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125 related items for PubMed ID: 17092461

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  • 8. [Mitochondrial myopathy and mitochondrial encephalomyopathy].
    Song D, Liu C, Lu Q, Shi J, Chen J, Zhang H, Zhang Y, Wang H, Zhang W, Li G.
    Zhonghua Yi Xue Za Zhi; 2002 Feb 10; 82(3):158-60. PubMed ID: 11953149
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  • 10. Proton MR spectroscopic characterization of differences in regional brain metabolic abnormalities in mitochondrial encephalomyopathies.
    Mathews PM, Andermann F, Silver K, Karpati G, Arnold DL.
    Neurology; 1993 Dec 10; 43(12):2484-90. PubMed ID: 8255444
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  • 11. Histochemical and molecular genetic study of MELAS and MERRF in Korean patients.
    Kim DS, Jung DS, Park KH, Kim IJ, Kim CM, Lee WH, Rho SK.
    J Korean Med Sci; 2002 Feb 10; 17(1):103-12. PubMed ID: 11850598
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  • 12. G8363A mutation in the mitochondrial DNA transfer ribonucleic acidLys gene: another cause of Leigh syndrome.
    Shtilbans A, Shanske S, Goodman S, Sue CM, Bruno C, Johnson TL, Lava NS, Waheed N, DiMauro S.
    J Child Neurol; 2000 Nov 10; 15(11):759-61. PubMed ID: 11108511
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  • 13. SPECT findings in mitochondrial encephalomyopathy.
    Watanabe Y, Hashikawa K, Moriwaki H, Oku N, Seike Y, Kodaka R, Ono J, Uehara T, Kusuoka H, Nishimura T.
    J Nucl Med; 1998 Jun 10; 39(6):961-4. PubMed ID: 9627326
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  • 14. Molecular epidemiologic study of mitochondrial DNA mutations in patients with mitochondrial diseases in Taiwan.
    Pang CY, Huang CC, Yen MY, Wang EK, Kao KP, Chen SS, Wei YH.
    J Formos Med Assoc; 1999 May 10; 98(5):326-34. PubMed ID: 10420700
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  • 17. MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes.
    Nakamura M, Yabe I, Sudo A, Hosoki K, Yaguchi H, Saitoh S, Sasaki H.
    J Med Genet; 2010 Oct 10; 47(10):659-64. PubMed ID: 20610441
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  • 18. Systemic and ocular findings in 100 patients with optic nerve hypoplasia.
    Garcia ML, Ty EB, Taban M, David Rothner A, Rogers D, Traboulsi EI.
    J Child Neurol; 2006 Nov 10; 21(11):949-56. PubMed ID: 17092460
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  • 19. Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype.
    Melone MA, Tessa A, Petrini S, Lus G, Sampaolo S, di Fede G, Santorelli FM, Cotrufo R.
    Arch Neurol; 2004 Feb 10; 61(2):269-72. PubMed ID: 14967777
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  • 20. Mitochondrial myopathies with necrotizing encephalopathy of the Leigh type.
    Peiffer J, Kustermann-Kuhn B, Mortier W, Poremba M, Roggendorf W, Scholte HR, Schröder JM, Wendtland B, Wessel K, Zimmermann C.
    Pathol Res Pract; 1988 Nov 10; 183(6):706-16. PubMed ID: 3222173
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