ライフサイエンスコーパス: congenital long QT syndrome

1 he genetics and the phenotypic expression of congenital long QT syndrome.

2 iated with variants (LQT-1 and LQT-5) of the congenital long QT syndrome.

3 nt sudden cardiac death in patients with the congenital long QT syndrome.

4 thmias and sudden death in families with the congenital long QT syndrome.

5 pathy, and prevention of sudden death in the congenital long QT syndrome.

6 set of spontaneous torsade de pointes in the congenital long QT syndrome.

7 he causes of the chromosome 7-linked form of congenital long QT syndrome.

8 minK are now recognized as one cause of the congenital long-QT syndrome.

9 er conditions mimicking the LQT1 form of the congenital long-QT syndrome.

10 Congenital long QT syndrome 2 (LQT2) is caused by loss-o

11 f sudden cardiac death in the young, whereas congenital long QT syndrome, affecting 1 in 5000 persons

12 in human KCNE1 cause congenital deafness and congenital long QT syndrome, an inherited predisposition

13 ted with inherited arrhythmia syndromes (eg, congenital long-QT syndrome and Brugada syndrome).

14 inergic polymorphic ventricular tachycardia, congenital long QT syndrome, and hypertrophic cardiomyop

15 olarization time, known to be altered in the congenital long-QT syndromes, and reflected in the diffe

16 The congenital long-QT syndrome, caused by mutations in card

17 Mutations in genes responsible for the congenital long-QT syndrome, especially SCN5A, have been

18 rious cardiac arrhythmia syndromes including congenital long QT syndrome, familial atrial fibrillatio

19 rocardiographic, and genetic features of the congenital long QT syndromes has emerged.

20 The congenital long QT syndrome is a potentially fatal, inhe

21 The congenital long QT syndrome is a potentially life-threat

22 Congenital long QT syndrome is a rare disease in which t

23 The congenital long QT syndrome is a rare disorder in which

24 Congenital long QT syndrome is a rare inherited conditio

25 The congenital long QT syndrome is an autosomal-dominant gen

26 Congenital long QT syndrome is caused by mutations in ge

27 The congenital long QT syndrome is characterized by abnormal

28 continually unraveling molecular biology of congenital long QT syndrome is discussed.

29 The congenital long-QT syndrome (LQT), an inherited cardiac

30 el alpha-subunit, is linked to 1 form of the congenital long-QT syndrome (LQT-3).

31 l alpha-subunit, are linked to 1 form of the congenital long-QT syndrome (LQT-3).

32 her-a-go-go-Related Gene (HERG) cause type 2 congenital long QT syndrome (LQT2) by disrupting traffic

33 The chromosome 7-linked form of congenital long QT syndrome (LQT2) is caused by mutation

34 Type 2 congenital long-QT syndrome (LQT2) results from KCNH2 mu

35 m (Na) channel gene (SCN5A) give rise to the congenital long-QT syndrome (LQT3) and the Brugada syndr

36 um (Na) channel, are linked to a form of the congenital long-QT syndrome (LQT3) that provokes lethal

37 Congenital long QT syndrome (LQTS) is a heterogeneous gr

38 Congenital Long QT syndrome (LQTS) is an arrhythmogenic

39 The congenital long QT syndrome (LQTS) is an inherited disor

40 The congenital long QT syndrome (LQTS) is an inherited disor

41 Congenital long QT syndrome (LQTS) is characterized by Q

42 s in the kcnq1 gene are the leading cause of congenital long QT syndrome (LQTS).

43 henotype on the yield of genetic testing for congenital long QT syndrome (LQTS).

44 Kr), account for a significant proportion of congenital long QT syndrome (LQTS).

45 to compare the efficacy of beta-blockers in congenital long QT syndrome (LQTS).

46 life-threatening cardiac arrhythmias such as congenital long-QT syndrome (LQTS) and catecholaminergic

47 Patients with congenital long-QT syndrome (LQTS) are susceptible to li

48 -threatening cardiac events in patients with congenital long-QT syndrome (LQTS) have focused mainly o

49 Congenital long-QT syndrome (LQTS) is a primary arrhythm

50 The congenital long-QT syndrome (LQTS) is an important cause

51 Congenital long-QT syndrome (LQTS) is an inherited condi

52 Congenital long-QT syndrome (LQTS) is caused by mutation

53 The congenital long-QT syndrome (LQTS) is characterized by p

54 beta-blockers are routinely prescribed in congenital long-QT syndrome (LQTS), but the effectivenes

55 patients referred for clinical evaluation of congenital long-QT syndrome (LQTS).

56 Specific ion channel mutations underlie the congenital long-QT syndrome (LQTS).

57 icking the LQT1, LQT2, and LQT3 forms of the congenital long-QT syndrome (LQTS).

58 micking HERG and SCN5A defects linked to the congenital long-QT syndrome (LQTS).

59 Variant 3 of the congenital long-QT syndrome (LQTS-3) is caused by mutati

60 ve, is commonly observed in the acquired and congenital long-QT syndromes (LQTS).

61 The congenital long QT syndrome may result from inherited de

62 voltage-gated sodium channel [NaV1.5]) cause congenital long-QT syndrome type 3 (LQT3).

63 gest that genotype-specific treatment of the congenital long QT syndrome will be feasible in the near

64 on an independent cohort of 82 subjects with congenital long-QT syndrome without an identified geneti