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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:
Authors:
Reem Mohamed ElSayed Mohamed Allam
Staff Zu Site
Abstract In Staff Site
Journal:
Alexandria Journal of Pediatrics Wolters Kluwer - Medknow
Volume:
Keywords :
Association between UGT-1A1 gene GLY71Arg polymorphism and
Abstract:
Introduction: 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 w
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Reem Mohamed ElSayed Mohamed Allam, "Influence of +299G>A and +62G˃A resistin gene promoter variants on cardiovascular risk in Egyptian women with systemic lupus erythematosus", Elsevier B.V, 2018
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Reem Mohamed ElSayed Mohamed Allam, "Association between HindIII (rs320) variant in the lipoprotein lipase gene and the presence of coronary artery disease and stroke among the Saudi population", Elsevier B.V, 2020
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Reem Mohamed ElSayed Mohamed Allam, "Genetic Association of rs10757278 on Chromosome 9p21 and Coronary Artery Disease in a Saudi Population", Dove Medical Press Limited, 2021
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Manal Mohamed Amin, " دراسة النيتريت فى البول وبعض مضادات الاكسدة فى الاطفال المصابين بالمتلازمة النفروزية ذات التغير البسيط", لايوجد, 1900
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Mona Elsayed Hashim Muhammad, "- Role of electrophysiological study and GAD65 in detection of Subclinical neuropathy in patients with recently diagnosed type 1 diabetes mellitus ", لايوجد, 1900
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Mohammed Issa Mohamed Sayed Ahmed, "Hemoglobin scavenger receptor (cluster of differentiation 163) role in acute leukemia", Web of Science, 2022
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Amany Mohamed Mohyldeen, "Neutrophil/lymphocyte ratio and platelet/lymphocyte ratio in Behçet’s disease: which and when to use?", International League of Associations for Rheumatology, 2018
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