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Journal Abstract Search

236 related items for PubMed ID: 9404143

  • 1. [A case of incomplete Kearns-Sayre syndrome with a stroke like episode].
    Furuya H, Sugimura T, Yamada T, Hayashi K, Kobayashi T.
    Rinsho Shinkeigaku; 1997 Aug; 37(8):680-4. PubMed ID: 9404143
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  • 2. Deletion of mitochondrial DNA in patients with combined features of Kearns-Sayre and MELAS syndromes.
    Zupanc ML, Moraes CT, Shanske S, Langman CB, Ciafaloni E, DiMauro S.
    Ann Neurol; 1991 Jun; 29(6):680-3. PubMed ID: 1892371
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  • 4. [A case of MELAS showing CSF pleocytosis associated with stroke-like episodes].
    Maruyama S, Yamada T, Ishimoto Y, Hara H, Taniwaki T, Kira J.
    Rinsho Shinkeigaku; 1998 Jul; 38(7):641-4. PubMed ID: 9868308
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  • 5. [Mitochondrial DNA deletions in Kearns-Sayre syndrome].
    Carod-Artal FJ, Lopez Gallardo E, Solano A, Dahmani Y, Herrero MD, Montoya J.
    Neurologia; 2006 Sep; 21(7):357-64. PubMed ID: 16977556
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  • 8. [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; 35(2):190-4. PubMed ID: 7781238
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  • 9. [Forty-six-year-old woman with progressive external ophthalmoplegia and limb weakness].
    Yamamoto T, Gotoh K, Sato T, Shiotsu H, Kuwabara N, Nagaoka M, Mizuno Y.
    No To Shinkei; 1993 Jan; 45(1):85-92. PubMed ID: 8476658
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  • 10. Patient with Kearns-Sayre syndrome exhibiting abnormal magnetic resonance image of the brain.
    Kamata Y, Mashima Y, Yokoyama M, Tanaka K, Goto Y, Oguchi Y.
    J Neuroophthalmol; 1998 Dec; 18(4):284-8. PubMed ID: 9858014
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  • 11. Auditory symptoms: a critical clue for diagnosis of MELAS.
    Tawankanjanachot I, Channarong NS, Phanthumchinda K.
    J Med Assoc Thai; 2005 Nov; 88(11):1715-20. PubMed ID: 16471125
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  • 12. Kearns-Sayre syndrome. A case report.
    Altunbaşak S, Bingöl G, Ozbarlas N, Akçören Z, Hergüner O.
    Turk J Pediatr; 1998 Nov; 40(2):255-9. PubMed ID: 9677732
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  • 13. [Cardiac involvement in mitochondrial disease: a clinical study of 38 patients].
    Anan R.
    Igaku Kenkyu; 1991 Sep; 61(2):49-61. PubMed ID: 1823506
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  • 14. Mitochondrial cytochrome b gene deletion in Kearns-Sayre syndrome associated with a subclinical type of peripheral neuropathy.
    Zanssen S, Molnar M, Buse G, Schröder JM.
    Clin Neuropathol; 1998 Sep; 17(6):291-6. PubMed ID: 9832255
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  • 16. A novel 7301-bp deletion in mitochondrial DNA in a patient with Kearns-Sayre syndrome, diabetes mellitus, and primary amenorrhoea.
    De Block CE, De Leeuw IH, Maassen JA, Ballaux D, Martin JJ.
    Exp Clin Endocrinol Diabetes; 2004 Feb; 112(2):80-3. PubMed ID: 15031771
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  • 17. [31P-NMR spectroscopy of mitochondrial myopathies: the relation between abnormal energy metabolism and muscle biopsy findings].
    Kawai M, Itoh M, Okazawa H, Kamakura K.
    Rinsho Shinkeigaku; 1989 Feb; 29(2):167-71. PubMed ID: 2546706
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  • 18. [MELAS associated with diabetes mellitus and point mutation in mitochondrial DNA].
    Onishi H, Inoue K, Osaka H, Nagatomo H, Ando N, Yamada Y, Suzuki K, Hanihara T, Kawamoto S, Okuda K.
    No To Shinkei; 1992 Mar; 44(3):259-64. PubMed ID: 1591103
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  • 19. [Mitochondrial DNA mutations in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome].
    Wang ZX, Yuan Y, Gao F, Qi Y, Shen DG, Chen QT.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):273-8. PubMed ID: 12903032
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  • 20. The neurological evolution of Pearson syndrome: case report and literature review.
    Lee HF, Lee HJ, Chi CS, Tsai CR, Chang TK, Wang CJ.
    Eur J Paediatr Neurol; 2007 Jul; 11(4):208-14. PubMed ID: 17434771
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