Diagnostic Accuracy of PET/CT-Guided Percutaneous Biopsies for Malignant Peripheral Nerve Sheath Tumors in Neurofibromatosis Type 1 Patients

por Brahmi, Mehdi, Thiesse, Philippe, Ranchere, Dominique, Mognetti, Thomas, Pinson, Stephane, Renard, Caroline, Decouvelaere, Anne-Valérie, Blay, Jean-Yves, Combemale, Patrick
Publicado 2015

Utility of 18F-FDG PET with a Semi-Quantitative Index in the Detection of Sarcomatous Transformation in Patients with Neurofibromatosis Type 1

por Combemale, Patrick, Valeyrie-Allanore, Laurence, Giammarile, Francesco, Pinson, Stephane, Guillot, Bernard, Goulart, Denis Mariano, Wolkenstein, Pierre, Blay, Jean Yves, Mognetti, Thomas
Publicado 2014

Human Radiosensitivity and Radiosusceptibility: What Are the Differences?

por El-Nachef, Laura, Al-Choboq, Joelle, Restier-Verlet, Juliette, Granzotto, Adeline, Berthel, Elise, Sonzogni, Laurène, Ferlazzo, Mélanie L., Bouchet, Audrey, Leblond, Pierre, Combemale, Patrick, Pinson, Stéphane, Bourguignon, Michel, Foray, Nicolas
Publicado 2021

The effect of methylphenidate on neurofibromatosis type 1: a randomised, double-blind, placebo-controlled, crossover trial

por Lion-François, Laurence, Gueyffier, François, Mercier, Catherine, Gérard, Daniel, Herbillon, Vania, Kemlin, Isabelle, Rodriguez, Diana, Ginhoux, Tiphanie, Peyric, Emeline, Coutinho, Virginie, Bréant, Valentine, des Portes, Vincent, Pinson, Stéphane, Combemale, Patrick, Kassaï, Behrouz
Publicado 2014

Genome profiling of chronic myelomonocytic leukemia: frequent alterations of RAS and RUNX1 genes

por Gelsi-Boyer, Véronique, Trouplin, Virginie, Adélaïde, José, Aceto, Nicola, Remy, Virginie, Pinson, Stephane, Houdayer, Claude, Arnoulet, Christine, Sainty, Danielle, Bentires-Alj, Mohamed, Olschwang, Sylviane, Vey, Norbert, Mozziconacci, Marie-Joëlle, Birnbaum, Daniel, Chaffanet, Max
Publicado 2008

Whole exome sequencing in three families segregating a pediatric case of sarcoidosis

por Calender, Alain, Rollat Farnier, Pierre Antoine, Buisson, Adrien, Pinson, Stéphane, Bentaher, Abderrazzaq, Lebecque, Serge, Corvol, Harriet, Abou Taam, Rola, Houdouin, Véronique, Bardel, Claire, Roy, Pascal, Devouassoux, Gilles, Cottin, Vincent, Seve, Pascal, Bernaudin, Jean-François, Lim, Clarice X., Weichhart, Thomas, Valeyre, Dominique, Pacheco, Yves, Clement, Annick, Nathan, Nadia
Publicado 2018

AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer

por Leclerc, Julie, Beaumont, Marie, Vibert, Roseline, Pinson, Stéphane, Vermaut, Catherine, Flament, Cathy, Lovecchio, Tonio, Delattre, Lucie, Demay, Christophe, Coulet, Florence, Guillerm, Erell, Hamzaoui, Nadim, Benusiglio, Patrick R., Brahimi, Afane, Cornelis, François, Delhomelle, Hélène, Fert‐Ferrer, Sandra, Fournier, Benjamin P. J., Hovnanian, Alain, Legrand, Clémentine, Lortholary, Alain, Malka, David, Petit, Florence, Saurin, Jean‐Christophe, Lejeune, Sophie, Colas, Chrystelle, Buisine, Marie‐Pierre
Publicado 2022

Primary hyperparathyroidism as first manifestation in multiple endocrine neoplasia type 2A: an international multicenter study

por Larsen, Louise Vølund, Mirebeau-Prunier, Delphine, Imai, Tsuneo, Alvarez-Escola, Cristina, Hasse-Lazar, Kornelia, Censi, Simona, Castroneves, Luciana A, Sakurai, Akihiro, Kihara, Minoru, Horiuchi, Kiyomi, Barbu, Véronique Dorine, Borson-Chazot, Francoise, Gimenez-Roqueplo, Anne-Paule, Pigny, Pascal, Pinson, Stephane, Wohllk, Nelson, Eng, Charis, Aydogan, Berna Imge, Saranath, Dhananjaya, Dvorakova, Sarka, Castinetti, Frederic, Patocs, Attila, Bergant, Damijan, Links, Thera P, Peczkowska, Mariola, Hoff, Ana O, Mian, Caterina, Dwight, Trisha, Jarzab, Barbara, Neumann, Hartmut P H, Robledo, Mercedes, Uchino, Shinya, Barlier, Anne, Godballe, Christian, Mathiesen, Jes Sloth
Publicado 2020