Skip Nav Destination
Close Modal
Update search
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
NARROW
Format
Subjects
Journal
Article Type
Issue Section
Date
Availability
1-5 of 5
Keywords: Corneal dystrophy
Close
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Sort by
Journal Articles
Subject Area:
Ophthalmology
Journal:
Ophthalmic Research
Ophthalmic Res (2023) 66 (1): 1114–1127.
Published Online: 25 July 2023
... recurrence was 17% (95% CI, 9%–24%) after trauma and 22% (95% CI, 11%–32%) in the corneal dystrophy group. Treatment-related adverse events included subepithelial haze, hyperopic shift, and decrease of the best spectacle-corrected visual acuity. In this study, the incidence of these events was 13% (95% CI, 6...
Journal Articles
Detailed Assessment of Renal Function in a Proband with Harboyan Syndrome Caused by a Novel Homozygous SLC4A11 Nonsense Mutation
Available to PurchaseSubject Area:
Ophthalmology
Petra Liskova, Lubica Dudakova, Vladimir Tesar, Vladimira Bednarova, Jana Kidorova, Katerina Jirsova, Alice E. Davidson, Alison J. Hardcastle
Journal:
Ophthalmic Research
Ophthalmic Res (2015) 53 (1): 30–35.
Published Online: 11 December 2014
... or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Harboyan syndrome SLC4A11 Corneal dystrophy Sensorineural hearing loss Kidney...
Journal Articles
Inherited Syndrome with Corneal Snowflake Dystrophy, Oculocutaneous Pigmentary Disturbances, Pseudoexfoliation and Malabsorption: Statistical Data of Some Symptoms
Available to PurchaseSubject Area:
Ophthalmology
Journal:
Ophthalmic Research
Ophthalmic Res (1987) 19 (5): 245–254.
Published Online: 04 December 2009
.... Corneal endothelium Corneal dystrophy Iris color Pseudoexfoliation Lactose intolerance Malabsorption Vitamin A Original Papers Ophthalmic Res. 19: 245-254 (1987) © 1987 S. Karger AG, Basel 0030-3747/87/0195-024 5$2.75/0 Inherited Syndrome with Corneal Snowflake Dystrophy, Oculocutaneous...
Journal Articles
Histopathogenic Study of the Macular Dystrophy of the Cornea: Fehr’s Dystrophy or Groenouw’s Type II
Available to PurchaseSubject Area:
Ophthalmology
Journal:
Ophthalmic Research
Ophthalmic Res (1975) 7 (4): 261–269.
Published Online: 03 December 2009
... or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Cornea Macular dystrophy Corneal dystrophy Histochemistry, Groenouw’s type II Fehr’s...
Journal Articles
Phenotype Associated with the H626P Mutation and Other Changes in the TGFBI Gene in Czech Families
Available to PurchaseSubject Area:
Ophthalmology
Petra Liskova, Gordon K. Klintworth, Brandy L. Bowling, Martin Filipec, Katerina Jirsova, Stephen J. Tuft, Shomi S. Bhattacharya, Alison J. Hardcastle, Neil D. Ebenezer
Journal:
Ophthalmic Research
Ophthalmic Res (2008) 40 (2): 105–108.
Published Online: 06 February 2008
... dominant corneal dystrophies. Methods: The coding sequence of the TGFBI gene was analysed in 22 affected Czech individuals from 7 apparently unrelated families. Comparison of phenotype to genotype was performed. Results: A H626P mutation, previously only described in a family with a variant of lattice...