbred C57BL Dependovirus Mice, Transgenic Dogs Mice, Knockout

Diseases26

Muscular Dystrophy, Duchenne Muscular Dystrophies Muscular Dystrophy, Animal Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Neuromuscular Diseases Disease Models, Animal Cardiomyopathies Fuchs' Endothelial Dystrophy Muscular Diseases Retinal Dystrophies Muscle Weakness Scoliosis Chromosome Deletion Syndrome Fibrosis Cardiomyopathy, Dilated Intellectual Disability Disease Progression Neuroaxonal Dystrophies Sarcoglycanopathies Walker-Warburg Syndrome

Chemicals and Drugs36

Dystrophin Utrophin Sarcoglycans Dystroglycans Dystrophin-Associated Proteins Creatine Kinase Dystrophin-Associated Protein Complex Muscle Proteins Pregnenediones Caveolin 3 Morpholinos Cytoskeletal Proteins Thymopoietins Collagen Type VI Laminin Glycerol Kinase Myostatin Membrane Proteins Oligonucleotides, Antisense Nitric Oxide Synthase Type I Integrin alpha Chains Oligoribonucleotides, Antisense Lamin Type A Poly(A)-Binding Protein II Evans Blue Mazindol DNA Codon, Nonsense DNA Probes Genetic Markers Phosphodiesterase 5 Inhibitors RNA, Messenger Calpain Protriptyline Oxadiazoles Membrane Glycoproteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment23

Heterozygote Detection Pedigree Genetic Therapy Disease Models, Animal Muscle Strength Prenatal Diagnosis Immunohistochemistry Biopsy Polymerase Chain Reaction Chromosome Mapping Injections, Intramuscular Genetic Testing Chromosome Banding Blotting, Western DNA Mutational Analysis Vital Capacity Electroretinography Neuromuscular Blockade Gene Transfer Techniques Respiratory Therapy Inspiratory Capacity Fluorescent Antibody Technique Chest Wall Oscillation

Psychiatry and Psychology5

Projective Techniques Stanford-Binet Test Sociology Intellectual Disability Mesopic Vision

Phenomena and Processes31

X Chromosome Exons Muscle Strength Regeneration Mutation Genetic Linkage Phenotype Heterozygote Muscle Development Chromosome Deletion Muscle Contraction Chromosomes, Human, Pair 4 Genes, Recessive Base Sequence Genetic Vectors Gene Deletion Reading Frames Polymorphism, Restriction Fragment Length Codon, Nonsense Vital Capacity Chromosomes, Human, 4-5 Dependent Ambulation Sequence Deletion Genetic Markers Time Factors Gene Expression Regulation Frameshift Mutation Mosaicism Mesopic Vision Inspiratory Capacity RNA Splicing

Disciplines and Occupations2

Genetic Counseling Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena1

Information Science2

Molecular Sequence Data Base Sequence

Health Care2

Genetic Counseling Genetic Testing

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 Dystrophy, Duchenne Muscular Dystrophies Dystrophin Muscular Dystrophy, Animal Mice, Inbred mdx Utrophin Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Muscle, Skeletal Sarcoglycans Dystroglycans Heterozygote Detection Muscular Dystrophy, Emery-Dreifuss Dystrophin-Associated Proteins Sarcolemma Corneal Dystrophies, Hereditary Creatine Kinase Muscle Fibers, Skeletal X Chromosome Muscular Dystrophy, Oculopharyngeal Exons Muscles Myoblasts Neuromuscular Diseases Dystrophin-Associated Protein Complex Pedigree Diaphragm Muscle Proteins Genetic Therapy Pregnenediones Disease Models, Animal Muscle Strength Cardiomyopathies Fuchs' Endothelial Dystrophy Caveolin 3 Regeneration Morpholinos Cytoskeletal Proteins Thymopoietins Mutation Genetic Linkage Mice, Inbred C57BL Muscular Diseases Retinal Dystrophies Collagen Type VI Phenotype Laminin Dependovirus Satellite Cells, Skeletal Muscle Heterozygote Glycerol Kinase Prenatal Diagnosis Muscle Weakness Muscle Development Scoliosis Genetic Counseling Myoblasts, Skeletal Chromosome Deletion Myostatin Syndrome Molecular Sequence Data Immunohistochemistry Muscle Contraction Membrane Proteins Oligonucleotides, Antisense Muscle Cells Nitric Oxide Synthase Type I Integrin alpha Chains Oligoribonucleotides, Antisense Chromosomes, Human, Pair 4 Projective Techniques Biopsy Fibrosis Lamin Type A Polymerase Chain Reaction Chromosome Mapping Genes, Recessive Base Sequence Poly(A)-Binding Protein II Evans Blue Mazindol Injections, Intramuscular Genetic Vectors Genetic Testing Mice, Transgenic Chromosome Banding Gene Deletion DNA Reading Frames Cardiomyopathy, Dilated Blotting, Western DNA Mutational Analysis Stanford-Binet Test Sociology Dogs Polymorphism, Restriction Fragment Length Codon, Nonsense Vital Capacity DNA Probes

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