ライフサイエンスコーパス: transposition of the great arteries

1 ally in patients with tetralogy of Fallot or transposition of the great arteries.

2 were men, and 28% had congenitally corrected transposition of the great arteries.

3 used by congenitally or surgically corrected transposition of the great arteries.

4 years) after atrial redirection surgery for transposition of the great arteries.

5 unoperated adult with congenitally corrected transposition of the great arteries.

6 ise capacity after the Mustard operation for transposition of the great arteries.

7 a after Mustard and Senning operations for d-transposition of the great arteries.

8 stence of a left-sided superior vena cava or transposition of the great arteries.

9 ed in most women with congenitally corrected transposition of the great arteries.

10 of coronary artery anatomy in patients with transposition of the great arteries.

11 to double-outlet right ventricle and dextro-transposition of the great arteries.

12 ion of the aorta; tetralogy of Fallot; and D-transposition of the great arteries.

13 the two-stage arterial switch operation for transposition of the great arteries.

14 diagnosis included single ventricle (36%), d-transposition of the great arteries (12%), right ventric

15 ptal defects (20%), (congenitally corrected) transposition of the great arteries (13%), and other (16

16 CHD, such as single ventricle (22.8%) and d-transposition of the great arteries (22.1%).

17 t ventricular outflow tract lesions (10%), l-transposition of the great arteries (8%), ventricular/at

18 astic function of the aorta in patients with transposition of the great arteries after arterial switc

19 operation and 2 by aortopulmonary shunts: d-transposition of the great arteries after Mustard/Sennin

20 ns with congenital heart disease--29 who had transposition of the great arteries and 12 who had singl

21 Among 153 patients (67% male), 96 had transposition of the great arteries and 57 had single ve

22 types of congenital heart disease---namely, transposition of the great arteries and double-outlet ri

23 lformations and indicates that some cases of transposition of the great arteries and double-outlet ri

24 r to Holt-Oram syndrome, and one family with transposition of the great arteries and heart situs anom

25 ion is a feasible strategy for patients with transposition of the great arteries and intact ventricul

26 al management of infants and children with d-transposition of the great arteries and left ventricular

27 ts, including double outlet right ventricle, transposition of the great arteries and persistent trunc

28 A total of 153 patients with transposition of the great arteries and single ventricle

29 ved for the CNVs identified in patients with transposition of the great arteries and tetralogy of Fal

30 defects ranging from tetralogy of Fallot to transposition of the great arteries and that decreased T

31 n preoperative brain injury in neonates with transposition of the great arteries and the performance

32 , including 76 coarctation of the aorta, 159 transposition of the great arteries, and 81 tetralogy of

33 n; 12 for Eisenmenger; 9 for Fontan; 9 for D-transposition of the great arteries; and 8 for tetralogy

34 ients with unoperated congenitally corrected transposition of the great arteries are often misdiagnos

35 es after the arterial switch operation for D-transposition of the great arteries are scarce.

36 Patients treated for transposition of the great arteries by atrial redirectio

37 utcome in adults with congenitally corrected transposition of the great arteries (CCTGA), with partic

38 gery in patients with congenitally corrected transposition of the great arteries (CCTGA).

39 sis and management of congenitally corrected transposition of the great arteries (ccTGA).

40 The outcome of patients with corrected transposition of the great arteries (CTGA) is variably a

41 ng-term impact on general health status of D-transposition of the great arteries (D-TGA) after the ar

42 s" in the management of patients with D-loop transposition of the great arteries (D-TGA) in the curre

43 ular septal defect, tetralogy of Fallot, and transposition of the great arteries decreased to zero fo

44 diagnosis of single ventricle physiology and transposition of the great arteries demonstrate less pre

45 with tetralogy of Fallot and 7 patients with transposition of the great arteries demonstrated compres

46 r arterial switch operation (ASO) for d-loop transposition of the great arteries (dTGA).

