RELIR un nouvel outil pour améliorer la prévention des incidents radiologiques von BIAU, A, GAURON, C, LEFAURE, C, RITTORE, D, CROUAIL, P

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Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte von Parry, David A., Logan, Clare V., Hayward, Bruce E., Shires, Michael, Landolsi, Hanène, Diggle, Christine, Carr, Ian, Rittore, Cécile, Touitou, Isabelle, Philibert, Laurent, Fisher, Rosemary A., Fallahian, Masoumeh, Huntriss, John D., Picton, Helen M., Malik, Saghira, Taylor, Graham R., Johnson, Colin A., Bonthron, David T., Sheridan, Eamonn G.

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NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage von Messaed, Christiane, Chebaro, Wafaa, Roberto, Raphael B Di, Rittore, Cecile, Cheung, Annie, Arseneau, Jocelyne, Schneider, Ariel, Chen, Moy Fong, Bernishke, Kurt, Surti, Urvashi, Hoffner, Lori, Sauthier, Philippe, Buckett, William, Qian, JianHua, Lau, Nga Man, Bagga, Rashmi, Engert, James C, Coullin, Philippe, Touitou, Isabelle, Slim, Rima

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Characterization of the TNFR1-d2 protein: Implication in TNF receptor associated periodic syndrome (TRAPS)? von Rittore, C, Sanchez, E, Soler, S, Ea, V, Genevieve, D, Touitou, I, Grandemange, S

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NLRP1 mutations cause autoinflammatory diseases in human von Grandemange, S, Sanchez, E, Louis-Plence, P, Rittore, C, Reed, JC, Touitou, I, Geneviève, D

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Le polymorphisme du TNFRII est associé à la réponse aux anti-TNFα dans la polyarthrite rhumatoïde chez les patients sans anticorps anti-CCP von Pers, Yves-Marie, Cadart, Doris, Rittore, Cécile, Ravel, Patrice, Daïen, Vincent, Fabre, Sylvie, Jorgensen, Christian, Touitou, Isabelle

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