Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Anas M. Elshreif"'
Publikováno v:
Open Access Macedonian Journal of Medical Sciences. 10:826-831
Aim: Iron deficiency anemia (IDA) is the most common cause of anemia in the Kingdom of Saudi Arabia. Thalassemia and sickle cell disease (SCD) are major concerns in several nations, including KSA. This study sought to investigate the prevalence of ID
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec4b87fbaf975f605150a48d2f925df6
https://doi.org/10.3889/oamjms.2022.9311
https://doi.org/10.3889/oamjms.2022.9311
Autor:
Mohamed A. Elkoumi, Sawsan H. Abdellatif, Dalia S. Fahmy, Sherif F Osman, A.A. Soliman, Naglaa F Boraey, Mohamed I. Alanwar, Nevin M. Waked, Rabab M. Saleh, Ahmed Salah, Alaa A. Sobieh, Mohamed A M Ibrahim, Sahbaa F. M. Hafez, Mohammed Soliman, Ahmed A. Elhewala, Mohamed Sayed Fahim, Naglaa A. Elshehawy, Adel M. Abdou, Nagwa E. Akeel, Ahmed A. Emam, Marwa M. Abdel-Aziz, Faisal Y. Mohamed, Ahmed Sherif, Mohamed H. Mashali, NourEldin M. Abdelaal, Amira A Abd El-Rahman Mosbah, Nancy M S Zeidan, Manal A. A. Youssef, Shaimaa S. A. Elashkar, Mervat T. Zakaria, Mustafa I.A. Hashem, Yasser Sedky, Ahmed A. Elshehawy, Mohamed M Shehab, Anas M. Elshreif, Mai M. Malek, Abdelrahman A. A. Ahmed
Publikováno v:
Pediatric Pulmonology. 55:1175-1183
BACKGROUND Pneumonia is the foremost cause of child death worldwide. M-ficolin is encoded by the FCN1 gene and represents a novel link between innate and adaptive immunity. OBJECTIVES To investigate the FCN1 -144 C/A (rs10117466) polymorphism as a po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c4198aa1d7fc499aa3d3731397ac891
https://doi.org/10.1002/ppul.24719
https://doi.org/10.1002/ppul.24719
Autor:
Mohamed A Elkoumi, Mayy AN Allah, Faisal Y Mohamed, Naglaa F Boraey, Sawsan H Abdellatif, Mohamed MM Shehab, Ahmed H Sherif, Nagwa E Akeel, Rabab M Saleh, Anas M Elshreif, Hind M Abdelrahman, Attia A Soliman, Ahmed A Emam, Manal AA Youssef, Dalia S Fahmy, Mohammad M Sallam, Abdalla M Nawara, Elsayed A Elgohary, Ali Ismael, Sameh MH El-Kaffas, Alaa A Sobeih, Lamya M Ibrahim, Mohamed AM Ibrahim, Adel M Abdou, Sherif M Yousry, Sherif F Osman, Fatma M El-Deeb, Ahmed A Elhewala, Sahbaa FM Hafez, Nevin M Waked, Hany AA Elbasyouni, Rania A Fouad, Nancy MS Zeidan, Mohamed Nashat, Mohsen AA Farghaly
Publikováno v:
Lupus. 29(7)
BackgroundRecently, the interleukin-17A ( IL-17A) gene has emerged as a potential candidate gene for autoimmune disorders, including systemic lupus erythematosus (SLE).ObjectivesThis study aimed to investigate whether IL-17A polymorphisms at rs227591
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c86039449928067b5dd8cf64b507b18
https://pubmed.ncbi.nlm.nih.gov/32380889
https://pubmed.ncbi.nlm.nih.gov/32380889