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Journal Abstract Search

91 related items for PubMed ID: 11596361

  • 1. [Fatal infantile mitochondrial disease].
    Murakami N.
    Ryoikibetsu Shokogun Shirizu; 2001; (36):173-5. PubMed ID: 11596361
    [No Abstract] [Full Text] [Related]

  • 2. [Complex I (NADH-ubiquinone oxidoreductase) deficiency].
    Nonaka I.
    Ryoikibetsu Shokogun Shirizu; 2001; (36):129-31. PubMed ID: 11596342
    [No Abstract] [Full Text] [Related]

  • 3. [Pure mitochondrial myopathy].
    Murakami N, Sakuta R.
    Ryoikibetsu Shokogun Shirizu; 2001; (36):186-9. PubMed ID: 11596366
    [No Abstract] [Full Text] [Related]

  • 4. [Mitochondrial diseases with recurrent myoglobinuria].
    Murakami N.
    Ryoikibetsu Shokogun Shirizu; 2001; (36):183-5. PubMed ID: 11596365
    [No Abstract] [Full Text] [Related]

  • 5. Respiratory chain complex I deficiency.
    Triepels RH, Van Den Heuvel LP, Trijbels JM, Smeitink JA.
    Am J Med Genet; 2001; 106(1):37-45. PubMed ID: 11579423
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  • 14. Benign reversible course in infants manifesting clinicopathological features of fatal mitochondrial myopathy due to m.14674 T>C mt-tRNAGlu mutation.
    Chen TH, Tu YF, Goto YI, Jong YJ.
    QJM; 2013 Oct; 106(10):953-4. PubMed ID: 23842486
    [No Abstract] [Full Text] [Related]

  • 15. [Complex IV (cytochrome c oxidase) deficiency].
    Nonaka I.
    Ryoikibetsu Shokogun Shirizu; 2001 Oct; (36):137-41. PubMed ID: 11596345
    [No Abstract] [Full Text] [Related]

  • 16. Mitochondrial complex I deficiency caused by a deleterious NDUFA11 mutation.
    Berger I, Hershkovitz E, Shaag A, Edvardson S, Saada A, Elpeleg O.
    Ann Neurol; 2008 Mar; 63(3):405-8. PubMed ID: 18306244
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  • 17. POLG1 mutations associated with progressive encephalopathy in childhood.
    Kollberg G, Moslemi AR, Darin N, Nennesmo I, Bjarnadottir I, Uvebrant P, Holme E, Melberg A, Tulinius M, Oldfors A.
    J Neuropathol Exp Neurol; 2006 Aug; 65(8):758-68. PubMed ID: 16896309
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  • 18. Congenital or late-onset myopathy in patients with the T14709C mtDNA mutation.
    Mancuso M, Ferraris S, Nishigaki Y, Azan G, Mauro A, Sammarco P, Krishna S, Tay SK, Bonilla E, Romansky SG, Hirano M, DiMauro S.
    J Neurol Sci; 2005 Jan 15; 228(1):93-7. PubMed ID: 15607216
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