28 research outputs found

    Improving keratoconus management with central corneal regularization and corneal collagen cross-linking protocol treatment

    Get PDF
    Purpose. To evaluate safety and efficacy of customized central corneal regularization (CCR), together with simultaneous accelerated corneal collagen cross-linking (A-CXL) - CCR-CXL protocol, to treat keratoconus-related corneal ectasia. Design. Retrospective, comparative observational case series. Methods. Patients that had undergone combined CCR-CXL protocol. Main inclusion criteria were keratoconus visual acuity deterioration and contact lens intolerance. All patients underwent complete ophthalmological evaluation, corrected distance visual acuity (CDVA) and Scheimpflug-corneal tomography. Central corneal regularization was performed by ablation using flying spot laser. Subsequently, the stroma was saturated with 0.17% riboflavin-5-phosphate added every 2 minutes, followed by A-CXL 9 mW/cm2 for 10 minutes. CDVA, medium keratometry value (Kmed), and total corneal morphological irregularity index (CMI) of patients were analyzed before surgery and after 1, 3 and 12 months. A P value of.05 or less was considered statistically significant. Results. 46 eyes of 39 keratoconus patients were treated. At 1 month, the mean CDVA (LogMar) increased from 0.19 ± 0.02 to 0.12 ± 0.02 (P < .05), and the difference remained stable at month 12. Kmax decrease was statistically significant from 57.02 ± 5.65 to 50.21 ± 4.48 (P < .05). CMI decreased significantly from 47.8 ± 2.84 to 30.1 ± 2.4 (P < .01). Conclusions. CCR-CXL protocol is safe and effective in arresting keratectasia progression and increasing corneal optic regularity in keratoconus. These findings showed a significant improvement in CDVA, keratometry values and corneal optical aberrations after being treated with the CCR-CXL protocol. Copyright © Società Editrice Universo (SEU

    Experimental evidence of s-wave superconductivity in bulk CaC6_{6}

    Full text link
    The temperature dependence of the in-plane magnetic penetration depth, λab(T)\lambda_{ab}(T), has been measured in a c-axis oriented polycrystalline CaC6_{6} bulk sample using a high-resolution mutual inductance technique. A clear exponential behavior of λab(T)\lambda_{ab}(T) has been observed at low temperatures, strongly suggesting isotropic s-wave pairing. Data fit using the standard BCS theory yields λab(0)=(720±80)\lambda_{ab}(0)=(720\pm 80) Angstroem and Δ(0)=(1.79±0.08)\Delta(0)=(1.79\pm 0.08) meV. The ratio 2Δ(0)/kBTc=(3.6±0.2)2\Delta(0)/k_{_B}T_{c}=(3.6\pm 0.2) gives indication for a conventional weakly coupled superconductor.Comment: To appear in Phys. Rev. Let

    Linear and nonlinear electrodynamic response of bulk CaC6 in the microwave regime

    Full text link
    The linear and nonlinear response to a microwave electromagnetic field of two c-axis oriented polycrystalline samples of the newly discovered superconductor CaC6 (Tc = 11.5 K) is studied in the superconducting state down to 2 K. The surface resistance Rs and the third order intermodulation distortion, arising from a two-tone excitation, have been measured as a function of temperature and microwave circulating power. Experiments are carried out using a dielectrically loaded copper cavity operating at 7 GHz in a "hot finger" configuration. The results confirm recent experimental findings that CaC6 behaves as a weakly-coupled, fully gapped, superconductor. The weak power dependence of Rs encourages a further investigation of this novel superconductor as a possible alternative to Nb in specific microwave applications.Comment: 8 pages, 4 figures, submitted to Appl. Phys. Let

    Lattice Corneal Dystrophy: a report of two cases in twin si- sters due to 3 mutations (T1620C, C1416T, A1924G) in the TGFBI (BIGH3) gene

    No full text
    Phenotypic characteristics associated with mutations in the tran- sforming growth factor beta-induced (TGFBI) gene in two twin sisters suffering from lattice corneal dystrophy are reported. Genomic DNA was extracted from peripheral blood and 3 new mutations in association with exons 11-12-14 of the TGFBI gene were found
    corecore