Inherited disorder muscular dystrophy duchenne. Medical search. Frequent questions

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Anatomy23

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

Organisms7

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

Diseases66

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Genetic Diseases, Inborn Fuchs' Endothelial Dystrophy Protoporphyria, Erythropoietic Syndrome Metabolism, Inborn Errors Disease Models, Animal Retinal Dystrophies Neuromuscular Diseases Granulomatous Disease, Chronic Muscular Diseases Cardiomyopathies Porphyria, Hepatoerythropoietic Jaundice, Chronic Idiopathic Amino Acid Metabolism, Inborn Errors Lipid Metabolism, Inborn Errors Hepatolenticular Degeneration Intellectual Disability Hemochromatosis Neuroaxonal Dystrophies Ichthyosis Walker-Warburg Syndrome Sarcoglycanopathies Hypophosphatasia Muscle Weakness Hemoglobinopathies Gitelman Syndrome Myositis Ichthyosiform Erythroderma, Congenital Abnormalities, Multiple Tooth Abnormalities Reflex Sympathetic Dystrophy Genetic Predisposition to Disease Cardiomyopathy, Dilated Purine-Pyrimidine Metabolism, Inborn Errors Myasthenic Syndromes, Congenital Photosensitivity Disorders Chromosome Deletion Vitelliform Macular Dystrophy Refsum Disease Malignant Hyperthermia Familial Mediterranean Fever Scoliosis Fibrosis Myotonic Disorders Muscular Atrophy Disease Progression Retinal Degeneration Substance-Related Disorders Long QT Syndrome Retinitis Pigmentosa Distal Myopathies Genetic Diseases, X-Linked Porphyria Cutanea Tarda Epidermolysis Bullosa Simplex Contracture Tic Disorders Necrosis

Chemicals and Drugs52

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment32

Pedigree Heterozygote Detection Disease Models, Animal DNA Mutational Analysis Genetic Therapy Prenatal Diagnosis Chromosome Mapping Genetic Testing Polymerase Chain Reaction Muscle Strength Immunohistochemistry Gene Transfer Techniques Biopsy Electroretinography Blotting, Western Models, Biological Fluorescent Antibody Technique Sequence Analysis, DNA Injections, Intramuscular Models, Genetic Transfection Cloning, Molecular Reverse Transcriptase Polymerase Chain Reaction Chromosome Banding Magnetic Resonance Imaging Severity of Illness Index Spin Trapping Blotting, Southern Case-Control Studies Electromyography Stem Cell Transplantation Neuromuscular Blockade

Psychiatry and Psychology21

Bipolar Disorder Mental Disorders Anxiety Disorders Mood Disorders Intellectual Disability Depressive Disorder, Major Attention Deficit Disorder with Hyperactivity Depressive Disorder Personal Construct Theory Obsessive-Compulsive Disorder Stress Disorders, Post-Traumatic Autistic Disorder Phobic Disorders Child Development Disorders, Pervasive Psychotic Disorders Substance-Related Disorders Cognition Disorders Projective Techniques Conduct Disorder Stanford-Binet Test Tic Disorders

Phenomena and Processes47

Mutation Exons Phenotype X Chromosome Genes, Recessive Genetic Linkage Heterozygote Genes, Dominant Base Sequence Mutation, Missense Frameshift Mutation Chromosomes, Human, Pair 4 Homozygote Codon, Nonsense Genotype Regeneration Muscle Strength Point Mutation Amino Acid Sequence Genetic Markers Muscle Development Gene Deletion Alleles Sequence Deletion Genetic Vectors Consanguinity Polymorphism, Restriction Fragment Length Lod Score Haplotypes Genetic Predisposition to Disease Gene Expression Chromosome Deletion Polymorphism, Single-Stranded Conformational Polymorphism, Genetic Muscle Contraction Gene Expression Regulation Trinucleotide Repeat Expansion Glycosylation Mosaicism Time Factors Reading Frames Transfection Transgenes RNA Splicing Necrosis Chromosomes, Human, X Cell Differentiation

Disciplines and Occupations2

Genetic Counseling Immunohistochemistry

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Diagnostic and Statistical Manual of Mental Disorders

Named Groups1

Infant, Newborn

Health Care6

Genetic Testing Age of Onset Genetic Counseling Family Health Severity of Illness Index Case-Control 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 Named Groups Health Care

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Dystrophin Mice, Inbred mdx Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Utrophin Sarcoglycans Dystroglycans Pedigree Corneal Dystrophies, Hereditary Muscle, Skeletal Muscular Dystrophy, Oculopharyngeal Heterozygote Detection Mutation Genetic Diseases, Inborn Exons Phenotype Fuchs' Endothelial Dystrophy Protoporphyria, Erythropoietic X Chromosome Dystrophin-Associated Proteins Syndrome Genes, Recessive Sarcolemma Thymopoietins Metabolism, Inborn Errors Creatine Kinase Genetic Linkage Disease Models, Animal Muscle Fibers, Skeletal Retinal Dystrophies Muscles Collagen Type VI Heterozygote DNA Mutational Analysis Myoblasts Muscle Proteins Genetic Therapy Molecular Sequence Data Dystrophin-Associated Protein Complex Neuromuscular Diseases Prenatal Diagnosis Bipolar Disorder Granulomatous Disease, Chronic Genes, Dominant Chromosome Mapping Caveolin 3 Base Sequence Muscular Diseases Genetic Testing Ferrochelatase Laminin Mutation, Missense Frameshift Mutation Chromosomes, Human, Pair 4 Membrane Proteins Homozygote Lamin Type A Codon, Nonsense Cytoskeletal Proteins Cardiomyopathies Mental Disorders Porphyria, Hepatoerythropoietic Mice, Inbred C57BL Poly(A)-Binding Protein II Polymerase Chain Reaction Anxiety Disorders Diaphragm Mood Disorders Jaundice, Chronic Idiopathic Amino Acid Metabolism, Inborn Errors Genotype Regeneration Lipid Metabolism, Inborn Errors Hepatolenticular Degeneration Muscle Strength Intellectual Disability Point Mutation Hemochromatosis Neuroaxonal Dystrophies Ichthyosis Amino Acid Sequence Mice, Transgenic Walker-Warburg Syndrome Sarcoglycanopathies Genetic Markers Calpain Muscle Development DNA Cells, Cultured Hypophosphatasia Muscle Weakness Pregnenediones Gene Deletion Age of Onset Alleles

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