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Journal Abstract Search

131 related items for PubMed ID: 3683878

  • 21.
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  • 23. Purpuric cutaneous manifestations in mitochondrial encephalomyopathy.
    Horiguchi Y, Fujii T, Imamura S.
    J Dermatol; 1991 May; 18(5):295-301. PubMed ID: 1939857
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  • 25. 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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  • 26. MELAS of infantile onset: mitochondrial angiopathy or cytopathy?
    Fujii T, Okuno T, Ito M, Mutoh K, Horiguchi Y, Tashiro H, Mikawa H.
    J Neurol Sci; 1991 May; 103(1):37-41. PubMed ID: 1865230
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  • 28. Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome.
    Ciafaloni E, Ricci E, Servidei S, Shanske S, Silvestri G, Manfredi G, Schon EA, DiMauro S.
    Neurology; 1991 Oct; 41(10):1663-4. PubMed ID: 1922812
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  • 34. [Complex I (NADH coenzyme-Q-reductase) deficiency, MELAS syndrome and hypertrophic cardiomyopathy].
    Márquez C, Bautista J, Arenas J, Segura D, Chinchón I, Rafel E, Campos Y, Huerta R.
    Neurologia; 1991 May; 6(5):185-7. PubMed ID: 1908255
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  • 37. [Mitochondrial abnormalities and diseases].
    Goto Y, Sugita H.
    Nihon Naika Gakkai Zasshi; 1991 May 10; 80(5):775-80. PubMed ID: 1651974
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  • 38. [Molecular biology of defects in the mitochondrial electron-transfer complexes].
    Tanaka M.
    Seikagaku; 1991 Mar 10; 63(3):169-87. PubMed ID: 2071965
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