Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Raghad Alhuthil"'
Autor:
Bayan Dubaie, Abdulaziz Aldayel, Shehana Alwethinani, Raghad Alhuthil, Fatimah Alhamlan, Salem Alghamdi, Mohammed Alsuhaibani, Suliman Aljumaah, Ohoud AlYabes, Esam AlBanyan, Sami Al-Hajjar
Publikováno v:
Journal of Infection and Public Health, Vol 17, Iss 6, Pp 961-966 (2024)
Background: The actual burden of the Omicron variants remains unclear. Therefore, this study aims to analyze the epidemiological and clinical features of Omicron-infected patients and investigate factors influencing hospital admission. Methods: This
Externí odkaz:
https://doaj.org/article/22108257e53c474b9601e65ea2b5ace7
Autor:
Deema Gashgarey, Mohammed Alsuhaibani, Raghad Alhuthil, Hattan Alhabshan, Azzam Alabdulqader, Rakan Badran, Abdulaziz Balhmar, Haifa Aldawood, Esam A. AlBanyan, Salem AlGhamdi, Suliman AlJumaah, Ohoud AlYabes, Sami Al-Hajjar
Publikováno v:
Journal of Epidemiology and Global Health, Vol 14, Iss 2, Pp 319-326 (2024)
Abstract Background The burden of respiratory syncytial virus (RSV) in high-risk pediatric patients remains unclear. Therefore, this study aims to characterize pediatric RSV cases from January 2019 to December 2022 and assess the impact of the COVID-
Externí odkaz:
https://doaj.org/article/b7ddad10bba34ab09e677995315802ef
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-5 (2024)
Abstract Background Graves’ disease is the autoimmune activation of the thyroid gland causing diffuse enlargement and hyperfunction of the gland. Manifestations of Graves’ disease are multisystemic and include thyroid orbitopathy; pretibial myxed
Externí odkaz:
https://doaj.org/article/3b4aee17c38a416e8095f051facd83a8
Autor:
Afaf Alsagheir, Abdullah Al-Ashwal, Amal Binladen, Raghad Alhuthil, Faisal Joueidi, Khushnooda Ramzan, Faiqa Imtiaz
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
IntroductionHereditary Vitamin D-dependent rickets type II (HVDDR-type II) is a rare autosomal recessive disorder caused by molecular variation in the gene encoding the vitamin D receptor (VDR). This study aims to evaluate phenotype and genotype char
Externí odkaz:
https://doaj.org/article/fae8c54f7b1844598ccccd5b82461701
Autor:
Mariam Abdelkarim, Dalal Alageel, Faridul Ahsan, Raghad Alhuthil, Haifa Alsarhani, Afaf Alsagheir
Publikováno v:
Bone Reports, Vol 19, Iss , Pp 101709- (2023)
Introduction: Hajdu-Cheney syndrome is a rare disorder caused by truncation mutations in exon 34 of the NOTCH2 gene. The main presentation includes acro-osteolysis, osteoporosis, and dysmorphism. This syndrome affects the other body systems as well.
Externí odkaz:
https://doaj.org/article/e5dea615acb24e619819472ded3d5f76
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-5 (2023)
Abstract Background Inappropriately high levels of insulin secretion can cause the potentially fatal condition of persistent hyperinsulinemic hypoglycemia of infancy. Our paper focuses on another cause of severe hypoglycemia, which can be easily miss
Externí odkaz:
https://doaj.org/article/b96b1bf14db1471cbd6180d57684b135
Autor:
Fadiah Alkhattabi, Nawaf Al Faryan, Manar Alsaleh, Maureen Long, Abdullah Alkhani, Salma Alwahibah, Margarita Frederico, Raghad Alhuthil
Publikováno v:
International Journal of Pediatrics and Adolescent Medicine. 9:209-215