Last Updated: Mar 07, 2016
- Molecular autopsy finds killer mutation- Sleuthing researchers focus genomic technology on unexplained deaths
San Diego Union Tribune, March 4, 2016 - Exercise restrictions for patients with inherited cardiac conditions: Current guidelines, challenges and limitations.
Hammond-Haley Matthew et al. International journal of cardiology 2016 Feb 209234-241 - [High incidence of sudden cardiac death in one family with type-3 long QT syndrome: molecular genetics and electrophysiology mechanism analysis].
Zhou Hui, et al. Zhonghua xin xue guan bing za zhi 2015 12 (12) 1046-50 - Association of the hERG mutation with long?QT syndrome type 2, syncope and epilepsy.
Li Guoliang, et al. Molecular medicine reports 2016 2 - 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 - 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 - 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 - 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 - The genetics underlying acquired long QT syndrome: impact for genetic screening.
Itoh Hideki, et al. European heart journal 2015 12 - 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 - Pennsylvania Genetic Services Program
Disease: Multiple Diseases; Type: General Information; State: Pennsylvania - 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 - 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 - 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 - Factors influencing uptake of familial long QT syndrome genetic testing.
Burns Charlotte et al. American journal of medical genetics. Part A 2015 Nov - Abnormal repolarization dynamics in a patient with KCNE1(G38S) who presented with torsades de pointes.
Yamaguchi Yoshiaki, et al. Journal of electrocardiology 2015 10 - Common Genotypes of Long QT Syndrome in China and the Role of ECG Prediction.
Gao Yuanfeng, et al. Cardiology 2016 0 (2) 73-8 - 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 - Mutational analysis of SCN5A gene in long QT syndrome.
Qureshi Sameera Fatima, et al. Meta gene 2015 12 26-35 - 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 - The Genetics of Cardiovascular Disease in Canadian and International Aboriginal Populations.
Arbour Laura et al. Can J Cardiol 2015 Sep (9) 1094-115 - 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 - Sports Participation in Genotype Positive Children With Long QT Syndrome.
Aziz Peter F, et al. JACC. Clinical electrophysiology 0 0 (1-2) 62-70 - Exome analysis of a family with Wolff-Parkinson-White syndrome identifies a novel disease locus.
Bowles Neil E, et al. American journal of medical genetics. Part A 2015 8 - Genetic screening in sudden cardiac death in the young can save future lives.
Stattin Eva-Lena et al. Int. J. Legal Med. 2015 Jul 31. - Physical and Psychological Consequences of Left Cardiac Sympathetic Denervation for Long QT Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia.
Waddell-Smith Kathryn E, et al. Circulation. Arrhythmia and electrophysiology 2015 7 - Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes.
Shigemizu Daichi, et al. PloS one 2015 0 (7) e0130329 - That's not it, either-neither polymorphisms in PHOX2B nor in MIF are involved in sudden infant death syndrome (SIDS).
Poetsch Micaela, et al. International journal of legal medicine 2015 9 (5) 985-9 - Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients.
Chang Ya-Sian, et al. International heart journal 2015 0 (4) 450-3 - A Common Mutation of Long QT Syndrome Type 1 in Japan.
Itoh Hideki, et al. Circulation journal : official journal of the Japanese Circulation Society 2015 8 (9) 2026-30
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