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Publications
10
Citations
1404
max across sources
Profile views
5
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Verification
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Overview
AI-generatedWalter Lisch (RTX-00000069) based in DE is a researcher on ResearchTrics. Lists research interests: corneal surgery and disorders, corneal surgery and treatments, liver disease diagnosis and treatment, metabolism and genetic disorders, ocular surface and contact lens. Has 10 publications recorded, including "IC3D Classification of Corneal Dystrophies—Edition 3" (2024), "Clinical and genetic update of corneal dystrophies" (2019), "IC3D Classification of Corneal Dystrophies—Edition 2" (2015).
An AI overview generated from this profile’s verified records — an interpretation, not a verified statement.
Research interests
- corneal surgery and disorders
- corneal surgery and treatments
- liver disease diagnosis and treatment
- metabolism and genetic disorders
- ocular surface and contact lens
Publications (20)
- IC3D Classification of Corneal Dystrophies—Edition 3102 cites
Cornea · 2024 · DOI
- IC3D Classification of Corneal Dystrophies—Edition 3102 cites
Cornea · 2024 · DOI
- Clinical and genetic update of corneal dystrophies54 cites
Experimental Eye Research · 2019 · DOI
- Clinical and genetic update of corneal dystrophies54 cites
Experimental Eye Research · 2019 · DOI
- IC3D Classification of Corneal Dystrophies—Edition 2518 cites
Cornea · 2015 · DOI
- IC3D Classification of Corneal Dystrophies—Edition 2518 cites
Cornea · 2015 · DOI
- Chameleon-like Appearance of Immunotactoid Keratopathy50 cites
Cornea · 2011 · DOI
- Chameleon-like Appearance of Immunotactoid Keratopathy50 cites
Cornea · 2011 · DOI
- Stage-Related Therapy of Corneal Dystrophies51 cites
Developments in ophthalmology · 2011 · DOI
- Stage-Related Therapy of Corneal Dystrophies51 cites
Developments in ophthalmology · 2011 · DOI
- The IC3D Classification of the Corneal Dystrophies351 cites
Cornea · 2008 · DOI
- The IC3D Classification of the Corneal Dystrophies351 cites
Cornea · 2008 · DOI
- Mutations in the<i>UBIAD1</i>Gene on Chromosome Short Arm 1, Region 36, Cause Schnyder Crystalline Corneal Dystrophy103 cites
Investigative Ophthalmology & Visual Science · 2007 · DOI
- Mutations in the<i>UBIAD1</i>Gene on Chromosome Short Arm 1, Region 36, Cause Schnyder Crystalline Corneal Dystrophy103 cites
Investigative Ophthalmology & Visual Science · 2007 · DOI
- A New, X-linked Endothelial Corneal Dystrophy60 cites
American Journal of Ophthalmology · 2006 · DOI
- A New, X-linked Endothelial Corneal Dystrophy60 cites
American Journal of Ophthalmology · 2006 · DOI
- Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to Xp22.357 cites
American Journal of Ophthalmology · 2000 · DOI
- Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to Xp22.357 cites
American Journal of Ophthalmology · 2000 · DOI
- A New, Band-shaped and Whorled Microcystic Dystrophy of the Corneal Epithelium58 cites
American Journal of Ophthalmology · 1992 · DOI
- A New, Band-shaped and Whorled Microcystic Dystrophy of the Corneal Epithelium58 cites
American Journal of Ophthalmology · 1992 · DOI
