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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

139 related items for PubMed ID: 8602857

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  • 23. [Enzyme complex defects of the mitochondrial respiratory chain].
    Rubio JC, Martín MA, del Hoyo P, de Bustos F, Campos Y, Arenas J.
    Rev Neurol; 1998 Apr; 26 Suppl 1():S15-20. PubMed ID: 9810586
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  • 27. Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitution.
    Hirata K, Nakagawa M, Higuchi I, Hashimoto K, Hanada K, Takahashi K, Niiyama T, Izumi K, Sakoda S, Yamada H, Osame M.
    J Hum Genet; 1999 Apr; 44(3):210-4. PubMed ID: 10319590
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  • 28. Mitochondrial myopathy with succinate dehydrogenase and aconitase deficiency. Abnormalities of several iron-sulfur proteins.
    Hall RE, Henriksson KG, Lewis SF, Haller RG, Kennaway NG.
    J Clin Invest; 1993 Dec; 92(6):2660-6. PubMed ID: 8254022
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  • 29. [From gene to disease; from SDHD, a defect in the respiratory chain, to paragangliomas and pheochromocytomas].
    Taschner PE, Bröcker-Vriends AH, van der Mey AG.
    Ned Tijdschr Geneeskd; 2002 Nov 16; 146(46):2188-90. PubMed ID: 12467161
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  • 30. Mutations in SDHD lead to autosomal recessive encephalomyopathy and isolated mitochondrial complex II deficiency.
    Jackson CB, Nuoffer JM, Hahn D, Prokisch H, Haberberger B, Gautschi M, Häberli A, Gallati S, Schaller A.
    J Med Genet; 2014 Mar 16; 51(3):170-5. PubMed ID: 24367056
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  • 33. Late-onset riboflavin-responsive myopathy with combined multiple acyl coenzyme A dehydrogenase and respiratory chain deficiency.
    Antozzi C, Garavaglia B, Mora M, Rimoldi M, Morandi L, Ursino E, DiDonato S.
    Neurology; 1994 Nov 16; 44(11):2153-8. PubMed ID: 7969976
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  • 35. Mitochondrial myopathies.
    DiMauro S, Bonilla E, Zeviani M, Servidei S, DeVivo DC, Schon EA.
    J Inherit Metab Dis; 1987 Nov 16; 10 Suppl 1():113-28. PubMed ID: 2824920
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  • 37. Dramatic improvement in mitochondrial cardiomyopathy following treatment with idebenone.
    Lerman-Sagie T, Rustin P, Lev D, Yanoov M, Leshinsky-Silver E, Sagie A, Ben-Gal T, Munnich A.
    J Inherit Metab Dis; 2001 Feb 16; 24(1):28-34. PubMed ID: 11286379
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  • 40. Kearns-Sayre syndrome and complex II deficiency.
    Rivner MH, Shamsnia M, Swift TR, Trefz J, Roesel RA, Carter AL, Yanamura W, Hommes FA.
    Neurology; 1989 May 16; 39(5):693-6. PubMed ID: 2710360
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