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Long QT Syndrome ► Public Health Genomics Knowledge Base (v1.0)
Public Health Genomics Knowledge Base (v1.0)
What's New
Last Updated: Feb 11, 2016
- Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases.
Neubauer Jacqueline, et al. International journal of legal medicine 2016 2 (From HuGE Literature Finder)
- Association of the hERG mutation with long?QT syndrome type 2, syncope and epilepsy.
Li Guoliang, et al. Molecular medicine reports 2016 2 (From HuGE Literature Finder)
- Pediatric Cohort With Long QT Syndrome?- KCNH2 Mutation Carriers Present Late Onset But Severe Symptoms.
Ozawa Junichi, et al. Circulation journal : official journal of the Japanese Circulation Society 2016 1(From HuGE Literature Finder)
- Time, frequency and information domain analysis of heart period and QT variability in asymptomatic long QT syndrome type 2 patients.
Bari Vlasta, et al. Conference proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual Conference 2015 8 294-7 (From HuGE Literature Finder)
- A novel technique to investigate the effect of ageing on ventricular repolarization characteristics in healthy and LQTS subjects.
Imam Mohammad H, et al. Conference proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual Conference 2015 8 2796-9 (From HuGE Literature Finder)
- The genetics underlying acquired long QT syndrome: impact for genetic screening.
Itoh Hideki, et al. European heart journal 2015 12 (From HuGE Literature Finder)
- Exome-based analysis of cardiac arrhythmia, respiratory control and epilepsy genes in sudden unexpected death in epilepsy.
Bagnall Richard D, et al. Annals of neurology 2015 12 (From HuGE Literature Finder)
- Pennsylvania Genetic Services Program
Disease: Multiple Diseases; Type: General Information; State: Pennsylvania (From Implementation Database)
- Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction.
Itoh Hideki, et al. European journal of human genetics : EJHG 2015 12 (From HuGE Literature Finder)
- Heat shock protein 70 gene polymorphisms' influence on the electrophysiology of long QT syndrome.
Ali Altaf, et al. Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing 2015 12 (From HuGE Literature Finder)
- Genetic Testing and Genetic Counseling in Patients With Sudden Death Risk Due to Heritable Arrhythmias.
Spoonamore Katherine G et al. Heart rhythm : the official journal of the Heart Rhythm Society 2015 Nov (From Genomics & Health Impact Scan Database)
- Factors influencing uptake of familial long QT syndrome genetic testing.
Burns Charlotte et al. American journal of medical genetics. Part A 2015 Nov (From Genomics & Health Impact Scan Database)
- Common Genotypes of Long QT Syndrome in China and the Role of ECG Prediction.
Gao Yuanfeng, et al. Cardiology 2016 0 (2) 73-8 (From HuGE Literature Finder)
- Abnormal repolarization dynamics in a patient with KCNE1(G38S) who presented with torsades de pointes.
Yamaguchi Yoshiaki, et al. Journal of electrocardiology 2015 10 (From HuGE Literature Finder)
- Too Young to Die: Impact of Sudden Cardiac Death of the Young in Michigan, 1999 - 2008[PDF 1.42 MB]
Disease: Sudden Cardiac Death; Type: Data|Program; State: Michigan (From Implementation Database)
- Mutational analysis of SCN5A gene in long QT syndrome.
Qureshi Sameera Fatima, et al. Meta gene 2015 12 26-35 (From HuGE Literature Finder)
- Prolonged QT: A rare cause of cardiac arrest.
Carlquist Jennifer, et al. JAAPA : official journal of the American Academy of Physician Assistants 2015 7 (7) 1-4 (From HuGE Literature Finder)
- The Genetics of Cardiovascular Disease in Canadian and International Aboriginal Populations.
Arbour Laura et al. Can J Cardiol 2015 Sep (9) 1094-115 (From Discoveries and Insights Database)
- A Systematic Review on the Cost-Effectiveness of Genetic and Electrocardiogram Testing for Long QT Syndrome in Infants and Young Adults.
Gonzalez Fernando Matias et al. Value Health 2015 Jul 18(5) 700-8 (From Genomics & Health Impact Scan Database)
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