How would you manage this small melanocytic choroidal tumour?

Por Papadopoulou, Domniki, Moulin, Alexandre P, Zografos, Leonidas, Schalenbourg, Ann
Publicado em 2012

Melanocytes and Pigmentation Are Affected in Dopachrome Tautomerase Knockout Mice

Por Guyonneau, Laurence, Murisier, Fabien, Rossier, Anita, Moulin, Alexandre, Beermann, Friedrich
Publicado em 2004

Derivation of Traceable and Transplantable Photoreceptors from Mouse Embryonic Stem Cells

Por Decembrini, Sarah, Koch, Ute, Radtke, Freddy, Moulin, Alexandre, Arsenijevic, Yvan
Publicado em 2014

Coxiella burnetii vascular graft infection

Por Senn, Laurence, Franciolli, Mario, Raoult, Didier, Moulin, Alexandre, Von Segesser, Ludwig, Calandra, Thierry, Greub, Gilbert
Publicado em 2005

UV light signature in conjunctival melanoma; not only skin should be protected from solar radiation

Por Rivolta, Carlo, Royer-Bertrand, Beryl, Rimoldi, Donata, Schalenbourg, Ann, Zografos, Leonidas, Leyvraz, Serge, Moulin, Alexandre
Publicado no J Hum Genet (2016)

Cone Genesis Tracing by the Chrnb4-EGFP Mouse Line: Evidences of Cellular Material Fusion after Cone Precursor Transplantation

Por Decembrini, Sarah, Martin, Catherine, Sennlaub, Florian, Chemtob, Sylvain, Biel, Martin, Samardzija, Marijana, Moulin, Alexandre, Behar-Cohen, Francine, Arsenijevic, Yvan
Publicado no Mol Ther (2017)

Adamts18 deletion results in distinct developmental defects and provides a model for congenital disorders of lens, lung, and female reproductive tract development

Por Ataca, Dalya, Caikovski, Marian, Piersigilli, Alessandra, Moulin, Alexandre, Benarafa, Charaf, Earp, Sarah E., Guri, Yakir, Kostic, Corinne, Arsenivic, Yvan, Soininen, Raija, Apte, Suneel S., Brisken, Cathrin
Publicado no Biol Open (2016)

Comprehensive Genetic Landscape of Uveal Melanoma by Whole-Genome Sequencing

Por Royer-Bertrand, Beryl, Torsello, Matteo, Rimoldi, Donata, El Zaoui, Ikram, Cisarova, Katarina, Pescini-Gobert, Rosanna, Raynaud, Franck, Zografos, Leonidas, Schalenbourg, Ann, Speiser, Daniel, Nicolas, Michael, Vallat, Laureen, Klein, Robert, Leyvraz, Serge, Ciriello, Giovanni, Riggi, Nicolò, Moulin, Alexandre P., Rivolta, Carlo
Publicado no Am J Hum Genet (2016)

Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects

Por Nikopoulos, Konstantinos, Farinelli, Pietro, Giangreco, Basilio, Tsika, Chrysanthi, Royer-Bertrand, Beryl, Mbefo, Martial K., Bedoni, Nicola, Kjellström, Ulrika, El Zaoui, Ikram, Di Gioia, Silvio Alessandro, Balzano, Sara, Cisarova, Katarina, Messina, Andrea, Decembrini, Sarah, Plainis, Sotiris, Blazaki, Styliani V., Khan, Muhammad Imran, Micheal, Shazia, Boldt, Karsten, Ueffing, Marius, Moulin, Alexandre P., Cremers, Frans P.M., Roepman, Ronald, Arsenijevic, Yvan, Tsilimbaris, Miltiadis K., Andréasson, Sten, Rivolta, Carlo
Publicado no Am J Hum Genet (2016)