BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 2176453)

  • 21. Defects in the cytochrome bc1 complex in mitochondrial diseases.
    Kennaway NG
    J Bioenerg Biomembr; 1988 Jun; 20(3):325-52. PubMed ID: 2841308
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Muscle pathology in mitochondrial myopathy].
    Nonaka I
    No To Hattatsu; 1987 Mar; 19(2):110-7. PubMed ID: 3030377
    [No Abstract]   [Full Text] [Related]  

  • 23. Heterogeneous tissue expression of enzyme defects in mitochondrial myopathies.
    Sperl W; Ruitenbeek W; Trijbels JM; Korenke GC; Sengers RC
    J Inherit Metab Dis; 1990; 13(3):359-62. PubMed ID: 2172646
    [No Abstract]   [Full Text] [Related]  

  • 24. Mitochondrial myopathy and encephalopathy: three cases--a deficiency of NADH-CoQ dehydrogenase?
    Holliday PL; Climie AR; Gilroy J; Mahmud MZ
    Neurology; 1983 Dec; 33(12):1619-22. PubMed ID: 6417559
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular defects of NADH-ubiquinone oxidoreductase (complex I) in mitochondrial diseases.
    Morgan-Hughes JA; Schapira AH; Cooper JM; Clark JB
    J Bioenerg Biomembr; 1988 Jun; 20(3):365-82. PubMed ID: 3136150
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [NADH-CoQ reductase deficiency].
    Sugiyama N; Kobayashi M
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):828-30. PubMed ID: 3152097
    [No Abstract]   [Full Text] [Related]  

  • 27. [Mitochondrial abnormalities and diseases].
    Goto Y; Sugita H
    Nihon Naika Gakkai Zasshi; 1991 May; 80(5):775-80. PubMed ID: 1651974
    [No Abstract]   [Full Text] [Related]  

  • 28. Myopathy with abnormal mitochondria, transient low electron transport capacity in the respiratory chain, and absence of energy transduction at sites 1 and 2 in vitro.
    Trockel U; Scholte HR; Toyka KV; Busch HF; Luyt-Houwen IE; Berden JA
    J Neurol Neurosurg Psychiatry; 1986 Jun; 49(6):645-50. PubMed ID: 3016196
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Neurological approach to mitochondrial abnormalities].
    Yokochi K
    No To Hattatsu; 1987 Mar; 19(2):118-24. PubMed ID: 3030378
    [No Abstract]   [Full Text] [Related]  

  • 30. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Mitochondrial myopathies].
    Scarlato G; Barbieri S
    Riv Neurol; 1988; 58(1):26-30. PubMed ID: 3047845
    [No Abstract]   [Full Text] [Related]  

  • 32. Familial mitochondrial complex I deficiency with an abnormal mitochondrial encoded protein.
    Barth PG; Bolhuis PA; Wijburg FA; Sinjorgo KM; Ruitenbeek W; Schutgens RB
    J Inherit Metab Dis; 1989; 12 Suppl 2():355-7. PubMed ID: 2512443
    [No Abstract]   [Full Text] [Related]  

  • 33. The molecular pathology of respiratory-chain dysfunction in human mitochondrial myopathies.
    Morgan-Hughes JA; Schapira AH; Cooper JM; Holt IJ; Harding AE; Clark JB
    Biochim Biophys Acta; 1990 Jul; 1018(2-3):217-22. PubMed ID: 2168209
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The genetics of metabolic disorders of muscle.
    Poulton J; Land J
    Baillieres Clin Endocrinol Metab; 1990 Sep; 4(3):621-64. PubMed ID: 2268229
    [No Abstract]   [Full Text] [Related]  

  • 35. 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]  

  • 36. Multiple defects of the mitochondrial respiratory chain in a mitochondrial encephalopathy (MERRF): a clinical, biochemical and molecular study.
    Bindoff LA; Desnuelle C; Birch-Machin MA; Pellissier JF; Serratrice G; Dravet C; Bureau M; Howell N; Turnbull DM
    J Neurol Sci; 1991 Mar; 102(1):17-24. PubMed ID: 1649912
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Control of oxidative phosphorylation in rat muscle mitochondria: implications for mitochondrial myopathies.
    Letellier T; Malgat M; Mazat JP
    Biochim Biophys Acta; 1993 Feb; 1141(1):58-64. PubMed ID: 8382080
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [A case of mitochondrial encephalomyopathy with a defect in electron transport at complex I and IV in skeletal muscle showing peripheral neuropathy].
    Ohnishi A; Nakano S; Hashimoto T; Tsuji S; Murai Y
    Rinsho Shinkeigaku; 1988 Jan; 28(1):107-11. PubMed ID: 2838209
    [No Abstract]   [Full Text] [Related]  

  • 39. A mitochondrial encephalomyopathy with cardiomyopathy. A case revealing a defect of complex I in the respiratory chain.
    Nishizawa M; Tanaka K; Shinozawa K; Kuwabara T; Atsumi T; Miyatake T; Ohama E
    J Neurol Sci; 1987 Apr; 78(2):189-201. PubMed ID: 3106581
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Favourable clinical course in an infant with severe deficiency of complex III of the respiratory chain combined with less severe deficiencies of complexes I, II and IV.
    Rubio-Gozalbo ME; Ruitenbeek W; Bentlage HA; Schägger H; Sengers RC; Trijbels JM; ter Laak HJ; Mariman EC; Bakker MM; de Jager J; Smeitink JA
    Eur J Pediatr; 1997 Dec; 156(12):931-4. PubMed ID: 9453375
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.