Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Ghaleb ElYamany"'
Autor:
Walaa Aboulkasem Shahin, Hayam Aldeeb, Majed Alsulami, Abdullah Tammas, Fatma Albatniji, Aljawhara Almanea, Abdalla Mohamed Zayed, Fahad Alabbas, Azzah Alzahrani, Tahani Bin Ali, Ghaleb Elyamany, Rana Hassan Almaghrabi, Huda Elfaraidi
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
BackgroundCOVID-19, the pandemic that hit the world in 2020, resulted in millions of deaths, with the elderly and adults succumbing to the disease more often than children. However, the presence of underlying morbidities increased the risk of death.
Externí odkaz:
https://doaj.org/article/d44d26a9892140daace49c7954e7f490
Autor:
Mansour S Aljabry, Fahad Alabbas, Ghaleb Elyamany, Qanita Sedick, Omar Alsuhaibani, Huda Elfaraidi, Azzah Alzahrani, Sultan Alotaibi, Mohammed S Alqahtani, Ahmad M Alshahrani, Mohammed Abdulaziz Alharbi, Hassan S Abusabah, Lulwa Alremali, Abdulmohsen Abduaziz Alameen, Mohammed Almohammadi
Publikováno v:
Journal of Applied Hematology, Vol 14, Iss 2, Pp 101-107 (2023)
BACKGROUND: Rare bleeding disorder (RBDs) encompasses a deficiency of one or more of FXIII, FXI, FX, FVII, FV, FII, and FI clotting factors, leading to bleeding disorders with variable presentations and outcomes ranging from none or minimal to life-t
Externí odkaz:
https://doaj.org/article/00193c4a102c4116adcb0a41bb41861f
Autor:
Ghaleb Elyamany, Hassan Rizwan, Ariz Akhter, Mansour S. Aljabry, Sultan Alotaibi, Mohammad A. Hameed Albalawi, Meer-Taher Shabani-Rad, Tariq Mahmood Roshan, Adnan Mansoor
Publikováno v:
Current Issues in Molecular Biology, Vol 45, Iss 1, Pp 604-613 (2023)
Dysregulated Wnt/β-catenin signal transduction is implicated in initiation, propagation, and poor prognosis in AML. Epigenetic inactivation is central to Wnt/β-catenin hyperactivity, and Wnt/β-catenin inhibitors are being investigated as targeted
Externí odkaz:
https://doaj.org/article/746f41bdca8942769698ebe1e6722423
Autor:
Mohammed Albalawi, Turki Alwasaidi, Mohammed Almohammadi, Ashraf Ahmad Alzarief, Ghaleb Elyamany
Publikováno v:
Clinical Case Reports, Vol 11, Iss 10, Pp n/a-n/a (2023)
Abstract COVID 19 is a serious infection that originated in Wuhan, China and has resulted in worldwide morbidity and mortality. It continues to be a major health concern in 2022, being associated with multiorgan failure. Although the pathophysiology
Externí odkaz:
https://doaj.org/article/639f129367c946d8902cb8da213ddea2
Autor:
Nawaf Alkhayat, Mohammad Alshahrani, Ghaleb Elyamany, Qanita Sedick, Walid Ibrahim, Hasna Hamzi, Amal Binhassan, Mohamed Othman, Saeed Alshieban, Mansour S. Aljabry, Shuaa Asiri, Muneerah Alzouman, Omar Alsuhaibani, Fahad Alabbas, Omar Alsharif, Yasser Elborai
Publikováno v:
Journal of the Egyptian National Cancer Institute, Vol 33, Iss 1, Pp 1-9 (2021)
Abstract Background Hodgkin lymphoma (HL) is lymphoid neoplasm usually affecting lymphatic system; it accounts 3.6% of cancers in Saudi Arabia. Modern treatment protocols had shown particular success rates in overall-survival (OS) and event-free-surv
Externí odkaz:
https://doaj.org/article/4be7a1fa2d86480c9736eca49e7c675a
Autor:
GHALEB ELYAMANY, Nawaf ALKHAYAT, Omar AL SHARIF, Yasser ELBORAI, Mohammad AL SHAHRANI, Omar ALSUHAIBANI
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S15-S16 (2022)
Objective: NOTCH1 is now established to play a key role in the prognosis of several hematological malignancies. Notch proteins are multifaceted and involved in several key cellular functions with extensive crosstalk with other critical pathways; ther
Externí odkaz:
https://doaj.org/article/695929ea8a774e3b938e9fa9efc6256d
Autor:
Ghaleb Elyamany, Ahmed Fouly, Abdulmalik Alqahtani, Assem Alrumeh, Shuaa Asiri, Salman Ali Faifi, Saeed Alshieban
Publikováno v:
Case Reports in Oncology, Vol 14, Iss 1, Pp 244-248 (2021)
Plasmablastic lymphoma (PBL) is a rare subtype of non-Hodgkin’s lymphoma that is associated with acquired immunodeficiency syndrome (AIDS), characterized by its association with Epstein-Barr virus (EBV), aggressive nature, and plasmacytic/plasmabla
Externí odkaz:
https://doaj.org/article/ff76571add254a559054e9ccaec9eb11
Autor:
Fahad Alabbas, Ghaleb Elyamany, Talal Alanzi, Tahani Bin Ali, Fatma Albatniji, Huda Alfaraidi
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-6 (2021)
Abstract Background Hemophagocytic lymphohistiocytosis (HLH) is a rare and potentially fatal syndrome that is characterized by strong activation of the immune system from hyperinflammatory cytokines. Symptoms of HLH patients include fever, hepatosple
Externí odkaz:
https://doaj.org/article/17afd9f92a2442b3ba0ee7fbec256247
Autor:
Aziz Alami Chentoufi, F. Aytül Uyar, Hiba A. Chentoufi, Khalid Alzahrani, Maria Paz, Ahmed Bahnassy, Ghaleb Elyamany, Assem Elghazaly
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Human leukocyte antigens (HLA) diversity has a tremendous impact on shaping the transplantation practices, transfusion-associated graft versus host disease prevention strategies, and host–pathogen interactions. Here, we conducted a retrospective st
Externí odkaz:
https://doaj.org/article/2209fa1e0fcd44f1be1464d9a22defc0
Autor:
Tarek Owaidah, Fahad Alabbas, Iman Alhazmi, Hussain Al Saeed, Saud Balelah, Ghaleb ElYamany, Ohoud Kashari, Mohamad Qari, Mahasen Saleh, Sherif Roushdy, Marwan ElBagoury
Publikováno v:
Journal of Applied Hematology, Vol 12, Iss 3, Pp 123-133 (2021)
Gaucher disease (GD) is a lysosomal storage disorder that occurs due to an inherited inborn error of metabolism. GD manifested due to the deficient activity of the glucocerebrosidase enzyme that results in the accumulation of the harmful glucocerebro
Externí odkaz:
https://doaj.org/article/960d7cb3617e4fce80e0455329ad818c