-
1
-
-
0344407030
-
Prevalence and triggers of syncope in medical students
-
Ganzeboom KS, Colman N, Reitsma JB, et al. Prevalence and triggers of syncope in medical students. Am J Cardiol 2003; 91:1006-1008.
-
(2003)
Am J Cardiol
, vol.91
, pp. 1006-1008
-
-
Ganzeboom, K.S.1
Colman, N.2
Reitsma, J.B.3
-
2
-
-
33748078740
-
Vasovagal syncope in medical students and their first-degree relatives
-
One of the first population-based studies of vasovagal syncope, this report used a standardized score to ascertain the diagnoses and a statistical approach to untangle sex-specific genetic effects
-
Serletis A, Rose S, Sheldon AG, Sheldon RS,. Vasovagal syncope in medical students and their first-degree relatives. Eur Heart J 2006; 27:1965-1970. One of the first population-based studies of vasovagal syncope, this report used a standardized score to ascertain the diagnoses and a statistical approach to untangle sex-specific genetic effects.
-
(2006)
Eur Heart J
, vol.27
, pp. 1965-1970
-
-
Serletis, A.1
Rose, S.2
Sheldon, A.G.3
Sheldon, R.S.4
-
3
-
-
33750081067
-
Lifetime cumulative incidence of syncope in the general population: A study of 549 Dutch subjects aged 35-60 years
-
Ganzeboom KS, Mairuhu G, Reitsma JB, et al.. Lifetime cumulative incidence of syncope in the general population: a study of 549 Dutch subjects aged 35-60 years. J Cardiovasc Electrophysiol 2006; 17:1172-1176.
-
(2006)
J Cardiovasc Electrophysiol
, vol.17
, pp. 1172-1176
-
-
Ganzeboom, K.S.1
Mairuhu, G.2
Reitsma, J.B.3
-
4
-
-
58149247404
-
Epidemiological aspects of transient loss of consciousness/syncope
-
Raviele A, editor, Berlin: Springer-Verlag;
-
Sheldon RS, Serletis A. Epidemiological aspects of transient loss of consciousness/syncope. In: Raviele A, editor. Cardiac arrhythmias. Berlin: Springer-Verlag; 2007. pp. 8-14.
-
(2007)
Cardiac arrhythmias
, pp. 8-14
-
-
Sheldon, R.S.1
Serletis, A.2
-
7
-
-
11144330897
-
Tilt testing for syncope: A reappraisal
-
Sheldon RS. Tilt testing for syncope: a reappraisal. Curr Opin Cardiol 2005; 20:38-41.
-
(2005)
Curr Opin Cardiol
, vol.20
, pp. 38-41
-
-
Sheldon, R.S.1
-
8
-
-
0141717974
-
Fainting in animals
-
van Dijk JG. Fainting in animals. Clin Auton Res 2003; 13:247-255.
-
(2003)
Clin Auton Res
, vol.13
, pp. 247-255
-
-
van Dijk, J.G.1
-
9
-
-
0038369764
-
Prevalence of family history in vasovagal syncope and haemodynamic response to head up tilt test in first degree relatives: Preliminary data for the Newcastle cohort
-
Newton JL, Kenny R, Lawson J, et al. Prevalence of family history in vasovagal syncope and haemodynamic response to head up tilt test in first degree relatives: preliminary data for the Newcastle cohort. Clin Auton Res 2003; 13:22-26.
-
(2003)
Clin Auton Res
, vol.13
, pp. 22-26
-
-
Newton, J.L.1
Kenny, R.2
Lawson, J.3
-
11
-
-
14044254800
-
Familial neurocardiogenic (vasovagal) syncope
-
Newton JL, Kerr S, Pairman J, et al. Familial neurocardiogenic (vasovagal) syncope. Am J Med Genet A 2005; 133:176-179.
-
(2005)
Am J Med Genet A
, vol.133
, pp. 176-179
-
-
Newton, J.L.1
Kerr, S.2
Pairman, J.3
-
12
-
-
30744460615
-
Diagnostic criteria for vasovagal syncope based on a quantitative history
-
Sheldon RS, Rose S, Connolly S, et al. Diagnostic criteria for vasovagal syncope based on a quantitative history. Eur Heart J 2006; 27:344-350.
