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Journal Abstract Search

119 related items for PubMed ID: 1810165

  • 1. Characteristic changes on brain CT in a case of Leigh encephalopathy with deficiency of pyruvate dehydrogenase.
    Arai Y, Miyasato Y, Koide H.
    Brain Dev; 1991 Nov; 13(6):457-8. PubMed ID: 1810165
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  • 4. Abnormalities of pyruvate dehydrogenase complex in brain disease.
    Sheu KF, Szabo P, Ko LW, Hinman LM.
    Ann N Y Acad Sci; 1989 Nov; 573():378-91. PubMed ID: 2517466
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  • 6. Pyruvate dehydrogenase activity is not deficient in the brain of three autopsied cases with Leigh disease (subacute necrotizing encephalomyelopathy, SNE).
    Kustermann-Kuhn B, Harzer K, Schröder R, Permanetter W, Peiffer J.
    Hum Genet; 1984 Nov; 68(1):51-3. PubMed ID: 6437963
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  • 8. [Leigh syndrome: serial CT and MR imaging findings].
    Ariga H, Takahashi S, Miyabayashi S, Ohnuma A, Higano S, Kurihara N, Sakamoto K.
    Nihon Igaku Hoshasen Gakkai Zasshi; 1996 Oct; 56(12):839-45. PubMed ID: 8940814
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  • 10. A family with pyruvate dehydrogenase complex deficiency due to a novel C>T substitution at nucleotide position 407 in exon 4 of the X-linked Epsilon1alpha gene.
    Tulinius M, Darin N, Wiklund LM, Holmberg E, Eriksson JE, Lissens W, De Meirleir L, Holme E.
    Eur J Pediatr; 2005 Feb; 164(2):99-103. PubMed ID: 15558317
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  • 13. Complex I (reduced nicotinamide-adenine dinucleotide-coenzyme Q reductase) deficiency in two patients with probable Leigh syndrome.
    Fujii T, Ito M, Okuno T, Mutoh K, Nishikomori R, Mikawa H.
    J Pediatr; 1990 Jan; 116(1):84-7. PubMed ID: 2104930
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  • 14. Subacute necrotizing encephalomyelopathy (Leigh disease): CT study.
    Paltiel HJ, O'Gorman AM, Meagher-Villemure K, Rosenblatt B, Silver K, Watters GV.
    Radiology; 1987 Jan; 162(1 Pt 1):115-8. PubMed ID: 3786750
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  • 15. Leigh syndrome: clinical features and biochemical and DNA abnormalities.
    Rahman S, Blok RB, Dahl HH, Danks DM, Kirby DM, Chow CW, Christodoulou J, Thorburn DR.
    Ann Neurol; 1996 Mar; 39(3):343-51. PubMed ID: 8602753
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  • 16. CT scan appearance in subacute necrotising encephalomyelopathy.
    Campistol J, Fernandez Alvarez E, Cusi V.
    Dev Med Child Neurol; 1984 Aug; 26(4):519-22. PubMed ID: 6479473
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  • 17. Subacute necrotizing encephalomyelopathy (Leigh's disease): clinical correlations with computerized tomography in the diagnosis of the juvenile and adult forms.
    Bianco F, Floris R, Pozzessere G, Rizzo PA.
    Acta Neurol Scand; 1987 Mar; 75(3):214-7. PubMed ID: 3577684
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  • 19. Leigh syndrome due to pyruvate dehydrogenase E1 alpha deficiency (point mutation R263G) in a Spanish boy.
    Briones P, López MJ, De Meirleir L, Ribes A, Rodés M, Martinez-Costa C, Peris M, Lissens W.
    J Inherit Metab Dis; 1996 Mar; 19(6):795-6. PubMed ID: 8982956
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