Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Saeed H Halawani"'
Autor:
Syed Najamuddin Farooq, Ammad Ahmed, Abdul Halim S Serafi, Saeed H Halawani, Muhammad Amir Mustafa, Muhammad Irfan Safi Rizvi
Publikováno v:
Annals of Abbasi Shaheed Hospital and Karachi Medical & Dental College, Vol 24, Iss 4 (2020)
Abstract Objective: Objective of the current study was to investigate the effect of obesity and positive family history of Cardiovascular Disease (CVD), Diabetes Mellitus (DM) on plasma C reactive protein (CRP) levels in apparently healthy young indi
Externí odkaz:
https://doaj.org/article/eb1e99aef7d44ea3a93439edd3e46be1
Autor:
Shahida A. Khan, Ghazi A. Damanhouri, Tahir J. Ahmed, Saeed H. Halawani, Ashraf Ali, Ahmad Makki, Sarah A. Khan
Publikováno v:
Jornal de Pediatria, Vol 98, Iss 5, Pp 513-518 (2022)
Objective: Sickle cell disease is characterized by clinical complications resulting in vaso-occlusive crisis with prominent attributes of oxidative stress, inflammation, and pain. Inflammation is an integral part of this disease which further exacerb
Externí odkaz:
https://doaj.org/article/35fb9739270d4653982a3de55678fb47
Autor:
Shahida A. Khan, Tahir Jameel Ahmed, Torki Al Zughaibi, Badrah S. Alghamdi, Saeed H. Halawani, Sarah A. Khan
Publikováno v:
Journal of King Saud University: Science, Vol 34, Iss 8, Pp 102338- (2022)
Background: Sickle cell disease (SCD) is one of the commonest prevalent blood inherited disorders, accompanied by inflammation, oxidative stress, pain and alterations in the membrane lipid composition. These have harmful impacts on the cardiovascular
Externí odkaz:
https://doaj.org/article/f124628f544e43f3926d4a72a1d8762a
Autor:
Mohammad Athar PhD, Zainularifeen Abduljaleel PhD, Ibrahim S. Ghita MD, Amani A. Albagenny MD, Saeed H. Halawani PhD, Mohammad M. Alkazmi MD, Wafa M. Elbjeirami PhD, Khalid Alquthami PhD, Mohammad M. Alkhuzae BLM, Fadel M. Ragab MS, Faisal A. Al-Allaf PhD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)
The rare Gln534 (Factor V Leiden; FVL) allele (1:169,519,049 T>C) is associated with an increased risk of venous thrombosis. The purpose of this study was to measure the prevalence of Factor V Leiden mutation in thrombophilia patients with deep vein
Externí odkaz:
https://doaj.org/article/e394647bb9664e38a5acbaa68b2fea43
Autor:
Hasan Ahmed H Baz, Saeed H. Halawani, Ibrahim Abdulaziz, Majid Ali, Nhal Ahmed Baz, Mohammed Jafal, Khaldoun Saleh
Publikováno v:
International Journal of Pharmaceutical Research And Allied Sciences. 11:24-32
Autor:
G. G. H. A. Shadab, Amani A. Albagenny, Mohammad M. Alkazmi, Neda M. Bogari, Mohammad M. Alkhuzae, Abdulaziz A. Althebyani, Khalid Alquthami, Saeed H. Halawani, Zainularifeen Abduljaleel, Mohammad Athar, Anas Dannoun, Ahmed Elsendiony, Ibrahim S. Ghita, Faisal A. Al-Allaf
Publikováno v:
Clinica Chimica Acta. 519:247-254
Background Thrombophilia is a substantial source of indisposition and mortality in several countries, including Arab populations. Deep venous thrombosis (DVT) with or without pulmonary embolism (PE) is the prevalent clinical manifestation of thrombop
Autor:
Saeed H. Halawani, Mohammad Athar, Mohammad M. Alkhuzae, Zainularifeen Abduljaleel, Ibrahim S. Ghita, Mohammad M. Alkazmi, Fadel M Ragab, Khalid Alquthami, Faisal A. Al-Allaf, Amani A. Albagenny, Wafa M. Elbjeirami
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis
Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)
Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)
The rare Gln534 (Factor V Leiden; FVL) allele (1:169,519,049 T>C) is associated with an increased risk of venous thrombosis. The purpose of this study was to measure the prevalence of Factor V Leiden mutation in thrombophilia patients with deep vein
Autor:
Amal Zaghloul, H. A. AL-Pakistani, T. A. M. A. Al-bukhari, Saeed H. Halawani, Maged Shalaby, Nada Bajuaifer, Shirin H. Teama
Publikováno v:
Diabetes Research and Clinical Practice. 106:597-604
Background and objective Endothelial dysfunction in diabetes mellitus (DM) is an important factor in the pathogenesis of micro and macrovascular complications. We aimed to measure soluble endothelial protein C receptor (sEPCR) and high sensitivity C
Autor:
Ghazi Al Harbi, Ghazi A. Damanhouri, Shahida A. Khan, Sarah A. Khan, Samy Marouf, Saeed H. Halawani, Ahmad Makki, Ashraf Ali, Aziz Khan, Ahmed Bakillah
Publikováno v:
Nutrition & Metabolism
Nutritional research in sickle cell disease has been the focus in recent times owing to not only specific nutritional deficiencies, but also the improvements associated with less painful episodes. Though hydroxyurea remains the drug of choice, certai
Autor:
Maged Shalaby, T. A. M. A. Al-bukhari, Saeed H. Halawani, Ghada A. Wassif, H. A. AL-Pakistani, Amal Zaghloul, Shirin H. Teama, Nada Bajuaifer
Publikováno v:
Hematology (Amsterdam, Netherlands). 21(6)
Many formulas from red blood cell (RCB) indices are instructed to differentiate between iron deficiency anemia (IDA) and beta thalassemia trait. None had 100% Youden index.To introduce two new formulas and evaluate them in the differentiation between