Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Agha M Rehan Khaliq"'
Autor:
Maram Al Banyan, Saad Al Shareef, Dina Mahmoud Ahmad Aljayar, Fayha Farraj Abothenain, Agha M Rehan Khaliq, Hassan Alrayes, Rand Arnaout, Farrukh Sheikh
Publikováno v:
Saudi Journal of Anaesthesia, Vol 15, Iss 4, Pp 377-382 (2021)
Background: Primary immune deficiency (PID) patients may develop acute or chronic pain. Pain has not been studied in this population until now. Objectives: This study systematically assessed the pain of various durations in PID patients using validat
Externí odkaz:
https://doaj.org/article/f2088487ce5c43d1ac245a555073734d
Autor:
Ashraf Al-Tarifi, Rand Arnaout, Abdulhadi Alqahtani, Farrukh Sheikh, Maram Al-Banyan, Bandar Al-Saud, Agha M. Rehan Khaliq, Hasan Al Rayes
Publikováno v:
American Journal of Infectious Diseases. 15:24-28
Autor:
Sulaiman Al Gazlan, Bander Al Saud, Saleh Al Mohsen, Abbas Hawwari, Latifa Al Shekaili, Ammar AlKawi, Mufarreh Al Zahrani, Abdulaziz Al Ghonaium, Agha M. Rehan Khaliq, Farrukh Sheikh, Hasan Al Dhekri, Hamoud Al Mousa, Safiah Al Sumayli, Rand Arnaout, Anas Dababo
Publikováno v:
Clinical Immunology. 178:39-44
Background Hyper-IgE syndrome (HIES) due to DOCK8 deficiency is an autosomal recessive (AR) primary combined immunodeficiency which results in significant morbidity and mortality at a young age. Different mutations in the DOCK8 gene can lead to varia
Autor:
Agha M. Rehan Khaliq, Hasan Al Dhekri, Sulaiman Al Gazlan, Hassan Al Rayes, Farrukh Sheikh, Safiah Hussain Sumayli, Rand Arnaout, Latifah Rashed Al Shekaili
Publikováno v:
Journal of Hematology. 4:174-177
Common variable immunodeficiency (CVID) is the second most prevalent primary immunodeficiency disorder following selective immunoglobulin A (IgA) deficiency but it is more complicated clinically. It causes a wide spectrum of symptoms and signs affect
Autor:
Anas M. Alazami, Safa Alhissi, Hasan Al Dhekri, Esteban Borrero, Abbas Hawwari, Farrukh Sheikh, Agha M. Rehan Khaliq, Lina El-Baik, Sulaiman Al Gazlan, Rand Arnaout, Hamoud Al-Mousa
Publikováno v:
Journal of clinical immunology. 37(6)
Non-homologous end joining gene 1 (NHEJ1) defect is a rare form of primary immune deficiency. Very few cases have been described from around the world. We are reporting the first family from the Arabian Gulf with three siblings presenting with combin
Autor:
Rashid Amin, Sulaiman Al Gazlan, Samia Al Hashim, Talal Al Otaibi, Farrukh Sheikh, Agha M. Rehan Khaliq
Publikováno v:
Asia Pacific Allergy
Background Anaphylaxis is a serious allergic reaction that may cause death. The signs and symptoms of anaphylaxis have not been examined in the Saudi population before. Objective The present study examined the signs, symptoms, triggers, and demograph