Jervell and Lange-Nielsen syndrome in cochlear implanted patients: Our experience and a review of literature
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
Reference25 articles.
1. Congenital long QT syndrome;Crotti;Orphanet J. Rare Dis.,2008
2. The genetic basis of long QT and short QT syndromes: a mutation update;Hedley;Hum. Mutat.,2009
3. Congenital deaf-mutism, functional heart disease with prolongation of the QT interval, and sudden death;Jervell;Am. Heart J.,1957
4. A new familial cardiac syndrome in children;Ward;J. Ir. Med. Assoc.,1964
5. Jervell and Lange-Nielsen syndrome in Norwegian children: aspects around cochlear implantation hearing, and balance;Siem;Ear Hear.,2008
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1. Pharmacogenomics of Pediatric Cardiac Arrest: Cisplatin Treatment Worsened by a Ryanodine Receptor 2 Gene Mutation;Cardiogenetics;2022-02-07
2. Cochlear implantation in a case of jervell and lange-nielsen syndrome presenting with absence seizure and anemia;Indian Journal of Otology;2022
3. Hearing Screening Combined with Target Gene Panel Testing Increased Etiological Diagnostic Yield in Deaf Children;Neural Plasticity;2021-07-23
4. Outcomes of Cochlear Implantation in Patients with Jervell and Lange-Nielsen Syndrome: A Systematic Review and Narrative Synthesis;The Journal of International Advanced Otology;2020-10-19
5. Genotype-Phenotype Correlation for Predicting Cochlear Implant Outcome: Current Challenges and Opportunities;Frontiers in Genetics;2020-07-14
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