Results 111 to 120 of about 7,292 (198)

Clinical manifestation of congenital aniridia in Ukrainian children and adolescents

Journal of Ophthalmology
Purpose: To investigate clinical manifestations of congenital aniridia (CA) in Ukrainian children and adolescents. Material and Methods: Twenty four children and adolescents (47 eyes; group 1 of children under 11 years and group 2 of adolescents aged 11
N. F. Bobrova, T. V. Romanova, G. M. Demnovetska, T. A. Sorochynska, K. S. Vdovichenko, O. D. Dovhan   +5 more
doaj   +1 more source

Contact-mediated control of radial migration of corneal epithelial cells [PDF]

, 2016
We thank Darrin Sheppard and other staff at the University of Aberdeen Medical Research Facility for specialist technical assistance. We thank Patsy D. Goast for overnight microscope monitoring.
Collinson, J Martin, Rajnicek, Ann M, Walczysko, Petr   +2 more
core   +1 more source

Early ocular surface and tear film status in congenital aniridia indicates a supportive treatment window. [PDF]

Br J Ophthalmol, 2023
Fries FN, Moslemani K, Utheim TP, Seitz B, Käsmann-Kellner B, Lagali NS.   +5 more
europepmc   +1 more source

A Novel PAX6 Frameshift Mutation Identified in a Large Chinese Family with Congenital Aniridia. [PDF]

J Pers Med, 2023
Wang C, Yang W, Li X, Zhou C, Liu J, Jin L, Jiang Q, Wang Y.   +7 more
europepmc   +1 more source

Corneal Opacification in Infancy [PDF]

, 1972
The purpose of this paper is to present a systematic classification of the more important conditions that can manifest as corneal opacification in early infancy and to state its differential diagnostic ...
Ching, Florencio C.
core   +1 more source

Gene expression study in the siRNA based aniridia cell model and in primary aniridia limbal epithelial cells following duloxetine and ritanserin treatment.

PLoS ONE
Progressive aniridia associated keratopathy is worsening visual acuity of congenital aniridia subjects lifelong. Restoration of PAX6 expression in PAX6 haploinsufficient limbal epithelial cells could be one therapeutic option.
Shweta Suiwal, Tanja Stachon, Zhen Li, Marta Corton, Mahsa Nastaranpour, Ning Chai, Maryam Amini, Berthold Seitz, Fabian N Fries, Thomas Tschernig, Nóra Szentmáry   +10 more
doaj   +1 more source

Co-Occurrence of Congenital Aniridia Due to Nonsense PAX6 Variant p.(Cys94*) and Chromosome 21 Trisomy in the Same Patient. [PDF]

Int J Mol Sci, 2023
Vasilyeva TA, Sukhanova NV, Marakhonov AV, Kuzina NY, Shilova NV, Kadyshev VV, Kutsev SI, Zinchenko RA.   +7 more
europepmc   +1 more source

Faktor-faktor Yang Berpengaruh Terhadap Kejadian Kelainan Kongenital Facio-oral Pada Neonatus [PDF]

, 2013
Latar belakang. Kelainan kongenital facio-oral merupakan kelainan pada struktur organ di wajah secara anatomi maupun fisiologis sejak lahir. Penelitian sebelumnya menemukan 40-60% orang dengan cacat lahir tidak diketahui penyebabnya.Tujuan.
Abidin, A. R. (Achmad), Suswihardhyono, A. N. (Adhie)   +1 more
core  

The Australian Corneal Graft Registry 2007 Report [PDF]

, 2007
The Australian Corneal Graft Registry opened in May 1985 and thus has now been in operation for over 22 years. The census date for this report was 01/09/2006. Over the years, we have collected data on more than 18,500 corneal grafts.
Bartlett, Christine Mary, Coster, Douglas John, Kelly, L, Lowe, Marie Therese, Williams, Keryn Anne   +4 more
core  

Rod and Cone Dark Adaptation in Congenital Aniridia and Its Association With Retinal Structure. [PDF]

Invest Ophthalmol Vis Sci, 2023
Pedersen HR, Gilson SJ, Landsend ECS, Utheim ØA, Utheim TP, Baraas RC.   +5 more
europepmc   +1 more source