These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


370 related items for PubMed ID: 25342614

  • 1. Pathogenic mitochondrial DNA mutations and associated clinical features in Korean patients with Leber's hereditary optic neuropathy.
    Yum HR, Chae H, Shin SY, Kim Y, Kim M, Park SH.
    Invest Ophthalmol Vis Sci; 2014 Oct 23; 55(12):8095-101. PubMed ID: 25342614
    [Abstract] [Full Text] [Related]

  • 2. Genotypic and phenotypic characteristics of Korean children with childhood-onset Leber's hereditary optic neuropathy.
    Ahn YJ, Park Y, Shin SY, Chae H, Kim M, Park SH.
    Graefes Arch Clin Exp Ophthalmol; 2020 Oct 23; 258(10):2283-2290. PubMed ID: 32506279
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Leber's Hereditary Optic Neuropathy is Associated with Compound Primary Mutations of Mitochondrial ND1 m.3635G > A and ND6 m.14502 T > C.
    Jin X, Wang L, Gong Y, Chen B, Wang Y, Chen T, Wei S.
    Ophthalmic Genet; 2015 Oct 23; 36(4):291-8. PubMed ID: 24417559
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. [A study of clinical and genetic characteristics of a Leber hereditary optic neuropathy family with the heteroplasmic m.14484T>C mutation].
    Sun Y, Lei K, Xu ZL, Geng Y.
    Zhonghua Yan Ke Za Zhi; 2018 Jul 11; 54(7):526-534. PubMed ID: 29996615
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Mitochondrial DNA mutations in Korean patients with Leber's hereditary optic neuropathy.
    Yang HK, Seong MW, Hwang JM.
    Sci Rep; 2024 Mar 08; 14(1):5702. PubMed ID: 38459091
    [Abstract] [Full Text] [Related]

  • 9. [Leber's hereditary optic neuropathy clinical features in patients with mitochondrial DNA m.13513G>A candidate mutation].
    Andreeva NA, Murakhovskaya YK, Tsygankova PG, Krilova TD, Sheremet NL.
    Vestn Oftalmol; 2022 Mar 08; 138(5. Vyp. 2):208-214. PubMed ID: 36287157
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy.
    Ji Y, Zhang J, Yu J, Wang Y, Lu Y, Liang M, Li Q, Jin X, Wei Y, Meng F, Gao Y, Cang X, Tong Y, Liu X, Zhang M, Jiang P, Zhu T, Mo JQ, Huang T, Jiang P, Guan MX.
    Hum Mol Genet; 2019 May 01; 28(9):1515-1529. PubMed ID: 30597069
    [Abstract] [Full Text] [Related]

  • 17. Leber's hereditary optic neuropathy with the 3434, 9011 mitochondrial DNA point mutation.
    Shidara K, Wakakura M.
    Jpn J Ophthalmol; 2012 Mar 01; 56(2):175-80. PubMed ID: 22183138
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Mitochondrial DNA Variation of Leber's Hereditary Optic Neuropathy in Western Siberia.
    Starikovskaya E, Shalaurova S, Dryomov S, Nazhmidenova A, Volodko N, Bychkov I, Mazunin I, Sukernik R.
    Cells; 2019 Dec 04; 8(12):. PubMed ID: 31817256
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 19.