-
1
-
-
0026466921
-
Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome. A multicenter report
-
P Brugada, and J Brugada Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report J Am Coll Cardiol 20 1992 1391 1396
-
(1992)
J Am Coll Cardiol
, vol.20
, pp. 1391-1396
-
-
Brugada, P.1
Brugada, J.2
-
2
-
-
13444300924
-
Brugada syndrome: Report of the second consensus conference: Endorsed by the Heart Rhythm Society and the European Heart Rhythm Association
-
C Antzelevitch, P Brugada, M Borggrefe, J Brugada, R Brugada, D Corrado, and et al. Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association Circulation 111 2005 659 670
-
(2005)
Circulation
, vol.111
, pp. 659-670
-
-
Antzelevitch, C.1
Brugada, P.2
Borggrefe, M.3
Brugada, J.4
Brugada, R.5
Corrado, D.6
-
3
-
-
0037133593
-
Natural history of Brugada syndrome: Insights for risk stratification and management
-
SG Priori, C Napolitano, M Gasparini, C Pappone, P Della Bella, U Giordano, and et al. Natural history of Brugada syndrome: insights for risk stratification and management Circulation 105 2002 1342 1347
-
(2002)
Circulation
, vol.105
, pp. 1342-1347
-
-
Priori, S.G.1
Napolitano, C.2
Gasparini, M.3
Pappone, C.4
Della Bella, P.5
Giordano, U.6
-
4
-
-
84891708821
-
Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes
-
SG Priori, AA Wilde, M Horie, Y Cho, ER Behr, C Berul, and et al. Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes Europace 15 2013 1389 1406
-
(2013)
Europace
, vol.15
, pp. 1389-1406
-
-
Priori, S.G.1
Wilde, A.A.2
Horie, M.3
Cho, Y.4
Behr, E.R.5
Berul, C.6
-
5
-
-
72449147774
-
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing
-
JD Kapplinger, DJ Tester, M Alders, B Benito, M Berthet, J Brugada, and et al. An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing Heart Rhythm 7 2010 33 46
-
(2010)
Heart Rhythm
, vol.7
, pp. 33-46
-
-
Kapplinger, J.D.1
Tester, D.J.2
Alders, M.3
Benito, B.4
Berthet, M.5
Brugada, J.6
-
7
-
-
2342523271
-
Human genomics and its impact on arrhythmias
-
DM Roden Human genomics and its impact on arrhythmias Trends Cardiovasc Med 14 2004 112 116
-
(2004)
Trends Cardiovasc Med
, vol.14
, pp. 112-116
-
-
Roden, D.M.1
-
8
-
-
77449091606
-
SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome
-
V Probst, AA Wilde, J Barc, F Sacher, D Babuty, P Mabo, and et al. SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome Circ Cardiovasc Genet 2 2009 552 557
-
(2009)
Circ Cardiovasc Genet
, vol.2
, pp. 552-557
-
-
Probst, V.1
Wilde, A.A.2
Barc, J.3
Sacher, F.4
Babuty, D.5
Mabo, P.6
-
9
-
-
84883461171
-
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
-
CR Bezzina, J Barc, Y Mizusawa, CA Remme, J-B Gourraud, F Simonet, and et al. Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death Nat Genet 45 2013 1044 1049
-
(2013)
Nat Genet
, vol.45
, pp. 1044-1049
-
-
Bezzina, C.R.1
Barc, J.2
Mizusawa, Y.3
Remme, C.A.4
Gourraud, J.-B.5
Simonet, F.6
-
10
-
-
84924929886
-
Brugada syndrome
-
R Brugada, O Campuzano, G Sarquella-Brugada, J Brugada, and P Brugada Brugada syndrome Methodist Debakey Cardiovasc J 10 2014 25 28
-
(2014)
Methodist Debakey Cardiovasc J
, vol.10
, pp. 25-28
-
-
Brugada, R.1
Campuzano, O.2
Sarquella-Brugada, G.3
Brugada, J.4
Brugada, P.5
-
11
-
-
0025666322
-
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
-
Y Goto, I Nonaka, and S Horai A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies Nature 348 1990 651 653
-
(1990)
Nature
, vol.348
, pp. 651-653
-
-
Goto, Y.1
Nonaka, I.2
Horai, S.3
-
