Results 161 to 170 of about 371,748 (188)
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[Mitochondrial encephalomyopathy].
Recenti progressi in medicina, 1990Modern concepts regarding mitochondrial encephalomyopathies (ME) are summarized. Utilizing recent techniques of molecular biology we studied some cases of ME referred to the Institute of Clinical Neurology of Milan University. With these techniques we demonstrated different mitochondrial DNA deletions either in patients' muscle or in culture.
G, Scarlato +4 more
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Mitochondrial encephalomyopathy with corticosteroid dependence
Medical Journal of Australia, 1989A 12-year-old boy with corticosteroid-responsive mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) is described. His mother proved to have an asymptomatic mitochondrial myopathy on examination of a muscle biopsy specimen.
S S, Gubbay +3 more
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Tachyduodenia in mitochondrial neurogastrointestinal encephalomyopathy
Neurogastroenterology & Motility, 2011AbstractIn a 38‐year‐old male patient diagnosed with mitochondrial neurogastrointestinal encephalomyopathy an abnormally high duodenal contraction frequency of 20 per minute was found to be present. It is speculated that this tachyduodenia is caused by a metabolic effect on Cajal cells.
Scheffer, R. C. H., Smout, A. J. P. M.
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[Mitochondrial encephalomyopathies].
Acta medica portuguesa, 1994Mitochondrial Encephalomyopathies are primary disorders of energy metabolism recently described. They are the result of mitochondrial abnormalities with a wide spectrum of syndromes implying a multisystemic but predominantly muscular and cerebral involvement.
R, Almeida, A, Sena, M, Gonçalves
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Mitochondrial encephalomyopathies
2002Salvatore Dimauro, Anthony H.V. Schapira
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Neuropathology of Mitochondrial Encephalomyopathies Due to Mitochondrial DNA Defects
Journal of Neuropathology and Experimental Neurology, 1993Eduardo Bonilla, M Sparaco, J M Powers
exaly
Mitochondrial encephalomyopathies.
Progress in clinical and biological research, 1989DiMauro, S +7 more
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