Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Zeina Baz"'
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:
Peter A. Nigrovic, Kelsey Stafstrom, Paul A. Brogan, Carla Irani, Pui Y. Lee, Christa Krupski, Janet Chou, Rasha El-Owaidy, Craig D. Platt, Sara Sebnem Kilic, Irit Tirosh, Eugene P. Chambers, Tali Stauber, Raif S. Geha, Raju Khubchandani, Zeina Baz, Z. Huang, M.R. Lokeshwar, Mohammed F. Alosaimi, Despina Eleftheriou, Wayne Bainter, Pallavi Pimpale, Michael B. Jordan, Ali Sobh, Erinn S. Kellner, Qing Zhou, Aaron R. Weiss, Somech Raz, Gérard Lefranc, Yuelong Huang, Elissa Furutani
Publikováno v:
J Allergy Clin Immunol
BACKGROUND: Deficiency of adenosine deaminase 2 (DADA2) is a syndrome with pleiotropic manifestations including vasculitis and hematologic compromise. A systematic definition of the relationship between ADA2 mutations and clinical phenotype remains u
Autor:
Fayhan Alroqi, Zeina Baz, Abduarahman Almutairi, Janet Chou, Sevgi Keles, Talal A. Chatila, Reem Mohammed, Pierre Mouawad, Fatima Ghandour, Louis-Marie Charbonnier, Rami Sabouneh, Raif S. Geha, Michel J. Massaad
The dedicator of cytokinesis 8 (DOCK8) deficiency is an autosomal recessive-combined immunodeficiency whose clinical spectra include recurrent infections, autoimmunity, malignancies, elevated serum IgE, eczema, and food allergies. Here, we report on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ae9b7063928e561521797620288942c
https://europepmc.org/articles/PMC5691358/
https://europepmc.org/articles/PMC5691358/
Autor:
Julie Sawalle-Belohradsky, Beate Hagl, H. Bobby Gaspar, Gundula Notheis, Ferah Genel, László Maródi, Abbas Hawwari, Stephan Ehl, Kirsten Bienemann, Fatih Mehmet Azik, Ilhan Tezcan, Deniz Cagdas Ayvaz, Zobaida Alsum, Larysa Kostyuchenko, Hans D. Ochs, Valerie Heinz, Oscar Porras, Waleed Al-Herz, Gregor Dückers, Daifulah Al-Zahrani, Sara Sebnem Kilic, Vincent Barlogis, Talal A. Chatila, Leena Kainulainen, Robbert G. M. Bredius, Joris M. van Montfrans, Betul Tavil, Karin R. Engelhardt, Benjamin Gathmann, Ashish R Kumar, Jens Thiel, Michael H. Albert, Alexandra F. Freeman, Andrew R. Gennery, Neslihan Edeer Karaca, Raif S. Geha, Sevgi Keles, Susanne Matthes-Martin, Roland C. Aydin, Ansgar Schulz, Sung-Yun Pai, Ayse Metin, Capucine Picard, Ozden Sanal, Marianne Ifversen, Bernd H. Belohradsky, Steven M. Holland, Manfred Hönig, Bodo Grimbacher, S. Aydin, Jordan S. Orange, Nima Rezaei, Helen Su, Ellen D. Renner, Carl Philipp Schwarze, Taco W. Kuijpers, Necil Kutukculer, Hamoud Al-Mousa, Jordan K. Abbott, Zeina Baz, Caner Aytekin, Luis Ignacio Gonzalez-Granado
Publikováno v:
Journal of Clinical Immunology, 35(2), 189. Springer New York
Journal of clinical immunology, 35(2), 189-198. Springer New York
Journal of clinical immunology, 35(2), 189-198. Springer New York
Mutations in DOCK8 result in autosomal recessive Hyper-IgE syndrome with combined immunodeficiency (CID). However, the natural course of disease, long-term prognosis, and optimal therapeutic management have not yet been clearly defined. In an interna
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf4afc46b4965adc66d9b22cce8a53cd
https://dspace.library.uu.nl/handle/1874/332865
https://dspace.library.uu.nl/handle/1874/332865
Autor:
