Disease: Corneal dystrophy- lattice- type 2
- A case of lattice corneal dystrophy type 1 with bilateral Mooren's ulcer
- A clinical and molecular genetic study of autosomal-dominant stromal corneal dystrophy in British population
- A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophy
- A new mutation (A546T) of the betaig-h3 gene responsible for a French lattice corneal dystrophy type IIIA
- A novel nonsense mutation with a compound heterozygous mutation in TGFBI gene in lattice corneal dystrophy type I
- Allelic homogeneity in Avellino corneal dystrophy due to a founder effect
- Alterations of epithelial adhesion molecules and basement membrane components in lattice corneal dystrophy (LCD)
- Amyloid fibril protein in familial amyloidosis with cranial neuropathy and corneal lattice dystrophy (FAP type IV) is related to transthyretin
- Amyloidosis and Ocular Involvement: an Overview
- An analysis of BIGH3 mutations in patients with corneal dystrophies in the Kyushu district of Japan
- Analyses of TGFBI gene mutation spectrum in four Chinese families with corneal dystrophy
- Benzalkonium chloride accelerates the formation of the amyloid fibrils of corneal dystrophy-associated peptides
- Case report of Cogan-like dystrophy diagnosed as confirmed type I lattice corneal dystrophy in a 10-year-old child
- Cell proliferation and apoptosis in stromal corneal dystrophies
- Changes of clinical manifestation of granular corneal deposits because of recurrent corneal erosion in granular corneal dystrophy types 1 and 2
- Classic lattice corneal dystrophy: a brief review and summary of treatment modalities
- Clinical and genetic features of TGFBI-linked corneal dystrophies in Mexican population: description of novel mutations and novel genotype-phenotype correlations
- Clinical outcome of eight BIGH3-linked corneal dystrophies
- Combined granular-lattice ('Avellino') corneal dystrophy
- Comparative Study of Anterior Eye Segment Measurements with Spectral Swept-Source and Time-Domain Optical Coherence Tomography in Eyes with Corneal Dystrophies
- Composition and proteolytic processing of corneal deposits associated with mutations in the TGFBI gene
- Corneal changes of uncertain etiology in mesoendemic onchocercal communities of Northern Nigeria
- Corneal dystrophies in the light of modern molecular genetic research
- Corneal Higher Order Aberrations in Granular, Lattice and Macular Corneal Dystrophies
- Corneal irregularity and visual function using anterior segment optical coherence tomography in TGFBI corneal dystrophy
- Corneal morphology and sensitivity in lattice dystrophy type II (familial amyloidosis, Finnish type)
- Danish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type)
- Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies Groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOX
- Destruction of amyloid fibrils of keratoepithelin peptides by laser irradiation coupled with amyloid-specific thioflavin T
- Detailed phenotypic description of stromal corneal dystrophy in a large pedigree carrying the uncommon TGFBI p.Ala546Asp pathogenic variant
- Development of a Transgenic Mouse with R124H Human TGFBI Mutation Associated with Granular Corneal Dystrophy Type 2
- Development of allele-specific gene-silencing siRNAs for TGFBI Arg124Cys in lattice corneal dystrophy type I
- Epigallocatechin Gallate Remodels Fibrils of Lattice Corneal Dystrophy Protein, Facilitating Proteolytic Degradation and Preventing Formation of Membrane-Permeabilizing Species
- Factors Affecting Formation of Type-1 and Type-2 Big Bubble during Deep Anterior Lamellar Keratoplasty
- Familial amyloid polyneuropathy type IV (Finnish type)--a clinicopathological study
- Fibrillin-2, tenascin-C, matrilin-2, and matrilin-4 are strongly expressed in the epithelium of human granular and lattice type I corneal dystrophies
- Frequency, distribution, and outcome of keratoplasty for corneal dystrophies at a tertiary eye care center in South India
- Gelsolin amyloidosis: genetics, biochemistry, pathology and possible strategies for therapeutic intervention
- Gelsolin immunoreactivity in corneal amyloid, wound healing, and macular and granular dystrophies
- Gene analysis of Japanese patients with familial amyloidotic polyneuropathy type IV
- Genetic refinement of the chromosome 5q lattice corneal dystrophy type I locus to within a 2 cM interval
- Genotypic Homogeneity in Distinctive Transforming Growth Factor-Beta Induced (TGFBI) Protein Phenotypes
- Haplotype analysis in gelsolin-related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and Japan
- Heterogeneity in granular corneal dystrophy: identification of three causative mutations in the TGFBI (BIGH3) gene-lessons for corneal amyloidogenesis
- Histopathological study of lattice corneal dystrophy with L 527 R mutation of transforming growth factor-beta induced gene
- Immunohistology of kerato-epithelin in corneal stromal dystrophies associated with R124 mutations of the BIGH3 gene
- Immunolocalization of beta ig-h3 protein in 5q31-linked corneal dystrophies and normal corneas
- In vitro amyloid aggregate forming ability of TGFBI mutants that cause corneal dystrophies
- In vitro creation of amyloid fibrils from native and Arg124Cys mutated betaIGH3((110-131)) peptides, and its relevance for lattice corneal amyloid dystrophy type I
- Inherited corneal amyloidosis predominantly manifested in one eye
- Intracorneal granulomatous inflammation
- Lattice corneal dystrophy type 1: an epithelial or stromal entity?
