Results 111 to 120 of about 246,741 (174)

Impact of <i>PAX6</i>-Related Congenital Aniridia on Corneal Diameter, Central Corneal Thickness and Keratometry. [PDF]

J Clin Med
Kormányos K, Csákány B, Csidey M, Náray A, Kéki-Kovács K, Németh O, Knézy K, Bausz M, Szigeti A, Csorba A, Szabó D, Corton M, Tory K, Jávorszky E, Nagy ZZ, Langenbucher A, Maka E, Szentmáry N.   +17 more
europepmc   +1 more source

Congenital aniridia: clinical profile of children seen at the University College Hospital, Ibadan, South-West Nigeria. [PDF]

Ther Adv Ophthalmol, 2021
Ugalahi MO, Ibukun FA, Olusanya BA, Baiyeroju AM.   +3 more
europepmc   +1 more source

Congenital aniridia: bilateral phacoemulsification and IOL implantation. [PDF]

Eye (Lond)
Yang L, Yang Y, Yang Y.
europepmc   +1 more source

Comprehensive Analysis of Congenital Aniridia and Differential Diagnoses: Genetic Insights and Clinical Manifestations. [PDF]

Ophthalmol Ther
Hall J, Corton M, Fries FN, Obst J, Grünauer-Kloevekorn C, Seitz B, Waizel MDV, Jávorszky E, Tory K, Maka E, Amini M, Suiwal S, Stachon T, Szentmáry N.   +13 more
europepmc   +1 more source

Response to spectral-domain optical coherence tomography foveal morphology as a prognostic factor for vision performance in congenital aniridia. [PDF]

Eur J Ophthalmol, 2022
Rufai SR, Thomas MG, Gottlob I.
europepmc   +1 more source

Reciprocal effects of conditioned medium on gene and protein expression of limbal epithelial cells and limbal fibroblasts in congenital aniridia. [PDF]

PLoS One
Berger M, Szentmáry N, Berger T, Zimmermann J, Trusen S, Seitz B, Fries FN, Suiwal S, Amini M, Stachon T.   +9 more
europepmc   +1 more source

Intraocular use of methotrexate (MTX) for the treatment of proliferative vitreoretinopathy (PVR) in congenital aniridia (CI) and a possible link to aniridia fibrosis syndrome (AFS) treatment. [PDF]

Am J Ophthalmol Case Rep
Ambati NR, Riemann CD.
europepmc   +1 more source

A sporadic case of congenital aniridia caused by pericentric inversion inv(11)(p13q14) associated with a 977 kb deletion in the 11p13 region. [PDF]

BMC Med Genomics, 2020
Vasilyeva TA, Marakhonov AV, Minzhenkova ME, Markova ZG, Petrova NV, Sukhanova NV, Koshkin PA, Pyankov DV, Kanivets IV, Korostelev SA, Krynskaya IA, Shilova NV, Kutsev SI, Kadyshev VV, Zinchenko RA.   +14 more
europepmc   +1 more source

Preferentially Paternal Origin of De Novo 11p13 Chromosome Deletions Revealed in Patients with Congenital Aniridia and WAGR Syndrome. [PDF]

Genes (Basel), 2020
Vasilyeva TA, Marakhonov AV, Sukhanova NV, Kutsev SI, Zinchenko RA.   +4 more
europepmc   +1 more source