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Journal Abstract Search

171 related items for PubMed ID: 1908255

  • 1. [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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  • 2. Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome.
    Kobayashi M, Morishita H, Sugiyama N, Yokochi K, Nakano M, Wada Y, Hotta Y, Terauchi A, Nonaka I.
    J Pediatr; 1987 Feb; 110(2):223-7. PubMed ID: 3100753
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  • 3. Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency.
    Koga Y, Nonaka I, Kobayashi M, Tojyo M, Nihei K.
    Ann Neurol; 1988 Dec; 24(6):749-56. PubMed ID: 3144939
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  • 4. Disproportionate deficiency of iron-sulfur clusters and subunits of complex I in mitochondrial encephalomyopathy.
    Ichiki T, Tanaka M, Kobayashi M, Sugiyama N, Suzuki H, Nishikimi M, Ohnishi T, Nonaka I, Wada Y, Ozawa T.
    Pediatr Res; 1989 Feb; 25(2):194-201. PubMed ID: 2493147
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  • 5. [A case of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes) with progressive cytochrome c oxidase deficiency].
    Sumi K, Nagaura T, Itagaki Y, Inui K, Abe J.
    Rinsho Shinkeigaku; 1989 Jul; 29(7):901-8. PubMed ID: 2553313
    [Abstract] [Full Text] [Related]

  • 6. Human mitochondrial respiratory chain deficiencies.
    Morgan-Hughes JA, Schapira AH, Cooper JM, Hayes DJ, Clark JB.
    Aust Paediatr J; 1988 Jul; 24 Suppl 1():55-7. PubMed ID: 2849394
    [Abstract] [Full Text] [Related]

  • 7. Vascular involvement in mitochondrial myopathy.
    Sakuta R, Nonaka I.
    Ann Neurol; 1989 Jun; 25(6):594-601. PubMed ID: 2500889
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  • 8. A mitochondrial encephalomyopathy with cardiomyopathy. A case revealing a defect of complex I in the respiratory chain.
    Nishizawa M, Tanaka K, Shinozawa K, Kuwabara T, Atsumi T, Miyatake T, Ohama E.
    J Neurol Sci; 1987 Apr; 78(2):189-201. PubMed ID: 3106581
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  • 10. Biochemical studies in mitochondrial encephalomyopathy.
    Goda S, Ishimoto S, Goto I, Kuroiwa Y, Koike K, Koike M, Nakagawa M, Reichmann H, DiMauro S.
    J Neurol Neurosurg Psychiatry; 1987 Oct; 50(10):1348-52. PubMed ID: 3681314
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  • 13. 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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  • 15. Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome and NADH-CoQ reductase deficiency.
    Kobayashi M, Morishita H, Sugiyama N, Yokochi K, Nakano M, Wada Y, Hotta Y, Terauchi A, Nonaka I.
    J Inherit Metab Dis; 1986 Jun; 9(3):301-4. PubMed ID: 3099078
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  • 17. [Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) associated with hypothalamo-pituitary hypofunction--a case report].
    Ishii A, Watanabe S, Ohkoshi N, Mizusawa H, Kanazawa I.
    Rinsho Shinkeigaku; 1991 Feb; 31(2):179-83. PubMed ID: 2060243
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  • 19. Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with special reference to the mechanism of cerebral manifestations.
    Seyama K, Suzuki K, Mizuno Y, Yoshida M, Tanaka M, Ozawa T.
    Acta Neurol Scand; 1989 Dec; 80(6):561-8. PubMed ID: 2515713
    [Abstract] [Full Text] [Related]

  • 20. Generalized mitochondrial microangiopathy and vascular cytochrome c oxidase deficiency. Occurrence in a case of MELAS syndrome with mitochondrial cardiomyopathy-myopathy and combined complex I/IV deficiency.
    Müller-Höcker J, Hübner G, Bise K, Förster C, Hauck S, Paetzke I, Pongratz D, Kadenbach B.
    Arch Pathol Lab Med; 1993 Feb; 117(2):202-10. PubMed ID: 8381271
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