Macular dystrophy in Heimler syndrome

Author： Lima Luiz H.   Barbazetto Irene A.   Chen Royce   Yannuzzi Lawrence A.   Tsang Stephen H.   Spaide Richard F.  

Publisher： Informa Healthcare

ISSN： 1381-6810

Source： Ophthalmic Genetics, Vol.32, Iss.2, 2011-06, pp. : 97-100

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Congenital Macular Dystrophy, Corpus Callosum Agenesis, Hippocampi Hypoplasia – A Novel Neuro-Ophthalmic Syndrome: Case Report

By Bitoun Pierre   Pipiras Eva   Rigaudiere Florence  

Ophthalmic Genetics, Vol. 33, Iss. 1, 2012-03 ,pp. : 39-43

Informa Healthcare

Access to resources Recommend Favorite

Natural History of Phenotypic Changes in Stargardt Macular Dystrophy

By Walia Saloni   Fishman Gerald  

Ophthalmic Genetics, Vol. 30, Iss. 2, 2009-06 ,pp. : 63-68

Informa Healthcare

Access to resources Recommend Favorite

Historical evolution in the understanding of Stargardt macular dystrophy

By Fishman Gerald Allen  

Ophthalmic Genetics, Vol. 31, Iss. 4, 2010-12 ,pp. : 183-189

Informa Healthcare

Access to resources Recommend Favorite

Best Macular Dystrophy in a Nigerian: A Case Report

By  

Case Reports in Ophthalmology, Vol. 3, Iss. 2, 2012-06 ,pp. : 205-208

Karger

Access to resources Recommend Favorite

Giant Macular Hole in Alport Syndrome

By  

Ophthalmic Genetics, Vol. 32, Iss. 1, 2011-03 ,pp. : 64-64

Informa Healthcare

Access to resources Recommend Favorite