THREE-DIMENSIONAL CHARACTERISTICS OF FOUR MACULAR INTRARETINAL LAYER THICKNESSES IN SYMPTOMATIC AND ASYMPTOMATIC CARRIERS OF G11778A MUTATION WITH LEBERʼS HEREDITARY OPTIC NEUROPATHY

Foveal pit morphological changes in asymptomatic carriers of the G11778A mutation with Leber’s hereditary optic neuropathy

International Journal of Ophthalmology ◽

10.18240/ijo.2020.05.11 ◽

2020 ◽

Vol 13 (5) ◽

pp. 766-772

Author(s):

Xin-Ting Liu

Keyword(s):

Optic Neuropathy ◽

Morphological Changes ◽

Asymptomatic Carriers ◽

G11778a Mutation ◽

Only male matrilineal relatives with Leber’s hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation

Biochemical and Biophysical Research Communications ◽

10.1016/j.bbrc.2005.01.062 ◽

2005 ◽

Vol 328 (4) ◽

pp. 1139-1145 ◽

Cited By ~ 28

Author(s):

Jia Qu ◽

Ronghua Li ◽

Yi Tong ◽

Yongwu Hu ◽

Xiangtian Zhou ◽

...

Keyword(s):

Mitochondrial Dna ◽

Optic Neuropathy ◽

Chinese Family ◽

G11778a Mutation ◽

Male Prevalence of Acquired Color Vision Defects in Asymptomatic Carriers of Leber’s Hereditary Optic Neuropathy

Investigative Opthalmology & Visual Science ◽

10.1167/iovs.06-0331 ◽

2007 ◽

Vol 48 (5) ◽

pp. 2362 ◽

Cited By ~ 42

Author(s):

Dora Fix Ventura ◽

Mirella Gualtieri ◽

Andre´ G. F. Oliveira ◽

Marcelo F. Costa ◽

Peter Quiros ◽

...

Keyword(s):

Color Vision ◽

Optic Neuropathy ◽

Asymptomatic Carriers ◽

Color Vision Defects ◽

Vision Defects ◽

The altered activity of complex III may contribute to the high penetrance of Leber's hereditary optic neuropathy in a Chinese family carrying the ND4 G11778A mutation

Mitochondrion ◽

10.1016/j.mito.2011.06.006 ◽

2011 ◽

Vol 11 (6) ◽

pp. 871-877 ◽

Cited By ~ 19

Author(s):

Yaping Qian ◽

Xiangtian Zhou ◽

Min Liang ◽

Jia Qu ◽

Min-Xin Guan

Keyword(s):

Optic Neuropathy ◽

Complex Iii ◽

Chinese Family ◽

High Penetrance ◽

G11778a Mutation ◽

Clinical phenotype and the G11778A mutation of mitochondrial DNA in patients with Leber’s hereditary optic neuropathy in Taiwan

Neuro-Ophthalmology ◽

10.1076/noph.26.4.207.15871 ◽

2001 ◽

Vol 26 (4) ◽

pp. 207-216

Author(s):

Chun-Che Chu ◽

Chin-Chang Huang ◽

Ling-Yuh Kao ◽

Hung-Chou Kuo ◽

Tzu-Ning Yu ◽

...

Keyword(s):

Mitochondrial Dna ◽

Optic Neuropathy ◽

Clinical Phenotype ◽

G11778a Mutation ◽

Variation in retinal nerve fiber layer thickness at different stages of Leber’s hereditary optic neuropathy in patients with the ND4 G11778A mutation

Seminars in Ophthalmology ◽

10.1080/08820538.2021.1986078 ◽

2021 ◽

pp. 1-6

Author(s):

Zhen Tian ◽

Xin Li ◽

Wu Zheng ◽

Bin Li ◽

Yong Zhang

Keyword(s):

Nerve Fiber ◽

Layer Thickness ◽

Optic Neuropathy ◽

Retinal Nerve Fiber Layer ◽

Fiber Layer ◽

Nerve Fiber Layer ◽

Nerve Fiber Layer Thickness ◽

G11778a Mutation ◽

Hereditary Optic Neuropathy ◽

Retinal Nerve Fiber

Phylogenetic Assessment of the Mitochondrial DNA Displacement Loop Haplotype in Japanese Patients with Leber’s Hereditary Optic Neuropathy Harboring the Mitochondrial DNA G11778A Mutation

Ophthalmic Research ◽

10.1159/000071174 ◽

2003 ◽

Vol 35 (4) ◽

pp. 224-231 ◽

Cited By ~ 7

Author(s):

Yasushi Isashiki ◽

Shozo Sonoda ◽

Shuji Izumo ◽

Taiji Sakamoto ◽

Hiroshi Tachikui ◽

...

Keyword(s):

Mitochondrial Dna ◽

Optic Neuropathy ◽

Japanese Patients ◽

G11778a Mutation ◽

Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation

Journal of Genetics and Genomics ◽

10.1016/s1673-8527(08)60086-7 ◽

2008 ◽

Vol 35 (11) ◽

pp. 649-655 ◽

Cited By ~ 31

Author(s):

Wanshi Cai ◽

Qun Fu ◽

Xiangtian Zhou ◽

Jia Qu ◽

Yi Tong ◽

...

Keyword(s):

Optic Neuropathy ◽

Phenotypic Manifestation ◽

G11778a Mutation ◽

Extremely Low Penetrance of Leber's Hereditary Optic Neuropathy in 8 Han Chinese Families Carrying the ND4 G11778A Mutation

Ophthalmology ◽

10.1016/j.ophtha.2008.10.022 ◽

2009 ◽

Vol 116 (3) ◽

pp. 558-564.e3 ◽

Cited By ~ 33

Author(s):

Jia Qu ◽

Xiangtian Zhou ◽

Juanjuan Zhang ◽

Fuxin Zhao ◽

Yan-Hong Sun ◽

...

Keyword(s):

Optic Neuropathy ◽

Han Chinese ◽

Chinese Families ◽

G11778a Mutation ◽

Very high penetrance and occurrence of Leber’s hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation

Molecular Genetics and Metabolism ◽

10.1016/j.ymgme.2010.04.013 ◽

2010 ◽

Vol 100 (4) ◽

pp. 379-384 ◽

Cited By ~ 20

Author(s):

Xiangtian Zhou ◽

Hongxing Zhang ◽

Fuxin Zhao ◽

Yanchun Ji ◽

Yi Tong ◽

...

Keyword(s):

Optic Neuropathy ◽

Han Chinese ◽

High Penetrance ◽

Very High ◽

G11778a Mutation ◽