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Results: 1-6 |
Results: 6

Authors: Dollfus, H Cantenot, L Rouault, F Philipp, N Flament, J
Citation: H. Dollfus et al., Bilateral iridoretinal colobomas in a child with a Noonan phenotype, CLIN DYSMOR, 10(4), 2001, pp. 299-300

Authors: Porto, FBO Mack, G Sterboul, MP Lewin, P Flament, J Sahel, J Dollfus, H
Citation: Fbo. Porto et al., Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation, AM J OPHTH, 132(6), 2001, pp. 935-937

Authors: Verbruggen, LA Dumarey, N Van de Velde, H Rebmann, V Flament, J Van Wayenberge, C Grosse-Wilde, H Demanet, C
Citation: La. Verbruggen et al., Soluble HLA-DR antigen levels in serum correlate with rheumatoid arthritisdisease activity and the presence of disease-associated epitopes, TISSUE ANTI, 56(5), 2000, pp. 436-440

Authors: Meyer, L Sahel, J Flament, J
Citation: L. Meyer et al., Central retinal vein occlusion and optociliary shunts: an angiographic diagnosis, J FR OPHTAL, 22(3), 1999, pp. 310-314

Authors: Szwarcberg, J Limacher, JM Fricker, JP Flament, J
Citation: J. Szwarcberg et al., Congenital hypertrophy of retinal pigment epithelium: a marker in familialadenomatous polyposis, J FR OPHTAL, 22(3), 1999, pp. 364-370

Authors: Mack, G Dolfus, H Flament, J Mohand-Said, S Sahel, J
Citation: G. Mack et al., A new mode of recording retinal activity: multifocal ERG, J FR OPHTAL, 22(2), 1999, pp. 221-225
Risultati: 1-6 |