Central retinal vein occlusion as the initial manifestation of LHON / MELAS overlap syndrome with mitochondrial DNA G13513A mutation——Case report and literature review

By Hsieh Yi-Ting   Yang Ming-Tao   Peng Yi-Jie   Hsu Wei-Cherng  

Ophthalmic Genetics, Vol. 32, Iss. 1, 2011-03 ,pp. : 31-38

Informa Healthcare

Access to resources Recommend Favorite

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

By  

Ophthalmic Research, Vol. 35, Iss. 4, 2003-06 ,pp. : 224-231

Karger

Access to resources Recommend Favorite

Prolidase deficiency associated with pathologic myopia

By Kiratli Hayyam   Satilmis Mücahit  

Ophthalmic Genetics, Vol. 19, Iss. 1, 1998-03 ,pp. : 49-53

Informa Healthcare

Access to resources Recommend Favorite

Intravitreal Ranibizumab for the Treatment of Choroidal Neovascularizations Associated with Pathologic Myopia: A Prospective Study

By  

Ophthalmologica, Vol. 233, Iss. 1, 2014-12 ,pp. : 2-7

Karger

Access to resources Recommend Favorite

Audiological and radiological characteristics of a family with T961G mitochondrial mutation

By Turchetta Rosaria   Mazzei Filippo   Celani Tiziana   Cammeresi Maria Gloria   Orlando Maria Patrizia   Altissimi Giancarlo   de Vincentiis Chiara   D'Ambrosio Ferdinando   Messineo Daniela   Ferraris Alessandro   Cianfrone Giancarlo  

International Journal of Audiology, Vol. 51, Iss. 12, 2012-12 ,pp. : 870-879

Informa Healthcare

Access to resources Recommend Favorite