- Lattice corneal dystrophy type II with familial amyloid polyneuropathy type IV
- Lattice corneal dystrophy type II with familial amyloid polyneuropathy type IV
- Lattice degeneration of the retina
- Low-Carbohydrate Diet Macronutrient Quality and Weight Change
- Mapping of Reis-Bucklers' corneal dystrophy to chromosome 5q
- Molecular genetic analysis of the BIGH3 gene in lattice type I (Biber-Haab-Dimmer) and granular type II (Avellino) corneal dystrophy: is indirect mutation analysis for hot spots recommended?
- Molecular genetic and histopathological examinations for genotype-phenotype analysis in patients with TGFBI-linked corneal dystrophy
- Mutation Analysis of the TGFBI Gene in Consecutive Korean Patients With Corneal Dystrophies
- Mutation hot spots in 5q31-linked corneal dystrophies
- Mutation in transforming growth factor beta induced protein associated with granular corneal dystrophy type 1 reduces the proteolytic susceptibility through local structural stabilization
- New mode of treatment for lattice corneal dystrophy type I: corneal epithelial debridement and fibronectin eye drops
- Novel and known mutations of TGFBI, their genotype-phenotype correlation and structural modeling in 3 Chinese families with lattice corneal dystrophy
- Novel mutation (V505D) of the TGFBI gene found in a Chinese family with lattice corneal dystrophy, type I
- On the role of kerato-epithelin in the pathogenesis of 5q31-linked corneal dystrophies
- Pathogenesis and treatments of TGFBI corneal dystrophies
- Pharmaceutical modulation of the proteolytic profile of Transforming Growth Factor Beta induced protein (TGFBIp) offers a new avenue for treatment of <em>TGFBI</em>-corneal dystrophy
- Pharmaceutical modulation of the proteolytic profile of Transforming Growth Factor Beta induced protein (TGFBIp) offers a new avenue for treatment of TGFBI-corneal dystrophy
- Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech families
- Phenotype-genotype correlations in patients with TGFBI-linked corneal dystrophies in Taiwan
- Pituicytoma with gelsolin amyloid deposition
- Polymicrobial Keratitis With Cryptococcus curvatus, Candida parapsilosis, and Stenotrophomonas maltophilia After Penetrating Keratoplasty: A Rare Case Report With Literature Review
- Prevalence of transforming growth factor beta-induced gene corneal dystrophies in Chinese refractive surgery candidates
- Prevalence of transforming growth factor β-induced gene corneal dystrophies in Chinese refractive surgery candidates
- Progressive cranial nerve involvement and grading of facial paralysis in gelsolin amyloidosis
- Protein Composition of TGFBI-R124C- and TGFBI-R555W-Associated Aggregates Suggests Multiple Mechanisms Leading to Lattice and Granular Corneal Dystrophy
- Rare stromal corneal dystrophic diseases in Oman: A clinical and histopathological analysis for accurate diagnosis
- Recurrence of the clinical signs of lattice corneal dystrophy (type I) in corneal transplants
- Recurrent Amyloid Material in Grafts Used in Patients with Lattice Corneal Dystrophy 2 (Meretoja's Syndrome)
- Spheroidal degeneration in H626R TGFBI variant lattice dystrophy: a multimodality analysis
- Surgical outcomes of re-excimer laser phototherapeutic keratectomy (re-PTK)
- Systemic investigation of keratoepithelin deposits in TGFBI/BIGH3-related corneal dystrophy
- TGFBI and CHST6 gene analysis in Chinese stromal corneal dystrophies
- TGFBI gene mutations analysis in Chinese families with corneal dystrophies
- TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients
- TGFBI gene mutations in a Korean population with corneal dystrophy
- TGFBI mutation screening and genotype-phenotype correlation in north Indian patients with corneal dystrophies
- TGFBI, CHST6, and GSN gene analysis in Mexican patients with stromal corneal dystrophies
- The First Argentinian Family with Familial Amyloidosis of the Finnish Type
- The Gelsolin Pathogenic D187N Mutant Exhibits Altered Conformational Stability and Forms Amyloidogenic Oligomers
- The molecular genetics of the corneal dystrophies--current status
- The pathogenesis and treatment of corneal disorders
- Topical Losartan: Practical Guidance for Clinical Trials in the Prevention and Treatment of Corneal Scarring Fibrosis and Other Eye Diseases and Disorders
- Transforming growth factor beta induced mutation-associated phenotype in a Chinese family exhibiting lattice corneal dystrophy
- Transforming growth factor β induced mutation-associated phenotype in a Chinese family exhibiting lattice corneal dystrophy
- Treatment of corneal dystrophies with phototherapeutic keratectomy
- Unilateral corneal lattice dystrophy
- Unique TGFBI protein in lattice corneal dystrophy
- What can we learn from molecular genetic analyses of inherited eye diseases?