-
1
-
-
1642363460
-
Hypertrophic obstructive cardiomyopathy
-
Nishimura RA, Holmes DR. Hypertrophic obstructive cardiomyopathy. N Engl J Med 2004; 350:1320-1327.
-
(2004)
N Engl J Med
, vol.350
, pp. 1320-1327
-
-
Nishimura, R.A.1
Holmes, D.R.2
-
2
-
-
1942436225
-
Assessing the risk of sudden cardiac death in a patient with hypertrophic cardiomyopathy
-
Frenneux MP. Assessing the risk of sudden cardiac death in a patient with hypertrophic cardiomyopathy. Heart 2004; 90:570-575. This article outlines the potential mechanisms of sudden death in HCM and provides a review of both clinically useful established risk factors as well as clinical markers of unproven clinical utility.
-
(2004)
Heart
, vol.90
, pp. 570-575
-
-
Frenneux, M.P.1
-
3
-
-
0642280767
-
Hypertrophic cardiomyopathy: From gene defect to clinical disease
-
Chung MW, Tsoutsman T, Semsarian C. Hypertrophic cardiomyopathy: from gene defect to clinical disease. Cell Res 2003; 13:9-20. This report provides a comprehensive outline of the molecular pathogenesis of HCM.
-
(2003)
Cell Res
, vol.13
, pp. 9-20
-
-
Chung, M.W.1
Tsoutsman, T.2
Semsarian, C.3
-
4
-
-
2942530660
-
Hypertrophic cardiomyopathy
-
Elliott P, McKenna WJ. Hypertrophic cardiomyopathy. Lancet 2004; 363: 1881-1891.
-
(2004)
Lancet
, vol.363
, pp. 1881-1891
-
-
Elliott, P.1
McKenna, W.J.2
-
5
-
-
0141719865
-
Mutations of the beta myosin heavy chain gene in hypertrophic cardiomyopathy: Critical functional sites determine prognosis
-
Woo A, Rakowski H, Liew JC, et al. Mutations of the beta myosin heavy chain gene in hypertrophic cardiomyopathy: critical functional sites determine prognosis. Heart 2003; 89:11 79-1185. This is a cohort study of HCM patients with the beta MHC genetic defect and their family members, noting heterogeneity of disease expression based on the type of genetic mutation.
-
(2003)
Heart
, vol.89
, pp. 1179-1185
-
-
Woo, A.1
Rakowski, H.2
Liew, J.C.3
-
6
-
-
0037454157
-
Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin gene in familial hypertrophic cardiomyopathy
-
Jongbloed RJ, Marcelis CL, Doevendans PA, et al. Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin gene in familial hypertrophic cardiomyopathy. J Am Coll Cardiol 2003; 41:994-996.
-
(2003)
J Am Coll Cardiol
, vol.41
, pp. 994-996
-
-
Jongbloed, R.J.1
Marcelis, C.L.2
Doevendans, P.A.3
-
7
-
-
0242522154
-
-
American College of Cardiology/European Society of Cardiology Clinical Expert Consensus Document on Hypertrophic Cardiomyopathy
-
Maron BJ, McKenna WJ. American College of Cardiology/European Society of Cardiology Clinical Expert Consensus Document on Hypertrophic Cardiomyopathy. J Am Coll Cardiol 2003; 42:1687-1713. This consensus document provides a comprehensive clinical treatment algorithm for the treatment of children with HCM, and addresses topics of controversy including the role of pacemaker management, implantable cardiac defibrillators, and alcohol septal ablation.
-
(2003)
J Am Coll Cardiol
, vol.42
, pp. 1687-1713
-
-
Maron, B.J.1
McKenna, W.J.2
-
8
-
-
12144288228
-
Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defects and the cardiac phenotype of hypertrophic cardiomyopathy
-
Tsybouleva N, Zhang L, Chen S, et al. Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defects and the cardiac phenotype of hypertrophic cardiomyopathy. Circulation 2004; 109:1284-1291. This report explores the clinical question of genetic heterogeneity with an emphasis on aldosterone as a potential modulator in disease expression.
-
(2004)
Circulation
, vol.109
, pp. 1284-1291
-
-
Tsybouleva, N.1
Zhang, L.2
Chen, S.3
-
9
-
-
4644346837
-
Prenatal molecular diagnosis in hypertrophic cardiomyopathy: Report of the first case
-
Charron P, Heron D, Gargiulo M, et al. Prenatal molecular diagnosis in hypertrophic cardiomyopathy: report of the first case. Prenat Diagn 2004; 24:701.
