Parkinson s disease and muscular dystrophy. Medical search. Frequent questions

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Anatomy27

Muscle, Skeletal Sarcolemma Myoblasts Muscle Fibers, Skeletal Muscles Chromosomes, Human, Pair 4 X Chromosome Diaphragm Substantia Nigra Lewy Bodies Satellite Cells, Skeletal Muscle Muscle Cells Myoblasts, Skeletal Brain Dopaminergic Neurons Subthalamic Nucleus Cells, Cultured Nuclear Envelope Cell Line Neurons Myocardium Neuromuscular Junction Fundus Oculi Sarcomeres Putamen Costameres Chromosomes, Human, Pair 2

Organisms7

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

Diseases50

Muscular Dystrophies Muscular Dystrophy, Duchenne Crohn Disease Muscular Dystrophy, Animal Parkinson Disease Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Fuchs' Endothelial Dystrophy Retinal Dystrophies Disease Models, Animal Muscular Diseases Neuromuscular Diseases Parkinsonian Disorders Neuroaxonal Dystrophies Sarcoglycanopathies Walker-Warburg Syndrome Cardiomyopathies Parkinson Disease, Secondary Reflex Sympathetic Dystrophy Muscle Weakness Vitelliform Macular Dystrophy Myositis Cardiomyopathy, Dilated Multiple System Atrophy Muscular Atrophy Myotonic Disorders Syndrome Retinal Degeneration Retinitis Pigmentosa Neurodegenerative Diseases Distal Myopathies Disease Progression Intellectual Disability Gait Disorders, Neurologic Lewy Body Disease MPTP Poisoning Supranuclear Palsy, Progressive Epidermolysis Bullosa Simplex Chromosome Deletion Genetic Predisposition to Disease Fibrosis Contracture Scoliosis Corneal Dystrophy, Juvenile Epithelial of Meesmann Myoglobinuria Lipodystrophy

Chemicals and Drugs51

Dystrophin Sarcoglycans Dystroglycans Utrophin Thymopoietins Collagen Type VI Dystrophin-Associated Proteins alpha-Synuclein Creatine Kinase Muscle Proteins Lamin Type A Dystrophin-Associated Protein Complex Laminin Caveolin 3 Poly(A)-Binding Protein II Antiparkinson Agents Cytoskeletal Proteins Calpain Plectin Membrane Proteins Connectin Levodopa Glucosylceramidase Myostatin Lamins Creatine Kinase, MM Form Mannosyltransferases Dopamine N-Acetylglucosaminyltransferases Poly(A)-Binding Protein I Membrane Glycoproteins Morpholinos 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine Oxepins Genetic Markers Oxidopamine Integrin alpha Chains Codon, Nonsense Pregnenediones Evans Blue Ubiquitin-Protein Ligases Caveolins RNA, Messenger Cardiotoxins DNA Nitric Oxide Synthase Type I Glycosyltransferases Oligoribonucleotides, Antisense Collagen Type VIII Glycerol Kinase Oligonucleotides, Antisense

Analytical, Diagnostic and Therapeutic Techniques and Equipment25

Duodenoscopy Pedigree Heterozygote Detection Disease Models, Animal DNA Mutational Analysis Genetic Therapy Chromosome Mapping Muscle Strength Immunohistochemistry Genetic Testing Deep Brain Stimulation Electroretinography Blotting, Western Biopsy Prenatal Diagnosis Polymerase Chain Reaction Electromyography Severity of Illness Index Fluorescent Antibody Technique Case-Control Studies Gait Dance Therapy Reverse Transcriptase Polymerase Chain Reaction Magnetic Resonance Imaging Models, Biological

Psychiatry and Psychology3

Intellectual Disability Lewy Body Disease Dance Therapy

Phenomena and Processes42

Mutation Chromosomes, Human, Pair 4 Exons Phenotype X Chromosome Genetic Linkage Genes, Recessive Consanguinity Muscle Development Regeneration Heterozygote Muscle Strength Mutation, Missense Genes, Dominant Base Sequence Trinucleotide Repeat Expansion Homozygote Glycosylation Genotype Amino Acid Sequence Gene Expression Regulation Frameshift Mutation Genetic Markers Codon, Nonsense Lod Score Gene Deletion Haplotypes Genetic Vectors Muscle Contraction Postural Balance Sequence Deletion Alleles Point Mutation Chromosome Deletion Genetic Predisposition to Disease Time Factors Tandem Repeat Sequences Gene Expression Gait Transgenes Chromosomes, Human, Pair 2 Founder Effect

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Humanities1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care6

Age of Onset Genetic Testing 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 Humanities Information Science Health Care

Muscular Dystrophies Duodenoscopy Muscular Dystrophy, Duchenne Crohn Disease Muscular Dystrophy, Animal Parkinson Disease Dystrophin Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Mice, Inbred mdx Muscular Dystrophy, Emery-Dreifuss Sarcoglycans Corneal Dystrophies, Hereditary Dystroglycans Muscular Dystrophy, Oculopharyngeal Utrophin Muscle, Skeletal Fuchs' Endothelial Dystrophy Thymopoietins Retinal Dystrophies Collagen Type VI Pedigree Dystrophin-Associated Proteins Sarcolemma Heterozygote Detection alpha-Synuclein Creatine Kinase Muscle Proteins Mutation Myoblasts Muscle Fibers, Skeletal Muscles Chromosomes, Human, Pair 4 Lamin Type A Dystrophin-Associated Protein Complex Laminin Exons Caveolin 3 Poly(A)-Binding Protein II Antiparkinson Agents Disease Models, Animal Muscular Diseases Phenotype X Chromosome Neuromuscular Diseases Parkinsonian Disorders Cytoskeletal Proteins Genetic Linkage Neuroaxonal Dystrophies Sarcoglycanopathies Walker-Warburg Syndrome Calpain Genes, Recessive Cardiomyopathies DNA Mutational Analysis Plectin Parkinson Disease, Secondary Genetic Therapy Membrane Proteins Consanguinity Connectin Muscle Development Regeneration Heterozygote Levodopa Molecular Sequence Data Reflex Sympathetic Dystrophy Muscle Weakness Chromosome Mapping Mice, Inbred C57BL Diaphragm Glucosylceramidase Muscle Strength Mutation, Missense Vitelliform Macular Dystrophy Substantia Nigra Lewy Bodies Dependovirus Age of Onset Myositis Myostatin Immunohistochemistry Genetic Testing Genes, Dominant Lamins Mice, Transgenic Satellite Cells, Skeletal Muscle Base Sequence Deep Brain Stimulation Genetic Counseling Mice, Knockout Cardiomyopathy, Dilated Electroretinography Multiple System Atrophy Muscular Atrophy Trinucleotide Repeat Expansion Muscle Cells Myotonic Disorders Homozygote

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