Suchergebnisse - Rand Arnaout
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Primary Immunodeficiency Diseases in Saudi Arabia: a Tertiary Care Hospital Experience over a Period of Three Years (2010–2013) von Bandar Al‐Saud, Hamoud Al‐Mousa, Sulaiman Al Gazlan, Abdulaziz Al‐Ghonaium, Rand Arnaout, Amal Al-Seraihy, Sahar Elshorbagi, Nazeema Elsayed, Jawad Afzal, Hasan Al‐Dhekri, Saleh Al‐Muhsen
Veröffentlicht 2015Artigo -
2
Novel CARMIL2 Mutations in Patients with Variable Clinical Dermatitis, Infections, and Combined Immunodeficiency von Anas M. Alazami, Maryam Al-Helale, Safa Alhissi, Bandar Al‐Saud, Huda Alajlan, Dorota Monies, Zeeshan Shah, Mohamed Abouelhoda, Rand Arnaout, Hasan Al‐Dhekri, Nouf S. Al‐Numair, Hazem Ghebeh, Farrukh Sheikh, Hamoud Al‐Mousa
Veröffentlicht 2018Artigo -
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A novel mutation in the POLE2 gene causing combined immunodeficiency von Francesco Frugoni, Kerry Dobbs, Kerstin Felgentreff, Hasan Al‐Dhekri, Bandar K. Al Saud, Rand Arnaout, Afshan A. Ali, Avinash Abhyankar, Fayhan Alroqi, Silvia Giliani, Mayra Martinez Ojeda, Erdyni N. Tsitsikov, Sung‐Yun Pai, Jean‐Laurent Casanova, Luigi D. Notarangelo, John P. Manis
Veröffentlicht 2015Carta -
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A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency von Haifa H. Jabara, Steven E. Boyden, Janet Chou, Narayanaswamy Ramesh, Michel J. Massaad, Halli Benson, Wayne Bainter, David Fraulino, Fedik Rahimov, Colin A. Sieff, Zhi-Jian Liu, Salem Alshemmari, Basel K. al-Ramadi, Hasan Al‐Dhekri, Rand Arnaout, Mohammad Abu-Shukair, Anant Vatsayan, Eli Silver, Sanjay Ahuja, E. Graham Davies, Martha Sola‐Visner, Toshiro K. Ohsumi, Nancy C. Andrews, Luigi D. Notarangelo, Mark D. Fleming, Waleed Al‐Herz, Louis M. Kunkel, Raif S. Geha
Veröffentlicht 2015Artigo -
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Hematopoietic Stem Cell Transplantation as Treatment for Patients with DOCK8 Deficiency von Susanne Aydin, Alexandra F. Freeman, Waleed Al‐Herz, Hamoud Al‐Mousa, Rand Arnaout, Roland C. Aydin, Vincent Barlogis, Bernd H. Belohradsky, Carmem Bonfim, Robbert G. M. Bredius, Julia Chu, Oana Ciocârlie, Figen Doğu, Hubert B. Gaspar, Raif S. Geha, Andrew R. Gennery, Fabian Hauck, Abbas Hawwari, Dennis D. Hickstein, Manfred Hoenig, Aydan İkincioğulları, Christoph Klein, Ashish Kumar, Marianne Ifversen, Susanne Matthes, Ayşe Metìn, Bénédicte Neven, Sung‐Yun Pai, Suhag Parikh, Capucine Pïcard, Ellen D. Renner, Özden Sanal, Ansgar Schulz, Friedhelm R. Schuster, Nirali N. Shah, Evan Shereck, Mary Slatter, Helen C. Su, Joris van Montfrans, Wilhelm Woessmann, John B. Ziegler, Michael H. Albert
Veröffentlicht 2018Artigo -