12
-
-
0036257834
-
Progressive cardiomyopathy as manifestation of mitochondrial disease
-
DN Nan, M Fernandez-Ayala, J Infante, P Matorras, and J Gonzalez-Macias Progressive cardiomyopathy as manifestation of mitochondrial disease Postgrad Med J 78 2002 298 299
-
(2002)
Postgrad Med J
, vol.78
, pp. 298-299
-
-
Nan, D.N.1
Fernandez-Ayala, M.2
Infante, J.3
Matorras, P.4
Gonzalez-Macias, J.5
-
13
-
-
58349095350
-
A mitochondrial mutation A4401G is involved in the pathogenesis of left ventricular hypertrophy in Chinese hypertensives
-
H-Y Zhu, S-W Wang, L Liu, Y-H Li, R Chen, L Wang, and et al. A mitochondrial mutation A4401G is involved in the pathogenesis of left ventricular hypertrophy in Chinese hypertensives Eur J Hum Genet 17 2009 172 178
-
(2009)
Eur J Hum Genet
, vol.17
, pp. 172-178
-
-
Zhu, H.-Y.1
Wang, S.-W.2
Liu, L.3
Li, Y.-H.4
Chen, R.5
Wang, L.6
-
14
-
-
0029835998
-
An additional mitochondrial tRNA(Ile) point mutation (A-to-G at nucleotide 4295) causing hypertrophic cardiomyopathy
-
F Merante, T Myint, I Tein, L Benson, and BH Robinson An additional mitochondrial tRNA(Ile) point mutation (A-to-G at nucleotide 4295) causing hypertrophic cardiomyopathy Hum Mutat 8 1996 216 222
-
(1996)
Hum Mutat
, vol.8
, pp. 216-222
-
-
Merante, F.1
Myint, T.2
Tein, I.3
Benson, L.4
Robinson, B.H.5
-
15
-
-
0029116474
-
A novel mtDNA point mutation in maternally inherited cardiomyopathy
-
C Casali, FM Santorelli, G D'Amati, P Bernucci, L DeBiase, and S DiMauro A novel mtDNA point mutation in maternally inherited cardiomyopathy Biochem Biophys Res Commun 213 1995 588 593
-
(1995)
Biochem Biophys Res Commun
, vol.213
, pp. 588-593
-
-
Casali, C.1
Santorelli, F.M.2
D'Amati, G.3
Bernucci, P.4
DeBiase, L.5
DiMauro, S.6
-
16
-
-
0031670876
-
Increased number of substitutions in the D-loop of mitochondrial DNA in the sudden infant death syndrome
-
SH Opdal, TO Rognum, A Vege, AK Stave, BM Dupuy, and T Egeland Increased number of substitutions in the D-loop of mitochondrial DNA in the sudden infant death syndrome Acta Paediatr 87 1998 1039 1044
-
(1998)
Acta Paediatr
, vol.87
, pp. 1039-1044
-
-
Opdal, S.H.1
Rognum, T.O.2
Vege, A.3
Stave, A.K.4
Dupuy, B.M.5
Egeland, T.6
-
17
-
-
0036325341
-
Possible role of mtDNA mutations in sudden infant death
-
SH Opdal, A Vege, T Egeland, MA Musse, and TO Rognum Possible role of mtDNA mutations in sudden infant death Pediatr Neurol 27 2002 23 29
-
(2002)
Pediatr Neurol
, vol.27
, pp. 23-29
-
-
Opdal, S.H.1
Vege, A.2
Egeland, T.3
Musse, M.A.4
Rognum, T.O.5
-
18
-
-
82455181638
-
Mutational analysis of the mitochondrial DNA detected in sudden cardiac death caused by cariomyopathy
-
M Kobayashi, S Nakamura, C Murakami, K Maeda, W Irie, and et al. Mutational analysis of the mitochondrial DNA detected in sudden cardiac death caused by cariomyopathy Kitasato Med J 41 2011 127 135
-
(2011)
Kitasato Med J
, vol.41
, pp. 127-135
-
-
Kobayashi, M.1
Nakamura, S.2
Murakami, C.3
Maeda, K.4
Irie, W.5
-
19
-
-
77957925524
-
Mitochondrial DNA variant discovery and evaluation in human cardiomyopathies through next-generation sequencing
-
MV Zaragoza, J Fass, M Diegoli, D Lin, and E Arbustini Mitochondrial DNA variant discovery and evaluation in human cardiomyopathies through next-generation sequencing PLoS One 5 2010 e12295
-
(2010)
PLoS One
, vol.5
-
-
Zaragoza, M.V.1
Fass, J.2
Diegoli, M.3
Lin, D.4
Arbustini, E.5
-
20
-
-
75149136664
-
Accumulation of mitochondrial genome variations in Persian LQTS patients: A possible risk factor?
