A new approach to the classification of neonatal corneal opacities
暂无分享,去创建一个
[1] M. Terry,et al. Successful Descemet’s stripping automated endothelial keratoplasty for congenital hereditary endothelial dystrophy in a pediatric patient , 2012, International Ophthalmology.
[2] J. Ko,et al. A Novel Mutation of the Decorin Gene Identified in a Korean Family With Congenital Hereditary Stromal Dystrophy , 2011, Cornea.
[3] R. Hennekam,et al. Digenic inheritance of mutations in FOXC1 and PITX2 : Correlating transcription factor function and axenfeld‐rieger disease severity , 2011, Human mutation.
[4] Eileen Wang,et al. Unilateral keratitis following death of a twin as the presenting sign of herpetic infection in a neonate. , 2011, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.
[5] W. Xu,et al. Two novel mutations of the PAX6 gene causing different phenotype in a cohort of Chinese patients , 2011, Eye.
[6] M. Bitner-Glindzicz,et al. CYP1B1-related anterior segment developmental anomalies novel mutations for infantile glaucoma and von Hippel's ulcer revisited. , 2011, Ophthalmology.
[7] D. Lazzaro,et al. Peters Anomaly: Review of the Literature , 2011, Cornea.
[8] N. Bhagat,et al. Corneal Autograft and Allograft in a 10-Month-Old Premature Boy With Acquired Bilateral Corneal Opacities , 2011, Cornea.
[9] J. Sowden,et al. Chromosome abnormalities and the genetics of congenital corneal opacification , 2011, Molecular vision.
[10] S. Minoshima,et al. A case of aniridia with unilateral Peters anomaly. , 2011, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.
[11] S. Harding,et al. Indications and outcomes of deep anterior lamellar keratoplasty in children. , 2010, Ophthalmology.
[12] M. McKibbin,et al. Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma , 2010, Molecular vision.
[13] O. Bergès,et al. Vitreoretinal Dysplasia Masquerading as Peters’ Anomaly , 2010, European journal of ophthalmology.
[14] Arif O. Khan,et al. High measured intraocular pressure in children with recessive congenital hereditary endothelial dystrophy. , 2010, Journal of pediatric ophthalmology and strabismus.
[15] S. Mittal,et al. Infectious keratitis in a newborn with goldenhar syndrome. , 2010, Journal of pediatric ophthalmology and strabismus.
[16] R. Niederer,et al. Phenotypic characterisation and ZEB1 mutational analysis in posterior polymorphous corneal dystrophy in a New Zealand population , 2009, Molecular vision.
[17] G. Mirza,et al. Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies , 2009, Human mutation.
[18] D. Mackey,et al. Null mutations in LTBP2 cause primary congenital glaucoma. , 2009, American journal of human genetics.
[19] C. Wolf,et al. A clinical and molecular genetic study of German patients with primary congenital glaucoma. , 2009, American journal of ophthalmology.
[20] F. Malecaze,et al. Descemet Stripping Automated Endothelial Keratoplasty in a Child With Descemet Membrane Breaks After Forceps Delivery , 2009, Cornea.
[21] S. Krishnaiah,et al. Outcome of Penetrating Keratoplasty for Peters Anomaly , 2008, Cornea.
[22] C. Wolf,et al. A novel mutation in the FOXC1 gene in a family with Axenfeld–Rieger syndrome and Peters’ anomaly , 2008, Clinical genetics.
[23] B. Seitz,et al. The IC3D classification of the corneal dystrophies. , 2008, Cornea.
[24] K. Nischal,et al. Congenital corneal opacities – a surgical approach to nomenclature and classification , 2007, Eye.
[25] Arif O. Khan,et al. Bilateral congenital stromal cyst of the cornea. , 2007, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.
[26] P. Garg,et al. Coexistent Congenital Hereditary Endothelial Dystrophy and Congenital Glaucoma , 2007, Cornea.
[27] G. Zaidman,et al. Long-term visual prognosis in children after corneal transplant surgery for Peters anomaly type I. , 2007, American journal of ophthalmology.
[28] R. Wolfs,et al. Newborn with bilateral hazy corneas. , 2007, Bulletin de la Societe belge d'ophtalmologie.
