Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Raymond Mikhael"'
Autor:
Rabi Hanna, Alexander A. Navarini, Janet Chou, Marc B. Bigler, Joeseph A. Church, Christoph Berger, Luigi D. Notarangelo, Polina Stepensky, Anne Valérie Burgener, Fariba Rezaee, Fabian Baldin, Mike Recher, Rebecca Higgins, Waleed Al-Herz, Florian Marquardsen, Gérard Lefranc, Shlomit Kfir-Erenfeld, Christoph Hess, Raif S. Geha, Benedikt J. Meyer, Florian Wunderer, Raymond Mikhael, Zeina Baz, Daniel Bloch, Annaïse Jauch
Publikováno v:
Journal of Clinical Immunology. 37:707-714
Mutations in Sp110 are the underlying cause of veno-occlusive disease with immunodeficiency (VODI), a combined immunodeficiency that is difficult to treat and often fatal. Because early treatment is critically important for patients with VODI, broadl
Autor:
Gunasekaran Ramakrishnan, Elie Choueiry, Raymond Mikhael, Mohammed Al-Tannir, Rodrigo DeAntonio, Mariam Rajab, Adlette Inati, Omar Salam, Ghassan Dbaibo
Publikováno v:
Trials in Vaccinology. 2:25-30
Background Rotavirus (RV) is a major cause of gastroenteritis (GE) in infants and young children globally, with rotavirus gastroenteritis (RVGE) causing dehydration due to diarrhea and frequently leading to hospitalization. Epidemiological data on RV
Autor:
Françoise Le Deist, Raif S. Geha, Raymond Mikhael, Haifa H. Jabara, Janet Chou, Michel J. Massaad, André Mégarbané, Pierre Portales, G Lefranc, Patrick Revy, Halli Benson, Toshiro K. Ohsumi, Jürgen Ruland, Hiroyuki Hosokawa, Andreas Gewies, Eliane Chouery, Toshinori Nakayama, Henry G. Herrod, Oliver Gorka
Publikováno v:
Journal of Allergy and Clinical Immunology
Background Combined immunodeficiency (CID) is characterized by severe recurrent infections with normal numbers of T and B lymphocytes but with deficient cellular and humoral immunity. Most cases are sporadic, but autosomal recessive inheritance has b
Autor:
Claudia Djambas Khayat, Capucine Picard, Ariane Chapgier, Guillaume Vogt, Alexandre Alcaïs, Nizar Mahlaoui, Jacinta Bustamante, Jacqueline Feinberg, Stéphanie Dupuis, Jean-Laurent Casanova, Christophe Lamaze, Jennifer M. Puck, Geneviève de Saint Basile, Raymond Mikhael, Laure Gineau
Publikováno v:
The Journal of Experimental Medicine
Germline mutations may cause human disease by various mechanisms. Missense and other in-frame mutations may be deleterious because the mutant proteins are not correctly targeted, do not function correctly, or both. We studied a child with mycobacteri
Autor:
Guillaume Vogt, Jacinta Bustamante, Ariane Chapgier, Jacqueline Feinberg, Stephanie Boisson Dupuis, Capucine Picard, Nizar Mahlaoui, Laure Gineau, Alexandre Alcaïs, Christophe Lamaze, Jennifer M. Puck, Geneviève de Saint Basile, Claudia Khayat, Raymond Mikhael, Jean-Laurent Casanova
Publikováno v:
The Journal of Cell Biology. 182:i6-i6