127 related articles for article (PubMed ID: 1623618)
21. Screening for the two most frequent mutations in Leber's hereditary optic neuropathy by duplex PCR based on allele-specific amplification.
Nørby S
Hum Mutat; 1993; 2(4):309-13. PubMed ID: 8401538
[TBL] [Abstract][Full Text] [Related]
22. Leber hereditary optic neuropathy associated with antiretroviral therapy for human immunodeficiency virus infection.
Shaikh S; Ta C; Basham AA; Mansour S
Am J Ophthalmol; 2001 Jan; 131(1):143-5. PubMed ID: 11162998
[TBL] [Abstract][Full Text] [Related]
23. Detection of the mtDNA 14484 mutation on an African-specific haplotype: implications about its role in causing Leber hereditary optic neuropathy.
Torroni A; Carelli V; Petrozzi M; Terracina M; Barboni P; Malpassi P; Wallace DC; Scozzari R
Am J Hum Genet; 1996 Jul; 59(1):248-52. PubMed ID: 8659531
[No Abstract] [Full Text] [Related]
24. A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.
Jun AS; Brown MD; Wallace DC
Proc Natl Acad Sci U S A; 1994 Jun; 91(13):6206-10. PubMed ID: 8016139
[TBL] [Abstract][Full Text] [Related]
25. Leber hereditary optic neuropathy.
Sadun AA; Sadun F
Ophthalmology; 1996 Feb; 103(2):201-2. PubMed ID: 8594500
[No Abstract] [Full Text] [Related]
26. The mitochondrial DNA mutation ND6*14,484C associated with leber hereditary optic neuropathy, leads to deficiency of complex I of the respiratory chain.
Oostra RJ; Van Galen MJ; Bolhuis PA; Bleeker-Wagemakers EM; Van den Bogert C
Biochem Biophys Res Commun; 1995 Oct; 215(3):1001-5. PubMed ID: 7488023
[TBL] [Abstract][Full Text] [Related]
27. Pathological significance of the mtDNA COX III mutation at nucleotide pair 9438 in Leber hereditary optic neuropathy.
Brown MD; Torroni A; Huoponen K; Chen YS; Lott MT; Wallace DC
Am J Hum Genet; 1994 Aug; 55(2):410-2. PubMed ID: 8037217
[No Abstract] [Full Text] [Related]
28. Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy.
Bolhuis PA; Bleeker-Wagemakers EM; Ponne NJ; Van Schooneveld MJ; Westerveld A; Van den Bogert C; Tabak HF
Biochem Biophys Res Commun; 1990 Aug; 170(3):994-7. PubMed ID: 2390098
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Leber hereditary optic neuropathy, progressive visual loss, and multiple-sclerosis-like symptoms.
Tran M; Bhargava R; MacDonald IM
Am J Ophthalmol; 2001 Oct; 132(4):591-3. PubMed ID: 11589893
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Single-cell analysis of intercellular heteroplasmy of mtDNA in Leber hereditary optic neuropathy.
Kobayashi Y; Sharpe H; Brown N
Am J Hum Genet; 1994 Jul; 55(1):206-9. PubMed ID: 8023848
[No Abstract] [Full Text] [Related]
33. Finger prick blood testing in Leber hereditary optic neuropathy.
Mackey D; Nasioulas S; Forrest S
Br J Ophthalmol; 1993 May; 77(5):311-2. PubMed ID: 8318469
[TBL] [Abstract][Full Text] [Related]
34. [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]
35. Predominance of the T14484C mutation in French-Canadian families with Leber hereditary optic neuropathy is due to a founder effect.
Macmillan C; Johns TA; Fu K; Shoubridge EA
Am J Hum Genet; 2000 Jan; 66(1):332-5. PubMed ID: 10631164
[No Abstract] [Full Text] [Related]
36. Development of reverse dot-blot system for screening of mitochondrial DNA mutations associated with Leber hereditary optic atrophy.
Schollen E; Vandenberk P; Cassiman JJ; Matthijs G
Clin Chem; 1997 Jan; 43(1):18-23. PubMed ID: 8990216
[TBL] [Abstract][Full Text] [Related]
37. The Leber hereditary optic neuropathy 14,484 mutation and X-linked adrenoleukodystrophy: a possible modifier of phenotypic expression?
Gray RG; Green SH; Davies P; Alger S; Green A
J Inherit Metab Dis; 1999 Aug; 22(6):760-1. PubMed ID: 10472539
[No Abstract] [Full Text] [Related]
38. Mitochondrial DNA mutation and heteroplasmy in type I Leber hereditary optic neuropathy.
Zhu DP; Economou EP; Antonarakis SE; Maumenee IH
Am J Med Genet; 1992 Jan; 42(2):173-9. PubMed ID: 1346348
[TBL] [Abstract][Full Text] [Related]
39. [Molecular genetic analysis for Leber's hereditary optic neuropathy (LHON)].
Tanno Y; Yoneda M; Tanaka K; Tsuji S
Nihon Rinsho; 1993 Sep; 51(9):2396-402. PubMed ID: 8411719
[TBL] [Abstract][Full Text] [Related]
40. A case-control study of tobacco and alcohol consumption in Leber hereditary optic neuropathy.
Kerrison JB; Miller NR; Hsu F; Beaty TH; Maumenee IH; Smith KH; Savino PJ; Stone EM; Newman NJ
Am J Ophthalmol; 2000 Dec; 130(6):803-12. PubMed ID: 11124301
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
