Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nourah Alruqaie"'
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Bacterial meningitis is one of the critical diseases that needs to be diagnosed and treated promptly. Recent diagnostics of high sensitivity and specificity rates, such as PCR, helped with such presentation, especially in cases with prior antibiotics
Externí odkaz:
https://doaj.org/article/2e206183f0cd4893a97b3b1186ef96c6
Publikováno v:
Journal of Fungi, Vol 8, Iss 9, p 930 (2022)
Paecilomyces/Purpureocillium has recently been recognized as an emerging human pathogen, causing serious infection in immunocompromised and immunocompetent patients. Several predisposing factors have been reported, including foreign body implants, pr
Externí odkaz:
https://doaj.org/article/093fd5d2d22f4f898f3d2f7776b4e739
Autor:
Lana A. Shaiba, Khalid Altirkawi, Adnan Hadid, Sara Alsubaie, Omar Alharbi, Hamad Alkhalaf, Musaed Alharbi, Nourah Alruqaie, Omar Alzomor, Fahad Almughaileth, Nasser Alyousef, Prakesh S. Shah
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
The objective of this study is to describe the clinical presentations, radiological and laboratory findings, and outcomes of COVID-19 disease in infants ≤ 90 days of age at presentation. We conducted a retrospective study of infants in this age gro
Externí odkaz:
https://doaj.org/article/f68380dfd5404d018bd8a0560595a77c
Autor:
Nourah Alruqaie, Majid Alfadhel
Publikováno v:
Journal of Biochemical and Clinical Genetics, Vol 1, Iss 2, Pp 87-92 (2018)
Background: Mitchell-Riley Syndrome (OMIM # 615710) is a rare autosomal recessive disorder, characterized by a genetic mutation in the RFX6 gene. Clinically it is presented with triad of neonatal diabetes, gall bladder agenesis/hypoplasia and intesti
Externí odkaz:
https://doaj.org/article/19fab7a79a3642ce99d912033387e94f
Autor:
Majid Alfadhel, Nourah Alruqaie
Publikováno v:
Journal of Biochemical and Clinical Genetics. :87-92
Background: Mitchell-Riley Syndrome (OMIM # 615710) is a rare autosomal recessive disorder, characterized by a genetic mutation in the RFX6 gene. Clinically it is presented with triad of neonatal diabetes, gall bladder agenesis/hypoplasia and intesti