These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 2279503)

  • 1. Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathies.
    Korenke GC; Bentlage HA; Ruitenbeek W; Sengers RC; Sperl W; Trijbels JM; Gabreels FJ; Wijburg FA; Wiedermann V; Hanefeld F
    Eur J Pediatr; 1990 Dec; 150(2):104-8. PubMed ID: 2279503
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lactic acidosis and mitochondrial myopathy associated with deficiency of several components of complex III of the respiratory chain.
    Kennaway NG; Buist NR; Darley-Usmar VM; Papadimitriou A; Dimauro S; Kelley RI; Capaldi RA; Blank NK; D'Agostino A
    Pediatr Res; 1984 Oct; 18(10):991-9. PubMed ID: 6093035
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fatal infantile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency.
    DiMauro S; Mendell JR; Sahenk Z; Bachman D; Scarpa A; Scofield RM; Reiner C
    Neurology; 1980 Aug; 30(8):795-804. PubMed ID: 6251406
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Muscle involvement in pyruvate dehydrogenase complex (PDHC) deficiency.
    Chung SJ; Asoh S; Yamanaka T; Okamura-Oho Y; Toshima K; Woo M; Nonaka I
    Brain Dev; 1987; 9(1):9-15. PubMed ID: 3111288
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mosaicism of mitochondria in mitochondrial myopathy: an electronmicroscopic analysis of cytochrome c oxidase.
    Haginoya K; Miyabayashi S; Iinuma K; Tada K
    Acta Neuropathol; 1990; 80(6):642-8. PubMed ID: 2177307
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Combined deficiencies of the pyruvate dehydrogenase complex and enzymes of the respiratory chain in mitochondrial myopathies.
    Sperl W; Ruitenbeek W; Sengers RC; Trijbels JM; Bentlage H; Wraith JE; Heilmann C; Stöckler S; Binder C; Korenke GC
    Eur J Pediatr; 1992 Mar; 151(3):192-5. PubMed ID: 1601011
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondrial myopathies.
    DiMauro S; Bonilla E; Zeviani M; Nakagawa M; DeVivo DC
    Ann Neurol; 1985 Jun; 17(6):521-38. PubMed ID: 3927817
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial myopathy with lactic acidosis and deficient activity of muscle succinate cytochrome-c-oxidoreductase.
    Behbehani AW; Goebel H; Osse G; Gabriel M; Langenbeck U; Berden J; Berger R; Schutgens RB
    Eur J Pediatr; 1984 Nov; 143(1):67-71. PubMed ID: 6096151
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsies.
    Zheng XX; Shoffner JM; Voljavec AS; Wallace DC
    Biochim Biophys Acta; 1990 Aug; 1019(1):1-10. PubMed ID: 2168748
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Enzyme activity analyses along ragged-red and normal single muscle fibres.
    Reichmann H
    Histochemistry; 1992 Sep; 98(2):131-4. PubMed ID: 1330995
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Morphometric analysis of skeletal muscle fibres and capillaries in mitochondrial myopathies.
    Scelsi R
    Pathol Res Pract; 1992 Jun; 188(4-5):607-11. PubMed ID: 1329053
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies.
    Müller-Höcker J; Ibel H; Paetzke I; Deufel T; Endres W; Kadenbach B; Gokel JM; Hübner G
    Virchows Arch A Pathol Anat Histopathol; 1991; 419(4):355-62. PubMed ID: 1659034
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital ocular motor apraxia associated with myopathy, external hydrocephalus and NADH dehydrogenase deficiency.
    Puñal JE; Rodríguez E; Pintos E; Campos Y; Castro-Gago M
    Brain Dev; 1998 Apr; 20(3):175-8. PubMed ID: 9628194
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A morphometric study of muscle mitochondria in cytochrome c oxidase deficiency.
    Chung S; Nonaka I
    J Neurol Sci; 1988 Feb; 83(2-3):269-82. PubMed ID: 2833575
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration.
    Yamamoto M; Sato T; Anno M; Ujike H; Takemoto M
    J Neurol Neurosurg Psychiatry; 1987 Nov; 50(11):1475-81. PubMed ID: 2826704
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fatal infantile mitochondrial myopathy due to cytochrome c oxidase deficiency.
    Minchom PE; Dormer RL; Hughes IA; Stansbie D; Cross AR; Hendry GA; Jones OT; Johnson MA; Sherratt HS; Turnbull DM
    J Neurol Sci; 1983; 60(3):453-63. PubMed ID: 6313867
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Benign mitochondrial myopathy with deficiency of NADH-CoQ reductase and cytochrome c oxidase.
    Roodhooft AM; Van Acker KJ; Martin JJ; Ceuterick C; Scholte HR; Luyt-Houwen IE
    Neuropediatrics; 1986 Nov; 17(4):221-6. PubMed ID: 3027606
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitochondrial myopathy with diffuse activation and focal deficiency of mitochondrial ATPase and carnitine deficiency.
    Müller-Höcker J; Paetzke I; Pongratz D; Hübner G
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1985; 48(2):185-96. PubMed ID: 2859691
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency.
    Koga Y; Nonaka I; Kobayashi M; Tojyo M; Nihei K
    Ann Neurol; 1988 Dec; 24(6):749-56. PubMed ID: 3144939
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Vascular involvement in mitochondrial myopathy.
    Sakuta R; Nonaka I
    Ann Neurol; 1989 Jun; 25(6):594-601. PubMed ID: 2500889
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.