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Journal Abstract Search

113 related items for PubMed ID: 2537772

  • 1.
    ; . PubMed ID:
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  • 2. Mitochondrial encephalomyopathy. Association with an NADH dehydrogenase deficiency.
    van Erven PM, Gabreëls FJ, Ruitenbeek W, Renier WO, Fischer JC.
    Arch Neurol; 1987 Jul; 44(7):775-8. PubMed ID: 3593065
    [Abstract] [Full Text] [Related]

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  • 5. [NMR tomographic aspect of encephalomyopathy].
    Henkes H, Sperner J, Stoltenburg-Didinger G.
    Rofo; 1987 Aug; 147(2):214-6. PubMed ID: 2819983
    [No Abstract] [Full Text] [Related]

  • 6. [Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children].
    Liu XL, Bao XH, Ma YN, Chang XZ, Qin J, Wu XR.
    Zhonghua Er Ke Za Zhi; 2013 Feb; 51(2):130-5. PubMed ID: 23527980
    [Abstract] [Full Text] [Related]

  • 7. MR findings in patients with subacute necrotizing encephalomyelopathy (Leigh syndrome): correlation with biochemical defect.
    Medina L, Chi TL, DeVivo DC, Hilal SK.
    AJR Am J Roentgenol; 1990 Jun; 154(6):1269-74. PubMed ID: 2159689
    [Abstract] [Full Text] [Related]

  • 8. Hereditary disorders including mitochondrial diseases.
    Lightowlers RN.
    Curr Opin Neurol Neurosurg; 1992 Jun; 5(3):368-74. PubMed ID: 1623266
    [Abstract] [Full Text] [Related]

  • 9. CT, MRI, and autopsy findings in brain of a patient with MELAS.
    Fujii T, Okuno T, Ito M, Motoh K, Hamazaki S, Okada S, Kusaka H, Mikawa H.
    Pediatr Neurol; 1990 Jun; 6(4):253-6. PubMed ID: 2119589
    [Abstract] [Full Text] [Related]

  • 10. Mitochondrial abnormalities in choroid plexus of Leigh disease.
    Ohama E, Ikuta F, Nakamura N.
    Brain Dev; 1988 Jun; 10(1):30-5. PubMed ID: 3285724
    [Abstract] [Full Text] [Related]

  • 11. Magnetic resonance imaging in subacute necrotizing encephalomyelopathy (Leigh's disease).
    Koch TK, Yee MH, Hutchinson HT, Berg BO.
    Ann Neurol; 1986 Jun; 19(6):605-7. PubMed ID: 3729315
    [Abstract] [Full Text] [Related]

  • 12. MELAS syndrome. Report of two patients, and comparison with data of 24 patients derived from the literature.
    van Hellenberg Hubar JL, Gabreëls FJ, Ruitenbeek W, Sengers RC, Renier WO, Thijssen HO, ter Laak HJ.
    Neuropediatrics; 1991 Feb; 22(1):10-4. PubMed ID: 1903852
    [Abstract] [Full Text] [Related]

  • 13. Familial Leigh's syndrome: association with a defect in oxidative metabolism probably restricted to brain.
    van Erven PM, Gabreëls FJ, Ruitenbeek W, Renier WO, Lamers KJ, Sloof JL.
    J Neurol; 1987 May; 234(4):215-9. PubMed ID: 3612192
    [Abstract] [Full Text] [Related]

  • 14. Intravenous pyruvate loading test in Leigh syndrome.
    Van Erven PM, Gabreëls FJ, Wevers RA, Doesburg WH, Ruitenbeek W, Renier WO, Lamers KJ.
    J Neurol Sci; 1987 Feb; 77(2-3):217-27. PubMed ID: 3819766
    [Abstract] [Full Text] [Related]

  • 15. Defect in succinate oxidation by isolated muscle mitochondria in a patient with symmetrical lesions in the basal ganglia.
    Martin JJ, Van de Vyver FL, Scholte HR, Roodhooft AM, Ceuterick C, Martin L, Luyt-Houwen IE.
    J Neurol Sci; 1988 Apr; 84(2-3):189-200. PubMed ID: 3379446
    [Abstract] [Full Text] [Related]

  • 16. [Leigh disease. Presentation of a clinical case].
    Coronado-Garza MA, Treviño-de Leal C, Murguía-Ibarra FJ.
    Bol Med Hosp Infant Mex; 1989 Jul; 46(7):494-6. PubMed ID: 2765163
    [Abstract] [Full Text] [Related]

  • 17. [X-ray CT and MRI findings in male siblings with Leigh's encephalopathy].
    Onuma A, Miyabayashi S, Iinuma K, Tada K.
    No To Hattatsu; 1986 Jan; 18(1):68-9. PubMed ID: 3718774
    [No Abstract] [Full Text] [Related]

  • 18. [A case of mitochondrial encephalomyopathy with myoclonic attacks, hyper-lactic-pyruvic acidemia, and decreased activities of complex II and cytochrome c oxidase].
    Harigaya Y, Shoji M, Okamoto K, Hirai S, Sato T.
    Rinsho Shinkeigaku; 1988 Jan; 28(1):24-31. PubMed ID: 2838211
    [No Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. [Leigh's syndrome].
    Sunohara N.
    Nihon Rinsho; 1990 Jul; 48(7):1568-72. PubMed ID: 2169544
    [No Abstract] [Full Text] [Related]

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