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232 related items for PubMed ID: 1532593

  • 1. Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation.
    Stone EM, Newman NJ, Miller NR, Johns DR, Lott MT, Wallace DC.
    J Clin Neuroophthalmol; 1992 Mar; 12(1):10-4. PubMed ID: 1532593
    [Abstract] [Full Text] [Related]

  • 2. Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA.
    Hotta Y, Fujiki K, Hayakawa M, Nakajima A, Kanai A, Mashima Y, Hiida Y, Shinoda K, Yamada K, Oguchi Y.
    Jpn J Ophthalmol; 1995 Mar; 39(1):96-108. PubMed ID: 7643491
    [Abstract] [Full Text] [Related]

  • 3. High incidence of visual recovery among four Japanese patients with Leber's hereditary optic neuropathy with the 14484 mutation.
    Yamada K, Mashima Y, Kigasawa K, Miyashita K, Wakakura M, Oguchi Y.
    J Neuroophthalmol; 1997 Jun; 17(2):103-7. PubMed ID: 9176781
    [Abstract] [Full Text] [Related]

  • 4. [Clinical manifestation and molecular identification of patients with Leber's hereditary optic neuropathy in a national reference center for neuro-ophthalmology in Cuba].
    Santiesteban-Freixas R, Rodríguez-Hernández M, Mendoza-Santiesteban CE, Carrero-Salgado M, Francisco-Plasencia M, Méndez-Larramendi I, Vidal-Casalís S, Rivero-Reyes R, Hirano M.
    Rev Neurol; 1997 Jun; 29(5):408-15. PubMed ID: 10584242
    [Abstract] [Full Text] [Related]

  • 5. 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; 5(4):233-40. PubMed ID: 8854108
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Leber's hereditary optic neuropathy.
    Letchavanakul A, Dechphongsaphilas W, Dhamcharee V.
    J Med Assoc Thai; 1999 Oct; 82(10):1051-5. PubMed ID: 10561972
    [Abstract] [Full Text] [Related]

  • 8. Preservation of photic blink reflex in Leber's hereditary optic neuropathy.
    Nakamura M, Sekiya Y, Yamamoto M.
    Invest Ophthalmol Vis Sci; 1996 Dec; 37(13):2736-43. PubMed ID: 8977489
    [Abstract] [Full Text] [Related]

  • 9. Clinical and genetical manifestations in 34 families with Leber's hereditary optic neuropathy (LHON).
    Meire GM, Cochaux P, Candaele C, Broux C.
    Bull Soc Belge Ophtalmol; 1994 Dec; 254():137-46. PubMed ID: 7493114
    [Abstract] [Full Text] [Related]

  • 10. Leber's hereditary optic neuropathy: clinical and molecular genetic aspects. Preliminary results in our families.
    Van Caelenberghe E, Meire F, Broux C, Vassart G, Cochaux P.
    Bull Soc Belge Ophtalmol; 1992 Dec; 243():139-46. PubMed ID: 1302143
    [Abstract] [Full Text] [Related]

  • 11. Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis.
    Kim JY, Hwang JM, Park SS.
    Ann Neurol; 2002 May; 51(5):630-4. PubMed ID: 12112111
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Late-onset Leber's hereditary optic neuropathy.
    Ajax ET, Kardon R.
    J Neuroophthalmol; 1998 Mar; 18(1):30-1. PubMed ID: 9532536
    [Abstract] [Full Text] [Related]

  • 14. Comparing pupil function with visual function in patients with Leber's hereditary optic neuropathy.
    Bremner FD, Shallo-Hoffmann J, Riordan-Eva P, Smith SE.
    Invest Ophthalmol Vis Sci; 1999 Oct; 40(11):2528-34. PubMed ID: 10509646
    [Abstract] [Full Text] [Related]

  • 15. Lack of differences among mitochondrial DNA in family members with Leber's hereditary optic neuropathy and differing visual outcomes.
    Mashima Y, Hiida Y, Oguchi Y.
    J Neuroophthalmol; 1995 Mar; 15(1):15-9. PubMed ID: 7780566
    [Abstract] [Full Text] [Related]

  • 16. Leber's hereditary optic neuropathy (LHON) with mitochondrial ND4 gene mutation (11778) in a Thai patient.
    Lertrit P, Ruangvaravate N, Trongpanich Y, Imsumran A, Mungkornkarn C, Neungton N.
    J Med Assoc Thai; 1999 Jan; 82(1):59-64. PubMed ID: 10087740
    [Abstract] [Full Text] [Related]

  • 17. Stargardt's type maculopathy in a patient with 11778 Leber's optic neuropathy.
    Yen MY, Wei YH, Liu JH.
    J Neuroophthalmol; 1996 Jun; 16(2):120-3. PubMed ID: 8797169
    [Abstract] [Full Text] [Related]

  • 18. Leber's hereditary optic neuropathy with childhood onset.
    Barboni P, Savini G, Valentino ML, La Morgia C, Bellusci C, De Negri AM, Sadun F, Carta A, Carbonelli M, Sadun AA, Carelli V.
    Invest Ophthalmol Vis Sci; 2006 Dec; 47(12):5303-9. PubMed ID: 17122117
    [Abstract] [Full Text] [Related]

  • 19. A multiple sclerosis-like illness in a man harboring the mtDNA 14484 mutation.
    Bhatti MT, Newman NJ.
    J Neuroophthalmol; 1999 Mar; 19(1):28-33. PubMed ID: 10098545
    [Abstract] [Full Text] [Related]

  • 20. [Leber's hereditary optic neuropathy with onset at the age of 54 years].
    Nakamura N, Furukawa Y, Fujiki K, Hayakawa M, Mizuno Y.
    Rinsho Shinkeigaku; 1994 Mar; 34(3):258-60. PubMed ID: 8200145
    [Abstract] [Full Text] [Related]

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