Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Caroline Lacombe"'
Autor:
Caroline Lacombe, Marine Perrier, Olivia Hentic, Hedia Brixi, Ophélie De Rycke, Jérôme Cros, Vinciane Rebours, Guillaume Cadiot, Philippe Ruszniewski, Louis de Mestier
Publikováno v:
Journal of Neuroendocrinology. 35
Neuroendocrine tumors (NETs) are highly vascularized neoplasms. While FOLFOX chemotherapy has shown efficacy in patients with advanced NETs, its combination with antiangiogenics has been scarcely described. Here, we report the efficacy and tolerance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcd8b99f2a8d309bc54d3f28412cdf79
https://doi.org/10.1111/jne.13227
https://doi.org/10.1111/jne.13227
Autor:
Ophélie De Rycke, Olivia Hentic, Louis de Mestier, Jérôme Cros, Gérard Zalcman, Philippe Ruszniewski, Anthony Turpin, Anne Couvelard, Caroline Lacombe, Aurélie Cazes, Valérie Gounant
Publikováno v:
Cancers
Volume 13
Issue 4
Cancers, Vol 13, Iss 643, p 643 (2021)
Volume 13
Issue 4
Cancers, Vol 13, Iss 643, p 643 (2021)
Etoposide-platinum (EP) chemotherapy has long been the reference treatment for grade 3 neuroendocrine neoplasms (G3 NEN). However, G3 NEN are heterogeneous, including well-differentiated tumors (NET) and poorly differentiated large (LCNEC) or small (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2988f74c0442fc864add90283c56a809
Autor:
M. Perrier, Guillaume Cadiot, H. Brixi, Caroline Lacombe, Olivia Hentic, Philippe Ruszniewski, Vinciane Rebours, L. de Mestier
Publikováno v:
Annals of Oncology. 32:S621
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3e3f539306f86898e958ea885e07c95
https://doi.org/10.1016/j.annonc.2021.08.703
https://doi.org/10.1016/j.annonc.2021.08.703
Autor:
Valérie Gounant, Caroline Lacombe, P. Ruszniewski, O. De Rycke, L. de Mestier, Olivia Hentic, Jerome Raffenne, Alain Sauvanet, Anne Couvelard, Jérôme Cros, Valérie Paradis, Gérard Zalcman
Publikováno v:
Pancreatology. 20:S84
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::971d310dd3d918ecaa917715271d4b6a
https://doi.org/10.1016/j.pan.2020.07.132
https://doi.org/10.1016/j.pan.2020.07.132
Autor:
Anne Couvelard, R. Chen, Caroline Lacombe, P. Ruszniewski, Olivia Hentic, Jérôme Cros, Nathalie Colnot, Gérard Zalcman, Aurélie Cazes, O. De Rycke, L. de Mestier
Publikováno v:
Pancreatology. 20:S111
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f58c5503a71c64854767f6cce4eab807
https://doi.org/10.1016/j.pan.2020.07.196
https://doi.org/10.1016/j.pan.2020.07.196
Publikováno v:
HPB. 22:792
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e81ac1d461ec81f7e97007cd4675868
https://doi.org/10.1016/j.hpb.2020.03.009
https://doi.org/10.1016/j.hpb.2020.03.009
Autor:
Cyril Gobinet, Mokhtar Zater, Roselyne Garnotel, Ganesh D. Sockalingum, Valérie Untereiner, Caroline Lacombe
Publikováno v:
The Analyst. 140(7)
Classic galactosemia is an autosomal recessive metabolic disease involving the galactose pathway, caused by the deficiency of galactose-1-phosphate uridyltransferase. Galactose accumulation induces in newborns many symptoms, such as liver disease, ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8425f3b649f4c0e879919df1bea85ad4
https://pubmed.ncbi.nlm.nih.gov/25622686
https://pubmed.ncbi.nlm.nih.gov/25622686