-
M Khatami, M Houshmand, M Sadeghizadeh, M Eftekharzadeh, MM Heidari, S Saber, and et al. Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor? Cardiovasc Pathol 19 2010 e21 e27
-
(2010)
Cardiovasc Pathol
, vol.19
, pp. e21-e27
-
-
Khatami, M.1
Houshmand, M.2
Sadeghizadeh, M.3
Eftekharzadeh, M.4
Heidari, M.M.5
Saber, S.6
-
21
-
-
84907435858
-
The mitochondrial DNA mutations associated with cardiac arrhythmia investigated in an LQTS family
-
F Khatami, M Mehdi Heidari, and M Houshmand The mitochondrial DNA mutations associated with cardiac arrhythmia investigated in an LQTS family Iran J Basic Med Sci 17 2014 656 661
-
(2014)
Iran J Basic Med Sci
, vol.17
, pp. 656-661
-
-
Khatami, F.1
Mehdi Heidari, M.2
Houshmand, M.3
-
22
-
-
0032868141
-
Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA
-
RM Andrews, I Kubacka, PF Chinnery, RN Lightowlers, DM Turnbull, and N Howell Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA Nat Genet 23 1999 147
-
(1999)
Nat Genet
, vol.23
, pp. 147
-
-
Andrews, R.M.1
Kubacka, I.2
Chinnery, P.F.3
Lightowlers, R.N.4
Turnbull, D.M.5
Howell, N.6
-
23
-
-
58349102189
-
MITOMASTER: A bioinformatics tool for the analysis of mitochondrial DNA sequences
-
MC Brandon, E Ruiz-Pesini, D Mishmar, V Procaccio, MT Lott, KC Nguyen, and et al. MITOMASTER: a bioinformatics tool for the analysis of mitochondrial DNA sequences Hum Mutat 30 2009 1 6
-
(2009)
Hum Mutat
, vol.30
, pp. 1-6
-
-
Brandon, M.C.1
Ruiz-Pesini, E.2
Mishmar, D.3
Procaccio, V.4
Lott, M.T.5
Nguyen, K.C.6
-
24
-
-
0026468520
-
Point mutations in mitochondrial DNA in patients with hypertrophic cardiomyopathy
-
T Obayashi, K Hattori, S Sugiyama, M Tanaka, T Tanaka, S Itoyama, and et al. Point mutations in mitochondrial DNA in patients with hypertrophic cardiomyopathy Am Heart J 124 1992 1263 1269
-
(1992)
Am Heart J
, vol.124
, pp. 1263-1269
-
-
Obayashi, T.1
Hattori, K.2
Sugiyama, S.3
Tanaka, M.4
Tanaka, T.5
Itoyama, S.6
-
25
-
-
79956346332
-
Is 8860 variation a rare polymorphism or associated as a secondary effect in HCM disease?
