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Mitochondrial Encephalomyopathies (n.)
1.(MeSH)A heterogenous group of disorders characterized by alterations of mitochondrial metabolism that result in muscle and nervous system dysfunction. These are often multisystemic and vary considerably in age at onset (usually in the first or second decade of life), distribution of affected muscles, severity, and course. (From Adams et al., Principles of Neurology, 6th ed, pp984-5)
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Mitochondrial Encephalomyopathies (n.) (MeSH)
C05.651.460.620, C10.228.140.163.540, C10.668.491.500.500, C18.452.132.540, C18.452.660.560.620, Encephalomyopathies, Mitochondrial (MeSH)
⇨ Creatine Kinase, Mitochondrial • Creatine Kinase, Mitochondrial Form • DNA, Mitochondrial • Genes, Mitochondrial • Genome, Mitochondrial • Inner Mitochondrial Membrane • Kearn-Sayre Mitochondrial Cytopathy • Mitochondrial ADP, ATP Translocases • Mitochondrial ATP Synthase • Mitochondrial ATP Synthases • Mitochondrial Apoptosis-Inducing Factor • Mitochondrial Assembly Factor hsp60 • Mitochondrial Creatine Kinase • Mitochondrial DNA • Mitochondrial Diseases • Mitochondrial Disorders • Mitochondrial Electron Transport Chain Complex Proteins • Mitochondrial Electron Transport Chain Deficiencies • Mitochondrial Electron Transport Complex I • Mitochondrial Electron Transport Complex II • Mitochondrial Electron Transport Complex III • Mitochondrial Electron Transport Complex IV • Mitochondrial F(1)F(0) ATPase • Mitochondrial Genes • Mitochondrial Genome • Mitochondrial Heat Shock Protein 70 • Mitochondrial Inheritance • Mitochondrial Membrane Potential • Mitochondrial Membrane Transport Proteins • Mitochondrial Membrane, Inner • Mitochondrial Membrane, Outer • Mitochondrial Membranes • Mitochondrial Myopathies • Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode • Mitochondrial Ocular Myopathy • Mitochondrial Pore Protein • Mitochondrial Porin • Mitochondrial Protein • Mitochondrial Proteins • Mitochondrial Proton-Translocating ATPases • Mitochondrial Respiratory Chain Deficiencies • Mitochondrial Size • Mitochondrial Swelling • Mitochondrial Telomere-Binding Protein • Mitochondrial Telomere-Binding Proteins • Mitochondrial Thioredoxin-Dependent Antioxidant Protein SP-22 • Mitochondrial Transhydrogenase • Mitochondrial Volume • Mitochondrial myopathy, not elsewhere classified • Myopathies, Mitochondrial • Outer Mitochondrial Membrane • Proteins, Mitochondrial • VDAC Mitochondrial Porin
⇨ ATP synthase, H+ transporting, mitochondrial F1 complex, alpha 1 • Anti-mitochondrial antibody • Human mitochondrial DNA haplogroup • Human mitochondrial genetics • Human mitochondrial molecular clock • Inner mitochondrial membrane • MT-TV (mitochondrial) • Mitochondrial DNA • Mitochondrial DNA (journal) • Mitochondrial Eve • Mitochondrial apoptosis-induced channel • Mitochondrial biogenesis • Mitochondrial carrier • Mitochondrial complex IV • Mitochondrial cytopathy • Mitochondrial decay • Mitochondrial disease • Mitochondrial diseases • Mitochondrial encephalomyopathy • Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes • Mitochondrial ferritin • Mitochondrial inner membrane • Mitochondrial matrix • Mitochondrial membrane transport protein • Mitochondrial membrane transporter • Mitochondrial myopathy • Mitochondrial permeability pore • Mitochondrial permeability transition • Mitochondrial protein-transporting ATPase • Mitochondrial shuttle • Mitochondrial toxicity • Mitochondrial transport protein • Mitochondrial trifunctional protein • Mitochondrial trifunctional protein deficiency • Outer mitochondrial membrane • Transfer of mitochondrial and chloroplast DNA to the nucleus
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