Tim Niehues, Karin R. Engelhardt, Mehmet Kilic, Raif S. Geha, Necil Kutukculer, Zeina Baz, Sevgi Keles, Cristina Glocker, Caner Aytekin, Ozden Sanal, Ismail Reisli, Zahra Pourpak, Ferah Genel, Mustafa Yilmaz, Alison Jones, B Gaspar, Elena C. Sigmund, Nermeen Galal, Yildiz Camcioglu, Michel J. Massaad, Amos Etzioni, Turkan Patiroglu, Laura E. Graham, Maria Cristina Pietrogrande, Majed Dasouki, Andrew R. Gennery, S Weinspach, G Dueckers, Michael E. Gertz, Monia Khemiri, M. R. Barbouche, Mehdi Yeganeh, Imen Ben-Mustapha, Shiva Saghafi, Bodo Grimbacher, Salem Al-Tamemi, Andrew J. Cant, A. Sassi, Gérard Lefranc, Ayse Metin, Vassilios Lougaris, Ayper Somer, Fethi Mellouli, Ekrem Unal, Alexandra F. Freeman, Jeannette Boutros, Ruben Ceja, Jens Thiel, André Mégarbané, Sara Sebnem Kilic, Talal A. Chatila, Mohamed Bejaoui, Alejandro A. Schäffer, Ilhan Tezcan, Waleed Al-Herz, Peter D. Arkwright, Ilka Schulze
Publikováno v:
Journal of Allergy and Clinical Immunology: In Practice
Journal of Allergy and Clinical Immunology: In Practice, Elsevier, 2015, 136 (2), pp.402-12. ⟨10.1016/j.jaci.2014.12.1945⟩
Journal of Allergy and Clinical Immunology: In Practice, Elsevier, 2015, 136 (2), pp.402-12. ⟨10.1016/j.jaci.2014.12.1945⟩
PubMedID: 25724123 Background Mutations in dedicator of cytokinesis 8 (DOCK8) cause a combined immunodeficiency (CID) also classified as autosomal recessive (AR) hyper-IgE syndrome (HIES). Recognizing patients with CID/HIES is of clinical importance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08d8b23abc6c5a5d7f77d7ae3893d473
http://hdl.handle.net/11655/14451
http://hdl.handle.net/11655/14451
Publikováno v:
Annals of Allergy, Asthma & Immunology. 80:263-268
Interferon-gamma (IFN-gamma) is a potent cytokine that modulates IL-4-induced immune responses. Atopic dermatitis is associated with increased IgE levels and decreased IFN-gamma production. Recent phase I and phase II studies have suggested that shor
Autor:
Zeina Baz
Publikováno v:
Journal of Allergy and Clinical Immunology. 137:AB155
Autor:
Maria Grazia Roncarolo, Cristina Panaroni, Francesco Marangoni, Zeina Baz, Luigi D. Notarangelo, Sara Trifari, Silvana Martino, Loïc Dupré, Manuela Battaglia, Anna Villa, Alessandro Aiuti, Ayse Metin, Federica Cattaneo, Samantha Scaramuzza
Publikováno v:
The Journal of experimental medicine, vol 204, iss 2
204 (2007): :369–380.
info:cnr-pdr/source/autori:Marangoni F, Trifari S, Scaramuzza S, Panaroni C, Martino S, Notarangelo LD, Baz Z, Metin A, Cattaneo F, Villa A, Aiuti A, Battaglia M, Roncarolo MG, Dupré L/titolo:WASP regulates suppressor activity of human and murine CD4(+)CD25(+)FOXP3(+) natural regulatory T cells/doi:/rivista:/anno:2007/pagina_da::369/pagina_a:380/intervallo_pagine::369–380/volume:204
The Journal of Experimental Medicine
204 (2007): :369–380.
info:cnr-pdr/source/autori:Marangoni F, Trifari S, Scaramuzza S, Panaroni C, Martino S, Notarangelo LD, Baz Z, Metin A, Cattaneo F, Villa A, Aiuti A, Battaglia M, Roncarolo MG, Dupré L/titolo:WASP regulates suppressor activity of human and murine CD4(+)CD25(+)FOXP3(+) natural regulatory T cells/doi:/rivista:/anno:2007/pagina_da::369/pagina_a:380/intervallo_pagine::369–380/volume:204
The Journal of Experimental Medicine
A large proportion of Wiskott-Aldrich syndrome (WAS) patients develop autoimmunity and allergy. CD4(+)CD25(+)FOXP3(+) natural regulatory T (nTreg) cells play a key role in peripheral tolerance to prevent immune responses to self-antigens and allergen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76c89f722061bc09e1280bd25b6477eb
https://escholarship.org/uc/item/2rb70927
https://escholarship.org/uc/item/2rb70927