Disease: Schnyder Crystalline Corneal dystrophy
- A case of Schnyder corneal dystrophy with crystals
- A Mouse Model of Schnyder Corneal Dystrophy with the N100S Point Mutation
- A mutation in the UBIAD1 gene in a Han Chinese family with Schnyder corneal dystrophy
- A novel UBIAD1 mutation identified in a Chinese family with Schnyder crystalline corneal dystrophy
- Analysis of fifteen positional candidate genes for Schnyder crystalline corneal dystrophy
- Application of homozygosity haplotype analysis to genetic mapping with high-density SNP genotype data
- Central corneal mosaic opacities in Schnyder's crystalline dystrophy
- Chameleon-like appearance of immunotactoid keratopathy
- Cholesterol localization in ultrathin frozen sections in Schnyder's corneal crystalline dystrophy
- Cholesterol turnover in hereditary crystalline corneal dystrophy of Schnyder
- Chromosomal mapping and expression of the human B120 gene
- Clinical and histopathologic features of corneal dystrophies in Japan
- Clinical and para-clinical description of a novel mutation for Schnyder dystrophy in a French family
- Clinical and pathological features of a non-crystalline form of Schnyder corneal dystrophy
- Clinical diversity in patients with Schnyder corneal dystrophy-a novel and known UBIAD1 pathogenic variants
- Coincidental Occurrence of Schnyder Corneal Dystrophy and Posterior Polymorphous Corneal Dystrophy Type 3
- Corneal changes in the dislipoproteinaemias
- Corneal changes of uncertain etiology in mesoendemic onchocercal communities of Northern Nigeria
- Corneal dystrophies in the light of modern molecular genetic research
- Crystalline corneal dystrophy (Schnyder) in the presence of familial type IIa hyperlipoproteinaemia (author's transl)
- Crystalline corneal dystrophy in the dog. Histochemical and ultrastructural study
- CRYSTALLINE CORNEAL DYSTROPHY. REPORT OF A CASE
- Crystalline Keratopathy in Post-LASIK Ectasia: A Case Report
- Crystalline stromal dystrophy: histochemistry and ultrastructure of the cornea
- Crystalline subtype of pre-descemetic corneal dystrophy
- Deep phototherapeutic keratectomy for Schnyder corneal dystrophy
- Differential diagnosis of Schnyder corneal dystrophy
- Disappearance of crystals in Schnyder's crystalline corneal dystrophy after epithelial erosion
- Down-regulation of TERE1/UBIAD1 activated Ras-MAPK signalling and induced cell proliferation
- Effects of cholestanol feeding on corneal dystrophy in mice
- Ex vivo 3D human corneal stroma model for Schnyder corneal dystrophy - role of autophagy in its pathogenesis and resolution
- Fine mapping of the Schnyder's crystalline corneal dystrophy locus
- Functional study of SCCD pathogenic gene <em>UBIAD1</em> (Review)
- Genetic analysis of 14 families with Schnyder crystalline corneal dystrophy reveals clues to UBIAD1 protein function
- Geranylgeranyl-regulated transport of the prenyltransferase UBIAD1 between membranes of the ER and Golgi
- High expression of Matrix Gla Protein in Schnyder corneal dystrophy patients points to an active role of vitamin K in corneal health
- Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy
- Identification of two novel mutations in the cornea-specific TGFBI gene causing unique phenotypes in patients with corneal dystrophies
- Identifying anterior segment crystals
- Images in clinical medicine. Schnyder's crystalline corneal dystrophy
- In vivo confocal microscopy of a family with Schnyder crystalline corneal dystrophy
- In vivo laser confocal microscopy findings and mutational analysis for Schnyder's crystalline corneal dystrophy
- LCAT, ApoD, and ApoA1 Expression and Review of Cholesterol Deposition in the Cornea
- Linkage analysis in granular corneal dystrophy (Groenouw I), Schnyder's crystalline corneal dystrophy, and Reis-Bücklers' corneal dystrophy
- Long-Term Outcome After Penetrating Keratoplasty in a Pedigree With the G177E Mutation in the UBIAD1 Gene for Schnyder Corneal Dystrophy
- Metabolic disorders and corneal changes (author's transl)
- Molecular Pathogenesis of Corneal Dystrophies: Schnyder Dystrophy and Granular Corneal Dystrophy type 2
- Morphological evaluation of Schnyder's central crystalline dystrophy by confocal microscopy before and after phototherapeutic keratectomy
- Morphological evaluation of Schnyder's crystalline corneal dystrophy by laser scanning confocal microscopy and Fourier-domain optical coherence tomography
