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Journal Abstract Search

247 related items for PubMed ID: 1467585

  • 21. [Mitochondrial DNA mutations and three major forms of mitochondrial myopathies: CPEO, MELAS and MERRF].
    Goto Y.
    Nihon Rinsho; 1997 Dec; 55(12):3259-64. PubMed ID: 9436447
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  • 23. [Clinical and investigative approaches in mitochondrial diseases. A review of 15 cases].
    Arpa J, Campos Y, Cruz Martínez A, Gutiérrez Molina M, Arenas J, Alonso M, Plaza I, Morales C, Palomo F, Barreiro P.
    Neurologia; 1994 Oct; 9(8):324-36. PubMed ID: 7803049
    [Abstract] [Full Text] [Related]

  • 24. [Comparison of clinical pictures of mitochondrial encephalomyopathy with tRNA(Leu(UUR)) mutation in 3243 with that in 3254].
    Mitsuoka T, Kawarai T, Watanabe C, Katayama S, Nakamura S.
    No To Shinkei; 1998 Dec; 50(12):1089-92. PubMed ID: 9989353
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  • 27. Peripheral neuropathy in mitochondrial encephalomyopathies.
    Chu CC, Huang CC, Fang W, Chu NS, Pang CY, Wei YH.
    Eur Neurol; 1997 Dec; 37(2):110-5. PubMed ID: 9058067
    [Abstract] [Full Text] [Related]

  • 28. Human mitochondrial diseases: answering questions and questioning answers.
    Howell N.
    Int Rev Cytol; 1999 Dec; 186():49-116. PubMed ID: 9770297
    [Abstract] [Full Text] [Related]

  • 29. Screening of common mitochondrial mutations in Chinese patients with mitochondrial encephalomyopathies.
    Qi Y, Zhang Y, Wang Z, Yang Y, Yuan Y, Niu S, Pei P, Wang S, Ma Y, Bu D, Zou L, Fang F, Xiao J, Sun F, Zhang Y, Wu Y, Wang S, Xiong H, Wu X.
    Mitochondrion; 2007 Dec; 7(1-2):147-50. PubMed ID: 17276742
    [Abstract] [Full Text] [Related]

  • 30. 74th ENMC international workshop: mitochondrial diseases 19-20 november 1999, Naarden, the netherlands.
    Poulton J, Turnbull DM.
    Neuromuscul Disord; 2000 Aug; 10(6):460-2. PubMed ID: 10899455
    [No Abstract] [Full Text] [Related]

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  • 32. Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies.
    Liu CS, Cheng WL, Lee CF, Ma YS, Lin CY, Huang CC, Wei YH.
    Acta Neurol Scand; 2006 May; 113(5):334-41. PubMed ID: 16629770
    [Abstract] [Full Text] [Related]

  • 33. Clinical and EEG findings in eleven patients affected by mitochondrial encephalomyopathy with MERRF-MELAS overlap.
    Serra G, Piccinnu R, Tondi M, Muntoni F, Zeviani M, Mastropaolo C.
    Brain Dev; 1996 May; 18(3):185-91. PubMed ID: 8836498
    [Abstract] [Full Text] [Related]

  • 34. Mitochondrial gene mutations and human diseases: a prolegomenon.
    Howell N.
    Am J Hum Genet; 1994 Aug; 55(2):219-24. PubMed ID: 8037201
    [No Abstract] [Full Text] [Related]

  • 35. Fibrous dysplasia in a child with mitochondrial A8344G mutation.
    Chen ST, Fan PC, Hwu WL, Wu MH.
    J Child Neurol; 2008 Dec; 23(12):1447-50. PubMed ID: 18772492
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  • 36.
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  • 37. A novel point mutation in the mitochondrial tRNA(Ser(UCN)) gene detected in a family with MERRF/MELAS overlap syndrome.
    Nakamura M, Nakano S, Goto Y, Ozawa M, Nagahama Y, Fukuyama H, Akiguchi I, Kaji R, Kimura J.
    Biochem Biophys Res Commun; 1995 Sep 05; 214(1):86-93. PubMed ID: 7669057
    [Abstract] [Full Text] [Related]

  • 38. Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome.
    Campos Y, Garcia-Silva T, Barrionuevo CR, Cabello A, Muley R, Arenas J.
    Pediatr Neurol; 1995 Jul 05; 13(1):69-72. PubMed ID: 7575854
    [Abstract] [Full Text] [Related]

  • 39. Progressive external ophthalmoplegia and multiple mitochondrial DNA deletions.
    Van Goethem G, Martin JJ, Van Broeckhoven C.
    Acta Neurol Belg; 2002 Mar 05; 102(1):39-42. PubMed ID: 12094562
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