These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

632 related items for PubMed ID: 17003408

  • 1. Mitochondrial abnormalities in patients with LHON-like optic neuropathies.
    Abu-Amero KK, Bosley TM.
    Invest Ophthalmol Vis Sci; 2006 Oct; 47(10):4211-20. PubMed ID: 17003408
    [Abstract] [Full Text] [Related]

  • 2. Sporadic bilateral optic neuropathy in children: the role of mitochondrial abnormalities.
    Bosley TM, Brodsky MC, Glasier CM, Abu-Amero KK.
    Invest Ophthalmol Vis Sci; 2008 Dec; 49(12):5250-6. PubMed ID: 18676632
    [Abstract] [Full Text] [Related]

  • 3. Mitochondrial changes in leukocytes of patients with optic neuritis.
    Bosley TM, Constantinescu CS, Tench CR, Abu-Amero KK.
    Mol Vis; 2007 Aug 29; 13():1516-28. PubMed ID: 17893651
    [Abstract] [Full Text] [Related]

  • 4. Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.
    Ferré M, Bonneau D, Milea D, Chevrollier A, Verny C, Dollfus H, Ayuso C, Defoort S, Vignal C, Zanlonghi X, Charlin JF, Kaplan J, Odent S, Hamel CP, Procaccio V, Reynier P, Amati-Bonneau P.
    Hum Mutat; 2009 Jul 29; 30(7):E692-705. PubMed ID: 19319978
    [Abstract] [Full Text] [Related]

  • 5. 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 29; 63(6):794-8. PubMed ID: 18496845
    [Abstract] [Full Text] [Related]

  • 6. Clinical, genetic, and biochemical characterization of a Leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations.
    Brown MD, Allen JC, Van Stavern GP, Newman NJ, Wallace DC.
    Am J Med Genet; 2001 Dec 15; 104(4):331-8. PubMed ID: 11754070
    [Abstract] [Full Text] [Related]

  • 7. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes.
    Hofmann S, Bezold R, Jaksch M, Obermaier-Kusser B, Mertens S, Kaufhold P, Rabl W, Hecker W, Gerbitz KD.
    Genomics; 1997 Jan 01; 39(1):8-18. PubMed ID: 9027481
    [Abstract] [Full Text] [Related]

  • 8. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
    Mao YJ, Qu J, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb 01; 25(1):45-9. PubMed ID: 18247303
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Influence of mutation type on clinical expression of Leber hereditary optic neuropathy.
    Spruijt L, Kolbach DN, de Coo RF, Plomp AS, Bauer NJ, Smeets HJ, de Die-Smulders CE.
    Am J Ophthalmol; 2006 Apr 01; 141(4):676-82. PubMed ID: 16564802
    [Abstract] [Full Text] [Related]

  • 11. [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 Apr 01; 59(10):777-9. PubMed ID: 12632910
    [Abstract] [Full Text] [Related]

  • 12. Assessing mitochondrial DNA nucleotide changes in spontaneous optic neuropathies.
    Bosley TM, Abu-Amero KK.
    Ophthalmic Genet; 2010 Dec 01; 31(4):163-72. PubMed ID: 21067478
    [Abstract] [Full Text] [Related]

  • 13. Prophylaxis for second eye involvement in leber hereditary optic neuropathy: an open-labeled, nonrandomized multicenter trial of topical brimonidine purite.
    Newman NJ, Biousse V, David R, Bhatti MT, Hamilton SR, Farris BK, Lesser RL, Newman SA, Turbin RE, Chen K, Keaney RP.
    Am J Ophthalmol; 2005 Sep 01; 140(3):407-15. PubMed ID: 16083844
    [Abstract] [Full Text] [Related]

  • 14. X-Inactivation patterns in females harboring mtDNA mutations that cause Leber hereditary optic neuropathy.
    Hudson G, Carelli V, Horvath R, Zeviani M, Smeets HJ, Chinnery PF.
    Mol Vis; 2007 Dec 21; 13():2339-43. PubMed ID: 18199976
    [Abstract] [Full Text] [Related]

  • 15. 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 Dec 21; 47(11):594-604. PubMed ID: 12436196
    [Abstract] [Full Text] [Related]

  • 16. 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 21; 47(12):5303-9. PubMed ID: 17122117
    [Abstract] [Full Text] [Related]

  • 17. Mitochondrial abnormalities in patients with primary open-angle glaucoma.
    Abu-Amero KK, Morales J, Bosley TM.
    Invest Ophthalmol Vis Sci; 2006 Jun 21; 47(6):2533-41. PubMed ID: 16723467
    [Abstract] [Full Text] [Related]

  • 18. A family with 3460G>A and 11778G>A mutations and haplogroup analysis of Polish Leber hereditary optic neuropathy patients.
    Tonska K, Kurzawa M, Ambroziak AM, Korwin-Rujna M, Szaflik JP, Grabowska E, Szaflik J, Bartnik E.
    Mitochondrion; 2008 Dec 21; 8(5-6):383-8. PubMed ID: 18801464
    [Abstract] [Full Text] [Related]

  • 19. [Sudden blindness: consider Leber's hereditary optic neuropathy].
    Schieving JH, de Vries BB, Hol F, Stroink H.
    Ned Tijdschr Geneeskd; 2008 Oct 25; 152(43):2313-6. PubMed ID: 19024058
    [Abstract] [Full Text] [Related]

  • 20. [Penetrance of Leber hereditary optic neuropathy individuals with mitochondrial DNA 11778 mutation in the Shanxi area].
    Zheng ML, Zhang GL, Hua AL, Zhang YL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr 25; 21(2):166-7. PubMed ID: 15079802
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 32.