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Hematopoietic stem cell transplantation for CD40 ligand deficiency: Results from an EBMT/ESID-IEWP-SCETIDE-PIDTC study von Francesca Ferrua, Stefania Galimberti, Virginie Courteille, Mary Slatter, Claire Booth, Despina Moshous, Bénédicte Neven, Stéphane Blanche, Marina Cavazzana, Alexandra Laberko, Anna Shcherbina, Dmitry Balashov, Elena Soncini, Fulvio Porta, Hamoud Al‐Mousa, Bandar Al‐Saud, Hasan Al‐Dhekri, Rand Arnaout, Renata Formánková, Yves Bertrand, Andrzej Lange, Joanne Smart, Beata Wolska‐Kuśnierz, Victor M. Aquino, Christopher C. Dvorak, Anders Fasth, Fanny Fouyssac, Carsten Heilmann, Manfred Hoenig, Catharina Schuetz, Jadranka Kelečić, Robbert G. M. Bredius, Arjan C. Lankester, Caroline A. Lindemans, Felipe Suárez, Kathleen E. Sullivan, Michael H. Albert, Krzysztof Kałwak, Vincent Barlogis, Monica Bhatia, Victoria Bordon, Wojciech Czogała, Laura Alonso, Figen Doğu, Jolanta Goździk, Aydan İkincioğulları, Gergely Kriván, Per Ljungman, Isabelle Meyts, Peter Mustillo, Angela R. Smith, Carsten Speckmann, Mikael Sundin, Steven J. Keogh, Peter J. Shaw, Jaap Jan Boelens, Ansgar Schulz, Petr Sedláček, Paul Veys, Nizar Mahlaoui, Aleš Janda, E. Graham Davies, Alain Fischer, Morton J. Cowan, Andrew R. Gennery
Veröffentlicht 2019Artigo -
7
Impaired IL-23–dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency von Masato Ogishi, Andrés A. Arias, Rui Yang, Ji Eun Han, Peng Zhang, Darawan Rinchai, Joshua Halpern, Jeanette Mulwa, Narelle Keating, Maya Chrabieh, Candice Lainé, Yoann Seeleuthner, Noé Ramírez-Alejo, Nioosha Nekooie‐Marnany, Andrea Guennoun, Ingrid Müller‐Fleckenstein, Bernhard Fleckenstein, Sara Şebnem Kılıç, Yoshiyuki Minegishi, Stephan Ehl, Petra Kaiser‐Labusch, Yasemin Kendir Demirkol, Flore Rozenberg, Abderrahmane Errami, Shen‐Ying Zhang, Qian Zhang, Jonathan Bohlen, Quentin Philippot, Anne Puel, Emmanuelle Jouanguy, Zahra Pourmoghaddas, Shahrzad Bakhtiar, André Willasch, Gerd Horneff, Genevieve Llanora, Lynette Pei‐Chi Shek, Louis Yi Ann Chai, Sen Hee Tay, Hamid Rahimi, Seyed Alireza Mahdaviani, Serdar Nepesov, Aziz Bousfiha, Emine Hafize Erdeniz, Adem Karbuz, Nico Marr, Carmen Navarrete, Mehdi Adeli, Lennart Hammarström, Hassan Abolhassani, Nima Parvaneh, Saleh Al Muhsen, Mohammed F. Alosaimi, Fahad Alsohime, Maryam Nourizadeh, Mostafa Moin, Rand Arnaout, Saad Alshareef, Jamila El Baghdadi, Ferah Genel, Roya Sherkat, Ayça Kıykım, Esra Yücel, Sevgi Keleş, Jacinta Bustamante, Laurent Abel, Jean‐Laurent Casanova, Stéphanie Boisson‐Dupuis
Veröffentlicht 2022Artigo -
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The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes von Dorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed, Zuhair N. Al‐Hassnan, Maha Alotaibi, Husam Kayyali, Mohammed Al‐Owain, Ayaz Shah, Zuhair Rahbeeni, Mohammad A. Al–Muhaizea, Hamad Alzaidan, Edward Cupler, Saeed Bohlega, Eissa Faqeih, Maha Faden, Banan Al‐Younes, Dyala Jaroudi, Ewa Goljan, Hadeel Elbardisy, Asma Akilan, Renad Albar, Hesham Aldhalaan, Shamshad Gulab, Aziza Chedrawi, Bandar K. Al Saud, Wesam Kurdi, Nawal Makhseed, Tahani