BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

289 related articles for article (PubMed ID: 17893651)

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

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [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; 30(7):E692-705. PubMed ID: 19319978
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial DNA content is decreased in autosomal dominant optic atrophy.
    Kim JY; Hwang JM; Ko HS; Seong MW; Park BJ; Park SS
    Neurology; 2005 Mar; 64(6):966-72. PubMed ID: 15781809
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genes.
    Wilichowski E; Ohlenbusch A; Hanefeld F
    Neuropediatrics; 1998 Dec; 29(6):307-12. PubMed ID: 10029350
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Characterization of the mitochondrial genome in childhood multiple sclerosis. I. Optic neuritis and LHON mutations.
    Ohlenbusch A; Wilichowski E; Hanefeld F
    Neuropediatrics; 1998 Aug; 29(4):175-9. PubMed ID: 9762692
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Optic nerve diffusion changes and atrophy jointly predict visual dysfunction after optic neuritis.
    Kolbe S; Chapman C; Nguyen T; Bajraszewski C; Johnston L; Kean M; Mitchell P; Paine M; Butzkueven H; Kilpatrick T; Egan G
    Neuroimage; 2009 Apr; 45(3):679-86. PubMed ID: 19162205
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Leber hereditary optic neuropathy and optic neuritis: similarities and differences of clinical characteristics].
    Lai CT; Wang Q; Li Z; Wang W; Zhu J; Lu Y; Zhang XJ; Yu HF
    Zhonghua Yan Ke Za Zhi; 2007 Sep; 43(9):793-7. PubMed ID: 18070523
    [TBL] [Abstract][Full Text] [Related]  

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

  • 11. Mitochondrial disorder with OPA1 mutation lacking optic atrophy.
    Milone M; Younge BR; Wang J; Zhang S; Wong LJ
    Mitochondrion; 2009 Jul; 9(4):279-81. PubMed ID: 19303950
    [TBL] [Abstract][Full Text] [Related]  

  • 12. mtDNA haplogroup J: a contributing factor of optic neuritis.
    Reynier P; Penisson-Besnier I; Moreau C; Savagner F; Vielle B; Emile J; Dubas F; Malthièry Y
    Eur J Hum Genet; 1999 Apr; 7(3):404-6. PubMed ID: 10234520
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nuclear and mitochondrial analysis of patients with primary angle-closure glaucoma.
    Abu-Amero KK; Morales J; Osman MN; Bosley TM
    Invest Ophthalmol Vis Sci; 2007 Dec; 48(12):5591-6. PubMed ID: 18055808
    [TBL] [Abstract][Full Text] [Related]  

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

  • 15. 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; 63(6):794-8. PubMed ID: 18496845
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Diagnostic potential of mitochondrial DNA assessment in patients with optic neuropathy.
    Feng X; Pu W; Gao D; Isashiki Y; Ohba N
    Chin Med J (Engl); 2000 Aug; 113(8):743-6. PubMed ID: 11776061
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation--A case report.
    Grazina MM; Diogo LM; Garcia PC; Silva ED; Garcia TD; Robalo CB; Oliveira CR
    Eur J Paediatr Neurol; 2007 Mar; 11(2):115-8. PubMed ID: 17254817
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 140(3):407-15. PubMed ID: 16083844
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Retinal atrophy using optical coherence tomography (OCT) in 15 patients with multiple sclerosis and comparison with healthy subjects].
    Jeanjean L; Castelnovo G; Carlander B; Villain M; Mura F; Dupeyron G; Labauge P
    Rev Neurol (Paris); 2008 Nov; 164(11):927-34. PubMed ID: 18808761
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.