BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

68 related articles for article (PubMed ID: 12013932)

  • 1. [Loss of visual acuity].
    Maeda K; Terada M; Mitsunami K
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():526-9. PubMed ID: 12013932
    [No Abstract]   [Full Text] [Related]  

  • 2. [LHON (Leber's hereditary optic neuropathy)].
    Mashima Y
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():282-6. PubMed ID: 12013866
    [No Abstract]   [Full Text] [Related]  

  • 3. [Optic atrophy/dystonia].
    Ishii A; Ohkoshi N
    Ryoikibetsu Shokogun Shirizu; 2001; (36):203-8. PubMed ID: 11596371
    [No Abstract]   [Full Text] [Related]  

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

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

  • 6. Rescue of a mitochondrial deficiency causing Leber Hereditary Optic Neuropathy.
    Guy J; Qi X; Pallotti F; Schon EA; Manfredi G; Carelli V; Martinuzzi A; Hauswirth WW; Lewin AS
    Ann Neurol; 2002 Nov; 52(5):534-42. PubMed ID: 12402249
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A MELAS-associated ND1 mutation causing leber hereditary optic neuropathy and spastic dystonia.
    Spruijt L; Smeets HJ; Hendrickx A; Bettink-Remeijer MW; Maat-Kievit A; Schoonderwoerd KC; Sluiter W; de Coo IF; Hintzen RQ
    Arch Neurol; 2007 Jun; 64(6):890-3. PubMed ID: 17562939
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Safety of rAAV2/2-ND4 Gene Therapy for Leber Hereditary Optic Neuropathy.
    Vignal C; Uretsky S; Fitoussi S; Galy A; Blouin L; Girmens JF; Bidot S; Thomasson N; Bouquet C; Valero S; Meunier S; Combal JP; Gilly B; Katz B; Sahel JA
    Ophthalmology; 2018 Jun; 125(6):945-947. PubMed ID: 29426586
    [No Abstract]   [Full Text] [Related]  

  • 9. Leber hereditary optic neuropathy and oxidative stress.
    Zhuo Y; Luo H; Zhang K
    Proc Natl Acad Sci U S A; 2012 Dec; 109(49):19882-3. PubMed ID: 23197830
    [No Abstract]   [Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 12. 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; 8(5-6):383-8. PubMed ID: 18801464
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Leber hereditary optic neuropathy mutations in the ND6 subunit of mitochondrial complex I affect ubiquinone reduction kinetics in a bacterial model of the enzyme.
    Pätsi J; Kervinen M; Finel M; Hassinen IE
    Biochem J; 2008 Jan; 409(1):129-37. PubMed ID: 17894548
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Partial mitochondrial complex I inhibition induces oxidative damage and perturbs glutamate transport in primary retinal cultures. Relevance to Leber Hereditary Optic Neuropathy (LHON).
    Beretta S; Wood JP; Derham B; Sala G; Tremolizzo L; Ferrarese C; Osborne NN
    Neurobiol Dis; 2006 Nov; 24(2):308-17. PubMed ID: 16959493
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Suppression of complex I gene expression induces optic neuropathy.
    Qi X; Lewin AS; Hauswirth WW; Guy J
    Ann Neurol; 2003 Feb; 53(2):198-205. PubMed ID: 12557286
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Leber hereditary optic neuropathy: biochemical lights in a blurry scenario.
    Hirano M; DiMauro S
    Arch Neurol; 2005 May; 62(5):711-2. PubMed ID: 15883256
    [No Abstract]   [Full Text] [Related]  

  • 17. Sequence homology of NADH CoQ reductase subunit IV with nucleotide-requiring enzymes.
    Isashiki Y; Ohba N; Uto M; Nakagawa M
    Jpn J Ophthalmol; 1993; 37(1):39-42. PubMed ID: 8320863
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Leber hereditary optic neuropathy--a disease with a known molecular basis but a mysterious mechanism of pathology.
    Mroczek-Tońska K; Kisiel B; Piechota J; Bartnik E
    J Appl Genet; 2003; 44(4):529-38. PubMed ID: 14617834
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A pedigree of Leber's hereditary optic neuropathy with mtDNA 14484 mutation].
    Tong Y; Wang Y; Jiang F; Liu B; Zhang S; Yang W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):531-3. PubMed ID: 18841565
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.