47 mes; at 16-year testing for individuals with transposition of the great arteries following the arteri

48 ng abnormalities were more frequent in the d-transposition of the great arteries group (33%) than in

49 None of the 45 patients with transposition of the great arteries had a deletion.

50 Only infants with transposition of the great arteries had smaller HC relat

51 Those with complete transposition of the great arteries have often had an at

52 e novo CNVs were identified in patients with transposition of the great arteries in contrast to coarc

53 y pesticides during the first trimester with transposition of the great arteries in their infants (TG

54 arteriosus, double-outlet right ventricle, L-transposition of the great arteries, interrupted aortic

55 Our data suggest that isolated transposition of the great arteries is a sporadic defect

56 Preoperative brain injury in neonates with transposition of the great arteries is associated with h

57 fspring of women with congenitally corrected transposition of the great arteries is uncertain.

58 var pulmonary stenosis, tetralogy of Fallot, transposition of the great arteries, muscular ventricula

59 ortic coarctation, but in no patients with D-transposition of the great arteries (n = 86) or valvar a

60 cluded double outlet right ventricle (n=36), transposition of the great arteries (n=14), and persiste

61 METHODS AND Infants with transposition of the great arteries (n=26) were retrospe

62 that of 15 fetuses with major heart defects: transposition of the great arteries (n=7), coarctation o

63 , the 22-year survival rate of patients with transposition of the great arteries operated on in 1953

64 patients with aortic stenosis, coarctation, transposition of the great arteries or tetralogy of Fall

65 resonance predicts outcomes in patients with transposition of the great arteries post atrial redirect

66 er complete situs inversus, dextrocardia, or transposition of the great arteries; similar cardiac abn

67 TPVR in patients with congenitally corrected transposition of the great arteries, subpulmonary left v

68 ong-term results of 358 patients with simple transposition of the great arteries surviving >30 days a

69 Other single-ventricle defects, transposition of the great arteries, tetralogy of Fallot

70 We included children with transposition of the great arteries, tetralogy of Fallot

71 control infants (n= 276) and infants with d-transposition of the great arteries (TGA) (n = 69), tetr

72 Patients with transposition of the great arteries (TGA) and systemic r

73 omes after the ASO in babies presenting with transposition of the great arteries (TGA) and Taussig-Bi

74 me after arterial switch operation (ASO) for transposition of the great arteries (TGA) have been hind

75 tle has been published regarding surgery for transposition of the great arteries (TGA) in the develop

76 haemodynamic effects of exercise training in transposition of the great arteries (TGA) patients with

77 n, the Mustard or Senning operation, for the transposition of the great arteries (TGA) was introduced

78 D-transposition of the great arteries (TGA) with left vent

79 (TOF), double outlet right ventricle (DORV), transposition of the great arteries (TGA), and truncus a

80 tive brain injury is common in neonates with transposition of the great arteries (TGA).

81 in patients with the congenital heart defect transposition of the great arteries (TGA).

82 se clinical outcome especially arrhythmia in transposition of the great arteries, thus LGE cardiovasc

83 rterial switch operation for correction of D-transposition of the great arteries, transient postopera

84 ed a retrospective review of neonates with D-transposition of the great arteries undergoing arterial

85 a variant of tetralogy of Fallot (n=36), or transposition of the great arteries, ventricular septal

86 Transposition of the great arteries was associated with

87 y Arrest Study involving 171 children with D-transposition of the great arteries, we explored the rel

88 ho had undergone arterial switch surgery for transposition of the great arteries were studied (mean a

89 Adolescents with d-transposition of the great arteries who have undergone t

90 Infants with D-transposition of the great arteries who underwent an art

91 sessments in children 16 years of age with d-transposition of the great arteries who underwent the ar

92 oot translocation plus arterial switch for d-transposition of the great arteries with left ventricula

93 A d-transposition of the great arteries with left ventricula

94 nslocation plus arterial switch to correct d-transposition of the great arteries with left ventricula

95 e preoperative brain injury in neonates with transposition of the great arteries with the performance

96 o have undergone arterial switch surgery for transposition of the great arteries, with no unexpected

97 ents with congenitally or atrially corrected transposition of the great arteries, worsening of the sy