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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1997 1
1998 1
1999 2
2000 1
2001 2
2002 1
2003 2
2007 1
2008 1
2011 1
2018 1
2023 1
2024 0

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14 results

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Page 1
Genetic predisposition to ocular surface disorders and opportunities for gene-based therapies.
Roshandel D, Semnani F, Rayati Damavandi A, Masoudi A, Baradaran-Rafii A, Watson SL, Morgan WH, McLenachan S. Roshandel D, et al. Ocul Surf. 2023 Jul;29:150-165. doi: 10.1016/j.jtos.2023.05.003. Epub 2023 May 14. Ocul Surf. 2023. PMID: 37192706 Free article. Review.
Gene defects may result in congenital ocular or systemic disorders with prominent ocular surface involvement. Examples include epithelial corneal dystrophies, aniridia, ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome, xeroderma pigmentosum (XP), and heredi …
Gene defects may result in congenital ocular or systemic disorders with prominent ocular surface involvement. Examples include epithelial
Stage-related therapy of corneal dystrophies.
Seitz B, Lisch W. Seitz B, et al. Dev Ophthalmol. 2011;48:116-153. doi: 10.1159/000324081. Epub 2011 Apr 26. Dev Ophthalmol. 2011. PMID: 21540634 Review.
Corneal dystrophies typically result in a gradual bilateral loss of vision in a primary 'white eye' - often in conjunction with epithelial defects in later stages. ...The therapy of endothelial dystrophies depends on diagnosis and age: Fuchs endothelial corneal
Corneal dystrophies typically result in a gradual bilateral loss of vision in a primary 'white eye' - often in conjunction with ep
[Recurrent Corneal Erosions in Epithelial Corneal Dystrophies].
Geerling G, Lisch W, Finis D. Geerling G, et al. Klin Monbl Augenheilkd. 2018 Jun;235(6):697-701. doi: 10.1055/a-0611-5783. Epub 2018 Jun 12. Klin Monbl Augenheilkd. 2018. PMID: 29895083 Review. German.
Epithelial basement membrane dystrophy (EBMD), epithelial recurrent erosion dystrophy (ERED) and Francheschetti and Meesmann's epithelial corneal dystrophy (MECD) can all - besides other signs and symptoms - result in more o
Epithelial basement membrane dystrophy (EBMD), epithelial recurrent erosion dystrophy (ERED) and Francheschetti
Phenotypic variability in Meesmann's dystrophy: clinical review of the literature and presentation of a family genetically identical to the original family.
Ehlers N, Hjortdal J, Nielsen K, Thiel HJ, Ørntoft T. Ehlers N, et al. Acta Ophthalmol. 2008 Feb;86(1):40-4. doi: 10.1111/j.1600-0420.2007.00931.x. Epub 2007 Nov 6. Acta Ophthalmol. 2008. PMID: 17986293 Free article. Review.
PURPOSE: To describe the phenotypic variability in Meesmann's microcystic dystrophy of the corneal epithelium based on a review of the literature and the presentation of a Danish family. ...The remaining 15% demonstrated variants with microcysts in the upper …
PURPOSE: To describe the phenotypic variability in Meesmann's microcystic dystrophy of the corneal epithelium based on …
Unilateral Meesmann's dystrophy.
Goldberg A, Schlötzer-Schrehardt U, Seiler T. Goldberg A, et al. Int Ophthalmol. 1997;21(3):117-20. doi: 10.1023/a:1026456232212. Int Ophthalmol. 1997. PMID: 9587826 Review.
We report the first case of a unilateral microcystic Meesmann's epithelial dystrophy, observed in the left cornea of a 43-year-old patient. The diagnosis was verified histologically by the unilateral occurrence of a 'peculiar substance' within epithelial
We report the first case of a unilateral microcystic Meesmann's epithelial dystrophy, observed in the left cornea of a …
Characteristics of the human ocular surface epithelium.
Kinoshita S, Adachi W, Sotozono C, Nishida K, Yokoi N, Quantock AJ, Okubo K. Kinoshita S, et al. Prog Retin Eye Res. 2001 Sep;20(5):639-73. doi: 10.1016/s1350-9462(01)00007-6. Prog Retin Eye Res. 2001. PMID: 11470454 Review.
Here, we review five important aspects of the human ocular surface epithelium. First, we recognize the discovery of corneal epithelial stem cells, and note how the palisades of Vogt have been suggested as a clinical marker of their presence. ...Third, we touch upon …
Here, we review five important aspects of the human ocular surface epithelium. First, we recognize the discovery of corneal epithe
The molecular genetics of the corneal dystrophies--current status.
Klintworth GK. Klintworth GK. Front Biosci. 2003 May 1;8:d687-713. doi: 10.2741/1018. Front Biosci. 2003. PMID: 12700042 Review.
The pertinent literature on inherited corneal diseases is reviewed in terms of the chromosomal localization and identification of the responsible genes. Disorders affecting the cornea have been mapped to human chromosome 1 (central crystalline corneal dystrophy
The pertinent literature on inherited corneal diseases is reviewed in terms of the chromosomal localization and identification of the …
The molecular genetics of keratin disorders.
Smith F. Smith F. Am J Clin Dermatol. 2003;4(5):347-64. doi: 10.2165/00128071-200304050-00005. Am J Clin Dermatol. 2003. PMID: 12688839 Review.
Keratins are the type I and II intermediate filament proteins which form a cytoskeletal network within all epithelial cells. They are expressed in pairs in a tissue- and differentiation-specific fashion. ...These include ichthyosis bullosa of Siemens (K2e), epidermolytic p …
Keratins are the type I and II intermediate filament proteins which form a cytoskeletal network within all epithelial cells. They are …
Structure, development and function of cytoskeletal elements in non-neuronal cells of the human eye.
Kivelä T, Uusitalo M. Kivelä T, et al. Prog Retin Eye Res. 1998 Jul;17(3):385-428. doi: 10.1016/s1350-9462(98)00001-9. Prog Retin Eye Res. 1998. PMID: 9695798 Review.
Nevertheless, potentially meaningful changes have already been observed in corneal dystrophies (Meesmann's dystrophy, posterior polymorphous dystrophy and iridocorneal endothelial syndrome), degenerations (pterygium) and inflammatory diseases (Pseudomo …
Nevertheless, potentially meaningful changes have already been observed in corneal dystrophies (Meesmann's dystrophy, p …
[Corneal dystrophies in the light of modern molecular genetic research].
Auw-Hädrich C, Witschel H. Auw-Hädrich C, et al. Ophthalmologe. 2002 Jun;99(6):418-26. doi: 10.1007/s00347-002-0645-6. Ophthalmologe. 2002. PMID: 12125408 Review. German.
Lattice dystrophy Type II is part of the Meretoja syndrome, a systemic amyloidosis, and is caused by a mutation of the gelsoline gene on chromosome 9 (9q34). Gelsoline is also predominantly expressed in the corneal epithelium. In addition, the responsible genes, the …
Lattice dystrophy Type II is part of the Meretoja syndrome, a systemic amyloidosis, and is caused by a mutation of the gelsoline gene …
14 results