Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Akram E. El-Sadek"'
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 29, Iss 4, Pp 852-862 (2018)
Acute kidney injury (AKI) is an independent predictor of morbidity and mortality for critically ill children at pediatric Intensive Care Units (PICU). It is proposed that heat shock protein 60 (HSP60) may be either a biomarker or a co-factor of survi
Externí odkaz:
https://doaj.org/article/b5cbde320be24e18b8caa0380a151bd2
Autor:
Waleed E. Abdelghani, Ashraf Hamed Al-shokary, Yehia Hamed Abdel Maksoud, Hatem Hamed Elshorbagy, Naglaa M. Kamal, Mohamed Gamal El Din Fathallah, Hany Abdelaziz Suliman, Asmaa Obada Ibrahim, Akram E. El-Sadek
Publikováno v:
Journal of Clinical Neuroscience. 94:237-243
Omega-3 may have a role in the treatment of drug- resistant epilepsy.To evaluate omega-3 supplementation in seizure control in children with attention deficit hyperactivity disorder (ADHD) and intractable epilepsy.Sixty children with ADHD and intract
Publikováno v:
Benha Journal of Applied Sciences. 6:213-217
Background: Meconium drawing is a life-threatening disorder. It is distinguished by significant respiratory difficulties. Lactate is a fast-paced variable, strongly related to difficulties and mortality in nearly every severely sick child. Our aim in
Autor:
Waleed E. Abdelghani, Yehia Hamed Abdel Maksoud, Hany Abdelaziz Suliman, Ashraf Hamed Al-shokary, Sanaa Mohammed Azab, Dalia M Nour El Din, Hatem Hamed Elshorbagy, Sameh Elsayed Abdulsamea, Akram E. El-Sadek, Naglaa M. Kamal, Iman M. Talaat, Naglaa Fathy Barseem
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
JCRPE, Vol 11, Iss 4, Pp 374-387 (2019)
JCRPE, Vol 11, Iss 4, Pp 374-387 (2019)
Objective: Neuron-specific enolase (NSE) and S100 calcium-binding protein B (S100B) are markers of different neurological disorders. The aim was to investigate the relationship between NSE and S100B serum concentrations and the severity of diabetic k
Publikováno v:
International Journal of Immunogenetics. 47:50-56
BACKGROUND Abnormal cytokine production derived from specific polymorphisms can have effect on development of respiratory distress syndrome (RDS). Therefore, the present study aimed to determine whether polymorphisms of IL10 in preterm newborn are as
Autor:
Waleed Abdellateef Abdelhalim, Ashraf Hamed Al-shokary, Waleed E. Abdelghani, Hany Abdelaziz Suliman, Yehia Hamed Abdel Maksoud, Akram E. El-Sadek, Asmaa Obada Ibrahim, Naglaa M. Kamal, Ahmed Mahmoud Attia, Naglaa FathyBarseem, Iman M. Talaat, Hatem Hamed Elshorbagy
Publikováno v:
Global Pediatric Health
Global Pediatric Health, Vol 8 (2021)
Global Pediatric Health, Vol 8 (2021)
Background: Perinatal asphyxia (PA) is a major cause of morbidity and mortality in which dramatic transient impairment in liver functions occurs in some patients. Objectives: We aimed to evaluate the state of the liver in cases of Perinatal asphyxia
Autor:
Hany Abdelaziz Suliman, Hatem Hamed Elshorbagy, Ashraf Hamed Al-shokary, Sanaa Mohammed Azab, Asmaa Obada Ibrahim, Naglaa M. Kamal, Waleed E. Abdelghani, Yehia Hamed Abdel Maksoud, Naglaa Fathy Barseem, Akram E. El-Sadek, Dalia M Nour El Din
Publikováno v:
Journal of Pediatric Neurosciences
Background: Attention-deficit hyperactivity disorder (ADHD) is a common disorder in children, but its etiology and pathogenesis are still unclear. Aims: The aims of this study were to measure the level of serum interleukin-6 (IL-6) and tumor necrosis
Publikováno v:
Benha Journal of Applied Sciences. 3:101-104
Kidney injury (KI) is a major contributor toward infants mortality and morbidity and is associated with greater long-term risk of chronic kidney disease.The current diagnostic approach of KI is based on an acute decrease of GFR, as reflected by an ac
Autor:
Waleed E. Abdulghany, Abdelfattah A. El-Kholy, Amal E. Mohammed, Akram E. El-Sadek, Dalia M. Mahmoud, Eman G. Behiry
Publikováno v:
Annals of Medicine and Surgery
Objective This study aims to investigate the association of neonatal indirect hyperbilirubinemia in exclusively breast-fed infants with UGT1A1 (Uridine Diphosphate-Glucuronyl transferase 1A1) polymorphism. Methods 50 neonates were classified into 2 g
Publikováno v:
Medical Research Journal. 15:48-56