Liste des publications
- 2010, 8 publications, 0 PDF
- 2009, 18 publications, 13 PDF
- 2008, 18 publications, 11 PDF
- 2007, 14 publications, 13 PDF
- 2006, 16 publications, 15 PDF
- 2005, 10 publications, 10 PDF
Recherche de publication
Dernières publications
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Pubmed
Modern cataract surgery for radiation-induced cataracts in retinoblastoma.
Osman IM, Abouzeid H, Balmer A, Gaillard MC, Othenin-Girard P, Pica A, Moeckli R, Schorderet DF, Munier FL.
Br J Ophthalmol. 2010 Jun 24. [Epub ahead of print] -
Pubmed
The PROM1 mutation p.R373C causes an autosomal dominant bull's eye maculopathy associated with rod, rod-cone and macular dystrophy.
Michaelides M, Gaillard MC, Escher P, Tiab L, Bedell M, Borruat FX, Barthelmes D, Carmona R, Zhang K, White E, McClements M, Robson AG, Holder G, Bradshaw K, Hunt DM, Webster A, Moore AT, Schorderet DF, Munier FL.
Invest Ophthalmol Vis Sci. 2010 Apr 14. [Epub ahead of print] -
Pubmed
A male with unilateral microphthalmia reveals a role for TMX3 in eye development.
Chao R, Nevin L, Agarwal P, Riemer J, Bai X, Delaney A, Akana M, JimenezLopez N, Bardakjian T, Schneider A, Chassaing N, Schorderet DF, FitzPatrick D, Kwok PY, Ellgaard L, Gould DB, Zhang Y, Malicki J, Baier H, Slavotinek A.
PLoS One. 2010 May 11;5(5):e10565. -
Pubmed
New insights into changes in corneal thickness in healthy mountaineers during a very-high-altitude climb to Mount Muztagh Ata.
Bosch MM, Barthelmes D, Merz TM, Knecht PB, Truffer F, Bloch KE, Thiel MA, Petrig BL, Turk AJ, Schoch OD, Hefti U, Landau K.
Arch Ophthalmol. 2010 Feb;128(2):184-9. -
Pubmed
Variable phenotypic expressivity in a Swiss family with autosomal dominant retinitis pigmentosa due to a T494M mutation in the PRPF3 gene.
Vaclavik V, Gaillard MC, Tiab L, Schorderet DF, Munier FL.
Mol Vis. 2010 Mar 19;16:467-75.
