Literature DB >> 2346203

Mitochondria and Leber's hereditary optic neuropathy.

N J Newman1, D C Wallace.   

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Year:  1990        PMID： 2346203     DOI： 10.1016/s0002-9394(14)72445-6

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN： 0002-9394            Impact factor:   5.258


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  10 in total

1.  Acquired mitochondrial impairment as a cause of optic nerve disease.

Authors:  A Sadun
Journal:  Trans Am Ophthalmol Soc       Date:  1998

2.  Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese families.

Authors:  Jia Qu; Ying Wang; Yi Tong; Xiangtian Zhou; Fuxin Zhao; Li Yang; Shoukang Zhang; Juanjuan Zhang; Constance E West; Min-Xin Guan
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-04-30       Impact factor: 4.799

3.  Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathy.

Authors:  C Carducci; V Leuzzi; M Scuderi; A M De Negri; C B Gabrieli; I Antonozzi; A Pontecorvi
Journal:  Hum Genet       Date:  1991-10       Impact factor: 4.132

4.  Central nervous system involvement in Leber's optic neuropathy.

Authors:  W Paulus; A Straube; W Bauer; A E Harding
Journal:  J Neurol       Date:  1993       Impact factor: 4.849

5.  Varying Clinical Phenotypes of Mitochondrial DNA T12811C Mutation: A Case Series Report.

Authors:  Qingdan Xu; Ping Sun; Chaoyi Feng; Qian Chen; Xinghuai Sun; Yuhong Chen; Guohong Tian
Journal:  Front Med (Lausanne)       Date:  2022-07-04

6.  Mechanisms of retinal ganglion specific-cell death in Leber hereditary optic neuropathy.

Authors:  Leonard A Levin
Journal:  Trans Am Ophthalmol Soc       Date:  2007

7.  Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation.

Authors:  Jia Qu; Xiangtian Zhou; Juanjuan Zhang; Fuxin Zhao; Yan-Hong Sun; Yi Tong; Qi-Ping Wei; Wansi Cai; Li Yang; Constance E West; Min-Xin Guan
Journal:  Ophthalmology       Date:  2009-01-22       Impact factor: 12.079

8.  Leber's hereditary optic neuropathy is associated with the T3866C mutation in mitochondrial ND1 gene in three Han Chinese Families.

Authors:  Xiangtian Zhou; Yaping Qian; Juanjuan Zhang; Yi Tong; Pingping Jiang; Min Liang; Xianning Dai; Huihui Zhou; Fuxin Zhao; Yanchun Ji; Jun Qin Mo; Jia Qu; Min-Xin Guan
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-07-09       Impact factor: 4.799

9.  ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait.

Authors:  Raed Behbehani; Motasem Melhem; Ghazi Alghanim; Kazem Behbehani; Osama Alsmadi
Journal:  Br J Ophthalmol       Date:  2014-02-25       Impact factor: 4.638

Review 10.  The Progress of Gene Therapy for Leber's Optic Hereditary Neuropathy.

Authors:  Yong Zhang; Zhen Tian; Jiajia Yuan; Chang Liu; Hong Li Liu; Si Qi Ma; Bin Li
Journal:  Curr Gene Ther       Date:  2017       Impact factor: 4.391
  10 in total

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