What does the future hold for the treatment of Fuchs endothelial dystrophy; will ‘keratoplasty’ still be a valid procedure?
暂无分享,去创建一个
C. Tong | G. Melles | M. Bruinsma | C. Tong | G. Melles
[1] J. Zavala,et al. Corneal endothelium: developmental strategies for regeneration , 2013, Eye.
[2] K. Goins,et al. Confirmation of the association between the TCF4 risk allele and Fuchs endothelial corneal dystrophy in patients from the Midwestern United States , 2013, Ophthalmic genetics.
[3] N. Koizumi,et al. The ROCK inhibitor eye drop accelerates corneal endothelium wound healing. , 2013, Investigative ophthalmology & visual science.
[4] J. Błasiak,et al. DNA damage and repair in Fuchs endothelial corneal dystrophy , 2012, Molecular Biology Reports.
[5] Nirubol Tosakulwong,et al. A Common Trinucleotide Repeat Expansion within the Transcription Factor 4 (TCF4, E2-2) Gene Predicts Fuchs Corneal Dystrophy , 2012, PloS one.
[6] P. Gain,et al. Revisited Microanatomy of the Corneal Endothelial Periphery: New Evidence for Continuous Centripetal Migration of Endothelial Cells in Humans , 2012, Stem cells.
[7] S. Iyengar,et al. Differing Roles for TCF4 and COL8A2 in Central Corneal Thickness and Fuchs Endothelial Corneal Dystrophy , 2012, PloS one.
[8] Cailing Liu,et al. Decline in DJ-1 and decreased nuclear translocation of Nrf2 in Fuchs endothelial corneal dystrophy. , 2012, Investigative ophthalmology & visual science.
[9] I. Dapena,et al. Recipient endothelium may relate to corneal clearance in descemet membrane endothelial transfer. , 2012, American journal of ophthalmology.
[10] N. Koizumi,et al. ROCK inhibitor converts corneal endothelial cells into a phenotype capable of regenerating in vivo endothelial tissue. , 2012, The American journal of pathology.
[11] David S. Parker,et al. Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy. , 2012, American journal of human genetics.
[12] U. Jurkunas,et al. Molecular bases of corneal endothelial dystrophies. , 2012, Experimental eye research.
[13] A. Hewitt,et al. Association of TCF4 and CLU polymorphisms with Fuchs’ endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process , 2012, European Journal of Human Genetics.
[14] T. Fuchsluger,et al. p53-regulated increase in oxidative-stress--induced apoptosis in Fuchs endothelial corneal dystrophy: a native tissue model. , 2011, Investigative ophthalmology & visual science.
[15] Laurence E. Frank,et al. Efficacy of descemet membrane endothelial keratoplasty: clinical outcome of 200 consecutive cases after a learning curve of 25 cases. , 2011, Archives of ophthalmology.
[16] Laurence E. Frank,et al. Patterns of corneal endothelialization and corneal clearance after descemet membrane endothelial keratoplasty for fuchs endothelial dystrophy. , 2011, American journal of ophthalmology.
[17] J. Mehta,et al. Association of TCF4 gene polymorphisms with Fuchs' corneal dystrophy in the Chinese. , 2011, Investigative ophthalmology & visual science.
[18] S. Gregory,et al. Replication of TCF4 through Association and Linkage Studies in Late-Onset Fuchs Endothelial Corneal Dystrophy , 2011, PloS one.
[19] N. Katsanis,et al. Replication of the TCF4 intronic variant in late-onset Fuchs corneal dystrophy and evidence of independence from the FCD2 locus. , 2011, Investigative ophthalmology & visual science.
[20] N. Koizumi,et al. Enhancement of corneal endothelium wound healing by Rho-associated kinase (ROCK) inhibitor eye drops , 2011, British Journal of Ophthalmology.
[21] R. Tandon,et al. Congenital hereditary endothelial dystrophy - mutation analysis of SLC4A11 and genotype-phenotype correlation in a North Indian patient cohort , 2010, Molecular vision.
[22] U. Jurkunas,et al. Evidence of oxidative stress in the pathogenesis of fuchs endothelial corneal dystrophy. , 2010, The American journal of pathology.
[23] N. Katsanis,et al. Missense mutations in the sodium borate cotransporter SLC4A11 cause late‐onset Fuchs corneal dystrophy a , 2010, Human mutation.
[24] U. Jurkunas,et al. Fuchs endothelial corneal dystrophy. , 2010, The ocular surface.
[25] Informatics,et al. E2-2 Protein and Fuchs's Corneal Dystrophy , 2022 .
[26] U. Stenevi,et al. Donor and recipient endothelial cell population of the transplanted human cornea: a two-dimensional imaging study. , 2010, Investigative ophthalmology & visual science.
[27] M. Srinivasan,et al. Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India , 2010, BMC ophthalmology.
