Muscular Dystrophy

Facioscapulohumeral muscular dystrophy

Polymorphism / Clinical Trial / Quality of life / Muscular Dystrophy / Therapy / Epigenetic / Clinical Sciences / Clinical Study / Biochemistry and cell biology / Muscle mass / Epigenetic / Clinical Sciences / Clinical Study / Biochemistry and cell biology / Muscle mass

A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy

Genetics / Science / Polyadenylation / Adolescent / Multidisciplinary / Humans / Haplotypes / Muscular Dystrophy / Female / Male / Young Adult / Aged / Middle Aged / Adult / Single Nucleotide Polymorphism / Transfection / Base Sequence / Humans / Haplotypes / Muscular Dystrophy / Female / Male / Young Adult / Aged / Middle Aged / Adult / Single Nucleotide Polymorphism / Transfection / Base Sequence

G.P.7.13 Gene expression profiling in a skeletal muscle cell model of oculopharyngeal muscular dystrophy reveals an extracellular matrix defect

Extracellular Matrix / Muscular Dystrophy / Medical Physiology / Clinical Sciences / Skeletal Muscle / Neuromuscular Disorders / Neurosciences / Neuromuscular Disorders / Neurosciences

Distal anterior compartment myopathy: A dysferlin mutation causing a new muscular dystrophy phenotype

Magnetic Resonance Imaging / Membrane Proteins / Humans / Mutation / Muscular Dystrophy / Female / Muscular Dystrophies / Male / Muscles / Pedigree / Phenotype / Clinical Sciences / Adult / Annals / Neurosciences / Female / Muscular Dystrophies / Male / Muscles / Pedigree / Phenotype / Clinical Sciences / Adult / Annals / Neurosciences

Efecto De Un Suplemento Parenteral Con Selenito De Sodio en La Mortalidad De Corderos y Los Valores Hemáticos De Selenio Effect of Parenteral Supplement with Sodium Selenite on Lamb Mortality and Hematic Values of Selenium

Muscular Dystrophy / soil pH

Deletion of Integrin-Linked Kinase from Skeletal Muscles of Mice Resembles Muscular Dystrophy Due to α7β1-Integrin Deficiency

Skeletal muscle biology / Mutation / Mice / Muscular Dystrophy / Muscular Dystrophies / Animals / American / Integrins / Skeletal Muscle / Focal Adhesions / Animals / American / Integrins / Skeletal Muscle / Focal Adhesions

Distal anterior compartment myopathy: A dysferlin mutation causing a new muscular dystrophy phenotype

Magnetic Resonance Imaging / Membrane Proteins / Humans / Mutation / Muscular Dystrophy / Female / Muscular Dystrophies / Male / Muscles / Pedigree / Phenotype / Clinical Sciences / Adult / Annals / Neurosciences / Female / Muscular Dystrophies / Male / Muscles / Pedigree / Phenotype / Clinical Sciences / Adult / Annals / Neurosciences

DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1

Multidisciplinary / DNA / Humans / Muscular Dystrophy / Base Sequence

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