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Journal Abstract Search

123 related items for PubMed ID: 1322508

  • 1. Mitochondrial angiopathy in a family with MELAS.
    Förster C, Hübner G, Müller-Höcker J, Pongratz D, Baierl P, Senger R, Ruitenbeek W.
    Neuropediatrics; 1992 Jun; 23(3):165-8. PubMed ID: 1322508
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  • 7. Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
    Hasegawa H, Matsuoka T, Goto Y, Nonaka I.
    Ann Neurol; 1991 Jun; 29(6):601-5. PubMed ID: 1892363
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  • 12. Clinical and autopsy findings in two cases of MELAS presenting with stroke-like episodes but without clinical myopathy.
    Nicoll JA, Moss TH, Love S, Campbell MJ, Schutt WH.
    Clin Neuropathol; 1993 Jun; 12(1):38-43. PubMed ID: 8382573
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  • 16. [Myopathy with carnitine deficiency and lactic acidosis. A contribution to differential diagnosis of carnitine deficiency myopathies and mitochondrial myopathies].
    Cammann R, Dunker H, Schumacher H, Ruitenbeek W, Sperner J.
    Z Arztl Fortbild (Jena); 1992 Jul 10; 86(13):667-71. PubMed ID: 1642019
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  • 19. Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) gene.
    Inui K, Fukushima H, Tsukamoto H, Taniike M, Midorikawa M, Tanaka J, Nishigaki T, Okada S.
    J Pediatr; 1992 Jan 10; 120(1):62-6. PubMed ID: 1370535
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  • 20. Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin.
    Boustany RN, Aprille JR, Halperin J, Levy H, DeLong GR.
    Ann Neurol; 1983 Oct 10; 14(4):462-70. PubMed ID: 6314875
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