Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Haroon A Javaid"'
Autor:
Abdulaziz A. Barakat, Omar Mobarak, Haroon Ahmed Javaid, Mhd Rasheed Awad, Karam Hamweyah, Abderrahman Ouban, Selwa A. F. Al-Hazzaa
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
IntroductionDiabetic retinopathy (DR) is the leading cause of preventable blindness in Saudi Arabia. With a prevalence of up to 40% of patients with diabetes, DR constitutes a significant public health burden on the country. Saudi Arabia has not yet
Externí odkaz:
https://doaj.org/article/19a1c2c926834c799733be6fa974ed98
Autor:
Bayan Duabie, Areej Alfattani, Sahar Althawadi, Abdullah Taha, Haroon Ahmed Javaid, Omar Mobarak, Esam Albanyan
Publikováno v:
International Journal of Pediatrics and Adolescent Medicine. 9:153-159
Since the initial emergence of the novel SARS-CoV-2 coronavirus responsible for the 2019 coronavirus disease (COVID-19) pandemic, many studies have been exploring the nature and characteristics of this virus and its associated clinical manifestations
Autor:
Touqa Khalil, Faaezuddin Syed, Basant Elaasser, Haroon A Javaid, Usama I Othman, Nabil Shehata
Publikováno v:
Cureus.
Autor:
Linah H Zaman, Haroon A Javaid, Nader A Fawzy, Safwan Abbasi, Usama I Othman, Samira M Ghallab, Nabil Shehata
Publikováno v:
Cureus.
Publikováno v:
Cureus.
Autor:
Ahmed M Hamed, Haroon A Javaid, Safwan Abbasi, Ahsan Amanullah, Majed Ramadan, Ismail M Shakir, Noara AlHusseini
Publikováno v:
Cureus. 14(7)
Background Physical inactivity has been identified as a major factor in developing and progressing chronic non-communicable diseases such as obesity. The Kingdom of Saudi Arabia ranks high worldwide in rates of obesity. During the coronavirus disease
Autor:
Muhammad Zaeem Khalid, Maria Iftikhar Raja, Junaid Azad, Haroon Javaid Javaid, Muhammad Imran Anwar
Publikováno v:
European Journal of Surgical Oncology. 49:e84
Publikováno v:
Cureus
Adenosine deaminase t-RNA-specific 3 (ADAT3) gene, present on chromosome 19, encodes for an enzyme responsible for deamination of adenosine to inosine. Individuals with ADAT3 mutation display microcephaly, dysmorphic features, neurological, behaviour