57 results on '"ANIRIDIA"'
Search Results
2. Phenotypic Spectrum and Natural History of Gillespie Syndrome. An Updated Literature Review with 2 New Cases
3. Analysis of Phenotypes Associated with Deficiency of PAX6 Haplotypes in Chinese Aniridia Families
4. Effects of miR-204-5p modulation on PAX6 regulation and corneal inflammation
5. Modified technique for sutured scleral fixated intraocular lens in a patient with post-traumatic aniridia and aphakia: a case report
6. Outcome of illuminated microcatheter-assisted circumferential trabeculotomy following failed angle surgery in PAX6 aniridic glaucoma: a case report and literature review
7. Short Communication: Lived experience perspectives on genetic testing for a rare eye disease
8. A novel microdeletion of 517 kb downstream of the PAX6 gene in a Chinese family with congenital aniridia
9. A novel PAX6 variant as the cause of aniridia in a Chinese patient with SRRRD
10. ABE8e Corrects Pax6-Aniridic Variant in Humanized Mouse ESCs and via LNPs in Ex Vivo Cortical Neurons
11. Surgical correction of corneal opacity and aniridia with penetrating keratoplasty and a new iris prosthesis implant
12. Aniridia-related keratopathy relevant cell signaling pathways in human fetal corneas
13. Clinical outcomes and visual prognostic factors in congenital aniridia
14. Detection of a novel PAX6 variant in a Chinese family with multiple ocular abnormalities
15. Pupillenrekonstruktion mit einer künstlichen Iris
16. Improving long-term intraocular pressure and visual outcomes in eyes with aniridic glaucoma
17. Versorgung von vaskularisierten Hochrisikoaugen mittels Boston-Keratoprothese
18. First observation of secondary childhood glaucoma in Coffin-Siris syndrome: a case report and literature review
19. A novel variant in PAX6 as the cause of aniridia in a Chinese family
20. Indikationen und Operationsmethoden für die Implantation der Artificial Iris®
21. „Blaue Augen“ – Fallbericht über die Risiken von kosmetischen Irisimplantaten
22. Prognostic factors of pediatric glaucoma: a retrospective study
23. Expanding the phenotype of CRYAA nucleotide variants to a complex presentation of anterior segment dysgenesis
24. Functional outcomes after combined iris and intraocular lens implantation in various iris and lens defects
25. Identification of a novel PAX6 mutation in a Chinese family with aniridia
26. Mild aniridia phenotype: an under-recognized diagnosis of a severe inherited ocular disease
27. Implication of non-coding PAX6 mutations in aniridia
28. Topical bevacizumab treatment in aniridia
29. The genetics of aniridia — simple things become complicated
30. Outer retinal deformity detected by optical coherence tomography in eyes with foveal hypoplasia
31. Aniridia and Boston KPro: Is It a Long-Term Option?
32. Long-term results after artificial iris implantation in patients with aniridia
33. Abnormal cone ERGs in a family with congenital nystagmus and photophobia harboring a p.X423Lfs mutation in the PAX6 gene
34. A novel duplication in the PAX6 gene in a North Indian family with aniridia
35. Isolated foveal hypoplasia without nystagmus
36. Intraocular pressure control with Ahmed glaucoma drainage device in patients with cicatricial ocular surface disease-associated or aniridia-related glaucoma
37. 11p13 deletions can be more frequent than the PAX6 gene point mutations in Polish patients with aniridia
38. Clinical characteristics of high grade foveal hypoplasia
39. Künstliche Iris
40. Irisprothetik
41. Glaukome bei primären Irisveränderungen: Axenfeld-Rieger-Syndrome, ICE-Syndrome (essenzielle Irisatrophie, Chandler-Syndrom, Cogan-Reese-Syndrom), Aniridie
42. Genotype/phenotype association in Indian congenital aniridia
43. Combined pars plana vitrectomy and artificial iris diaphragm implant after globe rupture
44. Corneal Epithelial Stem Cells: Deficiency and Regulation
45. Three novel mutations of the PAX6 gene in Japanese aniridia patients
46. Klinische Erfahrungen bei der Verwendung eines Irisdiaphragmas
47. Recent progress in the biology and treatment of Wilms’ tumor
48. Billateral Polycystic Kidneys in a Girl with WAGR Syndrome
49. Retinal detachment with giant oral dialysis in an eye with congenital aniridia
50. De novo deletions in the paired domain of PAX6 in south Indian aniridic patients
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