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Journal Abstract Search

136 related items for PubMed ID: 28711503

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  • 23. [A clinical case of Li syndrome caused by a mitochondrial DNA mutation].
    Zhadanov SI, Grechanina EIa, Grechanina IuB, Gusar VA, Fedoseeva NP, Shurr TG.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2008; 108(5):80-3. PubMed ID: 18666358
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  • 24. Leigh disease with mitochondrial DNA A8344G mutation: case report and brief review.
    Tsao CY, Herman G, Boué DR, Prior TW, Lo WD, Atkin JF, Rusin J.
    J Child Neurol; 2003 Jan; 18(1):62-4. PubMed ID: 12661941
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  • 26. Biochemical and genetic analysis of Leigh syndrome patients in Korea.
    Chae JH, Lee JS, Kim KJ, Hwang YS, Hirano M.
    Brain Dev; 2008 Jun; 30(6):387-90. PubMed ID: 18155376
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  • 30. [A case of Leigh syndrome associated with respiratory chain complex I deficiency due to mitochondrial gene 13513G>A mutation].
    Wei XQ, Kong QP, Zhang Y, Yang YL, Chang XZ, Qi Y, Qi ZY, Xiao JX, Qin J, Wu XR.
    Zhongguo Dang Dai Er Ke Za Zhi; 2009 May; 11(5):333-6. PubMed ID: 19470250
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  • 32. [MELAS-Leigh superposition syndrome: a case report].
    Yang S, Sun C, Zhu WH.
    Zhonghua Nei Ke Za Zhi; 2020 Feb 01; 59(2):140-143. PubMed ID: 32074688
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  • 34. De novo mtDNA nt 8993 (T-->G) mutation resulting in Leigh syndrome.
    Takahashi S, Makita Y, Oki J, Miyamoto A, Yanagawa J, Naito E, Goto Y, Okuno A.
    Am J Hum Genet; 1998 Mar 01; 62(3):717-9. PubMed ID: 9556461
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  • 35. The mitochondrial DNA A8344G mutation in Leigh syndrome revealed by analysis in paraffin-embedded sections: revisiting the past.
    Santorelli FM, Tanji K, Shanske S, Krishna S, Schmidt RE, Greenwood RS, DiMauro S, De Vivo DC.
    Ann Neurol; 1998 Dec 01; 44(6):962-4. PubMed ID: 9851442
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  • 36. Mitochondrial disorders.
    DiMauro S, Andreu AL, De Vivo DC.
    J Child Neurol; 2002 Dec 01; 17 Suppl 3():3S35-45; discussion 3S46-7. PubMed ID: 12597054
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  • 40. LEIGH SYNDROME: A CASE REPORT WITH A MITOCHONDRIAL DNA MUTATION.
    Lopes T, Coelho M, Bordalo D, Bandeira A, Bandeira A, Vilarinho L, Fonseca P, Carvalho S, Martins C, Oliveira JG.
    Rev Paul Pediatr; 2018 Dec 01; 36(4):519-523. PubMed ID: 30379275
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