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Journal Abstract Search

700 related items for PubMed ID: 11995959

  • 21. Spectrum of the mitochondrial DNA mutations of Leber's hereditary optic neuropathy in Koreans.
    Kim JY, Hwang JM, Chang BL, Park SS.
    J Neurol; 2003 Mar; 250(3):278-81. PubMed ID: 12638016
    [Abstract] [Full Text] [Related]

  • 22. [Diagnostic and differential diagnostic potential of mitochondrial DNA assessment in patients with Leber's hereditary optic neuropathy].
    Feng X, Pu W, Gao D.
    Zhonghua Yan Ke Za Zhi; 2001 May; 37(3):174-7. PubMed ID: 11864415
    [Abstract] [Full Text] [Related]

  • 23. Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man.
    La Russa A, Cittadella R, Andreoli V, Valentino P, Trecroci F, Caracciolo M, Gallo O, Gambardella A, Quattrone A.
    Mult Scler; 2011 Jun; 17(6):763-6. PubMed ID: 21685233
    [Abstract] [Full Text] [Related]

  • 24. Neuropathology of white matter disease in Leber's hereditary optic neuropathy.
    Kovács GG, Höftberger R, Majtényi K, Horváth R, Barsi P, Komoly S, Lassmann H, Budka H, Jakab G.
    Brain; 2005 Jan; 128(Pt 1):35-41. PubMed ID: 15483043
    [Abstract] [Full Text] [Related]

  • 25. 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]

  • 26. The genetics of leber hereditary optic neuropathy--prototype of an inherited optic neuropathy with mitochondrial dysfunction.
    Eichhorn-Mulligan K, Cestari DM.
    Semin Ophthalmol; 2008 Jan; 23(1):27-37. PubMed ID: 18214789
    [Abstract] [Full Text] [Related]

  • 27. Rapid quantification of the heteroplasmy of mutant mitochondrial DNAs in Leber's hereditary optic neuropathy using the Invader technology.
    Mashima Y, Nagano M, Funayama T, Zhang Q, Egashira T, Kudho J, Shimizu N, Oguchi Y.
    Clin Biochem; 2004 Apr; 37(4):268-76. PubMed ID: 15003728
    [Abstract] [Full Text] [Related]

  • 28. Leber's hereditary optic neuroretinopathy (LHON) associated with mitochondrial DNA point mutation G11778A in two Croatian families.
    Martin-Kleiner I, Gabrilovac J, Bradvica M, Vidović T, Cerovski B, Fumić K, Boranić M.
    Coll Antropol; 2006 Mar; 30(1):171-4. PubMed ID: 16617593
    [Abstract] [Full Text] [Related]

  • 29. [Clinical examination of Leber hereditary optic neuropathy in patients with the same gene mutation].
    Chelstowska J, Mroczek K, Niebudek D, Małecka-Idzikowska A, Bartnik E, Hanna Nizankowska M, Sasiadek M.
    Przegl Lek; 2002 Mar; 59(10):777-9. PubMed ID: 12632910
    [Abstract] [Full Text] [Related]

  • 30. Latent, acute, and chronic Leber's hereditary optic neuropathy.
    Kerrison JB.
    Ophthalmology; 2005 Jan; 112(1):1-2. PubMed ID: 15629812
    [No Abstract] [Full Text] [Related]

  • 31. [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
    [Abstract] [Full Text] [Related]

  • 32. 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 22; 24(1):107-11. PubMed ID: 19247386
    [Abstract] [Full Text] [Related]

  • 33. Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation.
    Shoffner JM, Brown MD, Stugard C, Jun AS, Pollock S, Haas RH, Kaufman A, Koontz D, Kim Y, Graham JR.
    Ann Neurol; 1995 Aug 22; 38(2):163-9. PubMed ID: 7654063
    [Abstract] [Full Text] [Related]

  • 34. Leber's hereditary optic neuropathy is associated with the mitochondrial ND6 T14484C mutation in three Chinese families.
    Sun YH, Wei QP, Zhou X, Qian Y, Zhou J, Lu F, Qu J, Guan MX.
    Biochem Biophys Res Commun; 2006 Aug 18; 347(1):221-5. PubMed ID: 16806060
    [Abstract] [Full Text] [Related]

  • 35. [Leber's optic neuropathy: a mitochondrial disease revealing its secret].
    Nikoskelainen E, Savontaus ML.
    Duodecim; 1998 Aug 18; 114(3):303-6. PubMed ID: 10895506
    [No Abstract] [Full Text] [Related]

  • 36. Hereditary optic neuropathies share a common mitochondrial coupling defect.
    Chevrollier A, Guillet V, Loiseau D, Gueguen N, de Crescenzo MA, Verny C, Ferre M, Dollfus H, Odent S, Milea D, Goizet C, Amati-Bonneau P, Procaccio V, Bonneau D, Reynier P.
    Ann Neurol; 2008 Jun 18; 63(6):794-8. PubMed ID: 18496845
    [Abstract] [Full Text] [Related]

  • 37. m.3635G>A mutation as a cause of Leber hereditary optic neuropathy.
    Kodroń A, Krawczyński MR, Tońska K, Bartnik E.
    J Clin Pathol; 2014 Jul 18; 67(7):639-41. PubMed ID: 24747208
    [Abstract] [Full Text] [Related]

  • 38. Retinal nerve fiber layer evaluation by optical coherence tomography in unaffected carriers with Leber's hereditary optic neuropathy mutations.
    Savini G, Barboni P, Valentino ML, Montagna P, Cortelli P, De Negri AM, Sadun F, Bianchi S, Longanesi L, Zanini M, Carelli V.
    Ophthalmology; 2005 Jan 18; 112(1):127-31. PubMed ID: 15629832
    [Abstract] [Full Text] [Related]

  • 39. Multiple sclerosis associated with Leber's Hereditary Optic Neuropathy.
    Palace J.
    J Neurol Sci; 2009 Nov 15; 286(1-2):24-7. PubMed ID: 19800080
    [Abstract] [Full Text] [Related]

  • 40. Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.
    Sudoyo H, Suryadi H, Lertrit P, Pramoonjago P, Lyrawati D, Marzuki S.
    J Hum Genet; 2002 Nov 15; 47(11):594-604. PubMed ID: 12436196
    [Abstract] [Full Text] [Related]

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