An analytical mechanical model to describe the response of NiTi rotary endodontic files in a curved root canal von Leroy, Agnès Marie Françoise, Bahia, Maria Guiomar de Azevedo, Ehrlacher, Alain, Buono, Vicente Tadeu Lopes

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Maintenance darunavir/ritonavir monotherapy to prevent perinatal HIV transmission, ANRS-MIE 168 MONOGEST study von Mandelbrot, Laurent, Tubiana, Roland, Frange, Pierre, Peytavin, Gilles, Le Chenadec, Jerome, Canestri, Ana, Morlat, Philippe, Brunet-Cartier, Cécile, Sibiude, Jeanne, Peretti, Delphine, Chambrin, Véronique, Chabrol, Amélie, Bui, Eida, Simon-Toulza, Caroline, Marchand, Lucie, Paul, Christelle, Delmas, Sandrine, Avettand-Fenoel, Véronique, Warszawski, Josiane

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Psychiatric symptoms and mortality in older adults with major psychiatric disorders: results from a multicenter study von Chene, Margaux, Sánchez-Rico, Marina, Blanco, Carlos, De Raykeer, Rachel Pascal, Hanon, Cécile, Vandel, Pierre, Limosin, Frédéric, Hoertel, Nicolas

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Performance and cost efficiency of KRAS mutation testing for metastatic colorectal cancer in routine diagnosis: the MOKAECM study, a nationwide experience von Blons, Hélène, Rouleau, Etienne, Charrier, Nathanaël, Chatellier, Gilles, Côté, Jean-François, Pages, Jean-Christophe, de Fraipont, Florence, Boyer, Jean-Christophe, Merlio, Jean Philippe, Morel, Alain, Gorisse, Marie-Claude, de Cremoux, Patricia, Leroy, Karen, Milano, Gérard, Ouafik, L'houcine, Merlin, Jean-Louis, Le Corre, Delphine, Aucouturier, Pascaline, Sabourin, Jean-Christophe, Nowak, Frédérique, Frebourg, Thierry, Emile, Jean-François, Durand-Zaleski, Isabelle, Laurent-Puig, Pierre

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SFBC working group "Biochemical markers of COVID-19" von Beauvieux, Marie-Christine, Bérard, Annie M, Aimone-Gastin, Isabelle, Barbé, Françoise, Barguil, Yann, Collin-Chavagnac, Delphine, Delacour, Hervé, Delevallée, Céline, Nivet-Antoine, Valérie, Peoc'h, Katell, Poupon, Carole, Schmitt, François, Piéroni, Laurence, Sapin, Vincent

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Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness von Audo, Isabelle, Bujakowska, Kinga, Orhan, Elise, Poloschek, Charlotte M., Defoort-Dhellemmes, Sabine, Drumare, Isabelle, Kohl, Susanne, Luu, Tien D., Lecompte, Odile, Zrenner, Eberhart, Lancelot, Marie-Elise, Antonio, Aline, Germain, Aurore, Michiels, Christelle, Audier, Claire, Letexier, Mélanie, Saraiva, Jean-Paul, Leroy, Bart P., Munier, Francis L., Mohand-Saïd, Saddek, Lorenz, Birgit, Friedburg, Christoph, Preising, Markus, Kellner, Ulrich, Renner, Agnes B., Moskova-Doumanova, Veselina, Berger, Wolfgang, Wissinger, Bernd, Hamel, Christian P., Schorderet, Daniel F., De Baere, Elfride, Sharon, Dror, Banin, Eyal, Jacobson, Samuel G., Bonneau, Dominique, Zanlonghi, Xavier, Le Meur, Guylene, Casteels, Ingele, Koenekoop, Robert, Long, Vernon W., Meire, Francoise, Prescott, Katrina, de Ravel, Thomy, Simmons, Ian, Nguyen, Hoan, Dollfus, Hélène, Poch, Olivier, Léveillard, Thierry, Nguyen-Ba-Charvet, Kim, Sahel, José-Alain, Bhattacharya, Shomi S., Zeitz, Christina

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Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness von Audo, Isabelle, Bujakowska, Kinga, Orhan, Elise, Poloschek, Charlotte M, Defoort-Dhellemmes, Sabine, Drumare, Isabelle, Kohl, Susanne, Luu, Tien D, Lecompte, Odile, Zrenner, Eberhart, Lancelot, Marie-Elise, Antonio, Aline, Germain, Aurore, Michiels, Christelle, Audier, Claire, Letexier, Mélanie, Saraiva, Jean-Paul, Leroy, Bart P, Munier, Francis L, Mohand-Saïd, Saddek, Lorenz, Birgit, Friedburg, Christoph, Preising, Markus, Kellner, Ulrich, Renner, Agnes B, Moskova-Doumanova, Veselina, Berger, Wolfgang, Wissinger, Bernd, Hamel, Christian P, Schorderet, Daniel F, De Baere, Elfride, Sharon, Dror, Banin, Eyal, Jacobson, Samuel G, Bonneau, Dominique, Zanlonghi, Xavier, Le Meur, Guylene, Casteels, Ingele, Koenekoop, Robert, Long, Vernon W, Meire, Francoise, Prescott, Katrina, de Ravel de l'Argentière, Thomy, Simmons, Ian, Nguyen, Hoan, Dollfus, Hélène, Poch, Olivier, Léveillard, Thierry, Nguyen-Ba-Charvet, Kim, Sahel, José-Alain, Bhattacharya, Shomi S, Zeitz, Christina

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Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness von Audo, Isabelle, Bujakowska, Kinga, Orhan, Elise, Poloschek, Charlotte M, Defoort-Dhellemmes, Sabine, Drumare, Isabelle, Kohl, Susanne, Luu, Tien D, Lecompte, Odile, Zrenner, Eberhart, Lancelot, Marie-Elise, Antonio, Aline, Germain, Aurore, Michiels, Christelle, Audier, Claire, Letexier, Mélanie, Saraiva, Jean-Paul, Leroy, Bart P, Munier, Francis L, Mohand-Saïd, Saddek, Lorenz, Birgit, Friedburg, Christoph, Preising, Markus, Kellner, Ulrich, Renner, Agnes B, Moskova-Doumanova, Veselina, Berger, Wolfgang, Wissinger, Bernd, Hamel, Christian P, Schorderet, Daniel F, De Baere, Elfride, Sharon, Dror, Banin, Eyal, Jacobson, Samuel G, Bonneau, Dominique, Zanlonghi, Xavier, Le Meur, Guylene, Casteels, Ingele, Koenekoop, Robert, Long, Vernon W, Meire, Francoise, Prescott, Katrina, de Ravel, Thomy, Simmons, Ian, Nguyen, Hoan, Dollfus, Hélène, Poch, Olivier, Léveillard, Thierry, Nguyen-Ba-Charvet, Kim, Sahel, José-Alain, Bhattacharya, Shomi S, Zeitz, Christina

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Évaluation de l’intérêt de la recherche des papillomavirus humains (HPV) dans le dépistage des lésions précancéreuses et cancéreuses du col de l’utérus

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Once upon a time: The World

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