-
(2006)
Eur Heart J
, vol.27
, pp. 344-350
-
-
Sheldon, R.S.1
Rose, S.2
Connolly, S.3
-
14
-
-
1942471150
-
Epigenetic regulation of mammalian genomic imprinting
-
Delaval K, Feil R. Epigenetic regulation of mammalian genomic imprinting. Curr Opin Genet Dev 2004; 14:188-195.
-
(2004)
Curr Opin Genet Dev
, vol.14
, pp. 188-195
-
-
Delaval, K.1
Feil, R.2
-
15
-
-
33845319792
-
Sex differences in brain expression of X- and Y-linked genes
-
Xu J, Disteche C. Sex differences in brain expression of X- and Y-linked genes. Brain Res 2006; 1126:50-55.
-
(2006)
Brain Res
, vol.1126
, pp. 50-55
-
-
Xu, J.1
Disteche, C.2
-
16
-
-
20344380424
-
Angiotensin converting enzyme insertion/deletion polymorphisms in vasovagal syncope
-
Newton JL, Donaldson P, Parry S, et al. Angiotensin converting enzyme insertion/deletion polymorphisms in vasovagal syncope. Europace 2005; 7:396-399.
-
(2005)
Europace
, vol.7
, pp. 396-399
-
-
Newton, J.L.1
Donaldson, P.2
Parry, S.3
-
17
-
-
34547927626
-
The Arg389Gly betal-adrenergic receptor gene polymorphism and susceptibility to faint during head-up tilt test
-
This allele of the β1-adrenoceptor may in some way confer sensitivity to fainting during tilt testing
-
Márquez MF, Hernandez-Pacheco G, Hermosillo AG, et al. The Arg389Gly betal-adrenergic receptor gene polymorphism and susceptibility to faint during head-up tilt test. Europace 2007; 9:585-588. This allele of the β1-adrenoceptor may in some way confer sensitivity to fainting during tilt testing.
-
(2007)
Europace
, vol.9
, pp. 585-588
-
-
Márquez, M.F.1
Hernandez-Pacheco, G.2
Hermosillo, A.G.3
-
18
-
-
28244477593
-
The Arg389Gly Betaradrenoceptor polymorphism and catecholamine effects on plasma-renin activity
-
Bruck H, Leineweber K, Temme T, et al. The Arg389Gly Betaradrenoceptor polymorphism and catecholamine effects on plasma-renin activity. J Am Coll Cardiol 2005;46:2111-2115.
-
(2005)
J Am Coll Cardiol
, vol.46
, pp. 2111-2115
-
-
Bruck, H.1
Leineweber, K.2
Temme, T.3
-
20
-
-
34447107791
-
Vasovagal syncope patients and the C825T GNB3 polymorphism
-
A silent SNP has an unusual prevalence in patients with 'atypical' vasovagal syncope
-
Lelonek M, PietruchaT, Stanczyk A, Goch JH. Vasovagal syncope patients and the C825T GNB3 polymorphism. Anadolu Kardiyol Derg 2007; 7 (Suppl 1): 206-208. A silent SNP has an unusual prevalence in patients with 'atypical' vasovagal syncope.
-
(2007)
Anadolu Kardiyol Derg
, vol.7
, Issue.SUPPL. 1
, pp. 206-208
-
-
Lelonek, M.1
Pietrucha, T.2
Stanczyk, A.3
Goch, J.H.4
-
21
-
-
33846815156
-
The GNB3 C825T polymorphism and essential hypertension: A meta-analysis of 34 studies including 14,094 cases and 17,760 controls
-
This meta-analysis of an unusual genetic finding showed that this silent SNP is in linkage disequilibrium with and marker of other genetic variants
-
Bagos PG, Elefsinioti AL, Nikolopoulos GK, Hamodrakas SJ. The GNB3 C825T polymorphism and essential hypertension: a meta-analysis of 34 studies including 14,094 cases and 17,760 controls. J Hypertens 2007; 25:487-500. This meta-analysis of an unusual genetic finding showed that this silent SNP is in linkage disequilibrium with and marker of other genetic variants.
-
(2007)
J Hypertens
, vol.25
, pp. 487-500
-
-
Bagos, P.G.1
Elefsinioti, A.L.2
Nikolopoulos, G.K.3
Hamodrakas, S.J.4
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