ライフサイエンスコーパス: arrhythmogenic right ventricular dysplasia

1 erwent magnetic resonance imaging to exclude arrhythmogenic right ventricular dysplasia.

2 orphic ventricular tachycardia and a form of arrhythmogenic right ventricular dysplasia.

3 rces for arrhythmias, even in the absence of arrhythmogenic right ventricular dysplasia.

4 detailed echocardiography, in patients with arrhythmogenic right ventricular dysplasia.

5 r therapy in the management of patients with arrhythmogenic right-ventricular dysplasia.

6 gnetic resonance imaging in the diagnosis of arrhythmogenic right-ventricular dysplasia.

7 netically uncharacterized diseases including arrhythmogenic right ventricular dysplasia 3.

8 yopathy, left ventricular noncompaction, and arrhythmogenic right ventricular dysplasia; and delineat

9 lymorphic ventricular tachycardia (CPVT) and arrhythmogenic right ventricular dysplasia (ARVD) affect

10 etic resonance imaging (MRI) examinations of arrhythmogenic right ventricular dysplasia (ARVD) and to

11 The loci of several genes responsible for arrhythmogenic right ventricular dysplasia (ARVD) have b

12 Arrhythmogenic right ventricular dysplasia (ARVD) is an

13 Ventricular tachycardia ablation in arrhythmogenic right ventricular dysplasia (ARVD) is mor

14 Arrhythmogenic right ventricular dysplasia (ARVD), a fam

15 study was to reevaluate the ECG features of arrhythmogenic right ventricular dysplasia (ARVD).

16 es in probands who were newly diagnosed with arrhythmogenic right ventricular dysplasia (ARVD).

17 r tachycardia (VT) ablation in patients with arrhythmogenic right ventricular dysplasia (ARVD).

18 ve recently localized a gene responsible for arrhythmogenic right ventricular dysplasia (ARVD).

19 where we have mapped a locus responsible for arrhythmogenic right ventricular dysplasia (ARVD).

20 e applied to ventricular tachycardia (VT) in arrhythmogenic right ventricular dysplasia (ARVD).

21 Arrhythmogenic right-ventricular dysplasia (ARVD), a car

22 r structural abnormalities characteristic of arrhythmogenic right ventricular dysplasia, but right ve

23 earch has described the arrhythmic course of arrhythmogenic right ventricular dysplasia/cardiomyopath

24 entricular contractions (PVCs) are common in arrhythmogenic right ventricular dysplasia/cardiomyopath

25 Arrhythmogenic right ventricular dysplasia/cardiomyopath

26 We hypothesized that VT in arrhythmogenic right ventricular dysplasia/cardiomyopath

27 entricular arrhythmias in patients harboring arrhythmogenic right ventricular dysplasia/cardiomyopath

28 ermine how exercise influences penetrance of arrhythmogenic right ventricular dysplasia/cardiomyopath

29 hythmic risk stratification in patients with arrhythmogenic right ventricular dysplasia/cardiomyopath

30 The study population included 16 consecutive arrhythmogenic right ventricular dysplasia/cardiomyopath

31 acycline cardiomyopathy, cardiac tumors, and arrhythmogenic right ventricular dysplasia/cardiomyopath

32 r tachycardia (VT) ablation in patients with arrhythmogenic right ventricular dysplasia/cardiomyopath

33 Arrhythmogenic right ventricular dysplasia/cardiomyopath

34 Arrhythmogenic right ventricular dysplasia/cardiomyopath

35 ricular tachycardia (VT) among patients with arrhythmogenic right ventricular dysplasia/cardiomyopath

36 icular arrhythmias distinguish patients with arrhythmogenic right ventricular dysplasia/cardiomyopath

37 defibrillator (ICD) therapy in patients with arrhythmogenic right ventricular dysplasia/cardiomyopath

38 lying right ventricular (RV) dyssynchrony in arrhythmogenic right ventricular dysplasia/cardiomyopath

39 ent in individuals predisposed to developing arrhythmogenic right ventricular dysplasia/cardiomyopath

40 ion (RFA) of ventricular tachycardia (VT) in arrhythmogenic right ventricular dysplasia/cardiomyopath

41 s have been identified as the major cause of arrhythmogenic right ventricular dysplasia/cardiomyopath

42 Arrhythmogenic right ventricular dysplasia/cardiomyopath

43 Arrhythmogenic right ventricular dysplasia/cardiomyopath

44 Arrhythmogenic right ventricular dysplasia/cardiomyopath

45 Arrhythmogenic right ventricular dysplasia/cardiomyopath

46 Arrhythmogenic right ventricular dysplasia/cardiomyopath

47 M and they were diagnostic or suggestive for arrhythmogenic right ventricular dysplasia/cardiomyopath

48 utations among family members of people with arrhythmogenic right ventricular dysplasia/cardiomyopath

49 Arrhythmogenic right ventricular dysplasia/cardiomyopath

50 RI) for noninvasive detection of fibrosis in Arrhythmogenic right ventricular dysplasia/cardiomyopath

51 ow overlap in the clinical presentation with arrhythmogenic right ventricular dysplasia/cardiomyopath

52 Arrhythmogenic right ventricular dysplasia/cardiomyopath

53 m of this study was to assess the outcome of arrhythmogenic right ventricular dysplasia/cardiomyopath

54 Arrhythmogenic right ventricular dysplasia/cardiomyopath

55 ovirus (CMV), enterovirus and parvovirus, in arrhythmogenic right ventricular dysplasia/cardiomyopath

56 diomyopathy (ie, restrictive cardiomyopathy, arrhythmogenic right ventricular dysplasia/cardiomyopath

57 lete penetrance and variable expressivity of arrhythmogenic right ventricular dysplasia/cardiomyopath

58 can in turn facilitate ablation of the VT in arrhythmogenic right ventricular dysplasia/cardiomyopath

59 imaging in arrhythmic risk stratification of arrhythmogenic right ventricular dysplasia/cardiomyopath

60 Arrhythmogenic right ventricular dysplasia/cardiomyopath

61 The majority of patients with arrhythmogenic right ventricular dysplasia have abnormal

62 Mutations in PTPLa correlated with arrhythmogenic right ventricular dysplasia in humans and

63 d the pathogenesis of both Uhl's anomaly and arrhythmogenic right ventricular dysplasia; in each apop

64 Arrhythmogenic right-ventricular dysplasia is a rare dis

65 Arrhythmogenic right-ventricular dysplasia is a rare inh

66 nt new breakthroughs in the genetic basis of arrhythmogenic right-ventricular dysplasia; it now appea

67 Selected reports suggest that arrhythmogenic right ventricular dysplasia may be a more

68 pertrophic cardiomyopathy, and patients with arrhythmogenic right ventricular dysplasia or channelopa

69 This may explain why arrhythmogenic right-ventricular dysplasia preferentiall

70 Ten patients with the clinical diagnosis of arrhythmogenic right ventricular dysplasia were included