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Association between UGT-1A1 gene GLY71Arg polymorphism and severe unexplained indirect hyperbilirubinemia among neonates
Faculty
Medicine
Year:
2018
Type of Publication:
ZU Hosted
Pages:
10
Authors:
weSam Abdel Moneim Mokhtar Ahmed
Staff Zu Site
Abstract In Staff Site
Journal:
مجلة القطاع الهندسى لجامعة الازهر wolters kluwer medknow
Volume:
Keywords :
Association between UGT-1A1 gene GLY71Arg polymorphism
Abstract:
Neonatal jaundice is considered the most prevailing clinical health problem among neonates. Numerous etiological factors are responsible for the development of pathological neonatal jaundice. Almost half of the cases have no well-identified
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weSam Abdel Moneim Mokhtar Ahmed, "Reducing ventilator-associated pneumonia in neonatal intensive care unit using “VAP prevention Bundle”: a cohort study", Biomed central, 2015
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weSam Abdel Moneim Mokhtar Ahmed, "Association between adenosine receptor gene polymorphism and response to caffeine citrate treatment in apnea of prematurity; An Egyptian single-center study", elseiver, 2018
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weSam Abdel Moneim Mokhtar Ahmed, "Role of high resolution ultrasonography in diagnosing septic hip arthritis in premature neonates admitted to the neonatal intensive care unit", Elsevier, 2017
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weSam Abdel Moneim Mokhtar Ahmed, "Does implementing a regime of dexamethasone before planned cesarean section at term reduce admission with respiratory morbidity to neonatal intensive care unit? A randomized controlled trial.", Taylor and franscis, 2017
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