-
(2004)
Prenat Diagn
, vol.24
, pp. 701
-
-
Charron, P.1
Heron, D.2
Gargiulo, M.3
-
10
-
-
11144355765
-
Characterization of left ventricular diastolic function by tissue Doppler imaging and clinical status in children with hypertrophic cardiomyopathy
-
McMahon CJ, Nagueh SF, Pignatelli RH, et al. Characterization of left ventricular diastolic function by tissue Doppler imaging and clinical status in children with hypertrophic cardiomyopathy. Circulation 2004; 109:1756-1773. This is the first study to demonstrate abnormalities on tissue Doppler imaging in children with HCM, and to relate these abnormalities with other clinical variables.
-
(2004)
Circulation
, vol.109
, pp. 1756-1773
-
-
McMahon, C.J.1
Nagueh, S.F.2
Pignatelli, R.H.3
-
11
-
-
10744221470
-
Diagnostic value of abnormal Q waves for identification of preclinical carriers of hypertrophic cardiomyopathy based on a molecular genetic diagnosis
-
Konno T, Shimizu M, Ino H, et al. Diagnostic value of abnormal Q waves for identification of preclinical carriers of hypertrophic cardiomyopathy based on a molecular genetic diagnosis. Eur Heart J 2004; 25:246-251.
-
(2004)
Eur Heart J
, vol.25
, pp. 246-251
-
-
Konno, T.1
Shimizu, M.2
Ino, H.3
-
12
-
-
0042377368
-
Non-sustained ventricular tachycardia in hypertrophic cardiomyopathy: An independent marker of sudden death risk in young patients
-
Monserrat L, Elliot PM, Gimeno JR, et al. Non-sustained ventricular tachycardia in hypertrophic cardiomyopathy: an independent marker of sudden death risk in young patients. J Am Coll Cardiol 2003; 42:873-879, This report describes the identification of a new marker of sudden death risk for young patients with HCM.
-
(2003)
J Am Coll Cardiol
, vol.42
, pp. 873-879
-
-
Monserrat, L.1
Elliot, P.M.2
Gimeno, J.R.3
-
13
-
-
2542442547
-
Safety of stress testing in patients with hypertrophic cardiomyopathy
-
Drinko JK, Nash PJ, Lever HM, Asher CR. Safety of stress testing in patients with hypertrophic cardiomyopathy. Am J Cardiol 2004; 93:1443-1444. Many physicians fail to perform cardiopulmonary stress tests on children with HCM due to fear of adverse events. This paper demonstrates the safety of stress testing in a large number of patients with HCM.
-
(2004)
Am J Cardiol
, vol.93
, pp. 1443-1444
-
-
Drinko, J.K.1
Nash, P.J.2
Lever, H.M.3
Asher, C.R.4
-
14
-
-
4744354503
-
Delayed hyper-enhancement of myocardium in hypertrophic cardiomyopathy with asymmetrical septal hypertrophy. Comparison with global and regional cardiac MR image appearances
-
Amano Y, Takayama M, Takahama K, Kumazaki T. Delayed hyper-enhancement of myocardium in hypertrophic cardiomyopathy with asymmetrical septal hypertrophy. Comparison with global and regional cardiac MR image appearances. J Magn Reson Imaging 2004; 20:595.
-
(2004)
J Magn Reson Imaging
, vol.20
, pp. 595
-
-
Amano, Y.1
Takayama, M.2
Takahama, K.3
Kumazaki, T.4
-
15
-
-
0041864064
-
Myocardial bridging in adult patients with hypertrophic cardiomyopathy
-
Sorajja P, Ommen SR, Nishimura RA, et al. Myocardial bridging in adult patients with hypertrophic cardiomyopathy. J Am Coll Cardiol 2003; 99:889-894.
-
(2003)
J Am Coll Cardiol
, vol.99
, pp. 889-894
-
-
Sorajja, P.1
Ommen, S.R.2
Nishimura, R.A.3
-
16
-
-
3342982877
-
Outcomes after unroofing of a myocardial bridge of the left anterior descending coronary artery in children with hypertrophic cardiomyopathy
-
Downar J, Williams WG, McDonald C, et al. Outcomes after unroofing of a myocardial bridge of the left anterior descending coronary artery in children with hypertrophic cardiomyopathy. Pediatric Cardiol 2004 This is a follow-up paper of children with HCM and surgical myectomy of myocardial bridges of epicardial coronary arteries. Myocardial bridging has been suggested to be a cause of ischemia and an important risk factor for sudden death in children with HCM, and these authors provide evidence in a small case series of resolution of symptoms with unroofing.
-
(2004)
Pediatric Cardiol
-
-
Downar, J.1
Williams, W.G.2
McDonald, C.3
-
17
-
-
0041385743
-
Coronary microvascular dysfunction and prognosis in hypertrophic cardiomyopathy
-
Cecchi F, Olivotto I, Gistri R, et al. Coronary microvascular dysfunction and prognosis in hypertrophic cardiomyopathy. N Engl J Med 2003; 349:1027-1035.
