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Journal Abstract Search

159 related items for PubMed ID: 17900719

  • 21.
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  • 22. Management of mitochondrial disease on an intensive care unit.
    Howard RS, Russell S, Losseff N, Harding AE, Hughes JM, Wiles CM, Miller DH, Hirsch NP.
    QJM; 1995 Mar; 88(3):197-207. PubMed ID: 7767670
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  • 23. Kearns-Sayre syndrome. A case report.
    Altunbaşak S, Bingöl G, Ozbarlas N, Akçören Z, Hergüner O.
    Turk J Pediatr; 1998 Mar; 40(2):255-9. PubMed ID: 9677732
    [Abstract] [Full Text] [Related]

  • 24. Genetics of cerebrovascular disorders.
    Meschia JF, Brott TG, Brown RD.
    Mayo Clin Proc; 2005 Jan; 80(1):122-32. PubMed ID: 15667040
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  • 25. Treatment of Depression With Duloxetine in Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes.
    Cozart B, Diaz Vera J, Denham JD, Whiting WL.
    Clin Neuropharmacol; 2018 Jan; 41(3):103-105. PubMed ID: 29596118
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  • 26. A case of myoclonus epilepsy and lactic acidosis: difficulties in diagnosis and treatment of terminal mitochondrial cytopathy.
    Müllges W, Dorn T, Paulus W, Seibel P, Reichmann H.
    Intensive Care Med; 1994 Nov; 20(8):613-4. PubMed ID: 7706581
    [No Abstract] [Full Text] [Related]

  • 27. Letter to the Editor regarding "Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes diagnosed after metformin-triggered stroke-like episodes".
    Finsterer J.
    J Stroke Cerebrovasc Dis; 2023 Jun; 32(6):107094. PubMed ID: 37085391
    [No Abstract] [Full Text] [Related]

  • 28. Late-onset mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with bitemporal lesions.
    Kisanuki YY, Gruis KL, Smith TL, Brown DL.
    Arch Neurol; 2006 Aug; 63(8):1200-1. PubMed ID: 16908753
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  • 29. Severe lactic acidosis secondary to minocycline in a teenager with infectious mononucleosis and mitochondrial myopathy.
    Zoraster RM, Rison RA.
    Clin Neurol Neurosurg; 2008 Jun; 110(6):627-30. PubMed ID: 18440128
    [Abstract] [Full Text] [Related]

  • 30. [Mitochondrial encephalomyopathies: 3243 mutation as a central matter].
    Goto Y, Nonaka I.
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1425-6. PubMed ID: 8752418
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  • 31.
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  • 32. Fundus changes in patients with the mitochondrial DNA point mutation at position 3243.
    Bonte C, Leys A, Matthijs G, Missotten L.
    Bull Soc Belge Ophtalmol; 1996 Dec; 261():9-12. PubMed ID: 9009357
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  • 40. Congenital disorders of glycosylation (CDG) may be underdiagnosed when mimicking mitochondrial disease.
    Briones P, Vilaseca MA, García-Silva MT, Pineda M, Colomer J, Ferrer I, Artigas J, Jaeken J, Chabás A.
    Eur J Paediatr Neurol; 2001 Dec; 5(3):127-31. PubMed ID: 11589167
    [Abstract] [Full Text] [Related]

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