[28] Caroline L. Speck,et al. Unfolded protein response in fuchs endothelial corneal dystrophy: a unifying pathogenic pathway? , 2010, American journal of ophthalmology.
[29] Nicholas Katsanis,et al. Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p. , 2010, American journal of human genetics.
[30] N. Katsanis,et al. Linkage of a mild late-onset phenotype of Fuchs corneal dystrophy to a novel locus at 5q33.1-q35.2. , 2009, Investigative ophthalmology & visual science.
[31] G. Melles,et al. Spontaneous corneal clearance despite graft detachment in descemet membrane endothelial keratoplasty. , 2009, American journal of ophthalmology.
[32] U. Stenevi,et al. Survival of donor-derived cells in human corneal transplants. , 2009, Investigative ophthalmology & visual science.
[33] N. Joyce,et al. Relationship among oxidative stress, DNA damage, and proliferative capacity in human corneal endothelium. , 2009, Investigative ophthalmology & visual science.
[34] N. Joyce,et al. Differential protein expression in human corneal endothelial cells cultured from young and older donors , 2008, Molecular vision.
[35] T. Aung,et al. SLC4A11 mutations in Fuchs endothelial corneal dystrophy. , 2008, Human molecular genetics.
[36] F. Yu,et al. Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal hernia , 2007, American journal of medical genetics. Part A.
[37] D. Coster,et al. The Immunobiology of Corneal Transplantation , 2007, Transplantation.
[38] W. Green,et al. Advanced glycation end products and receptors in Fuchs' dystrophy corneas undergoing Descemet's stripping with endothelial keratoplasty. , 2007, Ophthalmology.
[39] M. Abramowicz,et al. Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy , 2007, Journal of Medical Genetics.
[40] G. Melles. Posterior lamellar keratoplasty: DLEK to DSEK to DMEK. , 2006, Cornea.
[41] K. Broman,et al. A common locus for late-onset Fuchs corneal dystrophy maps to 18q21.2-q21.32. , 2006, Investigative ophthalmology & visual science.
[42] M. Salto‐Tellez,et al. Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2) , 2006, Nature Genetics.
[43] M. Boehnke,et al. Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells. , 2005, American journal of human genetics.
[44] S. Lowe,et al. Control of apoptosis by p53 , 2003, Oncogene.
[45] Robert W. Thompson,et al. Long-term graft survival after penetrating keratoplasty. , 2003, Ophthalmology.
[46] K. Colby,et al. Mechanisms of disease: Fuchs' endothelial dystrophy. , 2002, Ophthalmology clinics of North America.
[47] M. Kenney,et al. Evidence of Oxidative Stress in Human Corneal Diseases , 2002, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.
[48] W. Green,et al. The role of apoptosis in the pathogenesis of Fuchs endothelial dystrophy of the cornea. , 2001, A M A Archives of Ophthalmology.
[49] M. Baudrimont,et al. Corneal endothelial cell apoptosis in patients with Fuchs' dystrophy. , 2000, Investigative ophthalmology & visual science.
[50] J. Bergmanson,et al. Fuchs' endothelial dystrophy: a fresh look at an aging disease , 1999, Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians.
[51] W. Green,et al. Analysis of sex-mismatched human corneal transplants by fluorescence in situ hybridization of the sex-chromosomes. , 1999, Experimental eye research.
[52] D. Hodge,et al. Ten-year postoperative results of penetrating keratoplasty. , 1998, Ophthalmology.
[53] A. Adamis,et al. Fuchs' endothelial dystrophy of the cornea. , 1993, Survey of ophthalmology.
[54] E. G. Olsen,et al. THE HEALING OF HUMAN CORNEAL ENDOTHELIUM An in vitro study , 1984, Acta ophthalmologica.
[55] Prof. Dr. Ernst Fuchs. Dystrophia epithelialis corneae , 1910, Albrecht von Graefe's Archiv fur Ophthalmologie.
[56] G. van Rij,et al. Spontaneous corneal clearing after Descemet's stripping. , 2013, Ophthalmology.
[57] S. Proulx,et al. Culture of human corneal endothelial cells isolated from corneas with Fuchs endothelial corneal dystrophy. , 2012, Experimental eye research.
[58] M. Moshirfar,et al. Descemet ’ s Membrane Endothelial Keratoplasty , 2011 .
[59] J. Guyette,et al. Strategies for regeneration of heart muscle. , 2010, Critical reviews in eukaryotic gene expression.
[60] J. Mehta,et al. Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset Fuchs endothelial corneal dystrophy. , 2008, Investigative ophthalmology & visual science.
[61] B. Seitz,et al. The IC3D classification of the corneal dystrophies. , 2008, Cornea.
[62] K. Broman,et al. Linkage of late-onset Fuchs corneal dystrophy to a novel locus at 13pTel-13q12.13. , 2006, Investigative ophthalmology & visual science.
[63] S. Wilson,et al. Fuchs' dystrophy. , 1988, Cornea.