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Journal Abstract Search

69 related items for PubMed ID: 2855956

  • 21.
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  • 22. Cytochrome c oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome).
    Hayasaka K, Brown GK, Danks DM, Droste M, Kadenbach B.
    J Inherit Metab Dis; 1989; 12(3):247-56. PubMed ID: 2559245
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  • 23. [Cytochrome c oxydase-deficient Leigh syndrome with homozygous mutation in SURF1 gene].
    Monnot S, Chabrol B, Cano A, Pellissier JF, Collignon P, Montfort MF, Paquis-Flucklinger V.
    Arch Pediatr; 2005 May; 12(5):568-71. PubMed ID: 15885549
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  • 26. A novel mutation in the mitochondrial tRNA Asn gene associated with a lethal disease.
    Coulbault L, Herlicoviez D, Chapon F, Read MH, Penniello MJ, Reynier P, Fayet G, Lombès A, Jauzac P, Allouche S.
    Biochem Biophys Res Commun; 2005 Apr 15; 329(3):1152-4. PubMed ID: 15752774
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  • 27. Leigh syndrome with cytochrome-c oxidase deficiency and a single T insertion nt 5537 in the mitochondrial tRNATrp gene.
    Tulinius M, Moslemi AR, Darin N, Westerberg B, Wiklund LM, Holme E, Oldfors A.
    Neuropediatrics; 2003 Apr 15; 34(2):87-91. PubMed ID: 12776230
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  • 31. 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 15; 117(2):202-10. PubMed ID: 8381271
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  • 32.
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  • 33. Cytochrome c oxidase deficiency.
    Comi GP, Strazzer S, Galbiati S, Bresolin N.
    Int Rev Neurobiol; 2002 Feb 15; 53():205-40. PubMed ID: 12512342
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  • 34. Saguenay Lac Saint Jean cytochrome oxidase deficiency: sequence analysis of nuclear encoded COX subunits, chromosomal localization and a sequence anomaly in subunit VIc.
    Lee N, Morin C, Mitchell G, Robinson BH.
    Biochim Biophys Acta; 1998 Feb 27; 1406(1):1-4. PubMed ID: 9545512
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  • 38. Murine cytomegalovirus infection exacerbates complex IV deficiency in a model of mitochondrial disease.
    Ferreira N, Andoniou CE, Perks KL, Ermer JA, Rudler DL, Rossetti G, Periyakaruppiah A, Wong JKY, Rackham O, Noakes PG, Degli-Esposti MA, Filipovska A.
    PLoS Genet; 2020 Mar 27; 16(3):e1008604. PubMed ID: 32130224
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  • 39. Immunochemical study in three patients with cytochrome c oxidase deficiency presenting Leigh's encephalomyelopathy.
    Miyabayashi S, Ito T, Abukawa D, Narisawa K, Tada K, Tanaka M, Ozawa T, Droste M, Kadenbach B.
    J Inherit Metab Dis; 1987 Mar 27; 10(3):289-92. PubMed ID: 2828763
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  • 40. Clinical and biochemical studies on cytochrome oxidase deficiencies.
    Schon EA, Bonilla E, Lombes A, Moraes CT, Nakase H, Rizzuto R, Zeviani M, DiMauro S.
    Ann N Y Acad Sci; 1988 Mar 27; 550():348-59. PubMed ID: 2854407
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