Rezultati pretrage - Abdullah Alangari

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  1. 1
    Genomic and non-genomic actions of glucocorticoids in asthma

    Genomic and non-genomic actions of glucocorticoids in asthma od Abdullah Alangari

    Izdano 2010
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  2. 2
    Clinical Features and Anaphylaxis in Children With Cold Urticaria

    Clinical Features and Anaphylaxis in Children With Cold Urticaria od Abdullah Alangari, Frank J. Twarog, Mei‐Chiung Shih, Lynda C. Schneider

    Izdano 2004
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  3. 3
    Treatment of Disseminated Mycobacterial Infection with High-Dose IFN-<i>γ</i>in a Patient with IL-12R<i>β</i>1 Deficiency

    Treatment of Disseminated Mycobacterial Infection with High-Dose IFN-<i>γ</i>in a Patient with IL-12R<i>β</i>1 Deficiency od Abdullah Alangari, Fahad Alzamil, Abdulrahman Almazrou, Saleh Al‐Muhsen, Stéphanie Boisson‐Dupuis, Sitalbanat Awadallah, A.M. Kambal, Jean‐Laurent Casanova

    Izdano 2010
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  4. 4
    LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency

    LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency od Abdullah Alangari, Abdulrahman Alsultan, Nouran Adly, Michel J. Massaad, Iram Shakir Kiani, Abdulrahman Aljebreen, Emad Raddaoui, Abdulkareem Al-Momen, Saleh Al‐Muhsen, Raif S. Geha, Fowzan S. Alkuraya

    Izdano 2012
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  5. 5
    Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked–like disorder caused by loss-of-function mutations in LRBA

    Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked–like disorder caused by loss-of-function mutations in LRBA od Louis‐Marie Charbonnier, Erin Janssen, Janet Chou, Toshiro K. Ohsumi, Sevgi Keleş, Joyce T. Hsu, Michel J. Massaad, Maria Garcia-Lloret, Rima Hanna‐Wakim, Ghassan Dbaibo, Abdullah Alangari, Abdulrahman Alsultan, Daifulah Al-Zahrani, Raif S. Geha, Talal A. Chatila

    Izdano 2014
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  6. 6
    Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells

    Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells od Marjorie Côte, Mickaël Ménager, Agathe Burgess, Nizar Mahlaoui, Capucine Pïcard, Catherine Schaffner, Fahad AlManjomi, Musa Alharbi, Abdullah Alangari, Françoise Le Deist, Andrew R. Gennery, Nathalie Prince, Astrid Cariou, Patrick Nitschké, Ulrich Blank, Gehad ElGhazali, Gaël Ménasché, Sylvain Latour, Alain Fischer, Geneviève de Saint Basile

    Izdano 2009
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  7. 7
    Accelerating matchmaking of novel dysmorphology syndromes through clinical and genomic characterization of a large cohort

    Accelerating matchmaking of novel dysmorphology syndromes through clinical and genomic characterization of a large cohort od Ranad Shaheen, Nisha Patel, Hanan E. Shamseldin, Fatema Alzahrani, Ruah Alyamany, Agaadir Al Moisheer, Nour Ewida, Shamsa Anazi, Maha Alnemer, Mohamed A. El‐Sheikh, Khaled Alfaleh, Muneera J. Alshammari, Amal Alhashem, Abdullah Alangari, Mustafa A. Salih, Martin Kircher, Riza M. Daza, Niema Ibrahim, Salma M. Wakil, Ahmed Alaqeel, Ikhlas Altowaijri, Jay Shendure, Amro Al-Habib, Eissa Faqieh, Fowzan S. Alkuraya

    Izdano 2015
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  8. 8
    JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency

    JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency od Fahad Alsohime, Marta Martín-Fernández, Mohamad‐Hani Temsah, Majed Alabdulhafid, Tom Le Voyer, Malak Alghamdi, Xueer Qiu, Najla Alotaibi, Areej Alkahtani, Sofija Buta, Emmanuelle Jouanguy, Ayman Al‐Eyadhy, Conor Gruber, Gamal Hasan, Fahad A. Bashiri, Rabih Halwani, Hamdy H. Hassan, Saleh Al‐Muhsen, Nouf Alkhamis, Zobaida Alsum, Jean‐Laurent Casanova, Jacinta Bustamante, Dusan Bogunovic, Abdullah Alangari

