Diagnosis muscular dystrophy duchenne. Medical search. Frequent questions

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Anatomy21

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

Organisms7

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

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 Syndrome Myositis Reflex Sympathetic Dystrophy Cardiomyopathy, Dilated Chromosome Deletion Vitelliform Macular Dystrophy Intellectual Disability Scoliosis Disease Progression Fibrosis Muscular Atrophy Myotonic Disorders Retinal Degeneration Retinitis Pigmentosa Distal Myopathies Necrosis Genetic Diseases, X-Linked Epidermolysis Bullosa Simplex Contracture

Chemicals and Drugs47

Dystrophin Utrophin Sarcoglycans Dystroglycans Dystrophin-Associated Proteins Creatine Kinase Thymopoietins 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 Codon, Nonsense Lamins Genetic Markers Membrane Glycoproteins DNA Nitric Oxide Synthase Type I DNA Probes Oligoribonucleotides, Antisense Oligonucleotides, Antisense RNA, Messenger Creatine Kinase, MM Form Mannosyltransferases N-Acetylglucosaminyltransferases Poly(A)-Binding Protein I Oxepins Deoxyribonuclease HindIII Mazindol Caveolins MyoD Protein Phosphodiesterase 5 Inhibitors DNA Primers Cardiotoxins

Analytical, Diagnostic and Therapeutic Techniques and Equipment40

Heterozygote Detection Pedigree Prenatal Diagnosis Disease Models, Animal Genetic Therapy Muscle Strength Biopsy Polymerase Chain Reaction DNA Mutational Analysis Immunohistochemistry Chromosome Mapping Delayed Diagnosis Genetic Testing Sensitivity and Specificity Early Diagnosis Electroretinography Retrospective Studies Blotting, Western Fluorescent Antibody Technique Magnetic Resonance Imaging Preimplantation Diagnosis Diagnosis Injections, Intramuscular Reproducibility of Results Reverse Transcriptase Polymerase Chain Reaction Chromosome Banding Follow-Up Studies Predictive Value of Tests Gene Transfer Techniques Blotting, Southern Treatment Outcome Case-Control Studies Diagnostic Errors Severity of Illness Index Stem Cell Transplantation Neuromuscular Blockade Tomography, X-Ray Computed Prospective Studies Electromyography Vital Capacity

Psychiatry and Psychology3

Intellectual Disability Projective Techniques Stanford-Binet Test

Phenomena and Processes46

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

Disciplines and Occupations2

Genetic Counseling Immunohistochemistry

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups1

Infant, Newborn

Health Care15

Genetic Counseling Genetic Testing Sensitivity and Specificity Retrospective Studies Age of Onset Reproducibility of Results Age Factors Follow-Up Studies Predictive Value of Tests Treatment Outcome Case-Control Studies Diagnostic Errors Severity of Illness Index Family Health Prospective 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 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 Pedigree Sarcolemma Creatine Kinase Thymopoietins Retinal Dystrophies Muscle Fibers, Skeletal Collagen Type VI Muscles Exons X Chromosome Myoblasts Muscle Proteins Dystrophin-Associated Protein Complex Prenatal Diagnosis Neuromuscular Diseases Mutation Caveolin 3 Muscular Diseases Laminin Phenotype Chromosomes, Human, Pair 4 Disease Models, Animal Cardiomyopathies Lamin Type A Cytoskeletal Proteins Genetic Linkage Poly(A)-Binding Protein II Genetic Therapy Diaphragm Regeneration Muscle Strength Neuroaxonal Dystrophies Biopsy Heterozygote Genes, Recessive Sarcoglycanopathies Walker-Warburg Syndrome Calpain Muscle Development Muscle Weakness Polymerase Chain Reaction Pregnenediones Mice, Inbred C57BL DNA Mutational Analysis Molecular Sequence Data Membrane Proteins Genetic Counseling Syndrome Myositis Immunohistochemistry Plectin Satellite Cells, Skeletal Muscle Myostatin Dependovirus Morpholinos Consanguinity Chromosome Mapping Delayed Diagnosis Base Sequence Connectin Genetic Testing Reflex Sympathetic Dystrophy Sensitivity and Specificity Cardiomyopathy, Dilated Myoblasts, Skeletal Early Diagnosis Muscle Cells Chromosome Deletion Vitelliform Macular Dystrophy Electroretinography Mice, Transgenic Genes, Dominant Frameshift Mutation Integrin alpha Chains Time Factors Evans Blue Glycerol Kinase Intellectual Disability Retrospective Studies Muscle Contraction Gene Deletion Codon, Nonsense

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