Zobrazeno 1 - 10
of 335
pro vyhledávání: '"S Gouda"'
Autor:
Hala M. Sakhr, Mohammed H. Hassan, Ahmed El-Abd Ahmed, Nagwan I. Rashwan, Rehab H. Abdel-Aziz, Amr S. Gouda, Rana Toghan
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Nutritional status assessment, including amino acids, carnitine, and acylcarnitine profile, is an important component of diabetes care management, influencing growth and metabolic regulation. A designed case–control research included 100 E
Externí odkaz:
https://doaj.org/article/8b4f5cc34c494161a8cc8abd558d22f3
Autor:
Reda.S. Salama, Mostafa S. Gouda, Mohamed F. Aly Aboud, Fares T. Alshorifi, A. A. El-Hallag, Ahmad K. Badawi
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-14 (2024)
Abstract Supercapacitors have emerged as highly efficient energy storage devices, relying on electrochemical processes. The performance of these devices can be influenced by several factors, with key considerations including the selection of electrod
Externí odkaz:
https://doaj.org/article/fed8adc34e4349c7ada25c84d0440e34
Autor:
Reda. S. Salama, Mostafa S. Gouda, Mohamed F. Aly Aboud, Fares T. Alshorifi, A. A. El‑Hallag, Ahmad K. Badawi
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/ebdd4ee418fa4478a50c609fc5495aea
Autor:
Walaa S Nazim, Ekram M Fateen, Amr S Gouda, Amira M Radwan, Mostafa I Al-sharkawi, Azza F Elbaz
Publikováno v:
Journal of the Arab Society for Medical Research, Vol 18, Iss 1, Pp 51-59 (2023)
Background/aim Inborn errors of metabolism (IEM) are a group of congenital disorders that result from deficiency of enzymes or transporters involved in different metabolic pathways in the human body. The most severe form of these disorders appears ea
Externí odkaz:
https://doaj.org/article/8d1d06a2e1ea4746aebc15e1bd1b2a17
Autor:
Amira M. Sultan, Nawal S. Gouda
Publikováno v:
Journal of Pure and Applied Microbiology, Vol 16, Iss 2, Pp 1179-1186 (2022)
Vancomycin resistant enterococci are challenging bacteria as they are difficult to be eradicated. Toxin-antitoxin (TA) systems are genetic elements located in most prokaryotic genomes. The mazEF TA system is harbored by a plasmid among Enterococcus f
Externí odkaz:
https://doaj.org/article/a198c2f98d134619a87c13508ef4b982
Autor:
Aly A. Aboulnasr, Khaled R. Gaber, Gamal Abdel Sameea, Amr S. Gouda, Mona M. Ibrahim, Taghreed A. Shalabi, Amr Elnouri
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-6 (2022)
Abstract Background Mucopolysaccharidosis VI (MPS VI) or Maroteaux–Lamy syndrome is an autosomal recessive lysosomal storage disorder. Clinical manifestations are related to progressive accumulation of dermatan sulfate (DS). Two-dimensional electro
Externí odkaz:
https://doaj.org/article/466717b4dfbe44e99656183ff89a8c29
Autor:
Philippe Nguyen, Lucie Chevillard, Ahmed S. Gouda, Hervé Gourlain, Laurence Labat, Isabelle Malissin, Nicolas Deye, Sebastian Voicu, Bruno Mégarbane
Publikováno v:
Annals of Intensive Care, Vol 12, Iss 1, Pp 1-13 (2022)
Abstract Background Valproic acid (VPA) poisoning is responsible for life-threatening neurological and metabolic impairments. Despite only low-level evidence of effectiveness, L-carnitine has been used for years to prevent or reverse VPA-related toxi
Externí odkaz:
https://doaj.org/article/7ad3a4dc710e4a938b223316e88989d8
Autor:
Rania Elkeeb, Anomeh Avartoomian, Amira S. Gouda, Ahmed M. Abdel-Megied, Ola Abdallah, Eman Atef
Publikováno v:
Scientia Pharmaceutica, Vol 91, Iss 3, p 38 (2023)
The aim of the study is to evaluate the effectiveness of the pediatric sofosbuvir weight-based dosing strategy in providing an equitable drug exposure compared to the marketed dose. The physiologically based pharmacokinetic (PBPK) modeling and simula
Externí odkaz:
https://doaj.org/article/0222117e208a4031bdb2e1edcebf0c4a
Autor:
Nouran B. AbdAllah, Eman A. Toraih, Essam Al Ageeli, Hala Elhagrasy, Nawal S. Gouda, Manal S. Fawzy, Ghada M. Helal
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract Toll-like receptor (TLR) family signature has been implicated in sepsis etiopathology. We aimed to evaluate the genetic profile of TLR pathway-related key genes; the myeloid differentiation protein 88 (MYD88), IL1 receptor-associated kinase
Externí odkaz:
https://doaj.org/article/cb878c7b4af8494cbf9939490a57a6c2
Autor:
Amr S. Gouda, Walaa S. Nazim
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
Abstract Background Phenylketonuria (PKU), inborn error of metabolism, results from phenylalanine hydroxylase deficiency. PKU leads to neurological manifestations, intellectual disability, and mental disorders. Treatment depends on phenylalanine-rest
Externí odkaz:
https://doaj.org/article/738fe6743fd04cf89a059de8098bdba0