Rimeporide muscular dystrophy duchenne. Medical search. Frequent questions

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Anatomy19

Muscle, Skeletal Sarcolemma Muscle Fibers, Skeletal Muscles Myoblasts X Chromosome Chromosomes, Human, Pair 4 Diaphragm Satellite Cells, Skeletal Muscle Myoblasts, Skeletal Muscle Cells Myocardium Cells, Cultured Facial Muscles Neuromuscular Junction Shoulder Nuclear Envelope Respiratory Muscles Cell Line

Organisms7

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

Diseases38

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Fuchs' Endothelial Dystrophy Retinal Dystrophies Neuromuscular Diseases Muscular Diseases Disease Models, Animal Cardiomyopathies Neuroaxonal Dystrophies Sarcoglycanopathies Walker-Warburg Syndrome Muscle Weakness Myositis Reflex Sympathetic Dystrophy Cardiomyopathy, Dilated Syndrome Vitelliform Macular Dystrophy Chromosome Deletion Scoliosis Intellectual Disability Fibrosis Muscular Atrophy Myotonic Disorders Retinal Degeneration Disease Progression Retinitis Pigmentosa Distal Myopathies Epidermolysis Bullosa Simplex Genetic Diseases, X-Linked Contracture Necrosis

Chemicals and Drugs46

Dystrophin Utrophin Sarcoglycans Dystroglycans Dystrophin-Associated Proteins Thymopoietins Creatine Kinase Collagen Type VI Muscle Proteins Dystrophin-Associated Protein Complex Caveolin 3 Laminin Lamin Type A Cytoskeletal Proteins Poly(A)-Binding Protein II Calpain Pregnenediones Membrane Proteins Plectin Myostatin Morpholinos Connectin Integrin alpha Chains Evans Blue Glycerol Kinase Lamins Codon, Nonsense Membrane Glycoproteins Nitric Oxide Synthase Type I Genetic Markers Oligoribonucleotides, Antisense DNA Oligonucleotides, Antisense Creatine Kinase, MM Form Mannosyltransferases DNA Probes N-Acetylglucosaminyltransferases RNA, Messenger Poly(A)-Binding Protein I Oxepins Deoxyribonuclease HindIII Mazindol Caveolins MyoD Protein Cardiotoxins Phosphodiesterase 5 Inhibitors

Analytical, Diagnostic and Therapeutic Techniques and Equipment21

Heterozygote Detection Pedigree Disease Models, Animal Genetic Therapy Muscle Strength DNA Mutational Analysis Prenatal Diagnosis Chromosome Mapping Immunohistochemistry Polymerase Chain Reaction Biopsy Electroretinography Genetic Testing Blotting, Western Fluorescent Antibody Technique Injections, Intramuscular Chromosome Banding Gene Transfer Techniques Reverse Transcriptase Polymerase Chain Reaction Blotting, Southern Neuromuscular Blockade

Psychiatry and Psychology3

Intellectual Disability Projective Techniques Stanford-Binet Test

Phenomena and Processes40

Exons X Chromosome Mutation Chromosomes, Human, Pair 4 Phenotype Genetic Linkage Regeneration Muscle Strength Genes, Recessive Muscle Development Heterozygote Consanguinity Base Sequence Chromosome Deletion Genes, Dominant Gene Deletion Muscle Contraction Frameshift Mutation Codon, Nonsense Genetic Markers Sequence Deletion Mutation, Missense Genetic Vectors Trinucleotide Repeat Expansion Gene Expression Regulation Homozygote Glycosylation Amino Acid Sequence Mosaicism Polymorphism, Restriction Fragment Length Reading Frames Point Mutation Genotype Transgenes RNA Splicing Haplotypes Alternative Splicing Alleles Gene Expression Necrosis

Disciplines and Occupations2

Genetic Counseling Immunohistochemistry

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care3

Genetic Counseling Genetic Testing Age of Onset

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 Dystrophy, Duchenne Muscular Dystrophy, Animal Dystrophin Mice, Inbred mdx Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Utrophin Sarcoglycans Dystroglycans Corneal Dystrophies, Hereditary Muscle, Skeletal Muscular Dystrophy, Oculopharyngeal Heterozygote Detection Fuchs' Endothelial Dystrophy Dystrophin-Associated Proteins Sarcolemma Thymopoietins Pedigree Creatine Kinase Muscle Fibers, Skeletal Retinal Dystrophies Collagen Type VI Muscles Exons Myoblasts X Chromosome Muscle Proteins Dystrophin-Associated Protein Complex Neuromuscular Diseases Caveolin 3 Mutation Laminin Muscular Diseases Disease Models, Animal Chromosomes, Human, Pair 4 Lamin Type A Cytoskeletal Proteins Cardiomyopathies Phenotype Genetic Linkage Poly(A)-Binding Protein II Genetic Therapy Diaphragm Regeneration Muscle Strength Neuroaxonal Dystrophies Sarcoglycanopathies Walker-Warburg Syndrome Genes, Recessive Muscle Development Calpain Heterozygote Pregnenediones Mice, Inbred C57BL Muscle Weakness Membrane Proteins Plectin Molecular Sequence Data Satellite Cells, Skeletal Muscle Myostatin Dependovirus Morpholinos Myositis DNA Mutational Analysis Prenatal Diagnosis Chromosome Mapping Genetic Counseling Consanguinity Connectin Reflex Sympathetic Dystrophy Immunohistochemistry Myoblasts, Skeletal Cardiomyopathy, Dilated Base Sequence Syndrome Muscle Cells Polymerase Chain Reaction Vitelliform Macular Dystrophy Biopsy Chromosome Deletion Mice, Transgenic Electroretinography Genetic Testing Integrin alpha Chains Evans Blue Glycerol Kinase Genes, Dominant Gene Deletion Lamins Muscle Contraction Frameshift Mutation Codon, Nonsense Mice, Knockout Scoliosis Membrane Glycoproteins Blotting, Western Intellectual Disability

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