[29] M. Walter,et al. Further support of the role of CYP1B1 in patients with Peters anomaly. , 2006, Molecular vision.
[30] U. Schlötzer-Schrehardt,et al. A new, X-linked endothelial corneal dystrophy. , 2006, American journal of ophthalmology.
[31] R. Melendez,et al. Isolated herpes simplex keratoconjunctivitis in a neonate born by cesarean delivery. , 2005, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.
[32] H. Grossniklaus,et al. Corneal perforation with secondary congenital aphakia in Peters anomaly. , 2002, Cornea.
[33] D. Rootman,et al. Corneal transplants for the treatment of congenital corneal opacities. , 2005, Journal of pediatric ophthalmology and strabismus.
[34] S. Golubović,et al. Surgical treatment of large corneal dermoid , 2005, Documenta Ophthalmologica.
[35] S. Yazdani,et al. Penetrating Keratoplasty in Young Children with Congenital Hereditary Endothelial Dystrophy , 2003, Cornea.
[36] Consultant Paediatrician,et al. Developmental outcome, including setback, in young children with severe visual impairment , 2002 .
[37] N. Dale,et al. Developmental outcome, including setback, in young children with severe visual impairment. , 2002, Developmental medicine and child neurology.
[38] M. Abdolell,et al. Outcome of lamellar keratoplasty for limbal dermoids in children. , 2002, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.
[39] J. Naor,et al. Clinicopathological correlation of congenital corneal opacification using ultrasound biomicroscopy , 2002, The British journal of ophthalmology.
[40] P. Carlsson,et al. A forkhead gene, FoxE3, is essential for lens epithelial proliferation and closure of the lens vesicle. , 2000, Genes & development.
[41] R. D. Stulting,et al. Long-term results of corneal graft survival in infants and children with peters anomaly. , 1999, Ophthalmology.
[42] M. Dana,et al. Corneal transplantation in young children with congenital hereditary endothelial dystrophy. Multicenter Pediatric Keratoplasty Study. , 1999, American journal of ophthalmology.
[43] T. Møller-Pedersen,et al. A morphological and functional study of Congenital Hereditary Endothelial Dystrophy. , 1998, Acta ophthalmologica Scandinavica.
[44] E. Bermejo,et al. Congenital eye malformations: clinical-epidemiological analysis of 1,124,654 consecutive births in Spain. , 1998, American journal of medical genetics.
[45] R. Dana,et al. Corneal Transplantation in Children with Peters Anomaly and Mesenchymal Dysgeneses , 1997 .
[46] D. Schaumberg,et al. Corneal transplantation in children with Peters anomaly and mesenchymal dysgenesis. Multicenter Pediatric Keratoplasty Study. , 1997, Ophthalmology.
[47] S. Bhattacharya,et al. Linkage of congenital hereditary endothelial dystrophy to chromosome 20. , 1995, Human molecular genetics.
[48] R. E. Smith,et al. Microbial keratitis in children. , 1986, Ophthalmology.
[49] G. Rogers,et al. Treatment of corneal opacification in mucolipidosis IV with conjunctival transplantation. , 1985, American journal of ophthalmology.
[50] J. H. Elliott,et al. Hereditary sclerocornea. , 1985, Archives of ophthalmology.
[51] P. Sonksen. THE ASSESSMENT OF ‘VISION FOR DEVELOPMENT’ IN SEVERELY VISUALLY HANDICAPPED BABIES , 1983, Acta ophthalmologica. Supplementum.
[52] S. Sanyal,et al. Dysgenetic lens (dyl)--a new gene in the mouse. , 1979, Investigative ophthalmology & visual science.
[53] I. Maumenee,et al. Clinical differentiation of recessive congenital hereditary endothelial dystrophy and dominant hereditary endothelial dystrophy. , 1978, American journal of ophthalmology.
[54] B. Johnson,et al. Peters' anomaly with the fetal transfusion syndrome. , 1976, American journal of ophthalmology-glaucoma.
[55] K. M. Zinn. Changes in corneal ultrastructure resulting from early lens removal in the developing chick embryo. , 1970, Investigative ophthalmology.