Zobrazeno 1 - 10
of 168
pro vyhledávání: '"Marc Polivka"'
Publikováno v:
Dubai Medical Journal, Vol 5, Iss 4, Pp 267-271 (2022)
We present 2 cases of isolated tumour of the calvaria that underwent a different management but, unexpectedly, the same very rare diagnosis of primary diffuse large B-cell lymphoma of the cranial vault. Unfortunately, the outcome was the opposite due
Externí odkaz:
https://doaj.org/article/6eb72f97ecd44bc7ac5b162ed4b626dc
Autor:
Arnault Tauziède-Espariat, Thibaut Pierre, Michel Wassef, David Castel, Florence Riant, Jacques Grill, Alexandre Roux, Johan Pallud, Edouard Dezamis, Damien Bresson, Sandro Benichi, Thomas Blauwblomme, Djallel Benzohra, Guillaume Gauchotte, Celso Pouget, Sophie Colnat-Coulbois, Karima Mokhtari, Corinne Balleyguier, Frédérique Larousserie, Volodia Dangouloff-Ros, Nathalie Boddaert, Marie-Anne Debily, Lauren Hasty, Marc Polivka, Homa Adle-Biassette, Alice Métais, Emmanuèle Lechapt, Fabrice Chrétien, Felix Sahm, Philipp Sievers, Pascale Varlet, the RENOCLIP-LOC
Publikováno v:
Acta Neuropathologica Communications, Vol 10, Iss 1, Pp 1-11 (2022)
Abstract The International Society for the Study of Vascular Anomalies (ISSVA) has defined four vascular lesions in the central nervous system (CNS): arteriovenous malformations, cavernous angiomas (also known as cerebral cavernous malformations), ve
Externí odkaz:
https://doaj.org/article/ea31d1f1e8ef422d8660512d17fda86d
Autor:
Thibault Passeri, Ahmed Dahmani, Julien Masliah-Planchon, Adnan Naguez, Marine Michou, Rania El Botty, Sophie Vacher, Rachida Bouarich, André Nicolas, Marc Polivka, Coralie Franck, Anne Schnitzler, Fariba Némati, Sergio Roman-Roman, Franck Bourdeaut, Homa Adle-Biassette, Hamid Mammar, Sébastien Froelich, Ivan Bièche, Didier Decaudin
Publikováno v:
Cancers, Vol 14, Iss 6, p 1486 (2022)
Chordomas are rare neoplasms characterized by a high recurrence rate and a poor long-term prognosis. Considering their chemo-/radio-resistance, alternative treatment strategies are strongly required, but their development is limited by the paucity of
Externí odkaz:
https://doaj.org/article/a67713347fb849e7a4912cb619b47179
Autor:
Shai Rosenberg, Iva Simeonova, Franck Bielle, Maite Verreault, Bertille Bance, Isabelle Le Roux, Mailys Daniau, Arun Nadaradjane, Vincent Gleize, Sophie Paris, Yannick Marie, Marine Giry, Marc Polivka, Dominique Figarella-Branger, Marie-Hélène Aubriot-Lorton, Chiara Villa, Alexandre Vasiljevic, Emmanuèle Lechapt-Zalcman, Michel Kalamarides, Ariane Sharif, Karima Mokhtari, Stefano Maria Pagnotta, Antonio Iavarone, Anna Lasorella, Emmanuelle Huillard, Marc Sanson
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-9 (2018)
Chordoid glioma is a slow growing diencephalic tumor whose mutational landscape is poorly characterized. Here, the authors perform whole-exome and RNA-sequencing and find that 15 of 16 chordoid glioma cases studied harbor the same PRKCA mutation whic
Externí odkaz:
https://doaj.org/article/47f7d121d4304c4ca98cb2dbb0a6edde
Autor:
Agnès Aghetti, Damien Sène, Marc Polivka, Natalia Shor, Sarah Lechtman, Hugues Chabriat, Eric Jouvent, Stéphanie Guey
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Cerebral amyloid angiopathy related inflammation (CAA-RI) is a rare form of CAA characterized by subacute encephalitic symptoms (cognitive decline, seizures, focal deficits) associated with extensive and confluent white matter lesions co-localizing w