-
M Houshmand, M Montazeri, N Kuchekian, F Noohi, G Nozar, and A Zamani Is 8860 variation a rare polymorphism or associated as a secondary effect in HCM disease? Arch Med Sci 7 2011 242 246
-
(2011)
Arch Med Sci
, vol.7
, pp. 242-246
-
-
Houshmand, M.1
Montazeri, M.2
Kuchekian, N.3
Noohi, F.4
Nozar, G.5
Zamani, A.6
-
26
-
-
0031257633
-
Point mutations in mitochondrial DNA of patients with dilated cardiomyopathy
-
YY Li, B Maisch, ML Rose, and C Hengstenberg Point mutations in mitochondrial DNA of patients with dilated cardiomyopathy J Mol Cell Cardiol 29 1997 2699 2709
-
(1997)
J Mol Cell Cardiol
, vol.29
, pp. 2699-2709
-
-
Li, Y.Y.1
Maisch, B.2
Rose, M.L.3
Hengstenberg, C.4
-
27
-
-
0034519248
-
The complete sequence of mtDNA genes in idiopathic dilated cardiomyopathy shows novel missense and tRNA mutations
-
J Marin-Garcia, MJ Goldenthal, R Ananthakrishnan, and ME Pierpont The complete sequence of mtDNA genes in idiopathic dilated cardiomyopathy shows novel missense and tRNA mutations J Card Fail 6 2000 321 329
-
(2000)
J Card Fail
, vol.6
, pp. 321-329
-
-
Marin-Garcia, J.1
Goldenthal, M.J.2
Ananthakrishnan, R.3
Pierpont, M.E.4
-
28
-
-
2142649184
-
Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome
-
V Ruppert, D Nolte, T Aschenbrenner, S Pankuweit, R Funck, and B Maisch Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome Biochem Biophys Res Commun 318 2004 535 543
-
(2004)
Biochem Biophys Res Commun
, vol.318
, pp. 535-543
-
-
Ruppert, V.1
Nolte, D.2
Aschenbrenner, T.3
Pankuweit, S.4
Funck, R.5
Maisch, B.6
-
29
-
-
62149127790
-
Mitochondrial DNA analysis by multiplex denaturing high-performance liquid chromatography and selective sequencing in pediatric patients with cardiomyopathy
-
I Schrijver, LM Pique, I Traynis, C Scharfe, and AJ Sehnert Mitochondrial DNA analysis by multiplex denaturing high-performance liquid chromatography and selective sequencing in pediatric patients with cardiomyopathy Genet Med 11 2009 118 126
-
(2009)
Genet Med
, vol.11
, pp. 118-126
-
-
Schrijver, I.1
Pique, L.M.2
Traynis, I.3
Scharfe, C.4
Sehnert, A.J.5
-
30
-
-
77958501429
-
Reactive oxygen species originating from mitochondria regulate the cardiac sodium channel
-
M Liu, H Liu, and SC Dudley Reactive oxygen species originating from mitochondria regulate the cardiac sodium channel Circ Res 107 2010 967 974
-
(2010)
Circ Res
, vol.107
, pp. 967-974
-
-
Liu, M.1
Liu, H.2
Dudley, S.C.3
-
31
-
-
78650415092
-
Elevated oxidative stress is associated with ventricular fibrillation episodes in patients with Brugada-type electrocardiogram without SCN5A mutation
-
M Tanaka, K Nakamura, KF Kusano, H Morita, K Ohta-Ogo, D Miura, and et al. Elevated oxidative stress is associated with ventricular fibrillation episodes in patients with Brugada-type electrocardiogram without SCN5A mutation Cardiovasc Pathol 20 2011 e37 e42
-
(2011)
Cardiovasc Pathol
, vol.20
, pp. e37-e42
-
-
Tanaka, M.1
Nakamura, K.2
Kusano, K.F.3
Morita, H.4
Ohta-Ogo, K.5
Miura, D.6
-
32
-
-
38349099238
-
NF-kappaB-dependent transcriptional regulation of the cardiac scn5a sodium channel by angiotensin II
-
