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Journal Abstract Search

251 related items for PubMed ID: 1611773

  • 1. [Vascular pathology in chronic progressive external ophthalmoplegia with ragged-red fibers].
    Hasegawa H, Matsuoka T, Goto Y, Nonaka I.
    Rinsho Shinkeigaku; 1992 Feb; 32(2):155-60. PubMed ID: 1611773
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  • 2. [Strongly succinate dehydrogenase-reactive blood vessels (SSV) in various neuromuscular diseases].
    Matsuoka T, Hasegawa H, Nonaka I.
    Rinsho Shinkeigaku; 1992 Jun; 32(6):645-7. PubMed ID: 1424348
    [Abstract] [Full Text] [Related]

  • 3. [Expressions of PDCD5 and other apoptosis-related proteins in muscle of patients with mitochondrial cytopathy].
    Li YF, Wang ZX, Gao XG, Hong DJ, Yuan Y.
    Zhonghua Yi Xue Za Zhi; 2009 Jun 16; 89(23):1593-6. PubMed ID: 19957502
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  • 4. Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M, Mita S, Sakuta R, Nonaka I, Araki S.
    Ann Neurol; 1993 Mar 16; 33(3):275-80. PubMed ID: 7684581
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  • 11. Extraocular muscle biopsy in chronic progressive external ophthalmoplegia.
    Ringel SP, Wilson WB, Barden MT.
    Ann Neurol; 1979 Oct 16; 6(4):326-39. PubMed ID: 554523
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  • 12. Dysfunction of the hypothalamic-pituitary system in mitochondrial encephalomyopathies.
    Ohkoshi N, Ishii A, Shiraiwa N, Shoji S, Yoshizawa K.
    J Med; 1998 Oct 16; 29(1-2):13-29. PubMed ID: 9704289
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  • 13. [Quantitative skeletal muscle pathology of aging regarding ragged-red fibers and cytochrome c oxidase-negative fibers].
    Suoh H, Sahashi K, Ibi T, Tashiro M, Mitsuma T.
    Rinsho Shinkeigaku; 1992 Apr 16; 32(4):381-4. PubMed ID: 1327605
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  • 14. Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
    Hasegawa H, Matsuoka T, Goto Y, Nonaka I.
    Ann Neurol; 1991 Jun 16; 29(6):601-5. PubMed ID: 1892363
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  • 15. [A case of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes) with progressive cytochrome c oxidase deficiency].
    Sumi K, Nagaura T, Itagaki Y, Inui K, Abe J.
    Rinsho Shinkeigaku; 1989 Jul 16; 29(7):901-8. PubMed ID: 2553313
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  • 16. [Chronic progressive external ophthalmoplegia (CPEO) with deleted mitochondrial DNA].
    Tanno Y, Yoneda M, Ohnishi Y, Miyatake T, Ozawa T.
    Rinsho Shinkeigaku; 1989 Sep 16; 29(9):1176-9. PubMed ID: 2598547
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  • 17. Contribution of muscle biopsy and genetics to the diagnosis of chronic progressive external opthalmoplegia of mitochondrial origin.
    Sundaram C, Meena AK, Uppin MS, Govindaraj P, Vanniarajan A, Thangaraj K, Kaul S, Kekunnaya R, Murthy JM.
    J Clin Neurosci; 2011 Apr 16; 18(4):535-8. PubMed ID: 21277779
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  • 18. Neuropathy and mitochondrial myopathy.
    Peyronnard JM, Charron L, Bellavance A, Marchand L.
    Ann Neurol; 1980 Mar 16; 7(3):262-8. PubMed ID: 6252825
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  • 19. Chronic progressive external ophthalmoplegia. Clinical, electrophysiological, histochemical and ultrastructural studies of 14 cases.
    Piccolo G, Cosi V, Poloni M, Moglia A, Marchetti C, Scelsi R.
    Schweiz Arch Neurol Neurochir Psychiatr; 1982 Mar 16; 131(2):161-74. PubMed ID: 6298931
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  • 20. [A case of Kearns-Sayre syndrome whose asymptomatic mother had abnormal mitochondria in skeletal muscle].
    Akaike M, Kawai H, Kashiwagi S, Kunishige M, Saito S.
    Rinsho Shinkeigaku; 1995 Feb 16; 35(2):190-4. PubMed ID: 7781238
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