Zobrazeno 1 - 10
of 29
pro vyhledávání: '"M. Aboelghar"'
Publikováno v:
Egyptian Journal of Remote Sensing and Space Sciences, Vol 14, Iss 2, Pp 81-89 (2011)
The objective of the current work is to generate statistical empirical rice yield estimation models under the local conditions of the Egyptian Nile delta. The methodology is based on regressing measured yield with satellite derived spectral informati
Externí odkaz:
https://doaj.org/article/5e77a856bc7d4a69a46712109d4d45c8
Publikováno v:
Egyptian Journal of Remote Sensing and Space Sciences, Vol 13, Iss 2, Pp 121-127 (2010)
A research project was conducted as collaboration between the National Authority for Remote Sensing and Space Sciences (NARSS) in Egypt and the Institute of Remote Sensing Applications (IRSA), Chinese Academy of Sciences. The objective of this study
Externí odkaz:
https://doaj.org/article/c484ae15594c41b691b5d92bd9242eab
Publikováno v:
Clinical and Experimental Pediatrics, Vol 66, Iss 9, Pp 403-411 (2023)
Background The optimal timing of parenteral nutrition (PN) initiation in critically ill children remains controversial. Purpose To identify the optimal timing of PN initiation in critically ill children. Methods This randomized clinical trial was con
Externí odkaz:
https://doaj.org/article/e0db3071a7bc4634a8f99893c54b46f8
Autor:
Nagwan Y. Saleh, Hesham M. Aboelghar, Sherif S. Salem, Reda A. Ibrahem, Fatma O. Khalil, Ahmed S. Abdelgawad, Asmaa A. Mahmoud
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-11 (2021)
Abstract Background Emergence of 2019-nCoV attracted global attention and WHO declared COVID-19 a public health emergency of international concern. Therefore we aimed to explore the severity and atypical manifestations of COVID-19 among children. Met
Externí odkaz:
https://doaj.org/article/8ddbd5a6c94a4af9bf87dcf3c5a3d263
Publikováno v:
Children, Vol 8, Iss 9, p 791 (2021)
Background: Sepsis is still the main etiology of mortality in pediatric intensive care units (PICUs). Therefore, we performed this study to evaluate the value of procollagen Type III amino-terminal propeptide (PIIINP) as a biomarker for sepsis severi
Externí odkaz:
https://doaj.org/article/6ed1eea2d20047fcadb815175ef2d15e
Publikováno v:
Pediatric Research.
Background We assessed serum concentrations of pancreatic stone protein (PSP), copeptin, and apolipoprotein A-V (APOA5) biomarkers for the diagnosis and prognosis of pediatric sepsis, a condition associated with high mortality. Methods This prospecti
Autor:
Asmaa A. Mahmoud, Hesham M. Aboelghar, Sabry Moawad Abdelmageed, Heba M. Abdallah, Mohamed I. Garib, Nahla M. S. Abd El Hady
Publikováno v:
Pediatric research. 92(6)
Background Epilepsy is a neurological disease that requires long-term antiepileptic drugs (AEDs). The old generation of AEDs may affect serum homocysteine and asymmetric dimethylarginine (ADMA) and disturb lipid levels. The aim of the study was to ev
Publikováno v:
Children, Vol 8, Iss 791, p 791 (2021)
Children
Volume 8
Issue 9
Children
Volume 8
Issue 9
Background: Sepsis is still the main etiology of mortality in pediatric intensive care units (PICUs). Therefore, we performed this study to evaluate the value of procollagen Type III amino-terminal propeptide (PIIINP) as a biomarker for sepsis severi
Autor:
Sherif S. Salem, Hesham M. Aboelghar, Ahmed S. Abdelgawad, Reda A Ibrahem, Fatma O. Khalil, Nagwan Y. Saleh, Asmaa A. Mahmoud
Publikováno v:
BMC Pediatrics
BMC Pediatrics, Vol 21, Iss 1, Pp 1-11 (2021)
BMC Pediatrics, Vol 21, Iss 1, Pp 1-11 (2021)
Background Emergence of 2019-nCoV attracted global attention and WHO declared COVID-19 a public health emergency of international concern. Therefore we aimed to explore the severity and atypical manifestations of COVID-19 among children. Methods This
Autor:
Tamer Hamouda, Ahmed F. Elmahrouk, Ahmed A. Jamjoom, Hesham M. Aboelghar, Mohamed Ismail, Nashwa Badawy, Abdulbadee Bugis
Publikováno v:
The Thoracic and Cardiovascular Surgeon Reports
The Thoracic & Cardiovascular Surgeon Reports, Vol 07, Iss 01, Pp e12-e15 (2018)
The Thoracic & Cardiovascular Surgeon Reports, Vol 07, Iss 01, Pp e12-e15 (2018)
Background Factor X deficiency (also known as Stuart–Prower factor deficiency) is an autosomal recessive extremely rare hereditary hematologic disorder, affecting around 1:1,000,000 of the general population. Case Presentation This case report desc