    Izdano 2020
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  9. 9
    Herpes simplex encephalitis in children with autosomal recessive and dominant TRIF deficiency

    Herpes simplex encephalitis in children with autosomal recessive and dominant TRIF deficiency od Vanessa Sancho‐Shimizu, Rebeca Pérez de Diego, Lazaro Lorenzo, Rabih Halwani, Abdullah Alangari, Elisabeth Israelsson, Sylvie Fabrega, Annabelle Cardon, Jérôme Maluenda, Megumi Tatematsu, Farhad Mahvelati, Melina Herman, Michael J. Ciancanelli, Yiqi Guo, Zobaida Alsum, Nouf Alkhamis, Abdulkarim S. Al-Makadma, Ata Ghadiri, Soraya Boucherit, Sabine Plancoulaine, Capucine Pïcard, Flore Rozenberg, Marc Tardieu, Pierre Lebon, Emmanuelle Jouanguy, Nima Rezaei, Tsukasa Seya, Misako Matsumoto, Damien Chaussabel, Anne Puel, Shen‐Ying Zhang, Laurent Abel, Saleh Al‐Muhsen, Jean‐Laurent Casanova

    Izdano 2011
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  10. 10
    Revisiting Human IL-12Rβ1 Deficiency

    Revisiting Human IL-12Rβ1 Deficiency od Ludovic de Beaucoudrey, Arina Samarina, Jacinta Bustamante, Aurélie Cobat, Stéphanie Boisson‐Dupuis, Jacqueline Feinberg, Saleh Al‐Muhsen, Lucile Jannière, Y Rose, Maylis de Suremain, Xiao‐Fei Kong, Orchidée Filipe‐Santos, Ariane Chapgier, Capucine Pïcard, Alain Fischer, Figen Doğu, Aydan İkincioğulları, Gönül Tanır, Sami Al-Hajjar, Suliman Aljumaah, Husn H. Frayha, Zobaida Alsum, Sulaiman Al-Ajaji, Abdullah Alangari, Abdulaziz Al‐Ghonaium, Parisa Adimi Naghan, Davood Mansouri, Imen Ben‐Mustapha, Judith Yancoski, Ben‐Zion Garty, Carlos Rodríguez‐Gallego, Isabel Caragol, Necil Kütükçüler, Dinakantha Kumararatne, Smita Y. Patel, Rainer Döffinger, Andrew Exley, Olle Jeppsson, Janine Reichenbach, David Nadal, Yaryna Boyko, Barbara Pietrucha, Suzanne T. Anderson, Michael Levin, Liliane Schandené, Kinda Schepers, André Efira, Françoise Mascart, Masao Matsuoka, Tatsunori Sakai, Claire‐Anne Siegrist, Klára Frecerová, Renate Blüetters-Sawatzki, Jutta Bernhöft, Joachim Freihorst, Ulrich Baumann, Darko Richter, Filomeen Haerynck, Frans De Baets, Vas Novelli, David A. Lammas, Christiane Vermylen, David Tuerlinckx, Chris Nieuwhof, Małgorzata Pac, W. Haas, Ingrid Müller‐Fleckenstein, Bernhard Fleckenstein, Jacob Levy, Revathi Raj, Aileen Cleary Cohen, David B. Lewis, Steven M. Holland, Kuender D. Yang, Xiaochuan Wang, Xiaohong Wang, Liping Jiang, Xiqiang Yang, Chaomin Zhu, Yuanyuan Xie, Pamela Lee, Koon Wing Chan, Tong‐Xin Chen, Gabriela Castro, Ivelisse Natera, Ana Codoceo, Alejandra King, Liliana Bezrodnik, Daniela Di Giovani, María Isabel Gaillard, Dewton de Moraes Vasconcelos, Anete Sevciovic Grumach, Alberto José da Silva Duarte, Ruth Aldana, Francisco Espinosa‐Rosales, Mohammed Bejaoui, Ahmed Aziz Bousfiha, Jamila El Baghdadi, Namık Yaşar Özbek, Güzide Aksu

    Izdano 2010
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