Results 41 to 50 of about 8,688 (228)

The significance of macrophage polarization subtypes for animal models of tissue fibrosis and human fibrotic diseases. [PDF]

, 2015
The systemic and organ-specific human fibrotic disorders collectively represent one of the most serious health problems world-wide causing a large proportion of the total world population mortality.
Ballater R, Beon M, Bryan N, Butterfield TA, Connolly MK, Desmoulière A, Fallowfield JA, Galván‐Peña S, Gordon S, Goumans M, Hu B, Ito T, Jimenez SA, Korns D, Krieg T, Lassen S, Lech M, Leibovich SJ, Lev B, Mantovani A, Mantovani A, Molumdar K, Nestle FO, O’Doherty U, Piera‐Velazquez S, Poland GA, Rafii R, Rigamonte E, Tacke F, Venbervliet B, Wang Y, Wick G, Wijesundera KK   +32 more
core   +2 more sources

Descemet membrane endothelial keratoplasty combined with secondary sulcus hydrophobic intraocular lens implantation

American Journal of Ophthalmology Case Reports
Purpose: To report a case of combined Descemet membrane endothelial keratoplasty (DMEK) and secondary sulcus hydrophobic intraocular lens (IOL) implantation for hyperopic correction in a pseudophakic eye with Fuchs’ endothelial corneal dystrophy ...
Colya N. Englisch, Philip Wakili, Clara E. Englisch, Karl T. Boden, Annekatrin Rickmann, Peter Szurman, André Messias   +6 more
doaj   +1 more source

Demographic profile and clinical characteristics of Fuchs' endothelial corneal dystrophy in a tertiary eye care center

Indian Journal of Ophthalmology, 2023
Purpose: This study was performed to determine the demographic profile and clinical characteristics in patients with Fuchs' endothelial corneal dystrophy (FECD) reporting to a tertiary eye care center in India.
Pratik Bhadra, Sonali Sahoo, Srikant K Sahu, Smrutirekha Priyadarshini, Amrita Mohanty, Sujata Das   +5 more
doaj   +1 more source

Hydrophilic intraocular lens opacification after posterior lamellar keratoplasty - a material analysis with special reference to optical quality assessment [PDF]

, 2017
Background: Laboratory analysis and optical quality assessment of explanted hydrophilic intraocular lenses (IOLs) with clinically significant opacification after posterior lamellar keratoplasty (DMEK and DSAEK).
Auerbach, Florian N., Auffarth, Gerd U., Choi, Chul Y., Giers, Bert C., Khoramnia, Ramin, Mayer, Christian, Sel, Saadettin, Tandogan, Tamer   +7 more
core   +1 more source

Increased Clusterin Expression in Fuchs’ Endothelial Dystrophy [PDF]

Investigative Opthalmology & Visual Science, 2008
To investigate the differential expression of the glycoprotein clusterin/apoJ (CLU) in normal and Fuchs' endothelial dystrophy (FED) corneal endothelium and to compare the expression of various forms of CLU in normal and FED tissue.FED and pseudophakic bullous keratopathy (PBK) corneal buttons were removed during transplantation, and normal corneas ...
Ula V, Jurkunas, Maya S, Bitar, Ian, Rawe, Deshea L, Harris, Kathryn, Colby, Nancy C, Joyce   +5 more
openaire   +2 more sources

Exploring the histopathological signature of repeat‐mediated Fuchs endothelial corneal dystrophy

Acta Ophthalmologica, EarlyView.
Abstract Purpose To determine the histological differences between Fuchs endothelial corneal dystrophy (FECD) cases with and without the most common genetic risk factor, expansion of a CTG repeat (CTG18.1) within the TCF4 gene. Methods Formalin‐fixed paraffin‐embedded corneal tissues were compared retrospectively, and CTG18.1 status was determined from
Anne‐Marie S. Kladny, Nihar Bhattacharyya, Marcos Abreu Costa, Stephen J. Tuft, Caroline Thaung, Alice E. Davidson   +5 more
wiley   +1 more source

Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy

Nature Communications, 2017
Fuchs endothelial corneal dystrophy (FECD) is one of the most common reasons for corneal transplantation, and is known to cluster in families. Here, the authors discover new genetic loci associated with FECD with sex-specific effects and implications for
Natalie A. Afshari, Robert P. Igo, Nathan J. Morris, Dwight Stambolian, Shiwani Sharma, V. Lakshmi Pulagam, Steven Dunn, John F. Stamler, Barbara J. Truitt, Jacqueline Rimmler, Abraham Kuot, Christopher R. Croasdale, Xuejun Qin, Kathryn P. Burdon, S. Amer Riazuddin, Richard Mills, Sonja Klebe, Mollie A. Minear, Jiagang Zhao, Elmer Balajonda, George O. Rosenwasser, Keith H Baratz, V. Vinod Mootha, Sanjay V. Patel, Simon G. Gregory, Joan E. Bailey-Wilson, Marianne O. Price, Francis W. Price, Jamie E. Craig, John H. Fingert, John D. Gottsch, Anthony J. Aldave, Gordon K. Klintworth, Jonathan H. Lass, Yi-Ju Li, Sudha K. Iyengar   +35 more
doaj   +1 more source

Génexpresszió Fuchs-dystrophiában, pseudophakiás bullosus keratopathiában és keratoconusban = Gene expression in Fuchs' dystrophy, pseudophakic bullous keratopathy and keratoconus [PDF]

, 2009
A Fuchs dystrophia (dystrophia corneae endo-, epithelialis) és a pseudophakiás bullosus keratopathia a hasonló klinikai képet mutat, mindkettő alapja a cornea endothelsejtjeinek degenerációja.
Szentmáry, Nóra, Süveges, Ildikó
core  

A comparison of endothelial and penetrating keratoplasty outcomes following failed penetrating keratoplasty: a registry study [PDF]

, 2016
Author version made available in accordance with publisher copyright policy.Purpose To compare graft survival and visual outcomes for endothelial keratoplasty (EK) after a first penetrating keratoplasty (PK), with outcomes of repeat PK after a first ...
Australian Corneal Graft Registry, Contributors, Coster, Douglas John, Galettis, Rachel A, Keane, Miriam Claire, Mills, Richard Arthur, Williams, Keryn Anne   +5 more
core   +1 more source

Fuchs' Endothelial and Myotonic Dystrophies: Corneal Dystrophy in Myotonic Patients [PDF]

Investigative Opthalmology & Visual Science, 2017
n ...
De Bernardo, Maddalena, Rosa, Nicola
openaire   +3 more sources