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 *

234 related articles for article (PubMed ID: 9339703)

  • 41. 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]  

  • 42. 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]  

  • 43. Molecular diagnosis of Leber's hereditary optic neuropathy.
    Yen MY; Liu JH; Pang CY; Wei YH
    J Formos Med Assoc; 1993 Jan; 92(1):42-5. PubMed ID: 8099825
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation.
    Olsen NK; Hansen AW; Nørby S; Edal AL; Jørgensen JR; Rosenberg T
    Acta Neurol Scand; 1995 May; 91(5):326-9. PubMed ID: 7639060
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Leber's hereditary optic neuropathy mitochondrial DNA mutations at nucleotides 11778 and 3460 in multiple sclerosis.
    Mojon DS; Herbert J; Sadiq SA; Miller JR; Madonna M; Hirano M
    Ophthalmologica; 1999; 213(3):171-5. PubMed ID: 10202290
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Detection of the G to A mitochondrial DNA mutation at position 11778 in German families with Leber's hereditary optic neuropathy.
    Kormann BA; Schuster H; Berninger TA; Leo-Kottler B
    Hum Genet; 1991 Nov; 88(1):98-100. PubMed ID: 1959931
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. 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]  

  • 49. A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy.
    Singh G; Lott MT; Wallace DC
    N Engl J Med; 1989 May; 320(20):1300-5. PubMed ID: 2566116
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Exclusive homoplasmic 11778 mutation in mitochondrial DNA of Chinese patients with Leber's hereditary optic neuropathy.
    Yen MY; Lee HC; Wang AG; Chang WL; Liu JH; Wei YH
    Jpn J Ophthalmol; 1999; 43(3):196-200. PubMed ID: 10413253
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Leber's hereditary optic neuropathy. Clinical manifestations of the 3460 mutation.
    Johns DR; Smith KH; Miller NR
    Arch Ophthalmol; 1992 Nov; 110(11):1577-81. PubMed ID: 1444915
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases.
    Brown MD; Voljavec AS; Lott MT; MacDonald I; Wallace DC
    FASEB J; 1992 Jul; 6(10):2791-9. PubMed ID: 1634041
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Mae III positively detects the mitochondrial mutation associated with type I Leber's hereditary optic neuropathy.
    Stone EM; Coppinger JM; Kardon RH; Donelson J
    Arch Ophthalmol; 1990 Oct; 108(10):1417-20. PubMed ID: 1977373
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Leber's hereditary optic neuropathy (LHON) with mitochondrial ND4 gene mutation (11778) in a Thai patient.
    Lertrit P; Ruangvaravate N; Trongpanich Y; Imsumran A; Mungkornkarn C; Neungton N
    J Med Assoc Thai; 1999 Jan; 82(1):59-64. PubMed ID: 10087740
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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]  

  • 56. The mitochondrial DNA mutation at position 11778 in Chinese families with Leber's hereditary optic neuropathy.
    Zhang L; Huang Y; Li F; Wang S; Zhu B; Zhang Z; Tong Y; Gao J
    Yan Ke Xue Bao; 1994 Sep; 10(3):151-6. PubMed ID: 7744206
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Mitochondrial DNA mutation in Leber's hereditary optic neuropathy.
    Yen MY; Yen TC; Pang CY; Liu JH; Wei YH
    Invest Ophthalmol Vis Sci; 1992 Jul; 33(8):2561-6. PubMed ID: 1634353
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [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]  

  • 59. Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutation.
    Oostra RJ; Bolhuis PA; Zorn-Ende I; de Kok-Nazaruk MM; Bleeker-Wagemakers EM
    Hum Genet; 1994 Sep; 94(3):265-70. PubMed ID: 8076942
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Lack of differences among mitochondrial DNA in family members with Leber's hereditary optic neuropathy and differing visual outcomes.
    Mashima Y; Hiida Y; Oguchi Y
    J Neuroophthalmol; 1995 Mar; 15(1):15-9. PubMed ID: 7780566
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.