-
(2003)
N Engl J Med
, vol.349
, pp. 1027-1035
-
-
Cecchi, F.1
Olivotto, I.2
Gistri, R.3
-
18
-
-
2942624120
-
AHA Scientific Statement. Recommendations for physical activity and recreational sports participation for young patients with genetic cardiovascular diseases
-
Maron BJ. AHA Scientific Statement. Recommendations for physical activity and recreational sports participation for young patients with genetic cardiovascular diseases. Circulation 2004; 109:2807-2816. This comprehensive panel statement summarizes the current recommendations for physical activity in children with HCM, long QT syndrome, Brugada syndrome, arrhythmogenic right ventricular dysplasia, and Marfan syndrome.
-
(2004)
Circulation
, vol.109
, pp. 2807-2816
-
-
Maron, B.J.1
-
19
-
-
0842325275
-
Extended septal myectomy for hypertrophic cardiomyopathy with anomalous mitral papillary muscle and chordae
-
Minikata K, Dearani JA, Nishimura RA, et al. Extended septal myectomy for hypertrophic cardiomyopathy with anomalous mitral papillary muscle and chordae. J Thorac Cardiovasc Surg 2004; 127:481-489. This report deals with the difficult topic of how to surgically address left ventricular outflow tract obstruction when the mitral valve apparatus is an integral part of the obstruction, and provides an alternative treatment strategy to mitral valve replacement.
-
(2004)
J Thorac Cardiovasc Surg
, vol.127
, pp. 481-489
-
-
Minikata, K.1
Dearani, J.A.2
Nishimura, R.A.3
-
20
-
-
0742324990
-
Implications of implantable cardioverter defibrillator therapy in congenital heart disease and pediatrics
-
Alexander MF, Cecchin F, Waish EP, et al. Implications of implantable cardioverter defibrillator therapy in congenital heart disease and pediatrics. J Cardiovasc Electrophysiol 2004; 15:77-78. This retrospective review documents a high incidence of complications in children who have had an implantable cardiac defibrillator.
-
(2004)
J Cardiovasc Electrophysiol
, vol.15
, pp. 77-78
-
-
Alexander, M.F.1
Cecchin, F.2
Waish, E.P.3
-
21
-
-
0141630291
-
Efficacy of implantable cardioverter defibrillator therapy for primary and secondary prevention of sudden cardiac death in hypertrophic cardiomyopathy
-
Begley DA, Mohiddin SA, Tripodi D, et al. Efficacy of implantable cardioverter defibrillator therapy for primary and secondary prevention of sudden cardiac death in hypertrophic cardiomyopathy. Pacing Clin Electrophysiol 2003; 26:1887-1896. This report outlines survival rates and therapeutic implantable cardiac defibrillator intervention-free rates for patients receiving a defibriilator for primary prevention or secondary prevention, and notes a higher rate of therapeutic implantable cardiac defibrillator intervention in patients aged less than 21 years.
-
(2003)
Pacing Clin Electrophysiol
, vol.26
, pp. 1887-1896
-
-
Begley, D.A.1
Mohiddin, S.A.2
Tripodi, D.3
-
22
-
-
1642561513
-
Implantable cardioverter defibrillator in a child using a single subcutaneous array lead and an abdominal active can
-
Luedemann M, Hund K, Stertmann W, et al. Implantable cardioverter defibrillator in a child using a single subcutaneous array lead and an abdominal active can. Pacing Clin Electrophysiol 2004; 27:117-119. This report describes a novel alternative to epicardial patches for implantable cardiac defibrillator placement in a small child.
-
(2004)
Pacing Clin Electrophysiol
, vol.27
, pp. 117-119
-
-
Luedemann, M.1
Hund, K.2
Stertmann, W.3
-
23
-
-
0842308255
-
Catheter-based therapy for hypertrophic cardiomyopathy. First in-hospital outcome analysis of German TASH registry
-
Kuhn H, Seggeweiss H, Gietzen FH, et al. Catheter-based therapy for hypertrophic cardiomyopathy. First in-hospital outcome analysis of German TASH registry. Z Kardiol 2004; 93:23-31.
-
(2004)
Z Kardiol
, vol.93
, pp. 23-31
-
-
Kuhn, H.1
Seggeweiss, H.2
Gietzen, F.H.3
-
24
-
-
1542287485
-
Ventricular septal rupture following nonsurgical septal reduction for hypertrophic cardiomyopathy: Treatment with percutaneous closure
-
Aroney CN, Goh TH, Hourigan LA, Dyer W. Ventricular septal rupture following nonsurgical septal reduction for hypertrophic cardiomyopathy: treatment with percutaneous closure. Catheter Cardiovasc Interv 2004; 61: 411-414.
-
(2004)
Catheter Cardiovasc Interv
, vol.61
, pp. 411-414
-
-
Aroney, C.N.1
Goh, T.H.2
Hourigan, L.A.3
Dyer, W.4
|