LL Shang, S Sanyal, AE Pfahnl, Z Jiao, J Allen, H Liu, and et al. NF-kappaB-dependent transcriptional regulation of the cardiac scn5a sodium channel by angiotensin II Am J Physiol Cell Physiol 294 2008 C372 C379
-
(2008)
Am J Physiol Cell Physiol
, vol.294
, pp. C372-C379
-
-
Shang, L.L.1
Sanyal, S.2
Pfahnl, A.E.3
Jiao, Z.4
Allen, J.5
Liu, H.6
-
33
-
-
0346957389
-
Cardiomyocyte mitochondrial KATP channels participate in the antiarrhythmic and antiinfarct effects of KATP activators during ischemia and reperfusion in an intact anesthetized rabbit model
-
B Das, and C Sarkar Cardiomyocyte mitochondrial KATP channels participate in the antiarrhythmic and antiinfarct effects of KATP activators during ischemia and reperfusion in an intact anesthetized rabbit model Pol J Pharmacol 55 2003 771 786
-
(2003)
Pol J Pharmacol
, vol.55
, pp. 771-786
-
-
Das, B.1
Sarkar, C.2
-
34
-
-
1042268063
-
Inherited arrhythmogenic diseases: The complexity beyond monogenic disorders
-
SG Priori Inherited arrhythmogenic diseases: the complexity beyond monogenic disorders Circ Res 94 2004 140 145
-
(2004)
Circ Res
, vol.94
, pp. 140-145
-
-
Priori, S.G.1
-
35
-
-
34247877574
-
Aqueous access pathways in ATP synthase subunit a. Reactivity of cysteine substituted into transmembrane helices 1, 3, and 5
-
CM Angevine, KAG Herold, OD Vincent, and RH Fillingame Aqueous access pathways in ATP synthase subunit a. Reactivity of cysteine substituted into transmembrane helices 1, 3, and 5 J Biol Chem 282 2007 9001 9007
-
(2007)
J Biol Chem
, vol.282
, pp. 9001-9007
-
-
Angevine, C.M.1
Herold, K.A.G.2
Vincent, O.D.3
Fillingame, R.H.4
-
36
-
-
33748039093
-
Functional mutations of the ABCA1 gene in subjects of French-Canadian descent with HDL deficiency
-
K Alrasadi, IL Ruel, M Marcil, and J Genest Functional mutations of the ABCA1 gene in subjects of French-Canadian descent with HDL deficiency Atherosclerosis 188 2006 281 291
-
(2006)
Atherosclerosis
, vol.188
, pp. 281-291
-
-
Alrasadi, K.1
Ruel, I.L.2
Marcil, M.3
Genest, J.4
-
37
-
-
84868612596
-
Exome sequencing identifies 2 rare variants for low high-density lipoprotein cholesterol in an extended family
-
MVPL Reddy, I Iatan, D Weissglas-Volkov, E Nikkola, BE Haas, M Juvonen, and et al. Exome sequencing identifies 2 rare variants for low high-density lipoprotein cholesterol in an extended family Circ Cardiovasc Genet 5 2012 538 546
-
(2012)
Circ Cardiovasc Genet
, vol.5
, pp. 538-546
-
-
Reddy, M.1
Iatan, I.2
Weissglas-Volkov, D.3
Nikkola, E.4
Haas, B.E.5
Juvonen, M.6
-
39
-
-
0034603445
-
Brugada syndrome and sudden cardiac death in children
-
SG Priori, C Napolitano, U Giordano, G Collisani, and M Memmi Brugada syndrome and sudden cardiac death in children Lancet 355 2000 808 809
-
(2000)
Lancet
, vol.355
, pp. 808-809
-
-
Priori, S.G.1
Napolitano, C.2
Giordano, U.3
Collisani, G.4
Memmi, M.5
-
40
-
-
18244408818
-
Near-miss SIDS due to Brugada syndrome
-
JR Skinner, SK Chung, D Montgomery, CH McCulley, J Crawford, J French, and et al. Near-miss SIDS due to Brugada syndrome Arch Dis Child 90 2005 528 529
-
(2005)
Arch Dis Child
, vol.90
, pp. 528-529
-
-
Skinner, J.R.1
Chung, S.K.2
Montgomery, D.3
McCulley, C.H.4
Crawford, J.5
French, J.6
-
41
-
-
12944278908
-
The sudden infant death syndrome gene: Does it exist?
