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Journal Abstract Search

649 related items for PubMed ID: 19181635

  • 1. Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects.
    De Paepe B, Smet J, Lammens M, Seneca S, Martin JJ, De Bleecker J, De Meirleir L, Lissens W, Van Coster R.
    J Clin Pathol; 2009 Feb; 62(2):172-6. PubMed ID: 19181635
    [Abstract] [Full Text] [Related]

  • 2. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
    Auré K, Fayet G, Leroy JP, Lacène E, Romero NB, Lombès A.
    Brain; 2006 May; 129(Pt 5):1249-59. PubMed ID: 16537564
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  • 3. Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy.
    Meulemans A, De Paepe B, De Bleecker J, Smet J, Lissens W, Van Coster R, De Meirleir L, Seneca S.
    Arch Neurol; 2007 Sep; 64(9):1339-43. PubMed ID: 17846276
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  • 4. Quantification of OXPHOS gene transcripts during muscle cell differentiation in patients with mitochondrial myopathies.
    Bonod-Bidaud C, Giraud S, Mandon G, Mousson B, Stepien G.
    Exp Cell Res; 1999 Jan 10; 246(1):91-7. PubMed ID: 9882518
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  • 5. Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNA.
    Kärppä M, Herva R, Moslemi AR, Oldfors A, Kakko S, Majamaa K.
    Brain; 2005 Aug 10; 128(Pt 8):1861-9. PubMed ID: 15857931
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  • 6. 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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  • 7. [Application of new techniques for locating the underlying molecular defects in patients with disorders of oxidative phosphorylation].
    Van Coster R, Smet J.
    Verh K Acad Geneeskd Belg; 2007 Jan 15; 69(4):197-211. PubMed ID: 17821958
    [Abstract] [Full Text] [Related]

  • 8. Mitochondrial tRNA gene mutations in patients having mitochondrial disease with lactic acidosis.
    Ueki I, Koga Y, Povalko N, Akita Y, Nishioka J, Yatsuga S, Fukiyama R, Matsuishi T.
    Mitochondrion; 2006 Feb 15; 6(1):29-36. PubMed ID: 16337222
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  • 9. Mitochondrial medicine--molecular pathology of defective oxidative phosphorylation.
    Fosslien E.
    Ann Clin Lab Sci; 2001 Jan 15; 31(1):25-67. PubMed ID: 11314862
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  • 12. Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies.
    Hess JF, Parisi MA, Bennett JL, Clayton DA.
    Nature; 1991 May 16; 351(6323):236-9. PubMed ID: 1755869
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  • 13. ["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data].
    Laforêt P, Ziegler F, Sternberg D, Rouche A, Frachon P, Fardeau M, Eymard B, Lombès A.
    Rev Neurol (Paris); 2000 Dec 16; 156(12):1136-47. PubMed ID: 11139730
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  • 15. The role of complex I genes in MELAS: a novel heteroplasmic mutation 3380G>A in ND1 of mtDNA.
    Horváth R, Reilmann R, Holinski-Feder E, Ringelstein EB, Klopstock T.
    Neuromuscul Disord; 2008 Jul 16; 18(7):553-6. PubMed ID: 18590963
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  • 16. Muscle computed tomography patterns in patients with the mitochondrial DNA mutation 3243A>G.
    Kärppä M, Mahjneh I, Karttunen A, Tolonen U, Majamaa K.
    J Neurol; 2004 May 16; 251(5):556-63. PubMed ID: 15164188
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  • 17. The genetics and pathology of oxidative phosphorylation.
    Smeitink J, van den Heuvel L, DiMauro S.
    Nat Rev Genet; 2001 May 16; 2(5):342-52. PubMed ID: 11331900
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  • 20. Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders.
    Sternberg D, Chatzoglou E, Laforêt P, Fayet G, Jardel C, Blondy P, Fardeau M, Amselem S, Eymard B, Lombès A.
    Brain; 2001 May 16; 124(Pt 5):984-94. PubMed ID: 11335700
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