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Journal Abstract Search

131 related items for PubMed ID: 8410073

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  • 4. Chronic progressive external ophthalmoplegia: a correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsies.
    Goto Y, Koga Y, Horai S, Nonaka I.
    J Neurol Sci; 1990 Dec; 100(1-2):63-9. PubMed ID: 1965208
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  • 6. Functional respiratory chain studies in subjects with chronic progressive external ophthalmoplegia and large heteroplasmic mitochondrial DNA deletions.
    Trounce I, Byrne E, Marzuki S, Dennett X, Sudoyo H, Mastaglia F, Berkovic SF.
    J Neurol Sci; 1991 Mar; 102(1):92-9. PubMed ID: 1677417
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  • 8. Severe mitochondrial cytopathy with complete A-V block, PEO, and mtDNA deletions.
    Marín-García J, Goldenthal MJ, Flores-Sarnat L, Sarnat HB.
    Pediatr Neurol; 2002 Sep; 27(3):213-6. PubMed ID: 12393131
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  • 10. Muscle fibres: applications for the study of the metabolic consequences of enzyme deficiencies in skeletal muscle.
    Vielhaber S, Kudin A, Schröder R, Elger CE, Kunz WS.
    Biochem Soc Trans; 2000 Feb; 28(2):159-64. PubMed ID: 10816119
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  • 11. Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.
    Shoffner JM, Lott MT, Voljavec AS, Soueidan SA, Costigan DA, Wallace DC.
    Proc Natl Acad Sci U S A; 1989 Oct; 86(20):7952-6. PubMed ID: 2554297
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  • 12. Mitochondrial encephalomyopathies.
    DiMauro S, Moraes CT.
    Arch Neurol; 1993 Nov; 50(11):1197-208. PubMed ID: 8215979
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  • 13. Distinct segregation of the pathogenic m.5667G>A mitochondrial tRNAAsn mutation in extraocular and skeletal muscle in chronic progressive external ophthalmoplegia.
    Schlapakow E, Peeva V, Zsurka G, Jeub M, Wabbels B, Kornblum C, Kunz WS.
    Neuromuscul Disord; 2019 May; 29(5):358-367. PubMed ID: 30962064
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  • 17. A point mutation in the cytb gene of cardiac mtDNA associated with complex III deficiency in ischemic cardiomyopathy.
    Marin-Garcia J, Hu Y, Ananthakrishnan R, Pierpont ME, Pierpont GL, Goldenthal MJ.
    Biochem Mol Biol Int; 1996 Oct; 40(3):487-95. PubMed ID: 8908357
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  • 19. A novel nonsense mutation (Q352X) in the mitochondrial cytochrome b gene associated with a combined deficiency of complexes I and III.
    Lamantea E, Carrara F, Mariotti C, Morandi L, Tiranti V, Zeviani M.
    Neuromuscul Disord; 2002 Jan; 12(1):49-52. PubMed ID: 11731284
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  • 20. Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres.
    Oldfors A, Larsson NG, Holme E, Tulinius M, Kadenbach B, Droste M.
    J Neurol Sci; 1992 Jul; 110(1-2):169-77. PubMed ID: 1324295
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