About MEAJO | Editorial board | Search | Ahead of print | Current Issue | Archives | Instructions to authors | Online submission | Subscribe | Advertise | Contact | Login 
Middle East African Journal of Ophthalmology Middle East African Journal of Ophthalmology
Users Online: 1401   Home Print this page Email this page Small font sizeDefault font sizeIncrease font size

    Article Cited by others

OPHTHALMIC GENETICS UPDATE

Leber's hereditary optic neuropathy: The mitochondrial connection revisited

Abu-Amero Khaled K

Year : 2011| Volume: 18| Issue : 1 | Page no: 17-23

   This article has been cited by
 
1 Analyses of the mitochondrial mutations in the Chinese patients with sporadic Creutzfeldt–Jakob disease
Jin Zhang,Zhi-Xia Zhang,Peng-Chen Du,Wei Zhou,Su-Dong Wu,Qi-Ling Wang,Cao Chen,Qi Shi,Chen Chen,Chen Gao,Chan Tian,Xiao-Ping Dong
European Journal of Human Genetics. 2014;
[Pubmed]  [Google Scholar] [DOI]
2 Complete Mitochondrial Genome Analysis and Clinical Documentation of a Five-Generational Indian Family with Mitochondrial 1555A>G Mutation and Postlingual Hearing Loss
Mahalingam Subathra,Mathiyalagan Selvakumari,Arabandi Ramesh,Rajagopalan Ramakrishnan,Kalpita Rashmi Karan,Manpreet Kaur,Mayakannan Manikandan,C. R. Srikumari Srisailapathy
Annals of Human Genetics. 2014; : n/a
[Pubmed]  [Google Scholar] [DOI]
3 Neuro-Ophthalmology Annual Review
Angelina Espino Barros Palau,Michael L. Morgan,Sushma Yalamanchili,Andrew G. Lee
Asia-Pacific Journal of Ophthalmology. 2014; 3(2): 104
[Pubmed]  [Google Scholar] [DOI]
4 Clinical and electrophysiological recovery in Leber hereditary optic neuropathy with G3460A mutation
Sharkawi, E. and Oleszczuk, J.D. and Holder, G.E. and Raina, J.
Documenta Ophthalmologica. 2012; 125(1): 71-74
[Pubmed]  [Google Scholar]
5 Ophthalmic genetics: Moving forward
Abu-Amero, K.K.
Middle East African Journal of Ophthalmology. 2011; 18(1): 1
[Pubmed]  [Google Scholar]

 

Read this article