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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

104 related articles for article (PubMed ID: 1359290)

  • 1. Benzodiazepine sensitivity in Leber's hereditary optic neuroretinopathy.
    Nikoskelainen E; Asola M; Kalimo H; Savontaus ML; Majander A
    Lancet; 1992 Nov; 340(8829):1223-4. PubMed ID: 1359290
    [No Abstract]   [Full Text] [Related]  

  • 2. Recent advances in Leber's hereditary optic neuroretinopathy.
    Nikoskelainen E; Vilkki J; Huoponen K; Savontaus ML
    Eye (Lond); 1991; 5 ( Pt 3)():291-3. PubMed ID: 1955049
    [No Abstract]   [Full Text] [Related]  

  • 3. [Genetic basis of Leber's hereditary optic neuroretinopathy].
    Krawczyński MR; Pecold K
    Klin Oczna; 1993 Jun; 95(6):219-22. PubMed ID: 8309190
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 'Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation.
    Lodi R; Montagna P; Cortelli P; Iotti S; Cevoli S; Carelli V; Barbiroli B
    Brain; 2000 Sep; 123 ( Pt 9)():1896-902. PubMed ID: 10960053
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis.
    Kellar-Wood H; Robertson N; Govan GG; Compston DA; Harding AE
    Ann Neurol; 1994 Jul; 36(1):109-12. PubMed ID: 8024249
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Evidence for a metabolic trigger for Leber's hereditary optic neuropathy. A case report.
    DuBois LG; Feldon SE
    J Clin Neuroophthalmol; 1992 Mar; 12(1):15-6. PubMed ID: 1532594
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondria and Leber's hereditary optic neuropathy.
    Newman NJ; Wallace DC
    Am J Ophthalmol; 1990 Jun; 109(6):726-30. PubMed ID: 2346203
    [No Abstract]   [Full Text] [Related]  

  • 8. Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathy.
    Yoneda M; Tsuji S; Yamauchi T; Inuzuka T; Miyatake T; Horai S; Ozawa T
    Lancet; 1989 May; 1(8646):1076-7. PubMed ID: 2566021
    [No Abstract]   [Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy.
    Holt IJ; Miller DH; Harding AE
    J Neurol Neurosurg Psychiatry; 1988 Aug; 51(8):1075-7. PubMed ID: 2905730
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial DNA mutations in Leber's optic neuropathy.
    Hurko O
    Ann Neurol; 1994 May; 35(5):636. PubMed ID: 7910006
    [No Abstract]   [Full Text] [Related]  

  • 12. De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy.
    Biousse V; Brown MD; Newman NJ; Allen JC; Rosenfeld J; Meola G; Wallace DC
    Neurology; 1997 Oct; 49(4):1136-8. PubMed ID: 9339703
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Mitochondrial DNA mutation in Leber's hereditary optic neuropathy in China].
    Zhang LS; Huang Y; Li FY
    Zhonghua Yi Xue Za Zhi; 1994 Jun; 74(6):349-51, 390. PubMed ID: 7994643
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The molecular genetics of Leber's hereditary optic neuropathy.
    Johns DR
    Arch Ophthalmol; 1990 Oct; 108(10):1405-7. PubMed ID: 2222273
    [No Abstract]   [Full Text] [Related]  

  • 15. Leber's hereditary optic neuropathy.
    Volpe NJ; Lessell S
    Int Ophthalmol Clin; 1993; 33(2):153-68. PubMed ID: 8325730
    [No Abstract]   [Full Text] [Related]  

  • 16. Changes in mitochondrial complex I activity and coenzyme Q binding site in Leber's hereditary optic neuropathy (LHON).
    Ghelli A; Degli Esposti M; Carelli V; Lenaz G
    Mol Aspects Med; 1997; 18 Suppl():S263-7. PubMed ID: 9266534
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new mitochondrial DNA mutation in the tRNA leucine 1 gene (C3275A) in a patient with Leber's hereditary optic neuropathy.
    Garcia-Lozano JR; Aguilera I; Bautista J; Nuñez-Roldan A
    Hum Mutat; 2000 Jan; 15(1):120-1. PubMed ID: 10612844
    [No Abstract]   [Full Text] [Related]  

  • 18. Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy.
    Poulton J; Deadman ME; Bronte-Stewart J; Foulds WS; Gardiner RM
    J Med Genet; 1991 Nov; 28(11):765-70. PubMed ID: 1770533
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [DNA diagnosis of Leber's hereditary optic neuropathy].
    Mashima Y; Oguchi Y; Uemura Y; Kudoh J; Sakai K; Shimizu N
    Nippon Ganka Gakkai Zasshi; 1990 Jul; 94(7):683-7. PubMed ID: 2220506
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical spectrum of Leber's hereditary optic neuropathy.
    Kerrison JB; Newman NJ
    Clin Neurosci; 1997; 4(5):295-301. PubMed ID: 9292259
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.