Authors:
Ellies, P
Anderson, D
Dighiero, P
Legeais, JM
Renard, G
Tseng, SS
Citation: P. Ellies et al., Human amniotic membrane transplantation in the treatment of corneal surface diseases, J FR OPHTAL, 24(5), 2001, pp. 546-556
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
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
Authors:
Bodaghi, B
Mougin, C
Michelson, S
Agut, H
Dighiero, P
Offret, H
Frau, E
Citation: B. Bodaghi et al., Acyclovir-resistant bilateral keratitis associated with mutations in the HSV-1 thymidine kinase gene, EXP EYE RES, 71(4), 2000, pp. 353-359
Authors:
Dighiero, P
Drunat, S
D'Hermies, F
Renard, G
Delpech, M
Valleix, S
Citation: P. Dighiero et al., A novel variant of granular corneal dystrophy caused by association of 2 mutations in the TGFBI Gene - R124L and Delta T125-Lambda E126, ARCH OPHTH, 118(6), 2000, pp. 814-818
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
Authors:
Dighiero, P
Ellies, P
Legeais, JM
Briat, B
Mayer, F
David, T
Saragouassi, JJ
Abenhaim, A
Assouline, M
D'Hermies, F
Pouliquen, Y
Renard, G
Citation: P. Dighiero et al., Phototherapeutic keratectomy in the treatment of corneal granular dystrophy Groenouw I, J FR OPHTAL, 22(2), 1999, pp. 176-179