Skip to main page content
U.S. flag

An official website of the United States government

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

1975
2025

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
1993 2
1994 1
1998 1
1999 2
2000 1
2002 3
2003 1
2004 1
2006 1
2008 2
2009 1
2013 2
2015 2
2016 1
2019 2
2020 1
2022 1
2023 1
2024 1
2025 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Search Results

27 results

Results by year

Filters applied: . Clear all
Page 1
Jervell and Lange-Nielsen syndrome in cochlear implanted patients: our experience and a review of literature.
Eftekharian A, Mahani MH. Eftekharian A, et al. Int J Pediatr Otorhinolaryngol. 2015 Sep;79(9):1544-7. doi: 10.1016/j.ijporl.2015.07.012. Epub 2015 Jul 14. Int J Pediatr Otorhinolaryngol. 2015. PMID: 26205899 Review.
OBJECTIVES: To share our experience in cochlear implanted patients with Jervell and Lange-Nielsen syndrome (JLNS), to review the literature results and to disclose precautions which have to be taken dealing with these patients. MATERIALS AND METHODS: Electrocardiogr …
OBJECTIVES: To share our experience in cochlear implanted patients with Jervell and Lange-Nielsen syndrome (JLNS), to review t …
[Jervell and Lange-Nielsen syndrome].
Zhang WJ, Sun Y, Kong WJ. Zhang WJ, et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2019 Sep;33(9):825-829. doi: 10.13201/j.issn.1001-1781.2019.09.007. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2019. PMID: 31446697 Review. Chinese.
Summary Jervell and Lange-Nielsen syndrome(JLNS) is an autosomal recessive hereditary disease characterized by congenital severe sensorineural hearing loss in both ears and severe arrhythmias with QT interval prolongation. ...
Summary Jervell and Lange-Nielsen syndrome(JLNS) is an autosomal recessive hereditary disease characterized by congenital seve …
The history of Jervell and Lange-Nielsen syndrome.
Hem E, Gjesdal KT, Tranebjærg L, Nylenna M. Hem E, et al. Tidsskr Nor Laegeforen. 2024 Dec 16;144(15). doi: 10.4045/tidsskr.24.0412. Print 2024 Dec 17. Tidsskr Nor Laegeforen. 2024. PMID: 39692650 Free article. Review. English, Norwegian.
One of the best-known Norwegian examples is Jervell and Lange-Nielsen syndrome. MATERIAL AND METHOD: We conducted a literature review using systematic database searches and historical analysis. RESULTS AND INTERPRETATION: The Norwegian internal medicine specialists …
One of the best-known Norwegian examples is Jervell and Lange-Nielsen syndrome. MATERIAL AND METHOD: We conducted a literature …
[Genetic deafness].
Marcolla A, Bouchetemble P, Lerosey Y, Marie JP, Dehesdin D. Marcolla A, et al. Ann Otolaryngol Chir Cervicofac. 2006 Jun;123(3):143-7. doi: 10.1016/s0003-438x(06)76655-5. Ann Otolaryngol Chir Cervicofac. 2006. PMID: 16840903 Review. French.
RESULTS: Genetic sensorineural syndromic deafness represents 30% of cases of genetic deafness. A frequent cause is Pendred syndrome, which associates congenital sensorineural deafness with goitre and malformations of the inner ear which can be identified on computed tomogr …
RESULTS: Genetic sensorineural syndromic deafness represents 30% of cases of genetic deafness. A frequent cause is Pendred syndrome, …
Outcomes of Cochlear Implantation in Patients with Jervell and Lange-Nielsen Syndrome: A Systematic Review and Narrative Synthesis.
Metcalfe C, Muzaffar J, Monksfield P, Bance M. Metcalfe C, et al. J Int Adv Otol. 2020 Dec;16(3):456-462. doi: 10.5152/iao.2020.9025. J Int Adv Otol. 2020. PMID: 33136028 Free PMC article.
Establish outcomes following cochlear implantation (CI) in patients with Jervell and Lange-Nielsen Syndrome (JLNS). Methods Systematic review and narrative synthesis. Databases searched on Medline, Pubmed, Embase, Web of Science, Cochrane Collection and ClinicalTria …
Establish outcomes following cochlear implantation (CI) in patients with Jervell and Lange-Nielsen Syndrome (JLNS). Methods Sy …
[Hereditary hearing loss].
Tropitzsch A, Schade-Mann T, Gamerdinger P. Tropitzsch A, et al. HNO. 2023 Feb;71(2):131-142. doi: 10.1007/s00106-022-01254-x. Epub 2022 Dec 16. HNO. 2023. PMID: 36526931 Review. German.
Some of the most common syndromes (Usher, Pendred, Jervell-Lange-Nielsen, Waardenburg, branchiootorenal, and Alport syndrome) are introductorily described. ...
Some of the most common syndromes (Usher, Pendred, Jervell-Lange-Nielsen, Waardenburg, branchiootorenal, and Alport …
Novel mutations of KCNQ1 in Long QT syndrome.
Qureshi SF, Ali A, Ananthapur V, Jayakrishnan MP, Calambur N, Thangaraj K, Nallari P. Qureshi SF, et al. Indian Heart J. 2013 Sep-Oct;65(5):552-60. doi: 10.1016/j.ihj.2013.08.025. Epub 2013 Sep 4. Indian Heart J. 2013. PMID: 24206879 Free PMC article. Review.
BACKGROUND: Autosomal recessive Long QT syndrome is characterized by prolonged QTc along with congenital bilateral deafness depends on mutations in K(+) channel genes. A family of a Long QT syndrome proband from India has been identified with novel indel variations. …
BACKGROUND: Autosomal recessive Long QT syndrome is characterized by prolonged QTc along with congenital bilateral deafness depends o …
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. Yanmei F, et al. Int J Pediatr Otorhinolaryngol. 2008 Nov;72(11):1723-9. doi: 10.1016/j.ijporl.2008.07.013. Epub 2008 Sep 20. Int J Pediatr Otorhinolaryngol. 2008. PMID: 18805595 Review.
Jervell and Lange-Nielsen syndrome is characterized by a long QT interval in electrocardiography, syncopal attacks and congenital sensorineural hearing loss. ...Cochlear implantation is indicated for hearing rehabilitation in this syndrome with profound deafn …
Jervell and Lange-Nielsen syndrome is characterized by a long QT interval in electrocardiography, syncopal attacks and congeni …
27 results