Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Mousa Abujbara"'
Autor:
Dana Hyassat, Saba Al-Saeksaek, Duha Naji, Awn Mahasneh, Yousef Khader, Mousa Abujbara, Mohammad El-Khateeb, Kamel Ajlouni
Publikováno v:
Frontiers in Public Health, Vol 10 (2022)
ObjectivesTo determine the prevalence and patterns of dyslipidemia and its associated risk factors among patients with type 2 diabetes attending the National Center for Diabetes, Endocrinology, and Genetics (NCDEG).MethodsA cross-sectional study was
Externí odkaz:
https://doaj.org/article/ea701770c572480a887b35d70ca86fe6
Autor:
Mohammed El-Khateeb, Yousef Khader, Anwer Batieha, Hashem Jaddou, Dana Hyassat, Nahla Khawaja, Mousa Abujbara, Kamel Ajlouni
Publikováno v:
SAGE Open Medicine, Vol 7 (2019)
Background: In Jordan, many studies reported various rates of vitamin D deficiency and insufficiency among different groups. This study aimed to determine the prevalence of low vitamin D level among Jordanian adults and determine its association with
Externí odkaz:
https://doaj.org/article/ab3a0abda0ae46aba2aaa1f6a22b3bbf
Autor:
Mousa Abujbara, Anwar Batieha, Yousef Khader, Hashem Jaddou, Mohammed El-Khateeb, Kamel Ajlouni
Publikováno v:
Journal of Lipids, Vol 2018 (2018)
Background. Dyslipidemia is one of the major modifiable risk factors for the development of cardiovascular disease and type two diabetes mellitus. Knowing the current prevalence of dyslipidemia is an important step for increasing awareness of the pro
Externí odkaz:
https://doaj.org/article/4f9e769904b9467487704faa5992b041
Autor:
Dana Hyassat, Mohammad El-Khateeb, Aladdin Dahbour, Saad Shunnaq, Duha Naji, Ehab Bani Ata, Mousa Abujbara, Nahla Khawaja, Anwar Batieha, Kamel Ajlouni
Publikováno v:
Eastern Mediterranean Health Journal. 29:247-253
Background: Post-COVID-19 syndrome covers a wide range of new, recurring or ongoing health conditions, which can occur in anyone who has recovered from COVID-19. The condition may affect multiple systems and organs. Aims: To evaluate the frequency an
Publikováno v:
International Journal of General Medicine. 15:6611-6619
Mousa Abujbara,1 Huda M Al Hourani,2 Reem Ibrahim Al-Raoush,1 Yousef S Khader,3 Kamel Ajlouni1 1The National Centre (Institute) for Diabetes, Endocrinology and Genetics, The University of Jordan, Amman, Jordan; 2Department of Clinical Nutrition and D
Publikováno v:
Current Diabetes Reviews. 19
Background: Toenail onychomycosis is common in patients with diabetes and it can increase the risk of secondary infections and foot complications. Despite several studies investigating the prevalence and associated factors of toenail onychomycosis fr
Publikováno v:
International Journal of General Medicine.
Mousa Abujbara,1 Eiman A Khreisat,2 Yousef Khader,3 Kamel M Ajlouni4 1Department of Diabetes and Endocrinology, the National Centre (Institute) for Diabetes, Endocrinology and Genetics/The University of Jordan, Amman, Jordan; 2Department of Nursing,
Autor:
Kamel Ajlouni, Zaineh M. Shahrure, Mohammad Al Shhab, Yacoub M. Irshaid, Khader N. Mustafa, Mousa Abujbara, Mohammed El-Khateeb
Publikováno v:
Current Reviews in Clinical and Experimental Pharmacology. 16:281-288
Background: The use of statins to lower high serum cholesterol levels may be associated with a number of adverse reactions, including severe myopathy. The solute carrier organic anion transporter 1B1 (SLCO1B1) gene, which encodes the organic anion-tr
Publikováno v:
Annals of Medicine & Surgery. 74
myopathy is a major side effect of statins that leads to statin intolerance and discontinuation. In this prospective cohort study, the main objective was to estimate the incidence of myopathy in patients receiving statins. In addition, we identified
Autor:
Mousa Abujbara, Kamel Ajlouni, Chao Xing, Hatem El-Shanti, Zhengyang Zhou, Mohammed El-Khateeb, Abhimanyu Garg, Anil K. Agarwal, Khadeja Al-Rashed
Publikováno v:
Journal of the Endocrine Society
Context Despite considerable progress in elucidating the molecular basis of various progeroid syndromes, some rare patients remain unexplained. Objective To elucidate molecular genetic basis of a novel autosomal recessive progeroid syndrome. Particip