Authors:
Hamel, CP
Griffoin, JM
Bazalgette, C
Lasquellec, L
Duval, PA
Bareil, C
Beaufrere, L
Bonnet, S
Eliaou, C
Marlhens, F
Schmitt-Bernard, CF
Tuffery, S
Claustres, M
Arnaud, B
Citation: Cp. Hamel et al., Molecular genetics of pigmentary retinopathies: Identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes, J FR OPHTAL, 23(10), 2000, pp. 985-995
Authors:
Schmitt-Bernard, CF
Guittard, C
Arnaud, B
Demaille, J
Argiles, A
Claustres, M
Tuffery-Giraud, S
Citation: Cf. Schmitt-bernard et al., BIGH3 exon 14 mutations lead to intermediate type I/IIIA of lattice corneal dystrophies, INV OPHTH V, 41(6), 2000, pp. 1302-1308
Authors:
Argiles, A
Mourad, G
Gouin-Charnet, A
Schmitt-Bernard, CF
Citation: A. Argiles et al., Antiproteases and cells in the pathogenesis of beta(2)-microglobulin amyloidosis: Role of alpha(2)-macroglobulin and macrophages, NEPHRON, 86(1), 2000, pp. 1-11
Authors:
Schmitt-Bernard, CF
Chavanieu, A
Derancourt, J
Arnaud, B
Demaille, JG
Calas, B
Argiles, A
Citation: Cf. Schmitt-bernard et al., In vitro creation of amyloid fibrils from native and Arg124Cys mutated beta IGH3((110-131)) peptides, and its relevance for lattice corneal amyloid dystrophy type I, BIOC BIOP R, 273(2), 2000, pp. 649-653