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- Association of IL-10 gene polymorphismsand susceptibility to juvenile idiopathic arthritis in Egyptian children and adolescents
Faculty
Medicine
Year:
2017
Type of Publication:
ZU Hosted
Pages:
Authors:
Nashwa Mohamed Abdalmabboud abas
Staff Zu Site
Abstract In Staff Site
Journal:
Italian journal of pediatrics IF 1.6 ( 2017) 43:9 Italian journal of pediatrics IF 1.6 ( 2017) 43:9
Volume:
Keywords :
, , , , , Association , IL-10 gene polymorphismsand susceptibility , juvenile
Abstract:
Background: Juvenile Idiopathic Arthritis (JIA) is the most common chronic arthritis in children worldwide. Among anti-inflammatory cytokines, interleukin-10 (IL-10) is a key immunosuppressive cytokine involved in the pathogenesis of JIA.
Author Related Publications
Nashwa Mohamed Abdalmabboud abas, "Adipocytokines in patiens with non alcoholic fatty liver and their contribution to its pathogenesis.", لايوجد, 1900
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Nashwa Mohamed Abdalmabboud abas, "Relation of serum adipocytokines concentration and hepatic steatosis in chronic hepatitis C infected patients", لايوجد, 1900
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Nashwa Mohamed Abdalmabboud abas, "Patterns of clinical and immunological experession in systemic lupus erythomatosis co-existing with chronic hepatitis C virus infection", لايوجد, 1900
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Nashwa Mohamed Abdalmabboud abas, "Effect of midazolam on human platelets", لايوجد, 1900
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Nashwa Mohamed Abdalmabboud abas, "Serum levels of nerve growth factor and tumor necrosis factor in &_", لايوجد, 1900
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Hanan Samer Ahmed Mouhamd, "Genetic polymorphism of methylenetetrahydrofolate reductase is associated with insulin resistance in Egyptian women with polycystic ovary syndrome", John Wiley & Sons, Ltd., 2019
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Mage Munir Hussein Fawzi, "A Comparative Study of MALDI-TOF MS and VITEK2 for Identification of Aerobic Gram Positive and Yeast Strains Isolated in Clinical Microbiology Laboratory", Egyptian Society of Medical Microbiology, 2019
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Mei Mahmoud Samy Ibraheem, "The Expression Level of Long Non-Coding RNA PVT1 as a Diagnostic Marker for Advanced Stages in Patients with Nonalcoholic Fatty Liver Disease", The Egyptian Journal of Hospital Medicine, 2022
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Doaa Metwally Abdelmoniem, "Relation between mutations in the 5′ UTR of ANKRD26 gene and inherited thrombocytopenia with predisposition to myeloid malignancies. An Egyptian study العلاقة بين طفرات جين ANKRD26 و نقص الصفائح الدموية الوراثي مع قابلية حدوث سرطانات الدم الميلودية: دراسـة مصريــة", Platelets, 2021
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