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Journal Abstract Search


209 related items for PubMed ID: 12013866

  • 1. [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]

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

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. [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
    [Abstract] [Full Text] [Related]

  • 5. [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]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Case report: A Thai patient with Leber's hereditary optic neuropathy linked to mitochondrial DNA 14484 mutation.
    Chuenkongkaew W, Lertrit P, Suphavilai R.
    Southeast Asian J Trop Med Public Health; 2004 Mar; 35(1):167-8. PubMed ID: 15272763
    [Abstract] [Full Text] [Related]

  • 9. Leber's hereditary optic neuropathy mutations in ethambutol-induced optic neuropathy.
    Hwang JM, Kim J, Park SS.
    J Neurol; 2003 Jan; 250(1):87-9. PubMed ID: 12527998
    [Abstract] [Full Text] [Related]

  • 10. 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; 38(2):163-9. PubMed ID: 7654063
    [Abstract] [Full Text] [Related]

  • 11. [Rapid genetic screening of Leber's hereditary optic neuropathy with mtDNA G11778A mutation by AS-PCR with whole blood].
    Yang JH, Tong Y, Li BH, Chen YK.
    Zhonghua Yan Ke Za Zhi; 2005 Mar; 41(3):243-5. PubMed ID: 15840367
    [Abstract] [Full Text] [Related]

  • 12. White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation.
    Lev D, Yanoov-Sharav M, Watemberg N, Leshinsky-Silver E, Lerman-Sagie T.
    Eur J Paediatr Neurol; 2002 Mar; 6(2):121-3. PubMed ID: 11995959
    [Abstract] [Full Text] [Related]

  • 13. Treatment of Leber's hereditary optic neuropathy: theory to practice.
    Johns DR, Colby KA.
    Semin Ophthalmol; 2002 Mar; 17(1):33-8. PubMed ID: 15513454
    [Abstract] [Full Text] [Related]

  • 14. A mutational hot spot in the mitochondrial ND6 gene in patients with Leber's hereditary optic neuropathy.
    Luberichs J, Leo-Kottler B, Besch D, Fauser S.
    Graefes Arch Clin Exp Ophthalmol; 2002 Feb; 240(2):96-100. PubMed ID: 11931086
    [Abstract] [Full Text] [Related]

  • 15. [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]

  • 16. 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; 24(1):107-11. PubMed ID: 19247386
    [Abstract] [Full Text] [Related]

  • 17. 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; 51(6):774-8. PubMed ID: 12112086
    [Abstract] [Full Text] [Related]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. Leber's hereditary optic neuropathy: a multifactorial disease.
    Yen MY, Wang AG, Wei YH.
    Prog Retin Eye Res; 2006 Jul; 25(4):381-96. PubMed ID: 16829155
    [Abstract] [Full Text] [Related]

  • 20. Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.
    Tharaphan P, Chuenkongkaew WL, Luangtrakool K, Sanpachudayan T, Suktitipat B, Suphavilai R, Srisawat C, Sura T, Lertrit P.
    J Neuroophthalmol; 2006 Dec; 26(4):264-7. PubMed ID: 17204919
    [Abstract] [Full Text] [Related]


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