Alqasim, Heba Y. El Khashab, Hamoud Al‐Mousa, Amal Alhashem, Imaduddin Kanaan, Talal Algoufi, Khalid A. Alsaleem, Talal A. Basha, Fathiya Al-Murshedi, Sameena Khan, Adila Al‐Kindy, Maha Alnemer, Sami Al-Hajjar, Suad Alyamani, Hasan Al‐Dhekri, Ali Almehaidib, Rand Arnaout, Omar Dabbagh, Mohammad Shagrani, Dieter Broering, Maha Tulbah, Amal AlQassmi, Maisoon Almugbel, Mohammed Alquaiz, Abdulaziz Alsaman, Khalid Al‐Thihli, Raashda A. Sulaiman, Wajeeh Aldekhail, Abeer Al‐Saegh, Fahad A. Bashiri, Alya Qari, Suzan Alhomadi, Hisham Alkuraya, Mohammed Al‐Sebayel, Muddathir H. Hamad, László Szönyi, Faisal Abaalkhail, Sulaiman M. Al‐Mayouf, Hamad Al‐Mojalli, Khalid Alqadi, Hussien Elsiesy, Taghreed Shuaib, Mohammed Zain Seidahmed, Ibraheem Abosoudah, Hana Akleh, Abdulaziz Al‐Ghonaium, Turki M. Al-Kharfy, Fuad Al Mutairi, Wafa Eyaid, Abdullah Alshanbary, Farrukh Sheikh, Fahad Alsohaibani, Abdullah Alsonbul, Saeed Al Tala, Soher Balkhy, Randa Bassiouni, Ahmed Alenizi, Maged H. Hussein, Saeed Hassan, Mohamed M.I. Khalil, Brahim Tabarki, Saad AlShahwan, Oshi Amira, Yasser Sabr, Saad Alsaadoun, Mustafa A. Salih, Sarar Mohamed, Habiba Sultana, Abdullah Tamim, Moayad El-Haj, Saif Alshahrani, Dalal Bubshait, Majid Alfadhel
Veröffentlicht 2017Artigo -
9
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population von Dorota Monies, Mohammed Abouelhoda, Mirna Assoum, Nabil Moghrabi, Rafiullah Rafiullah, Naif A. M. Almontashiri, Mohammed Al‐Owain, Hamad Alzaidan, Moeen Al-Sayed, Shazia Subhani, Edward Cupler, Maha Faden, Amal Alhashem, Alya Qari, Aziza Chedrawi, Hisham Aldhalaan, Wesam Kurdi, Sameena Khan, Zuhair Rahbeeni, Maha Alotaibi, Ewa Goljan, Hadeel Elbardisy, Mohamed El-Kalioby, Zeeshan Shah, Hibah Alruwaili, Amal Jaafar, Ranad Albar, Asma Akilan, Hamsa T. Tayeb, Asma I. Tahir, Fawzy Mohamed, Mohammed A. F. Nasr, Shaza Makki, Abdullah Alfaifi, Hanna Akleh, Suad Al Yamani, Dalal Bubshait, Mohammed Mahnashi, Talal A. Basha, Afaf Alsagheir, Musad Abu Khaled, Khalid A. Alsaleem, Maisoon Almugbel, Manal Badawi, Fahad A. Bashiri, Saeed Bohlega, Raashida Sulaiman, Ehab Tous, Syed A. Ahmed, Talal Algoufi, Hamoud Al‐Mousa, Emadia Alaki, Susan Alhumaidi, Hadeel Alghamdi, Malak Alghamdi, Ahmed N. Sahly, Shapar Nahrir, Ali Alahmari, Hisham Alkuraya, Ali Almehaidib, Mohammed Abanemai, Fahad Alsohaibaini, Bandar Al‐Saud, Rand Arnaout, Ghada M. H. Abdel‐Salam, Hasan Al‐Dhekri, Suzan A. AlKhater, Khalid Alqadi, Essam Al‐Sabban, Turki Alshareef, Khalid Awartani, Hanaa Banjar, Nada Alsahan, Ibraheem Abosoudah, Abdullah Al‐Ashwal, Wajeeh Aldekhail, Sami Al-Hajjar, Sulaiman M. Al‐Mayouf, Abdulaziz Alsemari, Walaa Alshuaibi, Saeed M Al-Tala, Abdulhadi Altalhi, Salah Baz, Muddathir H. Hamad, Tariq Abalkhail, Badi Alenazi, Alya Alkaff, Fahad Almohareb, Fuad Al Mutairi, Mona Alsaleh, Abdullah Alsonbul, Somaya Alzelaye, Shakir Bahzad, Abdulaziz Bin Manee, Ola Jarrad, Neama Meriki, Bassem Albeirouti, Amal Alqasmi, Mohammed Al Balwi, Nawal Makhseed
