163 related articles for article (PubMed ID: 26620341)
1. Association between the V Leiden G1691A mutation and sudden sensorineural hearing loss in Italian population: a meta-analysis.
Shu J; Si Y; Yin S; He M
Eur Arch Otorhinolaryngol; 2016 Sep; 273(9):2467-72. PubMed ID: 26620341
[TBL] [Abstract][Full Text] [Related]
2. Association between the prothrombin G20210A mutation and sudden sensorineural hearing loss in European population: a meta-analysis.
Shu J; Yin S; Tan AZ; He M
Thromb Res; 2015 Jan; 135(1):73-7. PubMed ID: 25466842
[TBL] [Abstract][Full Text] [Related]
3. Association between the methylenetetrahydrofolate reductase gene C677T polymorphism and sudden sensorineural hearing loss: a meta-analysis.
Shu J; Yin S; Tan AZ; He M
Eur Arch Otorhinolaryngol; 2015 Sep; 272(9):2267-74. PubMed ID: 25012704
[TBL] [Abstract][Full Text] [Related]
4. Lack of association between inherited thrombophilic risk factors and idiopathic sudden sensorineural hearing loss in Italian patients.
Cadoni G; Scipione S; Rocca B; Agostino S; La Greca C; Bonvissuto D; Paludetti G
Ann Otol Rhinol Laryngol; 2006 Mar; 115(3):195-200. PubMed ID: 16572609
[TBL] [Abstract][Full Text] [Related]
5. The role of factor V Leiden and prothrombin G20210A mutations in sudden sensorineural hearing loss.
Görür K; Tuncer U; Eskandari G; Ozcan C; Unal M; Ozsahinoglu C
Otol Neurotol; 2005 Jul; 26(4):599-601. PubMed ID: 16015153
[TBL] [Abstract][Full Text] [Related]
6. Role of genetic and acquired prothrombotic risk factors in genesis of sudden sensorineural hearing loss.
Fusconi M; Chistolini A; Angelosanto N; Pignoloni P; Tombolini M; De Virgilio A; Pagliarella M; de Vincentiis M
Audiol Neurootol; 2011; 16(3):185-90. PubMed ID: 20798492
[TBL] [Abstract][Full Text] [Related]
7. A preliminary study on the role of inherited prothrombotic risk factors in Taiwanese patients with sudden sensorineural hearing loss.
Lan MY; Shiao JY; Hsu YB; Lin FY; Lin JC
Eur Arch Otorhinolaryngol; 2011 Jun; 268(6):817-22. PubMed ID: 21170721
[TBL] [Abstract][Full Text] [Related]
8. Prothrombotic gene mutations in patients with sudden sensorineural hearing loss and cardiovascular thrombotic disease.
Capaccio P; Cuccarini V; Ottaviani F; Fracchiolla NS; Bossi A; Pignataro L
Ann Otol Rhinol Laryngol; 2009 Mar; 118(3):205-10. PubMed ID: 19374152
[TBL] [Abstract][Full Text] [Related]
9. Genetic Polymorphisms in Sudden Sensorineural Hearing Loss: An Update.
Corazzi V; Ciorba A; Bianchini C; Pelucchi S; Skarżyński PH; Hatzopoulos S
Ear Nose Throat J; 2021 Jun; 100(3_suppl):337S-342S. PubMed ID: 32804576
[TBL] [Abstract][Full Text] [Related]
10. Genetic and acquired prothrombotic risk factors and sudden hearing loss.
Capaccio P; Ottaviani F; Cuccarini V; Bottero A; Schindler A; Cesana BM; Censuales S; Pignataro L
Laryngoscope; 2007 Mar; 117(3):547-51. PubMed ID: 17334320
[TBL] [Abstract][Full Text] [Related]
11. Genetic Polymorphisms and Susceptibility to Sudden Sensorineural Hearing Loss: A Systematic Review.
Cao Z; Gao J; Huang S; Xiang H; Zhang C; Zheng B; Zhan X; Chen R; Chen B
Audiol Neurootol; 2019; 24(1):8-19. PubMed ID: 30870848
[TBL] [Abstract][Full Text] [Related]
12. Coexistence of IL-6 -572C/G and ICAM-1 K469E Polymorphisms among Patients with Sudden Sensorineural Hearing Loss.
Tian G; Zhang S; Yang J
Tohoku J Exp Med; 2018 May; 245(1):7-12. PubMed ID: 29695657
[TBL] [Abstract][Full Text] [Related]
13. Glutathione s-transferase gene polymorphisms in Italian patients with sudden sensorineural hearing loss.
Cadoni G; Boccia S; Scipione S; Arzani D; Cianfagna F; Ricciardi G; Paludetti G; Agostino S
Otol Neurotol; 2006 Dec; 27(8):1166-9. PubMed ID: 16788422
[TBL] [Abstract][Full Text] [Related]
14. Glutathione peroxidase 3 gene polymorphisms and the risk of sudden sensorineural hearing loss.
Chien CY; Huang TY; Tai SY; Chang NC; Wang HM; Wang LF; Ho KY
Kaohsiung J Med Sci; 2017 Jul; 33(7):359-364. PubMed ID: 28738977
[TBL] [Abstract][Full Text] [Related]
15. eNOS gene Glu298Asp variant confer risk in sudden sensorineural hearing loss.
Yazdani N; Kakavand Hamidi A; Soroush N; Jalili N; Vahidi A; Zarabi Ahrabi N; Tajdini A; Amoli M
Acta Otolaryngol; 2018 Oct; 138(10):904-908. PubMed ID: 30354859
[TBL] [Abstract][Full Text] [Related]
16. Role of factor V Leiden polymorphism or G20210A prothrombin variant in patients with sudden sensorineural hearing loss: a meta-analysis of the literature.
Spiezia L; Vasques F; Bovo R; Martini A; Simioni P
Thromb Res; 2015 Mar; 135(3):565-7. PubMed ID: 25538030
[No Abstract] [Full Text] [Related]
17. Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes.
Nishio N; Teranishi M; Uchida Y; Sugiura S; Ando F; Shimokata H; Sone M; Otake H; Kato K; Yoshida T; Tagaya M; Hibi T; Nakashima T
Gene; 2012 May; 499(1):226-30. PubMed ID: 22426290
[TBL] [Abstract][Full Text] [Related]
18. [A Meta-analysis of prothrombin G20210A polymorphism and its risk for sudden sensorineural hearing loss].
Liu B; Feng WJ; Peng XX; Yang J
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2013 May; 48(5):417-21. PubMed ID: 24016568
[TBL] [Abstract][Full Text] [Related]
19. Proinflammatory cytokine IL-1 β polymorphisms in sudden sensorineural hearing loss.
Um JY; Jang CH; Kim HL; Cho YB; Park J; Lee SJ; Kim YB; Kim HJ; Ahn KS; Jang HJ; Lee SG; Lee H; Lee KM; Kim SJ; Hong SH
Immunopharmacol Immunotoxicol; 2013 Feb; 35(1):52-6. PubMed ID: 23013363
[TBL] [Abstract][Full Text] [Related]
20. Sudden hearing loss followed by deep vein thrombosis and pulmonary embolism in a patient with factor V Leiden mutation.
Lovato A; Tormene D; Staffieri C; Breda S; Staffieri A; Marioni G
Int J Audiol; 2014 Sep; 53(9):625-8. PubMed ID: 24735015
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]