Externí odkaz:
https://doaj.org/article/e5f10bfb8efa4262bf8ba59c6a81570a
Autor:
Monique Boukobza, Marc Polivka
Publikováno v:
eNeurologicalSci, Vol 15, Iss , Pp - (2019)
Intracranial germinomas (IGs) are rare malignant germ cell tumors. The septum pellucidum (SP) is an extremely rare site of IGs. To our knowledge we report the first patient presenting with synchronous involvement of the SP and the sellar region. A 28
Externí odkaz:
https://doaj.org/article/799fc1c7923f4ce6971df4b83bac3bd9
Autor:
Aymeric Amelot, Patricia De Cremoux, Véronique Quillien, Marc Polivka, Homa Adle-Biassette, Jacqueline Lehmann-Che, Laurence Françoise, Antoine F Carpentier, Bernard George, Emmanuel Mandonnet, Sébastien Froelich
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0130596 (2015)
A very small proportion of patients diagnosed with glioblastoma (GBM) survive more than 3 years. Isocitrate dehydrogenase 1 or 2 (IDH1/2) mutations define a small subgroup of GBM patients with favourable prognosis. However, it remains controversial w
Externí odkaz:
https://doaj.org/article/307b679f7bc54168aa0f60adc1e68826
Autor:
Khê Hoang-Xuan, Karima Mokhtari, Yannick Marie, Marie-Laure Tanguy, Carole Soussain, Caroline Houillier, Sylvain Choquet, Emmanuel Gyan, Pierre Soubeyran, Olivier Chinot, Luc Taillandier, Vincent Delwail, Rémy Gressin, Hervé Ghesquières, Anne Vital, Catherine Miquel, Dominique Figarella-Branger, Clovis Adam, Marc Polivka, Anne Jouvet, Aurélie Bruno, Alice Laurenge, Marta Rossetto, Naïma Habbita, Blandine Boisselier, Ahmed Idbaih, Alberto Gonzalez-Aguilar
Purpose: Our objective was to identify the genetic changes involved in primary central nervous system lymphoma (PCNSL) oncogenesis and evaluate their clinical relevance.Experimental Design: We investigated a series of 29 newly diagnosed, HIV-negative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d78015b959a263eff3f72e0786996ebb
https://doi.org/10.1158/1078-0432.c.6522807
https://doi.org/10.1158/1078-0432.c.6522807
Autor:
Khê Hoang-Xuan, Karima Mokhtari, Yannick Marie, Marie-Laure Tanguy, Carole Soussain, Caroline Houillier, Sylvain Choquet, Emmanuel Gyan, Pierre Soubeyran, Olivier Chinot, Luc Taillandier, Vincent Delwail, Rémy Gressin, Hervé Ghesquières, Anne Vital, Catherine Miquel, Dominique Figarella-Branger, Clovis Adam, Marc Polivka, Anne Jouvet, Aurélie Bruno, Alice Laurenge, Marta Rossetto, Naïma Habbita, Blandine Boisselier, Ahmed Idbaih, Alberto Gonzalez-Aguilar
PDF file, 55K, Table S1: Recurrent chromosome region imbalances found in more than 20% of PCNSLs investigated by high resolution genomic arrays.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b02931ed89e77b3e1d0c7486bbe34189
https://doi.org/10.1158/1078-0432.22454634.v1
https://doi.org/10.1158/1078-0432.22454634.v1
Autor:
Thibault Passeri, Pierre-Olivier Champagne, Lorenzo Giammattei, Rosaria Abbritti, Jérôme Cartailler, Valentin Calugaru, Loïc Feuvret, Jean-Pierre Guichard, Marc Polivka, Homa Adle-Biassette, Hamid Mammar, Damien Bresson, Philippe Herman, Emmanuel Mandonnet, Bernard George, Sébastien Froelich
Publikováno v:
32nd Annual Meeting North American Skull Base Society.
OBJECTIVE Chordomas represent one of the most challenging subsets of skull base and craniovertebral junction (CVJ) tumors to treat. Despite extensive resection followed by proton-beam radiation therapy, the recurrence rate remains high, highlighting