Veröffentlicht 2019Artigo -
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Definition, aims, and implementation of GA<sup>2</sup>LEN/HAEi Angioedema Centers of Reference and Excellence von Marcus Maurer, Werner Aberer, Rosana Câmara Agondi, Mona Al‐Ahmad, Maryam Al‐Nesf, Ignacio J. Ansotegui, Rand Arnaout, L. Karla Arruda, Riccardo Asero, Emel Aygören‐Pürsün, Aleena Banerji, Andrea Bauer, Moshe Ben‐Shoshan, Alejandro Berardi, Jonathan A. Bernstein, Stephen Betschel, Carsten Bindslev‐Jensen, Mojca Bizjak, Isabelle Boccon‐Gibod, Konrad Bork, Laurence Bouillet, Henrik Balle Boysen, Nicholas Brodszki, Sigurd Broesby‐Olsen, Paula J. Busse, Thomas Buttgereit, Anette Bygum, Teresa Caballero, Régis A. Campos, Mauro Cancian, Iván Chérrez-Ojeda, Danny M. Cohn, Célia Costa, Timothy Craig, Paulo Ricardo Criado, Roberta Fachini Jardim Criado, Dorottya Csuka, Joachim Dissemond, A. Du‐Thanh, Luís Felipe Ensina, Ragıp Ertaş, J E Fabiani, Claudio Fantini, Henriette Farkas, Silvia Mariel Ferrucci, Ignasi Figueras‐Nart, Natalia Lorena Fili, Daria Fomina, Atsushi Fukunaga, Aslı Gelincik, Ana M. Giménez‐Arnau, Kiran Godse, Mark Gompels, Margarida Gonçalo, Maia Gotua, Richard Gower, Anete Sevciovic Grumach, Guillermo Guidos Fogelbach, Michihiro Hide, Natalia Ilina, Naoko Inomata, Thilo Jakob, Darío Josviack, Hye–Ryun Kang, Allen P. Kaplan, Alicja Kasperska−Zając, Constance H. Katelaris, Aharon Kessel, Andreas Kleinheinz, Emek Kocatürk, Mitja Košnik, Dorota Krasowska, Kanokvalai Kulthanan, Muthu Sendhil Kumaran, José Ignacio Larco Sousa, Hilary Longhurst, William Lumry, Andrew J. MacGinnitie, Markus Magerl, Michaël Makris, Alejandro Malbrán, Alexander Marsland, Inmaculada Martinez‐Saguer, Iris Medina, Raisa Meshkova, Martin Metz, Iman Nasr, Jan P. Nicolay, Chikako Nishigori, Isao Ohsawa, Kemal Özyurt, Nikolaos G. Papadopoulos, Claudio Alberto Salvador Parisi, Jonny Peter, Wolfgang Pfützner, Todor A. Popov, Nieves Prior, German D. Ramón, Adam Reich, Avner Reshef
Veröffentlicht 2020Artigo -
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The global impact of the COVID‐19 pandemic on the management and course of chronic urticaria von Emek Kocatürk, Andaç Salman, Iván Chérrez-Ojeda, Paulo Ricardo Criado, Jonny Peter, Elif Cömert-Özer, Mohamed Abuzakouk, Rosana Câmara Agondi, Mona Al‐Ahmad, Sabine Altrichter, Rand Arnaout, L. Karla Arruda, Riccardo Asero, Andrea Bauer, Moshe Ben‐Shoshan, Jonathan A. Bernstein, Mojca Bizjak, Isabelle Boccon‐Gibod, Hanna Bonnekoh, Laurence Bouillet, Zenon Brzoza, Paula J. Busse, Régis A. Campos, Emily Carne, Niall Conlon, Roberta Fachini Jardim Criado, Eduardo Magalhães de Souza Lima, Semra Demir, Joachim Dissemond, Sibel Doğan, Irina V. Dorofeeva, Luís Felipe Ensina, Ragıp Ertaş, Silvia Mariel Ferrucci, Ignasi Figueras‐Nart, Daria Fomina, Sylvie M. Franken, Atsushi Fukunaga, Ana M. Giménez‐Arnau, Kiran Godse, Margarida Gonçalo, Maia