Zobrazeno 1 - 10
of 160
pro vyhledávání: '"François, Labrousse"'
Autor:
Valère Belle Mbou, Florian Sanglier, Julia Pestre-Munier, Aurélien Descazeaud, François Labrousse
Publikováno v:
BMC Urology, Vol 22, Iss 1, Pp 1-9 (2022)
Abstract Background Multiple kidney tumours are frequently seen in hereditary syndromes and familial diseases. Renal collision tumours (RCT) are characterized by the simultaneous existence of different and unrelated tumour types within the same locat
Externí odkaz:
https://doaj.org/article/d83968e9e84b4085bfbcbcc86a0f5ce6
Autor:
Guillaume Friconnet, MD, Mathilde Duchesne, MD, PhD, Marcel Gueye, MD, François Caire, MD, PhD, Charbel Mounayer, MD, PhD, Jean-François Emile, MD, PhD, François Labrousse, MD, PhD, Aymeric Rouchaud, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 16, Iss 7, Pp 1613-1617 (2021)
Rosai–Dorfman disease is a non–Langherans cell histiocytosis typically revealed by a lymphadenopathy. Central nervous system involvement is rare, exceptionally isolated, and usually consists of dural masses mimicking meningioma. Very few reports
Externí odkaz:
https://doaj.org/article/341569116693430a9fc22d3ef73da85f
Autor:
Paul Carrier, Anne Guyot, Marilyne Debette‐Gratien, Fabien Fredon, Marie‐Pierre Teissier, François Labrousse, Véronique Loustaud‐Ratti
Publikováno v:
JGH Open, Vol 5, Iss 11, Pp 1316-1318 (2021)
Abstract We report the case of a 36‐year‐old patient who was initially managed for gynecomastia. The first biological analyses showed a moderately elevated alpha‐fetoprotein (AFP) level. After an endocrine etiology was excluded, an abdominal co
Externí odkaz:
https://doaj.org/article/aa96001a8ae64f198e8125608e795b71
Autor:
Henri Salle, Stéphanie Durand, Karine Durand, Sylvie Bourthoumieu, Leslie Lemnos, Sandrine Robert, Justine Pollet, Thibault Passeri, Wassim Khalil, Sébastien Froelich, Homa Adle-Biassette, François Labrousse
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 82:312-323
Chordomas are rare tumors of the axial skeleton that are refractory to conventional therapy. Few studies have compared the morphological and molecular characteristics of chordomas according to the skull base and sacral locations. Histopathological da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec6dbaef20cc96127995ae4359ec9ec9
https://doi.org/10.1093/jnen/nlad008
https://doi.org/10.1093/jnen/nlad008
Autor:
Camille Lemaçon, Thibaut Loupret, Philippe Bertin, Pascale Vergne Salle, François Labrousse, Pauline Vital, Henri Salle
Publikováno v:
Joint Bone Spine. 90:105545
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cededd737d8496295c77f3a9ce541804
https://doi.org/10.1016/j.jbspin.2023.105545
https://doi.org/10.1016/j.jbspin.2023.105545
Autor:
Mathilde Duchesne, François Labrousse, Guillaume Friconnet, Aymeric Rouchaud, François Caire, Charbel Mounayer, Jean-François Emile, Marcel Gueye
Publikováno v:
Radiology Case Reports, Vol 16, Iss 7, Pp 1613-1617 (2021)
Rosai–Dorfman disease is a non–Langherans cell histiocytosis typically revealed by a lymphadenopathy. Central nervous system involvement is rare, exceptionally isolated, and usually consists of dural masses mimicking meningioma. Very few reports
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b94de8111952ac6fe5461f45818f69f
https://doi.org/10.1016/j.radcr.2021.04.021
https://doi.org/10.1016/j.radcr.2021.04.021
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 80:96-100
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::420a240b87cad13090a0d575d37af7a8
https://doi.org/10.1093/jnen/nlaa123
https://doi.org/10.1093/jnen/nlaa123
Autor:
François Caire, François Labrousse, Mathilde Duchesne, Isabelle Pommepuy, Quoc Dat Nguyen, Anne Guyot
Publikováno v:
Annales de Pathologie. 38:391-394
Calcifying pseudoneoplasms of the neuraxis (CAPNON) are rare lesions of the central nervous system. To date, about 60 cases have been reported in literature. We present a case that had the peculiarity to occur in a pregnant woman. At 32 weeks of gest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::727e001e46bc45e23af9a43dd7f3fc8c
https://doi.org/10.1016/j.annpat.2018.04.006
https://doi.org/10.1016/j.annpat.2018.04.006
Autor:
Valère Belle Mbou, Florian Sanglier, Julia Pestre-Munier, Aurélien Descazeaud, François Labrousse
Publikováno v:
BMC urology. 22(1)
Background Multiple kidney tumours are frequently seen in hereditary syndromes and familial diseases. Renal collision tumours (RCT) are characterized by the simultaneous existence of different and unrelated tumour types within the same location in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4ed28466129fa3ca8cb16a396cbe4fd
https://pubmed.ncbi.nlm.nih.gov/35870918
https://pubmed.ncbi.nlm.nih.gov/35870918
Autor:
Ahmed Idbaih, François Ducray, Caroline Dehais, Célia Courdy, Catherine Carpentier, Simon de Bernard, Emmanuelle Uro-Coste, Karima Mokhtari, Anne Jouvet, Jérôme Honnorat, Olivier Chinot, Carole Ramirez, Patrick Beauchesne, Alexandra Benouaich-Amiel, Joël Godard, Sandrine Eimer, Fabrice Parker, Emmanuelle Lechapt-Zalcman, Philippe Colin, Delphine Loussouarn, Thierry Faillot, Phong Dam-Hieu, Selma Elouadhani-Hamdi, Luc Bauchet, Olivier Langlois, Caroline Le Guerinel, Denys Fontaine, Elodie Vauleon, Philippe Menei, Marie Janette Motsuo Fotso, Christine Desenclos, Pierre Verrelle, François Ghiringhelli, Georges Noel, François Labrousse, Antoine Carpentier, Frédéric Dhermain, Jean-Yves Delattre, Dominique Figarella-Branger
Publikováno v:
PLoS ONE, Vol 8, Iss 5 (2013)
Externí odkaz:
https://doaj.org/article/168c3627a3e44f19b96c8d6f8ea87b5e