Search Results - (Author, Cooperation:F. Carbonnel)
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1M. Vetizou ; J. M. Pitt ; R. Daillere ; P. Lepage ; N. Waldschmitt ; C. Flament ; S. Rusakiewicz ; B. Routy ; M. P. Roberti ; C. P. Duong ; V. Poirier-Colame ; A. Roux ; S. Becharef ; S. Formenti ; E. Golden ; S. Cording ; G. Eberl ; A. Schlitzer ; F. Ginhoux ; S. Mani ; T. Yamazaki ; N. Jacquelot ; D. P. Enot ; M. Berard ; J. Nigou ; P. Opolon ; A. Eggermont ; P. L. Woerther ; E. Chachaty ; N. Chaput ; C. Robert ; C. Mateus ; G. Kroemer ; D. Raoult ; I. G. Boneca ; F. Carbonnel ; M. Chamaillard ; L. Zitvogel
American Association for the Advancement of Science (AAAS)
Published 2015Staff ViewPublication Date: 2015-11-07Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: Adult ; Aged ; Aged, 80 and over ; Animals ; Anti-Bacterial Agents/pharmacology ; Antibodies, Monoclonal/adverse effects/*therapeutic use ; Bacteroides/*immunology ; CTLA-4 Antigen/*antagonists & inhibitors/immunology ; Dysbiosis/immunology ; Fecal Microbiota Transplantation ; Female ; Gastrointestinal Microbiome/drug effects/*immunology ; Germ-Free Life/immunology ; Humans ; Immunologic Memory ; Immunotherapy ; Intestines/immunology/microbiology ; Male ; Melanoma/*therapy ; Mice ; Mice, Inbred C57BL ; Middle Aged ; Skin Neoplasms/*therapy ; T-Lymphocytes/immunologyPublished by: -
2Staff View
Publication Date: 2018-01-10Publisher: BMJ Publishing GroupPrint ISSN: 0017-5749Electronic ISSN: 1468-3288Topics: MedicinePublished by: -
3Staff View
Publication Date: 2018-03-09Publisher: BMJ Publishing GroupPrint ISSN: 0017-5749Electronic ISSN: 1468-3288Topics: MedicinePublished by: -
4BEAUGERIE, L. ; CARBONNEL, F. ; HECKETSWEILER, B. ; DÉCHELOTTE, P. ; GENDRE, J.-P. ; COSNES, J.
Oxford, UK : Blackwell Science Ltd
Published 1997Staff ViewISSN: 1365-2036Source: Blackwell Publishing Journal Backfiles 1879-2005Topics: MedicineNotes: Aim: To compare the effects of a standard oral rehydration solution with a polymeric glucose isotonic solution enriched with glutamine on water and sodium absorption in the short bowel. Methods: Six patients with high jejunostomy were tested in a random order on 2 consecutive days with the standard solution (20 g/L glucose, 94 mmol/L sodium, 292 mOsm/kg osmolality) and a solution containing maltodextrins (18 g/L Glucidex 12; hydrolysis of 18 g of Glucidex 12 yields 20 g glucose) enriched with 14.6 g/L of glutamine (94 mmol/L sodium, 282 mOsm/kg osmolality). Solutions were administered via a naso-gastric tube at a rate of 2 mL/min. Jejunal effluent for each solution was collected during an 8-h period, after a 14-h equilibrium period. Results: The net 8-h fluid absorption was not significantly different between the standard solution and the solution with glutamine (333 ± 195 and 213 ± 251 mL, respectively (mean ± S.E.M.)). Net sodium absorption was higher for the standard solution than for the solution with glutamine (15 ± 15 vs. 2 ± 20 mmol, P 〈 0.05). The rate of glucose absorption was not different between the solutions. Conclusion: The replacement of glucose by maltodextrins and the addition of glutamine to the standard oral rehydration solution, without changing its sodium content or osmolality, results in a reduction of sodium absorption in the short-bowel syndrome.Type of Medium: Electronic ResourceURL: