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.
6. Jervell-Lange Nielsen syndrome in a family with the long QT syndrome (LQTS). Shanbag P. Indian J Pediatr; 2007 Jan; 74(1):90; author reply 90. PubMed ID: 17264466 [No Abstract] [Full Text] [Related]
10. Jervell-Lange Nielsen syndrome in a family with the long QT Syndrome (LQTS). Mondal RK, Karmakar B, Chandra PK, Sarkar UN. Indian J Pediatr; 2006 Jul; 73(7):623-5. PubMed ID: 16877859 [Abstract] [Full Text] [Related]
11. The Jervell and Lange-Nielsen syndrome. Cusimano F, Martines E, Rizzo C. Int J Pediatr Otorhinolaryngol; 1991 Jul; 22(1):49-58. PubMed ID: 1917338 [Abstract] [Full Text] [Related]
15. Cochlear implantation in patients with Jervell and Lange-Nielsen syndrome, and a review of literature. Yanmei F, Yaqin W, Haibo S, Huiqun Z, Zhengnong C, Dongzhen Y, Shankai Y. Int J Pediatr Otorhinolaryngol; 2008 Nov 02; 72(11):1723-9. PubMed ID: 18805595 [Abstract] [Full Text] [Related]
16. Cochlear implantation in children with Jervell, Lange-Nielsen syndrome. Daneshi A, Ghassemi MM, Talee M, Hassanzadeh S. J Laryngol Otol; 2008 Mar 02; 122(3):314-7. PubMed ID: 17498328 [Abstract] [Full Text] [Related]
17. Cochlear implantation in Jervell & Lange-Nielsen syndrome: a cautionary report. Broomfield SJ, Bruce IA, Henderson L, Green KM, Ramsden RT. Cochlear Implants Int; 2010 Jun 02; 11 Suppl 1():163-5. PubMed ID: 21756604 [No Abstract] [Full Text] [Related]
18. An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome. Bhuiyan ZA, Momenah TS, Amin AS, Al-Khadra AS, Alders M, Wilde AA, Mannens MM. Prog Biophys Mol Biol; 2008 Jun 02; 98(2-3):319-27. PubMed ID: 19027783 [Abstract] [Full Text] [Related]
19. Congenital hearing loss in Jervell and Lange-Nielsen syndrome. Jacobson J, Jacobson C, Francis P. J Am Acad Audiol; 1990 Jul 02; 1(3):171-3. PubMed ID: 1721555 [Abstract] [Full Text] [Related]
20. The combined novel KCNQ1 frameshift I145Sfs*92 and nonsense W392X variants caused Jervell and Lange-Nielsen syndrome in a Chinese infant presenting with sustained foetal bradycardia. Zhang Y, Li X, Yang Y, Wang J, Gao X, Fan M. Europace; 2020 Dec 23; 22(12):1880-1884. PubMed ID: 32830254 [Abstract] [Full Text] [Related] Page: [Next] [New Search]