Sudden infant death syndrome due to long QT syndrome: a brief review of the genetic substrate and prevalence
暂无分享,去创建一个
[1] Christina A Holcroft,et al. Incidence and determinants of sudden infant death syndrome: a population-based study on 37 million births , 2015, World Journal of Pediatrics.
[2] Euan A Ashley,et al. Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing. , 2014, Heart rhythm.
[3] Yingying Tang,et al. Cardiac channelopathy testing in 274 ethnically diverse sudden unexplained deaths. , 2014, Forensic science international.
[4] J. Skinner,et al. Long QT molecular autopsy in sudden infant death syndrome , 2014, Archives of Disease in Childhood.
[5] M. Horie,et al. Cardiac Channelopathies Associated with Infantile Fatal Ventricular Arrhythmias: From the Cradle to the Bench , 2014, Journal of cardiovascular electrophysiology.
[6] Michael J Ackerman,et al. Impact of genetics on the clinical management of channelopathies. , 2013, Journal of the American College of Cardiology.
[7] Kui Zhang,et al. Maternal smoking and increased risk of sudden infant death syndrome: a meta-analysis. , 2013, Legal medicine.
[8] Thomas Meitinger,et al. Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants , 2013, Circulation.
[9] P. Goldwater,et al. Maternal and perinatal risk factors for SIDS: a novel analysis utilizing pregnancy outcome data , 2013, European Journal of Pediatrics.
[10] H. Kinney,et al. Risk Factor Changes for Sudden Infant Death Syndrome After Initiation of Back-to-Sleep Campaign , 2012, Pediatrics.
[11] Michael J Ackerman,et al. HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA). , 2011, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.
[12] H. Calkins,et al. HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA). , 2011, Heart rhythm.
[13] J. Svendsen,et al. Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis , 2011, BMC Medical Genetics.
[14] D. Tester,et al. Sudden infant death syndrome-associated mutations in the sodium channel beta subunits. , 2010, Heart rhythm.
[15] W. Shimizu,et al. Clinical Characteristics and Genetic Background of Congenital Long-QT Syndrome Diagnosed in Fetal, Neonatal, and Infantile Life: A Nationwide Questionnaire Survey in Japan , 2010, Circulation. Arrhythmia and electrophysiology.
[16] C. January,et al. &agr;1-Syntrophin Mutations Identified in Sudden Infant Death Syndrome Cause an Increase in Late Cardiac Sodium Current , 2009, Circulation. Arrhythmia and electrophysiology.
[17] P. Goldwater,et al. Staphylococcal enterotoxin genes are common in Staphylococcus aureus intestinal flora in Sudden Infant Death Syndrome (SIDS) and live comparison infants. , 2009, FEMS immunology and medical microbiology.
[18] M. Gollob,et al. Rapid genetic testing facilitating the diagnosis of short QT syndrome. , 2009, The Canadian journal of cardiology.
[19] D. Malicier,et al. Contribution of Long-QT Syndrome Genetic Variants in Sudden Infant Death Syndrome , 2009, Pediatric Cardiology.
[20] H. Kinney,et al. The brainstem and serotonin in the sudden infant death syndrome. , 2009, Annual review of pathology.
[21] N. Makita,et al. Cardiac Ion Channel Gene Mutations in Sudden Infant Death Syndrome , 2008, Pediatric Research.
[22] A. R. Highet. An infectious aetiology of sudden infant death syndrome , 2008, Journal of applied microbiology.
[23] Michael J Ackerman,et al. Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3. , 2007, Heart rhythm.
[24] Peter J. Schwartz,et al. Prevalence of Long-QT Syndrome Gene Variants in Sudden Infant Death Syndrome , 2007, Circulation.
[25] S. Priori,et al. Cost-effectiveness of neonatal ECG screening for the long QT syndrome. , 2006, European heart journal.
[26] Michael J Ackerman,et al. Mutant Caveolin-3 Induces Persistent Late Sodium Current and Is Associated With Long-QT Syndrome , 2006, Circulation.
[27] B. Brinkmann,et al. The San Diego definition of SIDS: practical application and comparison with the GeSID classification , 2006, International Journal of Legal Medicine.
[28] Matthew W State,et al. A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y. , 2006, The Journal of clinical investigation.
[29] Roger W Byard,et al. Sudden infant death syndrome and unclassified sudden infant deaths: a definitional and diagnostic approach. , 2004, Pediatrics.
[30] A. Bozio,et al. Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations. , 2004, Journal of the American College of Cardiology.
[31] B. Maher,et al. Sudden infant death syndrome: Association with a promoter polymorphism of the serotonin transporter gene , 2003, American journal of medical genetics. Part A.
[32] J. Beckwith. Defining the sudden infant death syndrome. , 2003, Archives of pediatrics & adolescent medicine.
[33] W. Guntheroth,et al. The triple risk hypotheses in sudden infant death syndrome. , 2002, Pediatrics.
[34] P. Schwartz,et al. Guidelines for the interpretation of the neonatal electrocardiogram. A task force of the European Society of Cardiology. , 2002, European heart journal.
[35] J. Towbin,et al. Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome. , 2001, JAMA.
[36] G. Breithardt,et al. Life-threatening Arrhythmias Genotype-phenotype Correlation in the Long-qt Syndrome : Gene-specific Triggers for Genotype-phenotype Correlation in the Long-qt Syndrome Gene-specific Triggers for Life-threatening Arrhythmias , 2022 .
[37] S. Priori,et al. A molecular link between the sudden infant death syndrome and the long-QT syndrome. , 2000, The New England journal of medicine.
[38] J. Zupancic,et al. Cost-effectiveness and implications of newborn screening for prolongation of QT interval for the prevention of sudden infant death syndrome. , 2000, The Journal of pediatrics.
[39] H. Storm,et al. The amount of brainstem gliosis in sudden infant death syndrome (SIDS) victims correlates with maternal cigarette smoking during pregnancy , 1999, Acta paediatrica.
[40] E. Rosenthal,et al. Prolongation of the QT interval and the sudden infant death syndrome. , 1998, The New England journal of medicine.
[41] T. Rognum,et al. Use of new Nordic criteria for classification of SIDS to re‐evaluate diagnoses of sudden unexpected infant death in the Nordic countries , 1997, Acta paediatrica.
[42] L. S. James,et al. Defining the sudden infant death syndrome (SIDS): deliberations of an expert panel convened by the National Institute of Child Health and Human Development. , 1991, Pediatric pathology.
[43] P. Schwartz. The quest for the mechanisms of the sudden infant death syndrome: doubts and progress. , 1987, Circulation.
[44] M. Sakanoue. [Sudden infant death syndrome]. , 1985, [Kango gijutsu] : [Nursing technique].
[45] B. Maron,et al. Potential Role of QT Interval Prolongation in Sudden Infant Death Syndrome , 1976, Circulation.
[46] P. Schwartz. Cardiac sympathetic innervation and the sudden infant death syndrome. A possible pathogenetic link. , 1976, The American journal of medicine.
[47] M. Willinger. Defining the sudden infant death syndrome (SIDS) , 1991 .