Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Saleh Al Mohsen"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6e2a90197f35c08ece6e0e7d9a0c115
https://doi.org/10.1016/j.clim.2016.08.002
https://doi.org/10.1016/j.clim.2016.08.002
Publikováno v:
Lecture Notes in Civil Engineering ISBN: 9789811511929
The building enterprise in Iraq performs the greatest instance of energy, especially in residential section. Indeed, most of the residential constructions rely on traditional construction systems. In the past, the traditional system used to supply th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f19f837e73b4c09d63e738e6e371f981
https://doi.org/10.1007/978-981-15-1193-6_24
https://doi.org/10.1007/978-981-15-1193-6_24
Autor:
Ali Alasmari, Bandar Al-Saud, Yong Xiong, Emad B. Abboud, Banan Al-Younes, Abeer Al-Mostafa, Ranad Shaheen, Abdulelah AlIssa, Ewa A. Naim, Mohammed A. Aldahmesh, Dorota Monies, Olga Buzovetsky, Niema Ibrahim, Mohamed Abouelhoda, Nada Al-Tassan, Ghada M H Abdel-Salam, Saleh Al-mohsen, Hisham Alkuraya, Hadeel Alsharif, Mohammed Al-Owain, Arif O. Khan, Asma Sunker, Mais Hashem, Sawsan R. Nowilaty, Selwa A.F. Al-Hazzaa, Firdous Abdulwahab, Shamsa Anazi, Hamad Al-Zaidan, Nisha Patel, Fowzan S. Alkuraya
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 18(6)
Retinal dystrophies (RD) are heterogeneous hereditary disorders of the retina that are usually progressive in nature. The aim of this study was to clinically and molecularly characterize a large cohort of RD patients. We have developed a next-generat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46369cd13a60ce989ac6d1806e07cd4c
https://pubmed.ncbi.nlm.nih.gov/26355662
https://pubmed.ncbi.nlm.nih.gov/26355662