-
SH Opdal, and TO Rognum The sudden infant death syndrome gene: does it exist? Pediatrics 114 2004 e506 e512
-
(2004)
Pediatrics
, vol.114
, pp. e506-e512
-
-
Opdal, S.H.1
Rognum, T.O.2
-
42
-
-
0032859720
-
Mitochondrial DNA point mutations detected in four cases of sudden infant death syndrome
-
SH Opdal, TO Rognum, H Torgersen, and A Vege Mitochondrial DNA point mutations detected in four cases of sudden infant death syndrome Acta Paediatr 88 1999 957 960
-
(1999)
Acta Paediatr
, vol.88
, pp. 957-960
-
-
Opdal, S.H.1
Rognum, T.O.2
Torgersen, H.3
Vege, A.4
-
43
-
-
84860586157
-
Mitochondrial regulation of epigenetics and its role in human diseases
-
S Minocherhomji, TO Tollefsbol, and KK Singh Mitochondrial regulation of epigenetics and its role in human diseases Epigenetics 7 2012 326 334
-
(2012)
Epigenetics
, vol.7
, pp. 326-334
-
-
Minocherhomji, S.1
Tollefsbol, T.O.2
Singh, K.K.3
-
44
-
-
84866627877
-
Mitochondrial DNA coding and control region variants as genetic risk factors for type 2 diabetes
-
C-W Liou, J-B Chen, M-M Tiao, S-W Weng, T-L Huang, J-H Chuang, and et al. Mitochondrial DNA coding and control region variants as genetic risk factors for type 2 diabetes Diabetes 61 2012 2642 2651
-
(2012)
Diabetes
, vol.61
, pp. 2642-2651
-
-
Liou, C.-W.1
Chen, J.-B.2
Tiao, M.-M.3
Weng, S.-W.4
Huang, T.-L.5
Chuang, J.-H.6
-
45
-
-
65749119166
-
Mitochondrial DNA haplogroup T is associated with coronary artery disease and diabetic retinopathy: A case control study
-
B Kofler, EE Mueller, W Eder, O Stanger, R Maier, M Weger, and et al. Mitochondrial DNA haplogroup T is associated with coronary artery disease and diabetic retinopathy: a case control study BMC Med Genet 10 2009 35
-
(2009)
BMC Med Genet
, vol.10
, pp. 35
-
-
Kofler, B.1
Mueller, E.E.2
Eder, W.3
Stanger, O.4
Maier, R.5
Weger, M.6
-
46
-
-
79952408201
-
Mitochondrial haplogroups A and M7a confer a genetic risk for coronary atherosclerosis in the Japanese elderly: An autopsy study of 1,536 patients
-
M Sawabe, M Tanaka, K Chida, T Arai, Y Nishigaki, N Fuku, and et al. Mitochondrial haplogroups A and M7a confer a genetic risk for coronary atherosclerosis in the Japanese elderly: an autopsy study of 1,536 patients J Atheroscler Thromb 18 2011 166 175
-
(2011)
J Atheroscler Thromb
, vol.18
, pp. 166-175
-
-
Sawabe, M.1
Tanaka, M.2
Chida, K.3
Arai, T.4
Nishigaki, Y.5
Fuku, N.6
-
47
-
-
70350504284
-
Genetic modulation of Brugada syndrome by a common polymorphism
-
E Lizotte, MJ Junttila, MP Dube, K Hong, B Benito, M DEZ, and et al. Genetic modulation of Brugada syndrome by a common polymorphism J Cardiovasc Electrophysiol 20 2009 1137 1141
-
(2009)
J Cardiovasc Electrophysiol
, vol.20
, pp. 1137-1141
-
-
Lizotte, E.1
Junttila, M.J.2
Dube, M.P.3
Hong, K.4
Benito, B.5
Dez, M.6
-
48
-
-
84882451403
-
Genetics can contribute to the prognosis of Brugada syndrome: A pilot model for risk stratification
-
E Sommariva, C Pappone, F Martinelli Boneschi, C Di Resta, M Rosaria Carbone, E Salvi, and et al. Genetics can contribute to the prognosis of Brugada syndrome: a pilot model for risk stratification Eur J Hum Genet 21 2013 911 917
-
(2013)
Eur J Hum Genet
, vol.21
, pp. 911-917
-
-
Sommariva, E.1
Pappone, C.2
Martinelli Boneschi, F.3
Di Resta, C.4
Rosaria Carbone, M.5
Salvi, E.6
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