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Journal Abstract Search

153 related items for PubMed ID: 36774923

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    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Goldstein A, Falk MJ.
    ; 1993. PubMed ID: 20301382
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  • 4. SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletions.
    Hanisch F, Kornhuber M, Alston CL, Taylor RW, Deschauer M, Zierz S.
    J Neurol Neurosurg Psychiatry; 2015 Jun; 86(6):630-4. PubMed ID: 25143630
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  • 5. The clinical, myopathological, and genetic analysis of 155 Chinese mitochondrial ophthalmoplegia patients with mitochondrial DNA single large deletions.
    Zhao Y, Hou Y, Zhao X, Liufu T, Yu M, Zhang W, Xie Z, Zhang VW, Yuan Y, Wang Z.
    Mol Genet Genomic Med; 2024 Jan; 12(1):e2328. PubMed ID: 38018320
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  • 8. Ophthalmoplegia in Mitochondrial Disease.
    Lee SJ, Na JH, Han J, Lee YM.
    Yonsei Med J; 2018 Dec; 59(10):1190-1196. PubMed ID: 30450853
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  • 10. Genotypes of chronic progressive external ophthalmoplegia in a large adult-onset cohort.
    Heighton JN, Brady LI, Sadikovic B, Bulman DE, Tarnopolsky MA.
    Mitochondrion; 2019 Nov; 49():227-231. PubMed ID: 31521625
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  • 11. [A case of mitochondrial encephalomyopathy showing ophthalmoplegia, diabetes mellitus and hearing loss associated with the A3243G mutation of mitochondrial DNA].
    Hoshino S, Tamaoka A, Ohkoshi N, Shoji S, Goto Y.
    Rinsho Shinkeigaku; 1997 Apr; 37(4):326-30. PubMed ID: 9248343
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  • 12. Extraocular muscle atrophy and central nervous system involvement in chronic progressive external ophthalmoplegia.
    Yu-Wai-Man C, Smith FE, Firbank MJ, Guthrie G, Guthrie S, Gorman GS, Taylor RW, Turnbull DM, Griffiths PG, Blamire AM, Chinnery PF, Yu-Wai-Man P.
    PLoS One; 2013 Apr; 8(9):e75048. PubMed ID: 24086434
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  • 14. Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathies.
    Jean-Francois MJ, Lertrit P, Berkovic SF, Crimmins D, Morris J, Marzuki S, Byrne E.
    Aust N Z J Med; 1994 Apr; 24(2):188-93. PubMed ID: 8042948
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  • 19. Atheromatosis of the Scalp: A Novel Feature of Chronic Progressive External Ophthalmoplegia Plus Due to a Single Mitochondrial DNA Deletion.
    Finsterer J.
    Cureus; 2021 Dec; 13(12):e20641. PubMed ID: 35103203
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  • 20. Defects of mitochondrial DNA.
    Zeviani M, Antozzi C.
    Brain Pathol; 1992 Apr; 2(2):121-32. PubMed ID: 1341953
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