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Items: 1 to 20 of 123

1.

A Study of Human Killer Cell Immunoglobulin-Like Receptor and Multidrug Resistance Gene Polymorphisms in Children With Immune Thrombocytopenia.

El-Beblawy NM, Elbarbary NS, Kamal TM, Mahmoud PM.

Clin Appl Thromb Hemost. 2016 Jul;22(5):429-40. doi: 10.1177/1076029615576738. Epub 2015 Mar 18.

PMID:
25792670
2.

The role of PTPN22 gene polymorphism in childhood immune thrombocytopenic purpura.

Anis SK, Abdel Ghany EA, Mostafa NO, Ali AA.

Blood Coagul Fibrinolysis. 2011 Sep;22(6):521-5. doi: 10.1097/MBC.0b013e328347b064.

PMID:
21597364
3.

Cytokine gene polymorphism [tumor necrosis factor-alpha (-308), IL-10 (-1082), IL-6 (-174), IL-17F, 1RaVNTR] in pediatric patients with primary immune thrombocytopenia and response to different treatment modalities.

Mokhtar GM, El-Beblawy NM, Adly AA, Elbarbary NS, Kamal TM, Hasan EM.

Blood Coagul Fibrinolysis. 2016 Apr;27(3):313-23. doi: 10.1097/MBC.0000000000000431.

PMID:
27007229
4.

The presence of KIR2DS5 confers protection against adult immune thrombocytopenia.

Seymour LA, Nourse JP, Crooks P, Wockner L, Bird R, Tran H, Gandhi MK.

Tissue Antigens. 2014 Mar;83(3):154-60. doi: 10.1111/tan.12295. Epub 2014 Feb 12.

PMID:
24571473
5.

Relation between 3435C>T multidrug resistance 1 gene polymorphism with high dose methylprednisolone treatment of childhood acute idiopathic thrombocytopenic purpura.

Akin M, Turgut S, Ayada C, Polat Y, Balci YI, Erdoğan F.

Gene. 2011 Nov 1;487(1):80-3. doi: 10.1016/j.gene.2011.06.019. Epub 2011 Jun 21.

PMID:
21718764
6.

Cannabinoid CB2 receptor gene (CNR2) polymorphism is associated with chronic childhood immune thrombocytopenia in Egypt.

Mahmoud Gouda H, Mohamed Kamel NR.

Blood Coagul Fibrinolysis. 2013 Apr;24(3):247-51. doi: 10.1097/MBC.0b013e32835aba1d.

PMID:
23406660
7.

Decreased Frequency of IL-17F rs763780 Site Allele G is Associated With Genetic Susceptibility to Immune Thrombocytopenia in a Chinese Population.

Li H, Zhou Z, Tai W, Feng W, Zhang D, Gu X, Yang R.

Clin Appl Thromb Hemost. 2017 Jul;23(5):466-471. doi: 10.1177/1076029615618022. Epub 2015 Nov 30.

PMID:
26620416
8.

FcγRIIa and FcγRIIIa genetic polymorphisms in a group of pediatric immune thrombocytopenic purpura in Egypt.

Eyada TK, Farawela HM, Khorshied MM, Shaheen IA, Selim NM, Khalifa IA.

Blood Coagul Fibrinolysis. 2012 Jan;23(1):64-8. doi: 10.1097/MBC.0b013e32834ddf2f.

PMID:
22123287
9.

STAT1 single nucleotide polymorphisms and susceptibility to immune thrombocytopenia.

Chen Z, Guo Z, Ma J, Liu F, Gao C, Liu S, Wang A, Wu R.

Autoimmunity. 2015;48(5):305-12. doi: 10.3109/08916934.2015.1016218. Epub 2015 Feb 24.

PMID:
25707685
10.

The potential association of tumor necrosis factor-βeta (252 G/A) cytokine gene polymorphism with immune thrombocytopenic purpura among Egyptian children.

Morgan DS, Afifi RA, El-Hoseiny SM, Amin DG, Ibrahim SYG.

