Indexed keywords
ADULT;
ANAMNESIS;
ARTICLE;
CASE REPORT;
CLINICAL FEATURE;
DISEASE ASSOCIATION;
ECHOCARDIOGRAPHY;
ELECTRON MICROSCOPY;
HEART BLOCK;
HEART MUSCLE BIOPSY;
HEART PREEXCITATION;
HUMAN;
HUMAN TISSUE;
HYPERTROPHIC CARDIOMYOPATHY;
MALE;
NUCLEAR MAGNETIC RESONANCE IMAGING;
PACEMAKER;
PRIORITY JOURNAL;
ADOLESCENT;
ADULT;
BIOPSY;
CARDIOMYOPATHY, HYPERTROPHIC, FAMILIAL;
CHILD;
DEATH, SUDDEN;
ECHOCARDIOGRAPHY;
ELECTROCARDIOGRAPHY;
FEMALE;
HEART BLOCK;
HEART CONDUCTION SYSTEM;
HUMANS;
HYPERTROPHY, LEFT VENTRICULAR;
MAGNETIC RESONANCE IMAGING, CINE;
MALE;
MIDDLE AGED;
MYOCARDIUM;
PEDIGREE;
PHENOTYPE;
PRE-EXCITATION SYNDROMES;
1
14844309457
Familial congenital complete A-V heart blocks
Wendkos M.H., and Study R.S. Familial congenital complete A-V heart blocks. Am Heart J 34 (1947) 138-142
(1947)
Am Heart J
, vol.34
, pp. 138-142
Wendkos, M.H.1
Study, R.S.2
2
0013379304
Congenital arrhythmias and conduction abnormalities in a father and four children
Segall H.N. Congenital arrhythmias and conduction abnormalities in a father and four children. Canad Med Assoc J 84 (1961) 1283-1296
(1961)
Canad Med Assoc J
, vol.84
, pp. 1283-1296
Segall, H.N.1
3
2442719434
Abnormal His-Purkinje system conduction leading to complete atrioventricular block in patients with hypertrophic cardiomyopathy: a report of 3 cases
Doven O., Cicek D., Pekdemir H., et al. Abnormal His-Purkinje system conduction leading to complete atrioventricular block in patients with hypertrophic cardiomyopathy: a report of 3 cases. Jpn Heart J 45 (2004) 347-352
(2004)
Jpn Heart J
, vol.45
, pp. 347-352
Doven, O.1
Cicek, D.2
Pekdemir, H.3
4
1242317063
Familial hypertrophic cardiomyopathy complicated by complete atrioventricular block
Cicek D., Camsari A., and Doven O. Familial hypertrophic cardiomyopathy complicated by complete atrioventricular block. Acta Cardiol 59 (2004) 71-74
(2004)
Acta Cardiol
, vol.59
, pp. 71-74
Cicek, D.1
Camsari, A.2
Doven, O.3
5
0033206831
Rare association of hypertrophic cardiomyopathy and complete atrioventricular block with prompt disappearance of outflow gradient after DDD pacing
Yesil M., Bayata S., Susam I., Dinckal H., and Postaci N. Rare association of hypertrophic cardiomyopathy and complete atrioventricular block with prompt disappearance of outflow gradient after DDD pacing. Europace 1 (1999) 280-282
(1999)
Europace
, vol.1
, pp. 280-282
Yesil, M.1
Bayata, S.2
Susam, I.3
Dinckal, H.4
Postaci, N.5
6
0031425546
Hypertrophic cardiomyopathy presenting with 3rd-degree atrioventricular block
Rosen K.L., Cameron R.W., Bigham P.J., and Neish S.R. Hypertrophic cardiomyopathy presenting with 3rd-degree atrioventricular block. Tex Heart Inst J 24 (1997) 372-375
(1997)
Tex Heart Inst J
, vol.24
, pp. 372-375
Rosen, K.L.1
Cameron, R.W.2
Bigham, P.J.3
Neish, S.R.4
7
0019429768
Hypertrophic cardiomyopathy and complete heart block in infancy
Maron B.J., Connor T.M., and Roberts W.C. Hypertrophic cardiomyopathy and complete heart block in infancy. Am Heart J 101 (1981) 857-860
(1981)
Am Heart J
, vol.101
, pp. 857-860
Maron, B.J.1
Connor, T.M.2
Roberts, W.C.3
8
0035859215
Identification of a gene responsible for familial Wolff-Parkinson-White syndrome
Gollob M.H., Green M.S., Tang A.S., et al. Identification of a gene responsible for familial Wolff-Parkinson-White syndrome. N Engl J Med 344 (2001) 1823-1831
(2001)
N Engl J Med
, vol.344
, pp. 1823-1831
Gollob, M.H.1
Green, M.S.2
Tang, A.S.3
9
40949133956
Glycogen storage diseases presenting as hypertrophic cardiomyopathy
Arad M., Maron B.J., Gorham J.M., et al. Glycogen storage diseases presenting as hypertrophic cardiomyopathy. N Engl J Med 344 (2001) 1861-1864
(2001)
N Engl J Med
, vol.344
, pp. 1861-1864
Arad, M.1
Maron, B.J.2
Gorham, J.M.3
10
20044391423
Adenosine monophosphate-activated protein kinase disease mimics hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome
Murphy R.T., Mogensen J., McGarry K., et al. Adenosine monophosphate-activated protein kinase disease mimics hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome. J Am Coll Cardiol 45 (2005) 922-930
(2005)
J Am Coll Cardiol
, vol.45
, pp. 922-930
Murphy, R.T.1
Mogensen, J.2
McGarry, K.3
11
0003096674
Cardiac conduction defects associate with mutations in SCN5A
[Letter]
Schott J.J., Alshinawi C., Kyndt F., et al. Cardiac conduction defects associate with mutations in SCN5A. Nat Genet 23 (1999) 20-21 [Letter]
(1999)
Nat Genet
, vol.23
, pp. 20-21
Schott, J.J.1
Alshinawi, C.2
Kyndt, F.3