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289 related items for PubMed ID: 10202290

  • 1. Leber's hereditary optic neuropathy mitochondrial DNA mutations at nucleotides 11778 and 3460 in multiple sclerosis.
    Mojon DS, Herbert J, Sadiq SA, Miller JR, Madonna M, Hirano M.
    Ophthalmologica; 1999; 213(3):171-5. PubMed ID: 10202290
    [Abstract] [Full Text] [Related]

  • 2. Leber's hereditary optic neuropathy mitochondrial DNA mutations in familial multiple sclerosis.
    Mojon DS, Fujihara K, Hirano M, Miller C, Lincoff NS, Jacobs LD, Greenberg SJ.
    Graefes Arch Clin Exp Ophthalmol; 1999 Apr; 237(4):348-50. PubMed ID: 10208269
    [Abstract] [Full Text] [Related]

  • 3. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
    Pénisson-Besnier I, Moreau C, Jacques C, Roger JC, Dubas F, Reynier P.
    Rev Neurol (Paris); 2001 May; 157(5):537-41. PubMed ID: 11438773
    [Abstract] [Full Text] [Related]

  • 4. Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis.
    Vanopdenbosch L, Dubois B, D'Hooghe MB, Meire F, Carton H.
    J Neurol; 2000 Jul; 247(7):535-43. PubMed ID: 10993496
    [Abstract] [Full Text] [Related]

  • 5. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis.
    Kellar-Wood H, Robertson N, Govan GG, Compston DA, Harding AE.
    Ann Neurol; 1994 Jul; 36(1):109-12. PubMed ID: 8024249
    [Abstract] [Full Text] [Related]

  • 6. Leber's hereditary optic neuropathy mutations in Korean patients with multiple sclerosis.
    Hwang JM, Chang BL, Park SS.
    Ophthalmologica; 2001 Jul; 215(6):398-400. PubMed ID: 11741103
    [Abstract] [Full Text] [Related]

  • 7. Leber's hereditary optic neuropathy (LHON)-related mitochondrial DNA sequence changes in italian patients presenting with sporadic bilateral optic neuritis.
    Sartore M, Grasso M, Piccolo G, Fasani R, Bergamaschi R, Malaspina A, Ceroni M, Kobayashi M, Semeraro A, Arbustini E.
    Biochem Mol Med; 1995 Oct; 56(1):45-51. PubMed ID: 8593537
    [Abstract] [Full Text] [Related]

  • 8. Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran.
    Houshmand M, Sanati MH, Rashedi I, Sharifpanah F, Asghari E, Lotfi J.
    Eur Neurol; 2004 Oct; 51(2):68-71. PubMed ID: 14671420
    [Abstract] [Full Text] [Related]

  • 9. Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population.
    Dogulu CF, Kansu T, Seyrantepe V, Ozguc M, Topaloglu H, Johns DR.
    Eye (Lond); 2001 Apr; 15(Pt 2):183-8. PubMed ID: 11339587
    [Abstract] [Full Text] [Related]

  • 10. No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON.
    Gerbitz KD, Paprotta A, Obermaier-Kusser B, Rietschel M, Zerres K.
    FEBS Lett; 1992 Dec 21; 314(3):251-5. PubMed ID: 1361456
    [Abstract] [Full Text] [Related]

  • 11. Screening for Leber's hereditary optic neuropathy associated mitochondrial DNA mutations in patients with prominent optic neuritis.
    Kalman B, Rodriguez-Valdez JL, Bosch U, Lublin FD.
    Mult Scler; 1997 Jan 21; 2(6):279-82. PubMed ID: 9065918
    [Abstract] [Full Text] [Related]

  • 12. Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genes.
    Wilichowski E, Ohlenbusch A, Hanefeld F.
    Neuropediatrics; 1998 Dec 21; 29(6):307-12. PubMed ID: 10029350
    [Abstract] [Full Text] [Related]

  • 13. No evidence of association between optic neuritis and secondary LHON mtDNA mutations in patients with multiple sclerosis.
    Andalib S, Talebi M, Sakhinia E, Farhoudi M, Sadeghi-Bazargani H, Masoudian N, Vafaee MS, Gjedde A.
    Mitochondrion; 2017 Sep 21; 36():182-185. PubMed ID: 28802665
    [Abstract] [Full Text] [Related]

  • 14. Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy.
    Jacobi FK, Leo-Kottler B, Mittelviefhaus K, Zrenner E, Meyer J, Pusch CM, Wissinger B.
    Invest Ophthalmol Vis Sci; 2001 May 21; 42(6):1208-14. PubMed ID: 11328729
    [Abstract] [Full Text] [Related]

  • 15. Leber's hereditary optic neuropathy mitochondrial DNA mutations in normal-tension glaucoma.
    Opial D, Boehnke M, Tadesse S, Lietz-Partzsch A, Flammer J, Munier F, Mermoud A, Hirano M, Flückiger F, Mojon DS.
    Graefes Arch Clin Exp Ophthalmol; 2001 Jul 21; 239(6):437-40. PubMed ID: 11561792
    [Abstract] [Full Text] [Related]

  • 16. Nonfamilial and unusual cases of Leber's hereditary optic neuropathy identified by mitochondrial DNA analysis.
    Isashiki Y, Ohba N, Uto M, Nakagawa M, Nakano T, Kitahara K, Hotta A, Okamura R, Ozaki M, Futami Y.
    Jpn J Ophthalmol; 1992 Jul 21; 36(2):197-204. PubMed ID: 1513067
    [Abstract] [Full Text] [Related]

  • 17. Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.
    Leo-Kottler B, Christ-Adler M, Baumann B, Zrenner E, Wissinger B.
    Ger J Ophthalmol; 1996 Jul 21; 5(4):233-40. PubMed ID: 8854108
    [Abstract] [Full Text] [Related]

  • 18. [Analysis on the effect of secondary mutations on Leber's hereditary optic neuropathy].
    Wang Y, Tong Y, Hu SX, Wang JY, Shao JB, Zhang HX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug 21; 24(4):397-400. PubMed ID: 17680528
    [Abstract] [Full Text] [Related]

  • 19. The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.
    Chinnery PF, Brown DT, Andrews RM, Singh-Kler R, Riordan-Eva P, Lindley J, Applegarth DA, Turnbull DM, Howell N.
    Brain; 2001 Jan 21; 124(Pt 1):209-18. PubMed ID: 11133798
    [Abstract] [Full Text] [Related]

  • 20. Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathy.
    Matsumoto M, Hayasaka S, Kadoi C, Hotta Y, Fujiki K, Fujimaki T, Takeda M, Ishida N, Endo S, Kanai A.
    Ophthalmic Genet; 1999 Sep 21; 20(3):153-60. PubMed ID: 10520236
    [Abstract] [Full Text] [Related]

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