Cone-rod dystrophy - Open Access .click

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Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy

Documenta Ophthalmologica, 2019
T. Hayashi +8 more
semanticscholar +1 more source

Cone Rod Dystrophies

2009
Nils Peters +199 more
openaire +1 more source

Progressive human cone-rod dysfunction (dystrophy).

Transactions. Section on Ophthalmology. American Academy of Ophthalmology and Otolaryngology, 1976
The author has classified progressive human cone-rod dysfunction into primary and secondary types. The primary type, identified by early ERG cone and usually also rod abnormalities, was further subdivided into types 1 and 2 based on, amoung other distinguishing characteristics, the extent of associated retinal pigment epithelial defects. Secondary cone-
openaire +1 more source

Progressive Cone Dystrophy and Cone-Rod Dystrophy (XL, AD, and AR).

Advances in Experimental Medicine and Biology, 2018
S. Tsang, Tarun Sharma
semanticscholar +1 more source

Hypotrichosis with cone-rod dystrophy in a patient with cadherin 3 (CDH3) mutation