| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Atrial arrhythmias in inherited arrhythmogenic disorders
|
Hasdemir, Can
|
|
2016
|
32 |
5 |
p. 366-372
7 p.
|
artikel
|
| 2 |
Autonomic and cardio-respiratory responses to exercise in Brugada Syndrome patients
|
Chanavirut, Raoyrin
|
|
2016
|
32 |
5 |
p. 426-432
7 p.
|
artikel
|
| 3 |
Cardiac dynamics: Alternans and arrhythmogenesis
|
Tse, Gary
|
|
2016
|
32 |
5 |
p. 411-417
7 p.
|
artikel
|
| 4 |
Catheter ablation for ventricular tachyarrhythmia in patients with channelopathies
|
Murakoshi, Nobuyuki
|
|
2016
|
32 |
5 |
p. 404-410
7 p.
|
artikel
|
| 5 |
Characterization of the novel mutant A78T-HERG from a long QT syndrome type 2 patient: Instability of the mutant protein and stabilization by heat shock factor 1
|
Kondo, Takehito
|
|
2016
|
32 |
5 |
p. 433-440
8 p.
|
artikel
|
| 6 |
Current topics in catecholaminergic polymorphic ventricular tachycardia
|
Sumitomo, Naokata
|
|
2016
|
32 |
5 |
p. 344-351
8 p.
|
artikel
|
| 7 |
Editorial Board
|
|
|
2016
|
32 |
5 |
p. iii-iv
nvt p.
|
artikel
|
| 8 |
Erratum to ‘2015 HRS/EHRA/APHRS/SOLAECE expert consensus statement on optimal implantable cardioverter-defibrillator programming and testing’ [Journal of Arrhythmia 32/1 (2016) 1–28]
|
Wilkoff, Bruce L.
|
|
2016
|
32 |
5 |
p. 441-442
2 p.
|
artikel
|
| 9 |
Genetics of Brugada syndrome
|
Juang, Jyh-Ming Jimmy
|
|
2016
|
32 |
5 |
p. 418-425
8 p.
|
artikel
|
| 10 |
Inherited bradyarrhythmia: A diverse genetic background
|
Ishikawa, Taisuke
|
|
2016
|
32 |
5 |
p. 352-358
7 p.
|
artikel
|
| 11 |
J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge
|
Antzelevitch, Charles
|
|
2016
|
32 |
5 |
p. 315-339
25 p.
|
artikel
|
| 12 |
Left cardiac sympathetic denervation: An important treatment option for patients with hereditary ventricular arrhythmias
|
Cho, Yongkeun
|
|
2016
|
32 |
5 |
p. 340-343
4 p.
|
artikel
|
| 13 |
Molecular autopsy in victims of inherited arrhythmias
|
Semsarian, Christopher
|
|
2016
|
32 |
5 |
p. 359-365
7 p.
|
artikel
|
| 14 |
Molecular genetics have opened a new era for arrhythmia research, but also Pandora׳s box?
|
Horie, Minoru
|
|
2016
|
32 |
5 |
p. 313-314
2 p.
|
artikel
|
| 15 |
Molecular pathogenesis of long QT syndrome type 2
|
Smith, Jennifer L.
|
|
2016
|
32 |
5 |
p. 373-380
8 p.
|
artikel
|
| 16 |
Molecular pathogenesis of long QT syndrome type 1
|
Wu, Jie
|
|
2016
|
32 |
5 |
p. 381-388
8 p.
|
artikel
|
| 17 |
Recent advances in genetic testing and counseling for inherited arrhythmias
|
Mizusawa, Yuka
|
|
2016
|
32 |
5 |
p. 389-397
9 p.
|
artikel
|
| 18 |
The genetic background of arrhythmogenic right ventricular cardiomyopathy
|
Ohno, Seiko
|
|
2016
|
32 |
5 |
p. 398-403
6 p.
|
artikel
|
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