Dilated cardiomyopathy genetic muscular dystrophies limb girdle. Medical search. Frequent questions

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Anatomy36

Muscle, Skeletal Myoblasts Muscle Fibers, Skeletal Myocardium Limb Buds Scapula Extremities Sarcolemma Shoulder Muscles Chromosomes, Human, Pair 4 X Chromosome Animal Fins Heart Ventricles Sarcomeres Forelimb Pelvis Heart Septum Heart Clavicle Myocytes, Cardiac Diaphragm Hindlimb Muscle Cells Cells, Cultured Satellite Cells, Skeletal Muscle Myofibrils Myoblasts, Skeletal Lower Extremity Leg Endocardium Arm Pectoralis Muscles Nuclear Envelope Costameres Sacroiliac Joint

Organisms7

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

Diseases64

Muscular Dystrophies Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Duchenne Cardiomyopathy, Dilated Muscular Dystrophy, Animal Cardiomyopathy, Hypertrophic Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Cardiomyopathies Pelvic Girdle Pain Muscular Dystrophy, Emery-Dreifuss Corneal Dystrophies, Hereditary Cardiomyopathy, Restrictive Muscular Dystrophy, Oculopharyngeal Muscular Diseases Takotsubo Cardiomyopathy Distal Myopathies Cardiomyopathy, Hypertrophic, Familial Muscle Weakness Fuchs' Endothelial Dystrophy Chagas Cardiomyopathy Retinal Dystrophies Myositis, Inclusion Body Cardiomyopathy, Alcoholic Disease Models, Animal Neuromuscular Diseases Pelvic Pain Arrhythmogenic Right Ventricular Dysplasia Diabetic Cardiomyopathies Ventricular Dysfunction, Left Neuroaxonal Dystrophies Fibrosis Heart Failure Sarcoglycanopathies Walker-Warburg Syndrome Myocarditis Limb Deformities, Congenital Puerperal Disorders Reflex Sympathetic Dystrophy Ventricular Outflow Obstruction Syndrome Death, Sudden, Cardiac Phantom Limb Vitelliform Macular Dystrophy Myositis Heart Diseases Arrhythmias, Cardiac Brachial Plexus Neuritis Muscular Atrophy Tachycardia, Ventricular Disease Progression Endomyocardial Fibrosis Myocardial Ischemia Hypertrophy, Left Ventricular Myotonic Disorders Retinal Degeneration Ventricular Remodeling Retinitis Pigmentosa Intellectual Disability Contracture Cardiomegaly Glycogen Storage Disease Type IIb Lipodystrophy Death, Sudden

Chemicals and Drugs43

Sarcoglycans Dystrophin Dystroglycans Caveolin 3 Muscle Proteins Calpain Connectin Utrophin Creatine Kinase Cytoskeletal Proteins Caveolins Thymopoietins Collagen Type VI Membrane Proteins Lamin Type A Dystrophin-Associated Proteins Laminin Dystrophin-Associated Protein Complex Poly(A)-Binding Protein II Plectin Myosin Heavy Chains Lamins Cardiac Myosins Myostatin Desmin Codon, Nonsense Ventricular Myosins Creatine Kinase, MM Form Cardiotoxins RNA, Messenger Membrane Glycoproteins Plakophilins Mannosyltransferases Genetic Markers N-Acetylglucosaminyltransferases Troponin T Morpholinos Poly(A)-Binding Protein I Oxepins Integrin alpha Chains Pregnenediones Evans Blue DNA

Analytical, Diagnostic and Therapeutic Techniques and Equipment35

Pedigree DNA Mutational Analysis Biopsy Heterozygote Detection Echocardiography Disease Models, Animal Immunohistochemistry Electrocardiography Limb Salvage Genetic Therapy Stroke Volume Muscle Strength Chromosome Mapping Genetic Testing Treatment Outcome Electromyography Follow-Up Studies Polymerase Chain Reaction Magnetic Resonance Imaging Magnetic Resonance Imaging, Cine Echocardiography, Doppler Blotting, Western Prenatal Diagnosis Electroretinography Heart Transplantation Cineradiography Retrospective Studies Heart Function Tests Cardiac Pacing, Artificial Severity of Illness Index Case-Control Studies Reverse Transcriptase Polymerase Chain Reaction Fluorescent Antibody Technique Defibrillators, Implantable Prospective Studies

