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Journal Abstract Search

295 related items for PubMed ID: 8797169

  • 1. 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
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  • 2. Peripapillary fluorescein leakage in 11778 Leber's optic neuropathy.
    Yen MY, Wei YH, Liu JH.
    J Neuroophthalmol; 1996 Sep; 16(3):178-81. PubMed ID: 8865009
    [Abstract] [Full Text] [Related]

  • 3. Leber's hereditary optic neuropathy.
    Letchavanakul A, Dechphongsaphilas W, Dhamcharee V.
    J Med Assoc Thai; 1999 Oct; 82(10):1051-5. PubMed ID: 10561972
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  • 4. 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 Oct; 39(1):96-108. PubMed ID: 7643491
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  • 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
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  • 6. Difficulty differentiating Leber's from dominant optic neuropathy in a patient with remote visual loss.
    Jacobson DM, Stone EM.
    J Clin Neuroophthalmol; 1991 Sep; 11(3):152-7. PubMed ID: 1836796
    [Abstract] [Full Text] [Related]

  • 7. 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
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  • 10. A family with Leber's hereditary optic neuropathy with mitochondrial DNA heteroplasmy related to disease expression.
    Tanaka A, Kiyosawa M, Mashima Y, Tokoro T.
    J Neuroophthalmol; 1998 Jun; 18(2):81-3. PubMed ID: 9621260
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  • 11. [Correlation between clinical and molecular genetic findings in Leber's optic atrophy].
    Leo-Kottler B, Christ-Adler M, Reck B, Wissinger B, Zrenner E.
    Ophthalmologe; 1995 Feb; 92(1):86-92. PubMed ID: 7719084
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  • 13. [Leber's hereditary optic neuropathy].
    Konrádová V, Zeman J, Stratilová L, Hermanská J, Vseticka I, Misovicová N, Kurca E, Gerinec A, Houstĕk J.
    Cas Lek Cesk; 1999 Oct 20; 138(18):565-8. PubMed ID: 10596473
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  • 14. 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 20; 82(1):59-64. PubMed ID: 10087740
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  • 15. Clinical correlation of mitochondrial DNA heteroplasmy and Leber's hereditary optic neuropathy.
    Isashiki Y, Nakagawa M.
    Jpn J Ophthalmol; 1991 Jan 20; 35(3):259-67. PubMed ID: 1770665
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  • 16. [Leber's hereditary optic atrophy. A hereditary disease caused by mitochondrial DNA mutation].
    Nørby S, Rosenberg T.
    Ugeskr Laeger; 1990 Oct 22; 152(43):3149-52. PubMed ID: 2238193
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  • 19. [A pedigree of Leber's hereditary optic neuropathy with mtDNA 14484 mutation].
    Tong Y, Wang Y, Jiang F, Liu B, Zhang S, Yang W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct 22; 25(5):531-3. PubMed ID: 18841565
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  • 20. [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; 2008 Oct 22; 29(5):408-15. PubMed ID: 10584242
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