Hematology. 2018 Jun;23(5):299-303. doi: 10.1080/10245332.2017.1386429. Epub 2017 Oct 12.

PMID:
29020887
11.

Interleukin-18 gene promoter--607 A/C polymorphism and the risk of immune thrombocytopenia.

Zhao H, Zhang Y, Xiao G, Wu N, Xu J, Fang Z.

Autoimmunity. 2014 Nov;47(7):478-81. doi: 10.3109/08916934.2014.921812. Epub 2014 Jun 4.

PMID:
24897237
12.

Relation of interleukin-10 Promoter Polymorphisms to Adult Chronic Immune Thrombocytopenic Purpura in a Cohort of Egyptian Population.

El Ghannam D, Fawzy IM, Azmy E, Hakim H, Eid I.

Immunol Invest. 2015;44(7):616-26. doi: 10.3109/08820139.2015.1064948.

PMID:
26436850
13.

The KIR2DS2/DL2 genotype is associated with adult persistent/chronic and relapsed immune thrombocytopenia independently of FCGR3a-158 polymorphisms.

Nourse JP, Lea R, Crooks P, Wright G, Tran H, Catalano J, Brighton T, Grigg A, Marlton P, Gandhi MK.

Blood Coagul Fibrinolysis. 2012 Jan;23(1):45-50. doi: 10.1097/MBC.0b013e32834d7ce3.

PMID:
22024796
14.

Has-mir-146a rs2910164 polymorphism and risk of immune thrombocytopenia.

Zhao H, Zhang Y, Xue F, Xu J, Fang Z.

Autoimmunity. 2014 May;47(3):173-6. doi: 10.3109/08916934.2014.883503. Epub 2014 Feb 6.

PMID:
24502829
15.

Interleukin-23R gene polymorphism in pediatric Egyptian patients with primary immune thrombocytopenia.

Farawela HM, Botros SK, El-Ghamrawy M, Ebrahim EO.

Blood Coagul Fibrinolysis. 2016 Jun;27(4):374-7. doi: 10.1097/MBC.0000000000000450.

PMID:
26859125
16.

DNMT3B promoter polymorphism and risk of immune thrombocytopenic purpura in pediatric Egyptians.

Shaheen IA, Abukhalil RE, Ali DK, Afifi RA.

Blood Coagul Fibrinolysis. 2012 Oct;23(7):636-9.

PMID:
22885766
17.

The polymorphisms of T cell-specific TBX21 gene may contribute to the susceptibility of chronic immune thrombocytopenia in Chinese population.

Zhang D, Zhang X, Ge M, Xuan M, Li H, Yang Y, Fu R, Zhou F, Zheng Y, Yang R.

Hum Immunol. 2014 Feb;75(2):129-33. doi: 10.1016/j.humimm.2013.11.011. Epub 2013 Nov 18.

PMID:
24262372
18.

Assessment of IL-17F rs763780 gene polymorphism in immune thrombocytopenia.

Tolba FM, Diab SM, Abdelrahman AMN, Behairy OG, Almonaem ERA, Mogahed MM, Mohamed SA.

Blood Cells Mol Dis. 2019 Mar;75:20-25. doi: 10.1016/j.bcmd.2018.12.001. Epub 2018 Dec 14.

PMID:
30594845
19.

Multi-drug resistance-1 gene polymorphisms in nephrotic syndrome: impact on susceptibility and response to steroids.

Youssef DM, Attia TA, El-Shal AS, Abduelometty FA.

Gene. 2013 Nov 10;530(2):201-7. doi: 10.1016/j.gene.2013.08.045. Epub 2013 Aug 27.

PMID:
23994685
20.

Lack of association between NR3C1 polymorphism and glucocorticoid resistance in Chinese patients with immune thrombocytopenia.

Xuan M, Li H, Fu R, Yang Y, Zhang D, Zhang X, Yang R.

Platelets. 2014;25(2):125-8. doi: 10.3109/09537104.2013.779369. Epub 2013 Mar 25.

PMID:
23527567

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