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Journal Abstract Search

156 related items for PubMed ID: 3612192

  • 21. Metabolic acidosis versus a compensation of respiratory alkalosis in four children with Leigh's disease.
    Pronicka E, Halikowski B.
    J Inherit Metab Dis; 1984; 7 Suppl 2():113-4. PubMed ID: 6434858
    [No Abstract] [Full Text] [Related]

  • 22. Familial intermittent ataxia with possible X-linked recessive inheritance. Two patients with abnormal pyruvate metabolism and a response to acetazolamide.
    Livingstone IR, Gardner-Medwin D, Pennington RJ.
    J Neurol Sci; 1984 Apr; 64(1):89-97. PubMed ID: 6539810
    [Abstract] [Full Text] [Related]

  • 23. [Current knowledge on mitochondrial myopathies and encephalomyopathies].
    György I.
    Orv Hetil; 1987 Sep 13; 128(37):1923-7. PubMed ID: 3313180
    [No Abstract] [Full Text] [Related]

  • 24. Mitochondrial enzyme deficiency in cerebrotendinous xanthomatosis.
    Dotti MT, Manneschi L, Federico A.
    J Neurol Sci; 1995 Apr 13; 129(2):106-8. PubMed ID: 7608723
    [Abstract] [Full Text] [Related]

  • 25. Cytochrome c oxidase deficiency and long-chain acyl coenzyme A dehydrogenase deficiency with Leigh's subacute necrotizing encephalomyelopathy.
    Reichmann H, Scheel H, Bier B, Ketelsen UP, Zabransky S.
    Ann Neurol; 1992 Jan 13; 31(1):107-9. PubMed ID: 1311909
    [Abstract] [Full Text] [Related]

  • 26. Energy metabolism of spermatozoa. VII. Interactions between lactate, pyruvate and malate as oxidative substrates for rabbit sperm mitochondria.
    Storey BT, Kayne FJ.
    Biol Reprod; 1978 May 13; 18(4):527-36. PubMed ID: 207366
    [No Abstract] [Full Text] [Related]

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  • 28. [Leigh's encephalomyelopathy and its related diseases].
    Narisawa K.
    No To Shinkei; 1985 Nov 13; 37(11):1108-9. PubMed ID: 3935145
    [No Abstract] [Full Text] [Related]

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  • 31. Progressive external ophthalmoplegia. Evidence for a generalised mitochondrial disease with a defect in pyruvate metabolism.
    Reske-Nielsen E, Lou HC, Lowes M.
    Acta Ophthalmol (Copenh); 1976 Oct 13; 54(5):553-73. PubMed ID: 185877
    [Abstract] [Full Text] [Related]

  • 32. Molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome.
    Adams PL, Lightowlers RN, Turnbull DM.
    Ann Neurol; 1997 Feb 13; 41(2):268-70. PubMed ID: 9029077
    [Abstract] [Full Text] [Related]

  • 33. [Leigh's syndrome and mitochondrial myopathy].
    Nakase H.
    Nihon Rinsho; 1993 Sep 13; 51(9):2403-8. PubMed ID: 8411720
    [Abstract] [Full Text] [Related]

  • 34. Progressive cytochrome c oxidase deficiency in a case of Leigh's encephalomyelopathy.
    Koga Y, Nonaka I, Nakao M, Yoshino M, Tanaka M, Ozawa T, Nakase H, DiMauro S.
    J Neurol Sci; 1990 Jan 13; 95(1):63-76. PubMed ID: 2159985
    [Abstract] [Full Text] [Related]

  • 35. Confirmation that a T-to-C mutation at 9176 in mitochondrial DNA is an additional candidate mutation for Leigh's syndrome.
    Makino M, Horai S, Goto Y, Nonaka I.
    Neuromuscul Disord; 1998 May 13; 8(3-4):149-51. PubMed ID: 9631394
    [Abstract] [Full Text] [Related]

  • 36. Subacute necrotizing encephalomyelopathy (Leigh's disease): report of a case.
    Tsai ML, Hung KL, Chen TY.
    J Formos Med Assoc; 1990 Sep 13; 89(9):799-802. PubMed ID: 1982541
    [Abstract] [Full Text] [Related]

  • 37. Hypokinesia and rigidity as clinical manifestations of mitochondrial encephalomyopathy: report of three cases.
    van Erven PM, Renier WO, Gabreëls FJ, Thijssen HO, Ruitenbeek W, Horstink MW.
    Dev Med Child Neurol; 1989 Feb 13; 31(1):81-91. PubMed ID: 2537772
    [Abstract] [Full Text] [Related]

  • 38. Positron emission tomography using pyruvate-1-11C in two cases of mitochondrial encephalomyopathy.
    Toyoda M, Sakuragawa N, Arai Y, Yoshikawa H, Sugai K, Arima M, Hara T, Iio M, Satoyoshi E.
    Ann Nucl Med; 1989 Jul 13; 3(2):103-9. PubMed ID: 2641450
    [Abstract] [Full Text] [Related]

  • 39. High mitochondrial DNA T8993G mutation (<90%) without typical features of Leigh's and NARP syndromes.
    Tsao CY, Mendell JR, Bartholomew D.
    J Child Neurol; 2001 Jul 13; 16(7):533-5. PubMed ID: 11453454
    [Abstract] [Full Text] [Related]

  • 40. [Diagnostic criteria in classical infantile subacute necrotizing encephalomyelopathy (Leigh's disease)].
    Sperl W, Rumpl E, Rittinger F, Pillwein K, Wick H, Henn R, Plöchl E.
    Klin Padiatr; 1989 Jul 13; 201(2):86-92. PubMed ID: 2716238
    [Abstract] [Full Text] [Related]

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