« Previous
Next »
Journal of Forensic and Legal Medicine
Volume 14, Issue 7
, Pages 389-397
, October 2007
Changing times: DNA resequencing and the “nearly normal autopsy”
References
- . The human genome project. J R Soc Med. Dec. 2005;98(12):545
- . Sudden cardiac death. Cardiovasc Pathol. 2001;10(5):211–218
- Sudden death in young adults: a 25-year review of autopsies in military recruits. Ann Intern Med. 2004;141(11):829–834
- . Sudden death in the young. Heart Rhythm Dec. 2005;2(12):1277–1282
- Postmortem molecular screening in unexplained sudden death. J Am Coll Cardiol. 2004;43(9):1625–1629
- . Molecular screening of selected long QT syndrome (LQTS) mutations in 165 consecutive bodies found in water. Int J Legal Med. 2003;117(2):115–117
- Prevalence of long-QT syndrome gene variants in sudden infant death syndrome. Circulation. 2007;115(3):361–367
- Cardiac sodium channel dysfunction in sudden infant death syndrome. Circulation. 2007;115(3):368–376
- . Contribution of long-QT syndrome genes to sudden infant syndrome: is it time to consider newborn electrocardiographic screening?. Circulation. 2007;115(3):294–296
- Diagnosis of unexplained cardiac arrest: role of adrenaline and procainamide infusion. Circulation. 2005;112(15):2228–2234
- Prevalence of the long QT syndrome. Circulation. 2005;112(17):II–660
- Brugada syndrome: report of the second consensus conference. Heart Rhythm. 2005;2(4):429–440
- . Asymmetrical hypertrophy of the heart in young adults. Br Heart J. 1958;20(1):1–8
- A 12 gene DNA resequencing chip for fast and reliable molecular diagnosis of hypertrophic cardiomyopathy. Circulation. 2005;112(17):II–188
- . Pharmacogenomic genotyping methodologies. Clin Chem Lab Med. 2004;42(11):1256–1264
- Roberts R. Disrobing the emperor (heart) without destroying the dignity of super-normality. Circulation. 105:2934–2936.
- . Familial hypertrophic cardiomyopathy: the same mutation, different prognosis. Comparison of two families with a long follow-up. Rev Port Cardiol. 2003;22(12):1445–1461
- . New insights into the pathology of inherited cardiomyopathy. Heart. 2005;91(2):257–264
- Sudden cardiac death during anabolic steroid abuse: morphologic and toxicologic findings in two fatal cases of bodybuilders. Int J Legal Med. 2005;(November 15):1–6
- Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy. N Engl J Med. 1995;332(16):1058–1064
- . What clinicians should know about the QT interval. Jama. 2003;289(16):2120–2127
- . Pharmacogenetics and drug-induced arrhythmias. Cardiovasc Res. 2001;50(2):224–231
- Malignant entity of idiopathic ventricular fibrillation and polymorphic ventricular tachycardia initiated by premature extrasystoles originating from the right ventricular outflow tract. J Am Coll Cardiol. 2005;46(7):1288–1294
- . A gene locus for progressive familial heart block type II (PFHBII) maps to chromosome 1q32.2–q32.3. Hum Genet. 2005;118(1):133–137
- . The short QT syndrome as a paradigm to understand the role of potassium channels in ventricular fibrillation. J Intern Med. 2006;259(1):24–38
- . The molecular genetics of the long QT syndrome: genes causing fainting and sudden death. Annu Rev Med. 1998;49:263–274
- Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death. Nature. 2003;421(6923):634–639
- . Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice. JAMA. 2005;294:2975–2980
- . Efficient genotyping for congenital long QT syndrome. JAMA. 2005;294:3027–3028
- . Predicting drug-HERG channel interactions that cause acquired long QT syndrome. Trends Pharmacol Sci. 2005;26(3):119–124
- Cardiac histological substrate in patients with clinical phenotype of Brugada syndrome. Circulation. 2005;112(24):3680–3687
- . Acquired forms of the Brugada syndrome. J Electrocardiol. 2005;38(4 Suppl.):22–25
- Arrhythmogenic mutation-linked defects in ryanodine receptor autoregulation reveal a novel mechanism of Ca2+ release channel dysfunction. Circ Res. 2005;
- . Histologic findings in patients with clinical and instrumental diagnosis of sporadic arrhythmogenic right ventricular dysplasia. JACC. 2005;43(12):2305–2313
- Sudden unexpected death in persons less than 40 years of age. Am J Cardiol. 1991;68(13):1388–1392
- . Causes of sudden cardiac death in young Australians. Med J Aust. 2004;180(3):110–112
- . New non-invasive approaches for the diagnosis of cardiomyopathy: magnetic resonance imaging. Ernst Schering Res Found Workshop. 2006;(55):261–285
- Diagnosis and presentation of fatal myocarditis. Hum Pathol. 2005;36(9):1003–1007
- Diagnosis and presentation of fatal myocarditis. Human Pathology. 2005;36(9):1003–1007
- . The pathology and etiology of cocaine-induced heart disease. Arch Pathol Lab Med. 1988;112(3):225–230
- . Cocaine cardiovascular toxicity. South Med J. 2005;98(8):794–799
- . An ion channel ’addicted’ to ether, alcohol and cocaine: the HERG potassium channel. Cardiovasc Res. 2002;53(1):6–8
- . Toxicogenetics. In: Karch S editors. Drug abuse handbook. Boca Raton, Boston, London, New York: Taylor and Francis; 2006;
- CYP2D6 and CYP2C19 genotype-based dose recommendations for antidepressants: a first step towards subpopulationspecific dosages. Acta Psychiatr Scand. 2001;104(3):173–192
- Alterations in 5-HT1B Receptor Function by p11 in Depression-Like States. Science. 2006;311(January 6):77–81
- Priori SG, Napolitano C. Role of genetic analysis in cardiology: part I: mendelian disease: cardiac channelopathies. Circulation 2006 (February 28);113(8):1130–5.
PII: S1752-928X(07)00067-4
doi: 10.1016/j.jflm.2007.04.008
© 2007 Elsevier Ltd and FFLM. All rights reserved.
« Previous
Next »
Journal of Forensic and Legal Medicine
Volume 14, Issue 7
, Pages 389-397
, October 2007
