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Journal Abstract Search

139 related items for PubMed ID: 8051882

  • 1. [Atypical presentation of Leber's optic neuropathy].
    Borruat FX, Sanders MD.
    Klin Monbl Augenheilkd; 1994 May; 204(5):400-2. PubMed ID: 8051882
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Optic nerve sheath distention in Leber's optic neuropathy and the significance of the "Wallace mutation".
    Smith JL, Tse DT, Byrne SF, Johns DR, Stone EM.
    J Clin Neuroophthalmol; 1990 Dec; 10(4):231-8. PubMed ID: 2150839
    [Abstract] [Full Text] [Related]

  • 4. [Optic neuropathy caused by alcoholism and smoking: a diagnostic pitfall of Leber's optic neuropathy].
    Borruat FX, Hirt L, Regli F.
    Rev Neurol (Paris); 1994 Nov; 150(11):799-801. PubMed ID: 7597375
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. [Hyperintense optic nerve lesion on T2-weighted MRI imaging in the acute stage of Leber's hereditary optic neuropathy: a case report].
    Honda H, Tsujihata M, Ochi M, Satoh A, Tomita I, Fujikawa A.
    Rinsho Shinkeigaku; 2006 Apr; 46(4):294-6. PubMed ID: 16768101
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. 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]

  • 9. 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]

  • 10. 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]

  • 11. 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 Oct; 36(2):197-204. PubMed ID: 1513067
    [Abstract] [Full Text] [Related]

  • 12. White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation.
    Lev D, Yanoov-Sharav M, Watemberg N, Leshinsky-Silver E, Lerman-Sagie T.
    Eur J Paediatr Neurol; 2002 Oct; 6(2):121-3. PubMed ID: 11995959
    [Abstract] [Full Text] [Related]

  • 13. [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
    [Abstract] [Full Text] [Related]

  • 14. [Leber's optic neuropathy: a case report].
    Pato-Pato A, Cimas-Hernando I, Lorenzo-González JR.
    Rev Neurol; 1995 Feb; 42(1):22-4. PubMed ID: 16402322
    [Abstract] [Full Text] [Related]

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  • 17. [Leber's optic neuropathy: new diagnostic prospects].
    Pagot V, Malecaze F, Rötig A, Simorre V, Maillard P, Mathis A, Munnich A.
    J Fr Ophtalmol; 1992 Feb; 15(1):19-23. PubMed ID: 1602101
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  • 19. 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]

  • 20. 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]

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