BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 7611010)

  • 1. [Molecular genetic analysis of Leber's hereditary optic neuropathy with the 3460 mutation in Japanese pedigrees].
    Hiida Y; Mashima Y; Saga M; Shuu M; Akiya S; Kudoh J; Shimizu N; Oguchi Y
    Nippon Ganka Gakkai Zasshi; 1995 Jun; 99(6):728-34. PubMed ID: 7611010
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA.
    Hotta Y; Fujiki K; Hayakawa M; Nakajima A; Kanai A; Mashima Y; Hiida Y; Shinoda K; Yamada K; Oguchi Y
    Jpn J Ophthalmol; 1995; 39(1):96-108. PubMed ID: 7643491
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.
    Leo-Kottler B; Christ-Adler M; Baumann B; Zrenner E; Wissinger B
    Ger J Ophthalmol; 1996 Jul; 5(4):233-40. PubMed ID: 8854108
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. A family with Leber's hereditary optic neuropathy with mitochondrial 11778/ND4 and 4216/ND1 mutations.
    Hwang JM
    Korean J Ophthalmol; 2000 Jun; 14(1):45-8. PubMed ID: 10933019
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic analysis of Japanese pedigrees with Leber's hereditary optic neuropathy.
    Nakamura M
    Kobe J Med Sci; 1993 Dec; 39(5-6):171-82. PubMed ID: 8182918
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial DNA mutations associated with the 11778 mutation in Leber's disease.
    Sawano T; Tanaka M; Ohno K; Yoneda M; Ota Y; Terasaki H; Awaya S; Ozawa T
    Biochem Mol Biol Int; 1996 Apr; 38(4):693-700. PubMed ID: 8728098
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Homoplasmic and exclusive ND4 gene mutation in Japanese pedigrees with Leber's disease.
    Nakamura M; Fujiwara Y; Yamamoto M
    Invest Ophthalmol Vis Sci; 1993 Mar; 34(3):488-95. PubMed ID: 8449667
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Stargardt's type maculopathy in a patient with 11778 Leber's optic neuropathy.
    Yen MY; Wei YH; Liu JH
    J Neuroophthalmol; 1996 Jun; 16(2):120-3. PubMed ID: 8797169
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Genetic characteristics of Japanese pedigrees with Leber's hereditary optic neuropathy].
    Nakamura M; Yamamoto M
    Nippon Ganka Gakkai Zasshi; 1994 Apr; 98(4):319-26. PubMed ID: 8165962
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.
    Newman NJ; Lott MT; Wallace DC
    Am J Ophthalmol; 1991 Jun; 111(6):750-62. PubMed ID: 2039048
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Leber's hereditary optic neuropathy: implications of the sex ratio for linkage studies in families with the 3460 ND1 mutation.
    Black GC; Craig IW; Oostra RJ; Norby S; Rosenberg T; Morten K; Laborde A; Poulton J
    Eye (Lond); 1995; 9 ( Pt 4)():513-6. PubMed ID: 7498577
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Difficulty differentiating Leber's from dominant optic neuropathy in a patient with remote visual loss.
    Jacobson DM; Stone EM
    J Clin Neuroophthalmol; 1991 Sep; 11(3):152-7. PubMed ID: 1836796
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Leber's hereditary optic neuropathy.
    Letchavanakul A; Dechphongsaphilas W; Dhamcharee V
    J Med Assoc Thai; 1999 Oct; 82(10):1051-5. PubMed ID: 10561972
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathy.
    Nakamura M; Ara F; Yamada M; Hotta Y; Hayakawa M; Fujiki K; Kanai A; Sakai J; Inoue M; Yamamoto M
    Jpn J Ophthalmol; 1992; 36(1):56-61. PubMed ID: 1635296
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. High incidence of visual recovery among four Japanese patients with Leber's hereditary optic neuropathy with the 14484 mutation.
    Yamada K; Mashima Y; Kigasawa K; Miyashita K; Wakakura M; Oguchi Y
    J Neuroophthalmol; 1997 Jun; 17(2):103-7. PubMed ID: 9176781
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Leber's hereditary optic neuropathy. Clinical manifestations of the 14484 mutation.
    Johns DR; Heher KL; Miller NR; Smith KH
    Arch Ophthalmol; 1993 Apr; 111(4):495-8. PubMed ID: 8470982
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.