Results 121 to 130 of about 25,639 (292)

Combined aniridic intraocular lens implantation and vitreoretinal surgery

Indian Journal of Ophthalmology, 2007
A 45-year-old man presented with post-traumatic aniridia. We describe the combined surgery done to treat both aniridia and epiretinal membrane simultaneously. A combined aniridia intraocular lens and vitreoretinal surgery was done.
Mehta Hitendra, Mehta Hijab, Jayadev Chaitra, Natarajan S   +3 more
doaj  

Anterior chamber angle in aniridia with and without glaucoma

Clinical Ophthalmology, 2019
Asima Bajwa,1 Eitan Burstein,1 Robert M Grainger,1,2 Peter A Netland11Department of Ophthalmology, University of Virginia School of Medicine, Charlottesville, VA, USA; 2Department of Biology, University of Virginia, Charlottesville, VA, USAPurpose: We ...
Bajwa A, Burstein E, Grainger RM, Netland PA   +3 more
doaj  

PAX6 gene variations associated with aniridia in south India

BMC Medical Genetics, 2004
Background Mutations in the transcription factor gene PAX6 have been shown to be the cause of the aniridia phenotype. The purpose of this study was to analyze patients with aniridia to uncover PAX6 gene mutations in south Indian population. Methods Total
Shashikant Shetty, Vijayalakshmi Perumalsamy, Krishnadas Subbaiah, Neethirajan Guruswamy, Sundaresan Periasamy   +4 more
doaj   +1 more source

Bilateral Wilms tumour: a review of clinical and molecular features [PDF]

, 2017
Wilms tumour (WT) is the most common paediatric kidney cancer and affects approximately one in 10 000 children. The tumour is associated with undifferentiated embryonic lesions called nephrogenic rests (NRs) or, when diffuse, nephroblastomatosis. WT or
Bergeron, C, Charlton, J, Irtan, S, Pritchard-Jones, K   +3 more
core   +1 more source

PAX6 Genotypic and Retinal Phenotypic Characterization in Congenital Aniridia

Investigative Ophthalmology and Visual Science, 2020
Purpose To investigate the association between PAX6 genotype and macular morphology in congenital aniridia. Methods The study included 37 participants (15 males) with congenital aniridia (aged 10–72 years) and 58 age-matched normal controls (18 males ...
H. R. Pedersen, R. Baraas, E. Landsend, Ø. Utheim, T. Utheim, S. Gilson, M. Neitz   +6 more
semanticscholar   +1 more source

Jackknife and bootstrapping resampling techniques to evaluate the precision of lens formula constants

Acta Ophthalmologica, Volume 103, Issue 6, Page e422-e433, September 2025.
Abstract Purpose The purpose of this study was to develop a method for evaluating intraocular lens (IOL) formula constant uncertainties using two modern statistical techniques—jackknife and bootstrap resampling. Methods Using two datasets (dataset 1: 888 eyes treated with the aberration correcting Hoya Vivinex IOL, dataset 2: 821 eyes with the ...
Achim Langenbucher, Jascha Wendelstein, Alan Cayless, Thomas Olsen, Peter Hoffmann, Nóra Szentmáry   +5 more
wiley   +1 more source

Germline CRISPR/Cas9-Mediated Gene Editing Prevents Vision Loss in a Novel Mouse Model of Aniridia

Molecular Therapy: Methods & Clinical Development, 2020
Aniridia is a rare eye disorder, which is caused by mutations in the paired box 6 (PAX6) gene and results in vision loss due to the lack of a long-term vision-saving therapy.
Seyedeh Zeinab Mirjalili Mohanna, Jack W. Hickmott, Siu Ling Lam, Nina Y. Chiu, Tess C. Lengyell, Beatrice M. Tam, Orson L. Moritz, Elizabeth M. Simpson   +7 more
doaj   +1 more source

A European perspective on auditory processing disorder-current knowledge and future research focus [PDF]

, 2017
Current notions of \u201chearing impairment,\u201d as reflected in clinical audiological practice, do not acknowledge the needs of individuals who have normal hearing pure tone sensitivity but who experience auditory processing difficulties in everyday ...
Bamiou, Doris-Eva, Barajas, Jose, Brechmann, Andr\ue3\ua9, Callimachou, Marina, Deggouj, Na\ue3\uafma, Demanez, Laurent, Grech, Helen, Hedjever, Mladen, Iliadou, Vasiliki, Kiese-Himmel, Christiane, Konukseven, Ozlem, Kuske, Sandra, Martins, Jorge Humberto, Mattsson, Tone Stokkereit, Nickisch, Andreas, Pedersen, Ellen Raben, Ptok, Martin, Santarelli, Rosamaria, Sirimanna, Tony, Sliwinska-Kowalska, Mariola, Thai-Van, Hung, Veraguth, Dorothy, Veuillet, Evelyne   +22 more
core   +7 more sources

Limbal stem cell transplantation: clinical results, limits, and perspectives [PDF]

, 2018
Limbal stem cell deficiency (LSCD) is a clinical condition characterized by damage of cornea limbal stem cells, which results in an impairment of corneal epithelium turnover and in an invasion of the cornea by the conjunctival epithelium.
Bruscolini, Alice, Lambiase, Alessandro, Rama, Paolo, Sacchetti, Marta   +3 more
core   +1 more source

Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations [PDF]

, 2018
Smooth muscle dysfunction syndrome (SMDS) due to heterozygous ACTA2 arginine 179 alterations is characterized by patent ductus arteriosus, vasculopathy (aneurysm and occlusive lesions), pulmonary arterial hypertension, and other complications in smooth ...
A Kikuchi, Alan C Braverman, AN Moosa, Anji Yetman, Anna L Mitchell, Anne Child, Anthony Estrera, AT Yetman, Birgit Lorenz, BL Loeys, Cori Feist, Denver Sallee, Dianna M Milewicz, DJ Schneider, DM Milewicz, Ellen S Regalado, ES Regalado, ES Roach, FM Roulez, Glen Iannucci, Hiroko Morisaki, HU Moller, J de Grazia, J Richer, JL Anderson, John R Ostergaard, Julie De Backer, Julie Richer, Kathryn C Chatfield, Kathryn W Holmes, Lauren Mellor-Crummey, LC Ades, Lesley Ades, LW Fung, M Al-Mohaissen, M Elizabeth Brickner, M Keir, MC Brodsky, ME Meuwissen, MM Georgescu, MR Amans, Mustafa Tekin, NJ Ullrich, P Munot, Patricia Musolino, Paul Mark, Reed Pyeritz, RV Lacro, S Prabhu, Shaine A Morris, Sherene Shalhub, Susan Benedict, T Logeswaran, Takayuki Morisaki, Timothy J Bradley, Y Arlachov   +55 more
core   +3 more sources