Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Narimane Zeghbib"'
Autor:
Romain Salle, Olivier Chosidow, Vincent Fihman, Nicolas de Prost, Narimane Zeghbib, Paul‐Louis Woerther, Camille Hua
Publikováno v:
Journal of the European Academy of Dermatology and Venereology.
Autor:
Laura Giraud‐Kerleroux, Saskia Ingen‐Housz‐Oro, Nicolas De Prost, Narimane Zeghbib, Caroline Fiani, Margaux Mongereau, Charlotte Gary, Gaëlle Hirsch, Camille Hua, Tu‐Anh Duong
Publikováno v:
Journal of the European Academy of Dermatology and Venereology : JEADVREFERENCES.
Autor:
T.-A. Duong, Caroline Fiani, G. Hirsch, Laura Giraud-Kerleroux, Saskia Oro, Camille Hua, Margaux Mongereau, Narimane Zeghbib, Charlotte Gary, Nicolas De Prost
Publikováno v:
Annales de Dermatologie et de Vénéréologie - FMC. 1:A320-A321
Introduction En permettant l’acces a l’expertise dermatologique, la teledermatologie (TD) facilite la prise en charge des patients atteints de maladies rares eloignes des centres de reference (CR). L’objectif de notre etude etait d’analyser l
Autor:
Sonia Lehri-Boufala, Christophe Morin, Céline Laurencé, Michael Rivard, Philippe Le Corvoisier, Isabelle Lachaise, Thierry Martens, Laure Garrigue-Antar, Narimane Zeghbib, Caroline Barau
Publikováno v:
Biochemical Pharmacology
Biochemical Pharmacology, Elsevier, 2019, 160, pp.14-23. ⟨10.1016/j.bcp.2018.12.007⟩
Biochemical Pharmacology, Elsevier, 2019, 160, pp.14-23. ⟨10.1016/j.bcp.2018.12.007⟩
International audience; Pharmaceuticals and their by-products are increasingly a matter of concern, because of their unknown impacts on human health and ecosystems. The lack of information on these transformation products, which toxicity may exceed t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18a4ab93c1ab68da2d080234aa467b21
https://hal-enpc.archives-ouvertes.fr/hal-02267947
https://hal-enpc.archives-ouvertes.fr/hal-02267947
Publikováno v:
ChemInform. 47
The reaction tolerates a wide range of functional groups and delivers the arylpyridinium chloride products in generally high yields.
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2016, 81 (8), pp.3256-3262. ⟨10.1021/acs.joc.6b00208⟩
Journal of Organic Chemistry, American Chemical Society, 2016, 81 (8), pp.3256-3262. ⟨10.1021/acs.joc.6b00208⟩
The Zincke reaction allows the transformation of primary amines into their respective N-alkylated or N-arylated pyridinium salts. While nucleophilic primary amines (typically, aliphatic primary amines) often lead to quantitative reactions and has bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14b0a3e459b1aaf9de571c449e597de4
https://hal.archives-ouvertes.fr/hal-03124455
https://hal.archives-ouvertes.fr/hal-03124455
Autor:
Andrea Civra, Manuela Donalisio, Claire Laine, David Lembo, Elsa P. Bianchini, Valeria Cagno, Narimane Zeghbib, Kawthar Bouchemal
A new, simple and green method was developed for the manufacturing of heparin nanoassemblies active against the heparan sulfate-dependent viruses HSV-1, HSV-2, HPV-16 and RSV. These nanoassemblies were obtained by the auto-association of O-palmitoyl-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::070afea7bf770c6b0cc629fe942d244d
http://hdl.handle.net/2318/148746
http://hdl.handle.net/2318/148746