Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Rehab Y. Al‐Ansari"'
Autor:
Rehab Y. Al-Ansari, Leena Abdulrahman Almuhaish, Khaled Abdullah Hassan, Tawasoul Fadoul, Alexander Woodman
Publikováno v:
Case Reports in Dermatological Medicine, Vol 2024 (2024)
Background. A fixed drug eruption (FDE) is an immunological cutaneous adverse reaction, classified as a cutaneous adverse drug reaction (CADR) and characterized by well-defined lichenoid lesions that occur at the same site each time. Ceftriaxone is a
Externí odkaz:
https://doaj.org/article/0397a63f64b449458f3f90fa67c6c88c
Autor:
Maria E. M. Mariano, Alexander Woodman, Eidan M. Al Zahrani, Yaser A. Al Naam, Rory R. Farrelly, Lamiaa H. Al‐Jamea, Abbas Al Mutair, Rehab Y. Al‐Ansari, Jenifer V. Quiambao, Jeffhraim Balilla
Publikováno v:
Nursing Open, Vol 10, Iss 2, Pp 988-997 (2023)
Abstract Aim This study aimed to explore the association of turnover‐attachment motive with socio‐demographic data among Saudi and foreign nurses in a hospital in the Eastern Province of Saudi Arabia. Methods A cross‐sectional correlation study
Externí odkaz:
https://doaj.org/article/0e79a8ed5e904c6ea7981a9d5f9fa6a8
Autor:
Rehab Y. Al-Ansari MBBS, Atallah Fadel Alruwaili MD, Khalid Mohammed Alqahtani MD, Amal Faed Al-Harbi DMS, Alexander Woodman PhD
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 11 (2023)
Factor XI deficiency (FXI) is the third most common coagulation factor deficiency after hemophilia A and B, ie, in the hierarchy after factors VIII and IX, taking into account von Willebrand’s factor deficiency, as bleeding disorders are higher tha
Externí odkaz:
https://doaj.org/article/4bbd9d3e2baa4204b6892074ba41a1ff
Autor:
Rehab Y Al-Ansari, Leena M Abdalla, Yasmin A Qomawi, Laila J Alromaih, Mohanad O Bakkar, Amal S Shilash, Nawaf Y Zakary
Publikováno v:
Journal of Family and Community Medicine, Vol 29, Iss 1, Pp 71-78 (2022)
BACKGROUND: Sickle cell disease (SCD) is a group of hereditary diseases, inherited as autosomal recessive disorder, which causes mutation in the β-globin gene. As a result, there is a change in the sixth amino acid from glutamic acid to valine. The
Externí odkaz:
https://doaj.org/article/e793caba6f9d4348af35db0cba97fe0b
Publikováno v:
SAGE Open Medical Case Reports, Vol 11 (2023)
Kikuchi’s disease is an idiopathic self-limiting condition first reported in Japan in 1972. However, hemophagocytic lympho-histiocytosis is a condition that occurs due to overstimulation of the immune system. The presence of the two conditions is r
Externí odkaz:
https://doaj.org/article/590d526312a443688fb58da6264c93be
Publikováno v:
SAGE Open Medical Case Reports, Vol 10 (2022)
Factor X deficiency is one of the rarest coagulation disorders representing 10% of all rare bleeding diseases with a frequency of 1:1,000,000. A 39-year-old male patient with no previous medical conditions was admitted to the hospital with a left car
Externí odkaz:
https://doaj.org/article/f7a1d45659c147adb3e186cdb2fcc6ef
Publikováno v:
SAGE Open Medical Case Reports, Vol 10 (2022)
Factor XII deficiency is a rare autosomal recessive health condition usually discovered incidentally during routine coagulation screening before surgery after investigating a prolongation of the activated partial thromboplastin time. This is a case o
Externí odkaz:
https://doaj.org/article/8505a3e365354a3cb8af52d158b711da
Publikováno v:
Journal of Infection and Public Health, Vol 14, Iss 10, Pp 1389-1391 (2021)
Background: COVID-19 is a pandemic disease that has no definite treatment or preventive medication until late 2020 when vaccines were developed. Vaccines are a very useful new tool against COVID-19 that stimulate the immune system after recognition o
Externí odkaz:
https://doaj.org/article/b480695743a8423faa8ad85464d99f9f
Publikováno v:
SAGE Open Medical Case Reports, Vol 10 (2022)
AstraZeneca vaccine became one of the four vaccines that encode different forms of the SARS-CoV-2 spike glycoprotein. We report the case of an 18-year-old medically free female with progressive bruising of the upper and lower extremities for 1 week,
Externí odkaz:
https://doaj.org/article/ed4de38ca97143a4927d15e979325883
Publikováno v:
SAGE Open Medical Case Reports, Vol 9 (2021)
Essential thrombocythemia is one of the famous diseases under the category of myeloproliferative disorder. It is an end result of a genetic mutation of one or more of the most frequent oncogenes such as Janos kinase 2 (JAK2), MPL proto-oncogene, thro
Externí odkaz:
https://doaj.org/article/f4e645d1eab249c3af98ba6b54d96bf8