Gotua, Clive Grattan, Carole Guillet, Naoko Inomata, Thilo Jakob, Gül Karakaya, Alicja Kasperska−Zając, Constance H. Katelaris, Mitja Košnik, Dorota Krasowska, Kanokvalai Kulthanan, Muthu Sendhil Kumaran, Claudia Lang, José Ignacio Larco‐Sousa, Elisavet Lazaridou, Tabi A. Leslie, Undine Lippert, Oscar Calderón Llosa, Michaël Makris, Alexander Marsland, Iris Medina, Raisa Meshkova, Esther Bastos Palitot, Claudio Alberto Salvador Parisi, Julia Pickert, German D. Ramón, Mónica Rodríguez-González, Nelson Augusto Rosário Filho, Michael Rudenko, Krzysztof Rutkowski, Jorge Sánchez, Sibylle Schliemann, Bülent Enis Şekerel, Faradiba Sarquis Serpa, E. Serra‐Baldrich, Zhiqiang Song, A. Soria, Maria Staevska, Petra Staubach, Anna Tagka, Shunsuke Takahagi, Simon Francis Thomsen, Regina Treudler, Zahava Vadasz, Solange Oliveira Rodrigues Valle, Martijn B. A. van Doorn, Christian Vestergaard, Nicola Wagner, Dahu Wang, Liangchun Wang, Bettina Wedi, Paraskevi Xepapadaki, Esra Yücel, Anna Zalewska‐Janowska, Zuotao Zhao, Torsten Zuberbier, Marcus Maurer
Veröffentlicht 2020Artigo -
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Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population von Dorota Monies, Mohammed Abouelhoda, Mirna Assoum, Nabil Moghrabi, Rafiullah Rafiullah, Naif A. M. Almontashiri, Mohammed Al‐Owain, Hamad Alzaidan, Moeen Al-Sayed, Shazia Subhani, Edward Cupler, Maha Faden, Amal Alhashem, Alya Qari, Aziza Chedrawi, Hisham Aldhalaan, Wesam Kurdi, Sameena Khan, Zuhair Rahbeeni, Maha Alotaibi, Ewa Goljan, Hadeel Elbardisy, Mohamed El-Kalioby, Zeeshan Shah, Hibah Alruwaili, Amal Jaafar, Ranad Albar, Asma Akilan, Hamsa T. Tayeb, Asma I. Tahir, Mohamed Fawzy, Mohammed A. F. Nasr, Shaza Makki, Abdullah Alfaifi, Hanna Akleh, Suad Al Yamani, Dalal Bubshait, Mohammed Mahnashi, Talal A. Basha, Afaf Alsagheir, Musad Abu Khaled, Khalid A. Alsaleem, Maisoon Almugbel, Manal Badawi, Fahad A. Bashiri, Saeed Bohlega, Raashida Sulaiman, Ehab Tous, S. Faisal Ahmed, Talal Algoufi, Hamoud Al‐Mousa, Emadia Alaki, Susan Alhumaidi, Hadeel Alghamdi, Malak Alghamdi, Ahmed N. Sahly, Shapar Nahrir, Ali Alahmari, Hisham Alkuraya, Ali Almehaidib, Mohammed Abanemai, Fahad Alsohaibaini, Bandar Al‐Saud, Rand Arnaout, Ghada M. H. Abdel‐Salam, Hasan Al‐Dhekri, Suzan A. AlKhater, Khalid Alqadi, Essam Al‐Sabban, Turki Alshareef, Khalid Awartani, Hanaa Banjar, Nada Alsahan, Ibraheem Abosoudah, Abdullah Al‐Ashwal, Wajeeh Aldekhail, Sami Al-Hajjar, Sulaiman M. Al‐Mayouf, Abdulaziz Alsemari, Walaa Alshuaibi, Saeed M Al-Tala, Abdulhadi Altalhi, Salah Baz, Muddathir H. Hamad, Tariq Abalkhail, Badi Alenazi, Alya Alkaff, Fahad Almohareb, Fuad Al Mutairi, Mona Alsaleh, Abdullah Alsonbul, Somaya Alzelaye, Shakir Bahzad, Abdulaziz Bin Manee, Ola Jarrad, Neama Meriki, Bassem Albeirouti, Amal Alqasmi, Mohammed Al Balwi, Nawal Makhseed
Veröffentlicht 2019Errata/Corrigenda
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