Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Nervana Bayoumy"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Coronary artery disease is a leading cause of morbidity and mortality worldwide. It occurs due to a combination of genetics, lifestyle, and environmental factors. Premature coronary artery disease (PCAD) is a neglected clinical entity despit
Externí odkaz:
https://doaj.org/article/2b35d0a2682042798642678fe00c84a9
Autor:
Khalid A. AlSaleh, Nouf Al-Numair, Ayman AlSuliman, Mohammed Zolaly, Abdul Majeed Albanyan, Nouf AlOtaishan, Esra Abudouleh, Nervana Bayoumy, Ahmad Tarawah, Faisal AlZahrani, Faisal AlAllaf, Abdul kareem AlMomen, Raihan Sajid, Tarek M. Owaidah
Publikováno v:
TH Open, Vol 04, Iss 04, Pp e457-e462 (2020)
Introduction Inherited bleeding disorders vary in prevalence due to genetic disparity and ethnicity. Little is known about the prevalence of coagulation factor deficiency and bleeding disorders in middle-eastern population. Methods Young Saudi adults
Externí odkaz:
https://doaj.org/article/4752f5a6cf364245920ca92d4a5b1826
Autor:
Esra Abudouleh, Nervana Bayoumy, Faisal M. Alzahrani, Abdulkareem Al-Momen, Tarek Owaidah, Mohammed Zolaly, Ayman Al-Suliman, Ahmad M Tarawah, Nouf S. Al-Numair, Raihan Sajid, Faisal A. Al-Allaf, Abdul Majeed Albanyan, Nouf AlOtaishan, Khalid Alsaleh
Publikováno v:
TH Open: Companion Journal to Thrombosis and Haemostasis
TH Open, Vol 04, Iss 04, Pp e457-e462 (2020)
TH Open, Vol 04, Iss 04, Pp e457-e462 (2020)
Introduction Inherited bleeding disorders vary in prevalence due to genetic disparity and ethnicity. Little is known about the prevalence of coagulation factor deficiency and bleeding disorders in middle-eastern population. Methods Young Saudi adults
Autor:
Nervana Bayoumy
Publikováno v:
International Journal of Morphology. 38:876-881
Publikováno v:
Clinical and Experimental Hypertension. 39:764-768
This study was conducted to test the association between promoter DNA methylation of α-Adducin (ADD1) gene and the risk of essential hypertension (EH). A total of 150 EH patients and 100 aged- and gender-matched controls were investigated. DNA methy
Autor:
Hamdy Omar, Ola Farouk Leheta, Mohamed M. El-Shabrawi, Alaa El‐Din M. Abo El‐Ela, Nervana Bayoumy
Publikováno v:
Diabetes/metabolism research and reviewsREFERENCES. 36(5)
BACKGROUND AND OBJECTIVE Diabetic nephropathy (DN) is the most common cause of end stage renal failure or even death among patients with type 2 diabetes mellitus. Genetic predisposition is widely studied among these patients to identify manageable as
Publikováno v:
Nephrology Dialysis Transplantation. 34
Publikováno v:
Human fertility (Cambridge, England). 23(4)
The blood testicular barrier (BTB) is a barrier protecting the testes from damage. It also plays an important role in spermatogenesis. The intracellular adhesion molecule-1 (ICAM-1) is a member of the immunoglobulin cell adhesion molecule family and
Publikováno v:
Journal of Taibah University Medical Sciences. 11:478-484
Objectives Many patients undergoing antiplatelet therapy continue to experience thrombotic events and failure of therapy leading to so-called ‘resistance’ to antiplatelet therapy. Recently, there has been an increasing focus on in vitro laborator
Autor:
Abdel Galil Abdel Gader, Abdulmajeed Albanyan, Nervana Bayoumy, S. K. Al-Ouda, Farjah H. Algahtani
Publikováno v:
Transfusion Medicine. 26:220-224
SUMMARY Background Human platelet antigens (HPAs) are involved in the pathogenesis of several clinical conditions, such as platelet transfusion purpura (PTP), refractoriness to platelet transfusion and neonatal alloimmune thrombocytopenia (NAITP). Ty