Psychiatry and Psychology2

Phantom Limb Intellectual Disability

Phenomena and Processes45

Mutation Mutation, Missense Phenotype Exons Chromosomes, Human, Pair 4 X Chromosome Genes, Recessive Ventricular Function, Left Genetic Linkage Regeneration Heterozygote Genes, Dominant Consanguinity Homozygote Muscle Development Myocardial Contraction Stroke Volume Muscle Strength Time Factors Base Sequence Genotype Codon, Nonsense Peripartum Period Frameshift Mutation Amino Acid Sequence Gene Deletion Point Mutation Gene Expression Regulation Glycosylation Biomechanical Phenomena Trinucleotide Repeat Expansion Muscle Contraction Genetic Markers Pregnancy Sequence Deletion Hemodynamics Gene Expression Ventricular Remodeling Locomotion Diastole Lod Score Transgenes Polymorphism, Single-Stranded Conformational Genetic Vectors Haplotypes

Disciplines and Occupations3

Immunohistochemistry Genetic Counseling Paleontology

Anthropology, Education, Sociology and Social Phenomena2

Fossils Paleontology

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care10

Age of Onset Genetic Testing Treatment Outcome Follow-Up Studies Genetic Counseling Retrospective Studies Severity of Illness Index Case-Control Studies Prospective Studies Family Health

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 Dystrophies, Limb-Girdle Muscular Dystrophy, Duchenne Cardiomyopathy, Dilated Muscular Dystrophy, Animal Sarcoglycans Dystrophin Cardiomyopathy, Hypertrophic Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Dystroglycans Cardiomyopathies Mice, Inbred mdx Pelvic Girdle Pain Muscle, Skeletal Caveolin 3 Muscular Dystrophy, Emery-Dreifuss Muscle Proteins Calpain Corneal Dystrophies, Hereditary Connectin Cardiomyopathy, Restrictive Muscular Dystrophy, Oculopharyngeal Muscular Diseases Utrophin Takotsubo Cardiomyopathy Pedigree Distal Myopathies Mutation Creatine Kinase Myoblasts Cardiomyopathy, Hypertrophic, Familial Mutation, Missense Phenotype Muscle Fibers, Skeletal Muscle Weakness Cytoskeletal Proteins Fuchs' Endothelial Dystrophy Chagas Cardiomyopathy Caveolins Myocardium Thymopoietins Limb Buds Retinal Dystrophies Collagen Type VI Membrane Proteins DNA Mutational Analysis Lamin Type A Scapula Extremities Myositis, Inclusion Body Biopsy Sarcolemma Shoulder Muscles Heterozygote Detection Cardiomyopathy, Alcoholic Age of Onset Dystrophin-Associated Proteins Echocardiography Laminin Disease Models, Animal Exons Neuromuscular Diseases Immunohistochemistry Pelvic Pain Electrocardiography Chromosomes, Human, Pair 4 Arrhythmogenic Right Ventricular Dysplasia Dystrophin-Associated Protein Complex X Chromosome Poly(A)-Binding Protein II Genes, Recessive Ventricular Function, Left Genetic Linkage Diabetic Cardiomyopathies Animal Fins Ventricular Dysfunction, Left Mice, Transgenic Neuroaxonal Dystrophies Heart Ventricles Fibrosis Heart Failure Sarcomeres Regeneration Molecular Sequence Data Sarcoglycanopathies Walker-Warburg Syndrome Heterozygote Myocarditis Genes, Dominant Forelimb Limb Salvage Pelvis Heart Septum Genetic Therapy Heart Clavicle Consanguinity Mice, Inbred C57BL

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