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Journal Abstract Search

157 related items for PubMed ID: 23419312

  • 21. [Leber's hereditary optic neuropathy].
    Hilo W, Jabaly-Habib H, Modi N, Briscoe D.
    Harefuah; 2013 Aug; 152(8):486-9, 498, 497. PubMed ID: 24167936
    [Abstract] [Full Text] [Related]

  • 22. Progressive Bilateral Cecocentral Scotomata.
    Abalem MF, Johnson MW, Jayasundera T.
    JAMA Ophthalmol; 2019 Jan 01; 137(1):107-108. PubMed ID: 30347014
    [No Abstract] [Full Text] [Related]

  • 23. Multifocal VEP provide electrophysiological evidence of predominant dysfunction of the optic nerve fibers derived from the central retina in Leber's hereditary optic neuropathy.
    Ziccardi L, Parisi V, Giannini D, Sadun F, De Negri AM, Barboni P, La Morgia C, Sadun AA, Carelli V.
    Graefes Arch Clin Exp Ophthalmol; 2015 Sep 01; 253(9):1591-600. PubMed ID: 25773998
    [Abstract] [Full Text] [Related]

  • 24. Comparing EPI-743 treatment in siblings with Leber's hereditary optic neuropathy mt14484 mutation.
    Chicani CF, Chu ER, Miller G, Kelman SE, Sadun AA.
    Can J Ophthalmol; 2013 Oct 01; 48(5):e130-3. PubMed ID: 24093206
    [No Abstract] [Full Text] [Related]

  • 25. A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathy.
    Klopstock T, Yu-Wai-Man P, Dimitriadis K, Rouleau J, Heck S, Bailie M, Atawan A, Chattopadhyay S, Schubert M, Garip A, Kernt M, Petraki D, Rummey C, Leinonen M, Metz G, Griffiths PG, Meier T, Chinnery PF.
    Brain; 2011 Sep 01; 134(Pt 9):2677-86. PubMed ID: 21788663
    [Abstract] [Full Text] [Related]

  • 26. Clinical and electrophysiological recovery in Leber hereditary optic neuropathy with G3460A mutation.
    Sharkawi E, Oleszczuk JD, Holder GE, Raina J.
    Doc Ophthalmol; 2012 Aug 01; 125(1):71-4. PubMed ID: 22684678
    [Abstract] [Full Text] [Related]

  • 27. Microperimetry in a case of occult macular dystrophy.
    Freund PR, Macdonald IM.
    Can J Ophthalmol; 2013 Oct 01; 48(5):e101-3. PubMed ID: 24093195
    [No Abstract] [Full Text] [Related]

  • 28. Woman with atypical unilateral Leber's hereditary optic neuropathy with visual improvement.
    Sugisaka E, Ohde H, Shinoda K, Mashima Y.
    Clin Exp Ophthalmol; 2007 Dec 01; 35(9):868-70. PubMed ID: 18173420
    [Abstract] [Full Text] [Related]

  • 29. Leber's hereditary optic neuropathy associated with multiple sclerosis: Harding's syndrome.
    Parry-Jones AR, Mitchell JD, Gunarwardena WJ, Shaunak S.
    Pract Neurol; 2008 Apr 01; 8(2):118-21. PubMed ID: 18344382
    [Abstract] [Full Text] [Related]

  • 30. Comparison of retinal nerve fibre layers between 11778 and 14484 mutations in Leber's hereditary optic neuropathy.
    Seo JH, Hwang JM, Park SS.
    Eye (Lond); 2010 Jan 01; 24(1):107-11. PubMed ID: 19247386
    [Abstract] [Full Text] [Related]

  • 31. Visual observations of an American patient with Leber hereditary optic neuropathy after purported injections of stem cells in China.
    Abukhalil F, Lam BL, Guy J.
    Arch Ophthalmol; 2012 Apr 01; 130(4):532-4. PubMed ID: 22491931
    [No Abstract] [Full Text] [Related]

  • 32. Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy.
    Valentino ML, Avoni P, Barboni P, Pallotti F, Rengo C, Torroni A, Bellan M, Baruzzi A, Carelli V.
    Ann Neurol; 2002 Jun 01; 51(6):774-8. PubMed ID: 12112086
    [Abstract] [Full Text] [Related]

  • 33. Acute Bilateral Leber Hereditary Optic Neuropathy.
    Khetan V, Zanolli M, Levin AV.
    J Pediatr Ophthalmol Strabismus; 2015 Jun 01; 52(4):256. PubMed ID: 26214724
    [No Abstract] [Full Text] [Related]

  • 34. Evaluation of fixation pattern and reading ability in patients with Leber hereditary optic neuropathy.
    Altpeter EK, Blanke BR, Leo-Kottler B, Nguyen XN, Trauzettel-Klosinski S.
    J Neuroophthalmol; 2013 Dec 01; 33(4):344-8. PubMed ID: 24256876
    [Abstract] [Full Text] [Related]

  • 35. Functional retinal locus rather than multiple PRLs?
    Markowitz SN, Reyes SV, Shima N.
    Invest Ophthalmol Vis Sci; 2011 Feb 28; 52(2):1191; author reply 1191. PubMed ID: 21357412
    [No Abstract] [Full Text] [Related]

  • 36. Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy.
    Liang M, Jiang P, Li F, Zhang J, Ji Y, He Y, Xu M, Zhu J, Meng X, Zhao F, Tong Y, Liu X, Sun Y, Zhou X, Mo JQ, Qu J, Guan MX.
    Invest Ophthalmol Vis Sci; 2014 Mar 06; 55(3):1321-31. PubMed ID: 24398099
    [Abstract] [Full Text] [Related]

  • 37. Characteristics of the preferred retinal loci of better and worse seeing eyes of patients with a central scotoma.
    Kisilevsky E, Tarita-Nistor L, González EG, Mandelcorn MS, Brent MH, Markowitz SN, Steinbach MJ.
    Can J Ophthalmol; 2016 Oct 06; 51(5):362-367. PubMed ID: 27769327
    [Abstract] [Full Text] [Related]

  • 38. Myelinated retinal nerve fibres loss in Leber's hereditary optic neuropathy.
    Gicquel JJ, Salama B, Mercié M, Bonneau D, Dighiero P.
    Acta Ophthalmol Scand; 2005 Aug 06; 83(4):517-8. PubMed ID: 16029287
    [No Abstract] [Full Text] [Related]

  • 39. 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 06; 51(5):630-4. PubMed ID: 12112111
    [Abstract] [Full Text] [Related]

  • 40. Leber's hereditary optic neuropathy precipitated by tadalafil use for erectile dysfunction.
    Cornish KS, Barras C.
    Semin Ophthalmol; 2011 Jan 06; 26(1):7-10. PubMed ID: 21275598
    [Abstract] [Full Text] [Related]

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