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Journal Abstract Search

58 related items for PubMed ID: 12013880

  • 1. [Complex III deficiency due to mutations in the cytochrome b gene].
    Ishii A, Ohkoshi N.
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():337-40. PubMed ID: 12013880
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  • 2. [Complex III (ubiquinone-cytochrome c reductase) deficiency].
    Nonaka I.
    Ryoikibetsu Shokogun Shirizu; 2001 Apr; (36):135-6. PubMed ID: 11596344
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  • 5. A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiency.
    Valnot I, Kassis J, Chretien D, de Lonlay P, Parfait B, Munnich A, Kachaner J, Rustin P, Rötig A.
    Hum Genet; 1999 Jun; 104(6):460-6. PubMed ID: 10453733
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  • 8. Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA.
    Andreu AL, Hanna MG, Reichmann H, Bruno C, Penn AS, Tanji K, Pallotti F, Iwata S, Bonilla E, Lach B, Morgan-Hughes J, DiMauro S.
    N Engl J Med; 1999 Sep 30; 341(14):1037-44. PubMed ID: 10502593
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  • 13. [West syndrome associated with deficit of complex III of the respiratory mitochondrial chain].
    Castro-Gago M, Pavón Belinchón P, Fernández Seara J, Rodrigo Sáez E, Beiras Iglesias A, Pérez Sánchez A.
    An Esp Pediatr; 1993 Apr 30; 38(4):355-8. PubMed ID: 8386913
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  • 14. Clinical and biochemical spectrum of mitochondrial complex III deficiency caused by mutations in the BCS1L gene.
    Ramos-Arroyo MA, Hualde J, Ayechu A, De Meirleir L, Seneca S, Nadal N, Briones P.
    Clin Genet; 2009 Jun 30; 75(6):585-7. PubMed ID: 19508421
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  • 15. 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 30; 12(1):49-52. PubMed ID: 11731284
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  • 16. [Complex IV(cytochrome c oxidase)].
    Sugie K, Nishino I.
    Nihon Rinsho; 2002 Apr 30; 60 Suppl 4():490-4. PubMed ID: 12013921
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  • 18. [MNGIE--thymidine phosphorylase deficiency].
    Nishino I, Hirano M.
    Nihon Rinsho; 2002 Apr 30; 60 Suppl 4():349-52. PubMed ID: 12013883
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  • 19. Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient.
    Blázquez A, Gil-Borlado MC, Morán M, Verdú A, Cazorla-Calleja MR, Martín MA, Arenas J, Ugalde C.
    Neuromuscul Disord; 2009 Feb 30; 19(2):143-6. PubMed ID: 19162478
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  • 20. Are cytochrome b gene mutations the only cause of atovaquone resistance in Pneumocystis?
    Kaneshiro ES.
    Drug Resist Updat; 2001 Oct 30; 4(5):322-9. PubMed ID: 11991686
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