Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Ahmed Absi"'
Autor:
Feras Alfraih, Ahmed Absi, Mohamed Abuhaleeqa, Khalofa Alghamdi, Ahmad Alhuraiji, Murtadha Al‐Khabori, Zeyad Al‐Shaibani, Musa Alzahrani, Honar Cherif, Saleem Eldadah, Amr Hanbali, Ibraheem H. Motabi, Hind Salama
Publikováno v:
Cancer Reports, Vol 7, Iss 2, Pp n/a-n/a (2024)
Abstract Leukemia burden is growing in the Gulf Council Cooperation (GCC) countries. Nonetheless, there is no unified protocol for managing adult acute lymphoblastic leukemia (ALL) patients in the GCC‐countries. Therefore, the GCC Adult‐ALL Treat
Externí odkaz:
https://doaj.org/article/55f760154b6946a78d38acd42823c57f
Publikováno v:
Journal of Applied Hematology, Vol 13, Iss 3, Pp 157-161 (2022)
We describe two male patients with unique mutation of the CD40L gene, unlike the classic presentation of X-linked hyper immunoglobulin M immunodeficiency syndrome (XHIGM syndrome), both were healthy until presenting in their early twenties with a cha
Externí odkaz:
https://doaj.org/article/734fb5aab67a4e8f8e8942b07d884d8c
Autor:
Hind Abdin Salama, Ayman Yahya Alhejazi, Ahmed Absi, Saeed Alshieban, Mohsen Alzahrani, Ahmed Alaskar, Giamal Gmati, Moussab Damlaj, Khadega A Abuelgasim, Osama Ali, Abdulrahman Alghamdi, Bader Alahmari, Areej Almugairi, Hazza Alzahrani, Hanni ALhashmi, Abdul Rahman Jazieh
Publikováno v:
Journal of Applied Hematology, Vol 9, Iss 4, Pp 111-119 (2018)
BACKGROUND: Histiocytic disease is a diverse disease, characterized by multisystem involvement, diagnosis and management can be challenging. Guidelines are important tool to provide evidence-based management; however, guidelines for management of adu
Externí odkaz:
https://doaj.org/article/9af799ca6b2341c88ccfadac94240859
Autor:
Mubarak Al-Mansour, Saif Ahmed Saif, Ziyad Alharbi, Abdulrhman Salem Alhwaity, Ahmed Almasrahi, Waleed Alnejadi, Sarah Hussain, Syed Aga, Muhammad Khan, Roula Almufti, Ahmed Absi
Publikováno v:
Asian Pacific Journal of Cancer Prevention. 24:623-631
Publikováno v:
International Journal of Neuroscience. :1-5
Iron is an essential element for brain cells that is required for the transport of oxygen, energy generation, myelin synthesis, and production of neurotransmitters. Disturbances in the homeostatic mechanisms of iron metabolism may cause iron accumula
Autor:
Ahmed S Higazi, Ihab Y Hemaidi, Sameer Alamoudi, Roaa S Gassas, Ahmed Alsaeed, Amani S Ahmed, Abdulrahman Alghamdi, Mannar M Khalil, Saleem K Dadah, Majed Alahmadi, Walaa A Rajkhan, Ahmed Absi
Publikováno v:
Saudi Medical Journal. 42:847-852
Objectives: To assess local epidemiology and risk factors for bacterial, fungal, and viral infections among the autologous bone marrow transplant population. Methods: This study is a retrospective correlational cohort design comprising 150 adult pati
Autor:
Hind Salama, Saleem Eldadah, Mohamed H. Omer, Ayman Alhejazi, Luluh Bin Dayil, Ayman Almozaini, Roaa Reda Khalil, Areej Al Mugairi, Mohammed Snnallah, Moussab Damlaj, Ahmed Alaskar, Ahmad Alsaeed, Mohammed Mosa Bakkar, Bader Alahmari, Mohsen Alzahrani, Ihab Elhemaidi, Majed Alahmadi, Sameer Alamoudi, Walaa Rajkhan, Manar Khalil, Solaf Sami Kanfar, Abdullah S. Al Saleh, Abdulrahman Al Raizah, Ayman Ibrahim, Ahmed Absi
Publikováno v:
Leukemia Research. 130:107316
Autor:
Mubarak Al‑Μansour, Ahmed Absi, Roula Al‑Μufti, Majed Alahmadi, Ihab El‑Ηemaidi, Sameer Alamoudi, Saleem Eldadah, Syed Aga, Muhammed Khan, Ahmed Alsaeed
Publikováno v:
Molecular and clinical oncology. 17(6)
Central nervous system (CNS) relapse in patients with diffuse large B-cell lymphoma (DLBCL) is rare (2-5% of cases), but is a devastating complication with a poor survival rate. The administration of high-dose methotrexate (HDMTX) for CNS prophylaxis
Autor:
Alaa T Alsharif, Mohammed Aldawsari, Emad M Babateen, Meshaal A Kouther, Faisal F Aljahdali, Ahmed Absi, Taghreed Aldosary, Mohamed E Ahmed
Publikováno v:
Cureus. 14(5)
Background Hodgkin's lymphoma (HL) is a disease that affects lymphocytes, mostly B cells, and it is commonly diagnosed by the presence of Reed-Sternberg cells. The influence of obesity on the disease course of HL is still controversial. This study's
Autor:
Hazza A Alzahrani, Saeed Alshieban, Mohsen Alzahrani, Hind Salama, Ahmed Absi, Abdul Rahman Jazieh, Giamal Gmati, Khadega A. Abuelgasim, M.O.H. Musa, Moussab Damlaj, Areej Almugairi, Gaurav Goyal, Ayman Alhejazi, Ali Bazarbachi, Bader Alahmari, Ahmed Alaskar, Abdulrahman Alghamdi
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia
Clinical Lymphoma, Myeloma & Leukemia
Clinical Lymphoma, Myeloma & Leukemia
Histiocytic disorders are an exceptionally rare group of diseases with diverse manifestations and a paucity of approved treatments, thereby leading to various challenges in their diagnosis and management. With the discovery of novel molecular targets