- Multidrug-Resistant Stenotrophomonas maltophilia Keratitis in a Penetrating Keratoplasty Patient
- Mutation in the UBIAD1 gene of a Chinese family with Schnyder crystal corneal dystrophy
- Mutations in the UBIAD1 gene on chromosome short arm 1, region 36, cause Schnyder crystalline corneal dystrophy
- Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy
- Naturally occurring UBIAD1 mutations differentially affect menaquinone biosynthesis and vitamin K-dependent carboxylation
- Newly reported p.Asp240Asn mutation in UBIAD1 suggests central discoid corneal dystrophy is a variant of Schnyder corneal dystrophy
- Ocular lipid deposition and hyperlipoproteinaemia
- Ocular manifestation in LCAT deficiency--a clinicopathological correlation
- Ocular Manifestation of Mucopolysaccharidosis I-S (Scheie's Syndrome)
- Optical coherence tomography and confocal microscopy aspects of a Schnyder's corneal dystrophy case
- Oval corneal opacities in beagles. III. Histochemical demonstration of stromal lipids without hyperlipidemia
- Patterns of inheritance, not always easily visible
- Peripheral Center Sparing Presentation of Schnyder Corneal Dystrophy
- Phenotype-genotype correlation in patients with Schnyder corneal dystrophy
- Phototherapeutic keratectomy for Schnyder's central crystalline dystrophy
- Phototherapeutic keratectomy for Schnyder's crystalline corneal dystrophy
- Phototherapeutic keratectomy in Schnyder crystalline corneal dystrophy
- Possibilities of therapeutic photokeratotomy with the excimer laser in treatment of Schnyder crystalline corneal dystrophy
- Progressive Schnyder's corneal dystrophy
- Recurrence of corneal dystrophy after excimer laser phototherapeutic keratectomy
- Recurrence of corneal stromal dystrophies after penetrating keratoplasty
- Schnyder corneal crystalline dystrophy: description of a new family with evidence of abnormal lipid storage in skin fibroblasts
- Schnyder corneal dystrophy and associated phenotypes caused by novel and recurrent mutations in the UBIAD1 gene
- Schnyder corneal dystrophy and juvenile, systemic hypercholesteremia
- Schnyder Corneal Dystrophy in a Saudi Arabian Family with Heterozygous UBIAD1 Mutation (p.L121F)
- Schnyder corneal dystrophy-associated UBIAD1 inhibits ER-associated degradation of HMG CoA reductase in mice
- Schnyder corneal dystrophy-associated UBIAD1 is defective in MK-4 synthesis and resists autophagy-mediated degradation
- Schnyder corneal dystrophy-associated UBIAD1 mutations cause corneal cholesterol accumulation by stabilizing HMG-CoA reductase
- Schnyder Corneal Dystrophy: A Rare Case Report
- Schnyder crystalline dystrophy
- Schnyder crystalline dystrophy sine crystals. Recommendation for a revision of nomenclature
- Schnyder's crystalline corneal dystrophy
- Schnyder's crystalline corneal dystrophy in association with hyperlipoproteinemia: histopathological and ultrastructural findings
- Schnyder's crystalline corneal dystrophy. Further narrowing of the linkage interval at chromosome 1p34.1-p36?
- Schnyder's crystalline dystrophy of the cornea
- Schnyder's crystalline dystrophy. I. Study of a case by light and electron microscopy
- Schnyder's crystalline dystrophy. II. Association with genu valgum
- Schnyder's crystalline-like corneal dystrophy: a case report
- Schnyder's dystrophy of the cornea. A Swede-Finn connection
- Schnyder's dystrophy. Progression and metabolism
- Stromal corneal dystrophy (possible Schnyder's dystrophy) with peripheral corneal degeneration - diagnostic and therapeutic challenges
- Structure of a membrane-embedded prenyltransferase homologous to UBIAD1
- The bladder tumor suppressor protein TERE1 (UBIAD1) modulates cell cholesterol: implications for tumor progression
- The gene for schnyder's crystalline corneal dystrophy maps to human chromosome 1p34.1-p36
- The Oskar Fehr Lecture
- The UBIAD1 prenyltransferase links menaquinone-4 [corrected] synthesis to cholesterol metabolic enzymes
- Topical 1% cyclosporine eyedrops for the treatment of crystalline corneal dystrophy in dogs
- UbiA prenyltransferase domain-containing protein 1 (UBIAD1) variant c.695 A > G identified in a multigenerational Japanese family with Schnyder corneal dystrophy
- Ultrastructural changes in the posterior layers of the cornea in Schnyder's crystalline dystrophy
- Unesterified cholesterol in Schnyder's corneal crystalline dystrophy
- Visual morbidity in thirty-four families with Schnyder crystalline corneal dystrophy (an American Ophthalmological Society thesis)