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Results: 1-11 |
Results: 11
Treatment of ocular cicatricial pemphigoid with sulfasalazine
Authors: Doan, S Lerouic, JF Robin, H Prost, C Savoldelli, M Hoang-Xuan, T
Citation: S. Doan et al., Treatment of ocular cicatricial pemphigoid with sulfasalazine, OPHTHALMOL, 108(9), 2001, pp. 1565-1568
Histologic phenotype-genotype correlation of corneal dystrophies associated with eight distinct mutations in the TGFBI gene
Authors: Dighiero, P Niel, F Ellies, P D'Hermies, F Savoldelli, M Renard, G Delpech, M Valleix, S
Citation: P. Dighiero et al., Histologic phenotype-genotype correlation of corneal dystrophies associated with eight distinct mutations in the TGFBI gene, OPHTHALMOL, 108(4), 2001, pp. 818-823
Chemotactic penetration of keratocytes in ePTFE polymer in vitro
Authors: Dupuy, FP Savoldelli, M Robert, AM Robert, L Legeais, JM Renard, G
Citation: Fp. Dupuy et al., Chemotactic penetration of keratocytes in ePTFE polymer in vitro, J BIOMED MR, 56(4), 2001, pp. 487-493
Avellino corneal dystrophy
Authors: Dighiero, P Ellies, P Valleix, S D'Hermies, F Savoldelli, M Pouliquen, Y Legeais, JM Renard, G
Citation: P. Dighiero et al., Avellino corneal dystrophy, J FR OPHTAL, 23(7), 2000, pp. 735-737
Clinical, histologic, and ultrastructural features of the corneal dystrophy caused by the R124L, mutation of the BIGH3 gene
Authors: Dighiero, P Valleix, S D'Hermies, F Drunat, S Ellies, P Savoldelli, M Pouliquen, Y Delpech, M Legeais, JM Renard, G
Citation: P. Dighiero et al., Clinical, histologic, and ultrastructural features of the corneal dystrophy caused by the R124L, mutation of the BIGH3 gene, OPHTHALMOL, 107(7), 2000, pp. 1353-1357
EIU in the rat promotes the potential of syngeneic retinal cells injected.into the vitreous cavity to induce PVR
Authors: Behar-Cohen, FF Thillaye-Goldenberg, B de Bizemont, T Savoldelli, M Chauvaud, D de Kozak, Y
Citation: Ff. Behar-cohen et al., EIU in the rat promotes the potential of syngeneic retinal cells injected.into the vitreous cavity to induce PVR, INV OPHTH V, 41(12), 2000, pp. 3915-3924
A viscous bioerodible poly(ortho ester) as a new biomaterial for intraocular application
Authors: Einmahl, S Behar-Cohen, F Tabatabay, C Savoldelli, M D'Hermies, F Chauvaud, D Heller, J Gurny, R
Citation: S. Einmahl et al., A viscous bioerodible poly(ortho ester) as a new biomaterial for intraocular application, J BIOMED MR, 50(4), 2000, pp. 566-573
A new mutation (A546T) of the beta ig-h3 gene responsible for a French lattice corneal dystrophy type IIIA
Authors: Dighiero, P Drunat, S Ellies, P D'Hermies, F Savoldelli, M Legeais, JM Renard, G Delpech, M Grateau, G Valleix, S
Citation: P. Dighiero et al., A new mutation (A546T) of the beta ig-h3 gene responsible for a French lattice corneal dystrophy type IIIA, AM J OPHTH, 129(2), 2000, pp. 248-251
Retinal TUNEL-positive cells and high glutamate levels in vitreous humor of mutant quail with a glaucoma-like disorder
Authors: Dkhissi, O Chanut, E Wasowicz, M Savoldelli, M Nguyen-Legros, J Minvielle, F Versaux-Botteri, C
Citation: O. Dkhissi et al., Retinal TUNEL-positive cells and high glutamate levels in vitreous humor of mutant quail with a glaucoma-like disorder, INV OPHTH V, 40(5), 1999, pp. 990-995
Novel synthetic meshwork for glaucoma treatment. I. Design and preliminaryin vitro and in vivo evaluation of various expanded poly(tetrafluoroethylene) materials
Authors: Jallet, V Gautier, SE Parel, JM Matsui, T Haefliger, I Kondo, H Kato, H Savoldelli, M Pouliquen, Y
Citation: V. Jallet et al., Novel synthetic meshwork for glaucoma treatment. I. Design and preliminaryin vitro and in vivo evaluation of various expanded poly(tetrafluoroethylene) materials, J BIOMED MR, 47(2), 1999, pp. 260-269
Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144
Authors: Teh, EM Chisholm, JW Dolphin, PJ Pouliquen, Y Savoldelli, M de Gennes, JL Benlian, P
Citation: Em. Teh et al., Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144, ATHEROSCLER, 146(1), 1999, pp. 141-151
Risultati: 1-11 |