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Articles

Impact of serum immunoglobulins level and IL-18 promoter gene polymorphism among Egyptian patients with idiopathic thrombocytopenic purpura

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Mervat hesham, Tamer Hassan, Amal Fawzy, Noura Mohamed, Ebtihaj Alhejny, Manar Fathy, Sherief El Gebaly & Marwa Zakaria. (2021) PTPN22 gene polymorphism as a genetic risk factor for primary immune thrombocytopenia in Egyptian children. Expert Review of Hematology 14:9, pages 877-881.
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Sahar Najafi, MohammadAli Jalali Far, GholamAbbas Kaydani, Kaveh Jaseb & Najmaldin Saki. (2021) Role of platelet endothelial aggregation receptor 1 polymorphisms in idiopathic thrombocytopenic purpura: Is there an association?. Clinical Cancer Investigation Journal 10:5, pages 227.
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Zi Sheng, Ju Li, Yuanjian Wang, Song Li, Ming Hou, Jun Peng & Qi Feng. (2019) A CARD9 single-nucleotide polymorphism rs4077515 is associated with reduced susceptibility to and severity of primary immune thrombocytopenia. Annals of Hematology 98:11, pages 2497-2506.
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Ali Amin Asnafi, Mohammad bagher Mohammadi, Hadi Rezaeeyan, Nader Davari & Najmaldin Saki. (2019) Prognostic significance of mutated genes in megakaryocytic disorders. Oncology Reviews 13:2.
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Hadi Rezaeeyan, Kaveh Jaseb, Arash Alghasi, Ali Amin Asnafi & Najmaldin Saki. (2017) Association between gene polymorphisms and clinical features in idiopathic thrombocytopenic purpura patients. Blood Coagulation & Fibrinolysis 28:8, pages 617-622.
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