These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. 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]
6. 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]
7. 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]
8. Methylenetetrahydrofolate reductase C677T gene mutation as risk factor for sudden sensorineural hearing loss: association with plasma homocysteine, folate and cholesterol concentrations. Lee EJ; Cho YJ; Yoon YJ J Laryngol Otol; 2010 Dec; 124(12):1268-73. PubMed ID: 20492738 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
12. Association between Macrophage Migration Inhibitory Factor Gene Variation and Response to Glucocorticoid Treatment in Sudden Sensorineural Hearing Loss. Yazdani N; Kakavand Hamidi A; Ghazavi H; Rikhtegar MJ; Motesadi Zarandi M; Qorbani M; Amoli MM Audiol Neurootol; 2015; 20(6):376-82. PubMed ID: 26426302 [TBL] [Abstract][Full Text] [Related]
13. Phosphodiesterase 4D gene polymorphisms in sudden sensorineural hearing loss. Chien CY; Tai SY; Wang LF; Hsi E; Chang NC; Wang HM; Wu MT; Ho KY Eur Arch Otorhinolaryngol; 2016 Sep; 273(9):2403-9. PubMed ID: 26521189 [TBL] [Abstract][Full Text] [Related]
14. Association of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with primary glaucoma in Saudi population. Al-Shahrani H; Al-Dabbagh N; Al-Dohayan N; Arfin M; Al-Asmari M; Rizvi S; Al-Asmari A BMC Ophthalmol; 2016 Sep; 16(1):156. PubMed ID: 27585654 [TBL] [Abstract][Full Text] [Related]
15. 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]
17. MTHFR C677T, FII G20210A, FV Leiden G1691A, NOS3 intron 4 VNTR, and APOE epsilon4 gene polymorphisms are not associated with spontaneous cervical artery dissection. Jara-Prado A; Alonso ME; Martínez Ruano L; Guerrero Camacho J; Leyva A; López M; Gutierrez-Castrellon P; Arauz A Int J Stroke; 2010 Apr; 5(2):80-5. PubMed ID: 20446941 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. MTHFR polymorphism: associated intralabyrinthine hemorrhage. Braverman I; Ben David J; Shupak A Otolaryngol Head Neck Surg; 2009 Oct; 141(4):541-2. PubMed ID: 19786230 [No Abstract] [Full Text] [Related]
20. MTHFR (C677T) CT genotype and CT-apoE3/3 genotypic combination predisposes the risk of ischemic stroke. Vijayan M; Chinniah R; Ravi PM; Sivanadham R; Mosses Joseph AK; Vellaiappan NA; Krishnan JI; Karuppiah B Gene; 2016 Oct; 591(2):465-70. PubMed ID: 27378745 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]