ライフサイエンスコーパス: ventricular septal defect

1 nt mice have other cardiac defects including ventricular septal defect.

2 eltaI)/B(-) mice were born with a membranous ventricular septal defect.

3 viduals, as well as atrial septal defect and ventricular septal defect.

4 septum, and 6.4% for pulmonary atresia with ventricular septal defect.

5 entricular septum and 298 (38%) for TGA with ventricular septal defect.

6 ciation holds in patients with and without a ventricular septal defect.

7 etralogy of Fallot or pulmonary atresia with ventricular septal defect.

8 ocardial hypoplasia, hypertrabeculation, and ventricular septal defect.

9 poplasia, double-outlet right ventricle, and ventricular septal defect.

10 mal cardiac function, and had no evidence of ventricular septal defect.

11 ble outlet right ventricle with a concurrent ventricular septal defect.

12 ortly after birth with lung hypoplasia and a ventricular septal defect.

13 ning defects, pulmonary artery stenosis, and ventricular septal defects.

14 ing common arterial trunk and perimembranous ventricular septal defects.

15 eptal defects and between ozone and isolated ventricular septal defects.

16 p-helix factor (CHF)1Hey2 gene show isolated ventricular septal defects.

17 developed a cardiomyopathy but did not have ventricular septal defects.

18 rdiac outflow tract alignment and membranous ventricular septal defects.

19 ions and coarctations of the aortic arch and ventricular septal defects.

20 t obstruction and between sertraline use and ventricular septal defects.

21 uspid valve, and perimembranous and muscular ventricular septal defects.

22 ity alleles at different loci for atrial and ventricular septal defects.

23 ackground C57Bl/6 frequently have atrial and ventricular septal defects.

24 cular septal defects and C57Bl/6 to muscular ventricular septal defects.

25 mpaction, double outlet right ventricles and ventricular septal defects.

26 interventricular septum and display profound ventricular septal defects.

27 bryonic stage with thin ventricular wall and ventricular septal defects.

28 k, -0.41 (95% CI, -0.74 to -0.09); and major ventricular septal defects, -0.25 (95% CI, -0.35 to -0.1

29 confidence interval, -0.87 to -0.10); major ventricular septal defects, -0.41 (95% confidence interv

30 re pulmonary insufficiency (4), and residual ventricular septal defect (1).

31 This association was significant for ventricular septal defects (1.1% vs 0.6%; P = .001) and

32 s, 2 warfarin embryopathies, 1 stillbirth, 1 ventricular septal defect, 1 growth retardation) were re

33 68-1.57) or premature CAD (OR for CoA versus ventricular septal defect, 1.44; 95% CI, 0.79-2.64) afte

34 ssociated cardiovascular anomalies, of which ventricular septal defects (22/47, 47%), atrial septal d

35 Overall, 400 patients, 154 (38.3%) with a ventricular septal defect, 238 (59.5%) with an intact se

36 7) hair dye in multiple/multiplex membranous ventricular septal defect, 3.3%; and 8) urinary tract in

37 % for tetralogy of Fallot, 2.7% for isolated ventricular septal defect, 3.5% for coarctation of the a

38 CAD compared with 224 of 6481 patients with ventricular septal defect (4.9% versus 3.5%; P=0.04).

39 nd associated CHD (9 atrial septal defect, 7 ventricular septal defect, 4 transposition of the great

40 6) pesticide exposure in isolated membranous ventricular septal defect, 5.5%; 7) hair dye in multiple

41 12 had Taussig-Bing anomaly, 12 had multiple ventricular septal defects, 8 had right ventricular hypo

42 If AVVI is < 0.67 in the presence of a large ventricular septal defect, a single-ventricle approach t

43 nt of the neural crest such as cleft palate, ventricular septal defect, abnormal development of hypog

44 es, including pulmonic arterial stenosis and ventricular septal defects accompanied by high peak outf

45 eeks' gestation, with d-TGA, with or without ventricular septal defects, admitted to our institution

46 ere not significantly related to presence of ventricular septal defect, age at surgery, perfusion var

47 ouble outlet right ventricle, and atrial and ventricular septal defects, all occurring with variable

48 owed structural cardiac defects, including a ventricular septal defect, an aortic root that either st

49 s of 58 patients, 3 to 57 years of age, with ventricular septal defect and a marked increase in pulmo

50 n of Ets1(-/-) embryos revealed a membranous ventricular septal defect and an abnormal nodule of cart

51 , likely resulting from a profound subaortic ventricular septal defect and associated malalignment of

52 tissue defects, including liver hypotrophy, ventricular septal defect and haemorrhage.

53 cts in cardiovascular development, including ventricular septal defect and non-compaction, as well as

54 ing to left-to-right shunting in the form of ventricular septal defect and paradoxical thromboembolis

55 This pattern was also true for patients with ventricular septal defect and subaortic stenosis compare

56 stenosis and 12 patients with perimembranous ventricular septal defect and subaortic stenosis-and wer

57 uses, with high penetrance, large membranous ventricular septal defects and a bifid cardiac apex, and

58 fects or embryonic death, but does result in ventricular septal defects and a low incidence of semilu

59 study of the ontogeny and natural history of ventricular septal defects and cardiomyopathy.

60 nt article describes the clinical aspects of ventricular septal defects and current management strate

61 HDAC5 and HDAC9 show a propensity for lethal ventricular septal defects and thin-walled myocardium.

62 e tetralogy of Fallot, overriding aorta with ventricular septal defect, and bicuspid aortic valves.

63 elopment including hypoplasia of myocardium, ventricular septal defect, and disorganized morphology.

