Výsledky vyhledávání - Bandar Al‐Saud
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Primary Immunodeficiency Diseases in Saudi Arabia: a Tertiary Care Hospital Experience over a Period of Three Years (2010–2013) Autor 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
Vydáno 2015Artigo -
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Novel CARMIL2 Mutations in Patients with Variable Clinical Dermatitis, Infections, and Combined Immunodeficiency Autor 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
Vydáno 2018Artigo -
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Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies Autor Nisha Patel, Mohammed A. Aldahmesh, Hisham Alkuraya, Shamsa Anazi, Hadeel Alsharif, Arif O. Khan, Asma Sunker, Saleh Al-mohsen, Emad B. Abboud, Sawsan R. Nowilaty, Mohammed Al‐Owain, Hamad Alzaidan, Bandar Al‐Saud, Ali Alasmari, Ghada M. H. Abdel‐Salam, Mohamed Abouelhoda, Firdous Abdulwahab, Niema Ibrahim, Ewa A. Naim, Banan Al‐Younes, Abeer Al‐Mostafa, Abdulelah AlIssa, Mais Hashem, Olga Buzovetsky, Yong Xiong, Dorota Monies, Nada Al Tassan, Ranad Shaheen, Selwa A.F. Al-Hazzaa, Fowzan S. Alkuraya
Vydáno 2015Artigo -
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Human inherited complete STAT2 deficiency underlies inflammatory viral diseases Autor Giorgia Bucciol, Leen Moens, Masato Ogishi, Darawan Rinchai, Daniela Matuozzo, Mana Momenilandi, Nacim Kerrouche, Catherine M. Cale, Elsa Treffeisen, Mohammad Al Salamah, Bandar Al‐Saud, Alain Lachaux, Rémi Duclaux‐Loras, Marie Meignien, Aziz Bousfiha, Ibtihal Benhsaien, Anna Shcherbina, Anna Roppelt, Florian Gothe, Nadhira Houhou‐Fidouh, Scott J. Hackett, Lisa M. Bartnikas, Michelle C. Maciag, Mohammed F. Alosaimi, Janet Chou, Reem Mohammed, Bishara J. Freij, Emmanuelle Jouanguy, Shen‐Ying Zhang, Stéphanie Boisson‐Dupuis, Vivien Béziat, Qian Zhang, C.J. Duncan, Sophie Hambleton, Jean‐Laurent Casanova, Isabelle Meyts
Vydáno 2023Artigo -
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Genetic, Immunological, and Clinical Features of 32 Patients with Autosomal Recessive STAT1 Deficiency Autor Tom Le Voyer, Sonoko Sakata, Miyuki Tsumura, Taushif Khan, Ana Esteve‐Solé, Bandar Al‐Saud, Hatice Eke Güngör, Prasad Taur, Valentine Jeanne-Julien, Mette Christiansen, Lisa-Maria Köhler, Gehad ElGhazali, Jérémie Rosain, Shiho Nishimura, Fumiaki Sakura, Matthieu Bouaziz, Carmen Oleaga‐Quintas, Alejandro Nieto-Patlán, Àngela Deyà‐Martínez, Yasemin Altuner Torun, Anna‐Lena Neehus, Manon Roynard, Şefika Elmas Bozdemir, Nawal Al Kaabi, Moza Al Hassani, Irina Mersiyanova, Flore Rozenberg, Carsten Speckmann, Ina Hainmann, Fabian Hauck, Mohammed H. Al-Zahrani, Sami Al-Hajjar, Saleh Al‐Muhsen, Theresa Cole, Ramsay Fuleihan, Peter D. Arkwright, Raffaele Badolato, Laia Alsina, Laurent Abel, Mukesh Desai, Hamoud Al‐Mousa, Anna Shcherbina, Nico Marr, Stéphanie Boisson‐Dupuis, Jean‐Laurent Casanova, Satoshi Okada, Jacinta Bustamante
Vydáno 2021Carta -
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The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity Autor Safa Barış, Hassan Abolhassani, Michel J. Massaad, Maryam Al‐Nesf, Zahra Chavoshzadeh, Sevgi Keleş, İsmail Reisli, Azzeddine Tahiat, Hiba Shendi, Dalia Abd Elaziz, Brahim Belaid, Fatima Al Dhaheri, Şule Haskoloğlu, Figen Doğu, Imen Ben‐Mustapha, Ali Sobh, Nermeen Galal, Safa Meshaal, Rabab El Hawary, Aisha Elmarsafy, Fayhan Alroqi, Bandar Al‐Saud, Mona Al‐Ahmad, Tariq Al Farsi, Nashat Al Sukaiti, Salem Al‐Tamemi, Cybel Mehawej, Ghassan Dbaibo, Gehad ElGhazali, Sara Şebnem Kılıç, Ferah Genel, Ayça Kıykım, Uğur Muşabak, Hasibe Artaç, Şükrü Nail Güner, Rachida Boukari, Réda Djidjik, Nadia Kechout, Deniz Çağdaş, Zeinab A. El-Sayed, Elif Karakoç-Aydıner, Raed Alzyoud, Mohamed‐Ridha Barbouche, Mehdi Adeli, Rima Hanna Wakim, Shereen M. Reda, Aydan İkincioğulları, Ahmet Özen, Aziz Bousfiha, Hamoud Al‐Mousa, Nima Rezaei, Waleed Al‐Herz, Raif S. Geha
Vydáno 2022Revisão -
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Hematopoietic stem cell transplantation for CD40 ligand deficiency: Results from an EBMT/ESID-IEWP-SCETIDE-PIDTC study Autor 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
Vydáno 2019Artigo -
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Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population Autor 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
Vydáno 2019Artigo -
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Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population Autor 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
Vydáno 2019Errata/Corrigenda
Vyhledávací nástroje:
Související témata
Medicine
Biology
Consanguinity
Immunology
Genetics
Environmental health
Exome
Exome sequencing
Gene
Pediatrics
Population
Primary immunodeficiency
Disease
Epidemiology
Geography
Immune system
Internal medicine
Mutation
Newborn screening
Pathology
Phenotype
Allele
Allelic heterogeneity
Antibody
Archaeology
Cartography
Common variable immunodeficiency
Computational biology
Computer science
Dermatology