Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Soraya Sakhi"'
Autor:
Théophile Cocherie, Mathilda Bastide, Soraya Sakhi, Karen Zafilaza, Philippe Flandre, Valentin Leducq, Aude Jary, Sonia Burrel, Martine Louet, Vincent Calvez, Anne-Geneviève Marcelin, Stéphane Marot
Publikováno v:
Microbiology Spectrum, Vol 10, Iss 5 (2022)
ABSTRACT Large-scale screening for SARS-CoV-2 infection is an important tool for epidemic prevention and control. The appearance of new variants associated with specific mutations can call into question the effectiveness of rapid diagnostic tests (RD
Externí odkaz:
https://doaj.org/article/49a43e191b0a4cb6831f3cab592497b3
Autor:
Soraya Sakhi, Sophie Cholet, Samer Wehbi, Bertrand Isidor, Benjamin Cogne, Sandrine Vuillaumier-Barrot, Thierry Dupré, Trost Detleft, Emmanuelle Schmitt, Bruno Leheup, Céline Bonnet, François Feillet, Christine Muti, François Fenaille, Arnaud Bruneel
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 28, Iss , Pp 100775- (2021)
Congenital disorders of glycosylation (CDG) constitute an ever-growing group of genetic diseases affecting the glycosylation of proteins. CDG individuals usually present with severe multisystem disorders. MAN1B1-CDG is a CDG with nonspecific clinical
Externí odkaz:
https://doaj.org/article/034a12e529784f2f8fecf4cbb92a51e7
Autor:
Soraya Sakhi, Magalie Lodin, Marie-Liesse Étienne, Khadija Ouaziz, Mathilde Filser, Amandine François, Amandine Caillault, Lamia Rouabah, Zoé Guilbert, Margaux Cadenet, Morgane Ducastel, Mathilda Bastide, Emilie Guemas, Julie Brousseau, Mathilde Puel, Pierre Jatteau, Bérénice Schell, Mathilde Roche
Publikováno v:
Annales de biologie clinique.
Autor:
Sandrine Vuillaumier-Barrot, François Fenaille, Soraya Sakhi, Céline Bonnet, Trost Detleft, Sophie Cholet, Samer Wehbi, Bruno Leheup, Emmanuelle Schmitt, Benjamin Cogné, François Feillet, Bertrand Isidor, Christine Muti, Arnaud Bruneel, Thierry Dupré
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 28, Iss, Pp 100775-(2021)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Congenital disorders of glycosylation (CDG) constitute an ever-growing group of genetic diseases affecting the glycosylation of proteins. CDG individuals usually present with severe multisystem disorders. MAN1B1-CDG is a CDG with nonspecific clinical