64 including hypoplastic myocardium, membranous ventricular septal defect, and double outlet right ventr

65 uch as abnormalities of the tricuspid valve, ventricular septal defect, and pulmonary stenosis, occur

66 Of surviving embryos, 23% showed ventricular septal defects, and 11% showed neural tube d

67 ht ventricle, with obligatory perimembranous ventricular septal defects, and double-sided aortic arch

68 ar valve development, bicuspid aortic valve, ventricular septal defects, and embryonic lethality.

69 e Gsk3b(-/-) embryos had a double outlet RV, ventricular septal defects, and hypertrophic myopathy, w

70 efects overall, pulmonary-artery hypoplasia, ventricular septal defects, and hypoplastic left heart.

71 sgenesis of the aortic and pulmonary valves, ventricular septal defects, and other cardiac anomalies.

72 ovascular abnormalities including atrial and ventricular septal defects, and tetralogy of Fallot, res

73 rch arteries, double-outlet right ventricle, ventricular septal defects, and thin-walled myocardium.

74 ls severe cardiac defects such as atrial and ventricular septal defects, and valvular defects includi

75 ns, including double outlet right ventricle, ventricular-septal defects, and pericardial edema.

76 formations (aOR = 1.28; 95% CI: 1.03, 1.61), ventricular septal defect (aOR = 1.19; 95% CI: 1.00, 1.4

77 ght ventricle, transposition, and membranous ventricular septal defects), aortic sac (persistent trun

78 Ventricular septal defects are common in human infants,

79 Ventricular septal defects are either isolated small def

80 Because congenital ventricular septal defects are of different sizes and lo

81 Ventricular septal defects are the most common congenita

82 le device closure and closure of postinfarct ventricular septal defects, are also discussed.

83 of the aorta (aRR, 0.77; 95% CI, 0.61-0.96), ventricular septal defects (aRR, 0.85; 95% CI, 0.75-0.96

84 x37 and found a high incidence of atrial and ventricular septal defects at birth.

85 ube defects, transposition of great vessels, ventricular septal defect, atrial septal defect, tetralo

86 Severe nonchromosomal CHD (ie, excluding ventricular septal defects, atrial septal defects, and p

87 Mortality rates for coarctation, ventricular septal defect, atrioventricular septal defec

88 k; (b) the transcatheter closure of muscular ventricular septal defects; (c) the transcatheter closur

89 A type of ventricular septal defect called the Gerbode defect, whi

90 Postinfarction ventricular septal defect carries a grim prognosis.

91 mentation (n=5), mitral valvuloplasty (n=5), ventricular septal defect closure (n=4), apicoaortic con

92 c stenosis resection/Konno procedure (n=10), ventricular septal defect closure (n=8), apical aortic c

93 s associated with death after postinfarction ventricular septal defect closure included the following

94 of Fallot by the traditional technique with ventricular septal defect closure through a ventriculoto

95 Postinfarction ventricular septal defect closure was attempted in 53 pa

96 with the modified technique with transatrial ventricular septal defect closure, a short infundibular

97 , aortoplasty, subaortic stenosis resection, ventricular septal defect closure, and ascending aorta r

98 ioventricular block and operations involving ventricular septal defect closure.

99 lthough transcatheter valve replacements and ventricular septal defect closures have already been per

100 The associations with major ventricular septal defects, common arterial trunk, and a

101 nce of congenital cardiac malformations like ventricular septal defects, common atrioventricular cana

102 This review discusses the different types of ventricular septal defects commonly seen in adults in th

103 ar ventricular septal defect, perimembranous ventricular septal defect, conotruncal defects, left ven

104 for trabecular and papillary muscle defects, ventricular septal defects, conotruncal ridge defects, a

105 lar chamber (chamber hypoplasia and muscular ventricular septal defects), conotruncus (double-outlet

106 t ventricular hypertrophy, overriding aorta, ventricular septal defects, coronary vessel abnormalitie

107 ntal abnormalities include overriding aorta, ventricular septal defects, cranial nerve, and craniofac

108 the transcatheter closure of perimembranous ventricular septal defects; (d) the placement of biopros

109 The Amplatz ventricular septal defect device appears highly efficaci

110 eptal defects using the Amplatzer membranous ventricular septal defect device have been encouraging.

111 on of the delivery system for the membranous ventricular septal defect device that is aimed to overco

112 is study was to close MVSDs with the Amplatz ventricular septal defect device.

113 verall, we observed an accuracy of 89.8% for ventricular septal defect diagnosis.

114 decreasing NMII-B by 80% results in cardiac (ventricular septal defect, double outlet of the right ve

115 g Jun in Isl1-expressing progenitors display ventricular septal defects, double outlet right ventricl

116 e flow measurements of mitral regurgitation, ventricular septal defect flow and aortic regurgitation.

117 s, such as operative urgency and postinfarct ventricular septal defect, have been relatively stable o

118 ) and of a tunnel type in 7, with associated ventricular septal defect in 28 (37%).

119 s associated with ventricular hypoplasia and ventricular septal defects in beta-myosin heavy chain-mi

120 Because we observed ventricular septal defects in embryos that are null for

121 hereas deletion of both miRNAs causes lethal ventricular-septal defects in approximately half of doub

122 Percutaneous closure of postinfarction ventricular septal defect is a reasonably effective trea

123 significantly increased by the presence of a ventricular septal defect, left ventricular outflow obst

124 Repair of muscular ventricular septal defects (MVSDs) has always been chall

125 The cardiac diagnoses included ventricular septal defect (n = 11), tetralogy of Fallot

126 fetal/newborn mice revealed an abundance of ventricular septal defects (n=307).

127 mbryos showed heart malformations, including ventricular septal defect, noncompaction of the ventricu

128 test odds of offspring with a perimembranous ventricular septal defect (odds ratio = 3.23, 95% confid

129 1.43, 3.60), and sulfur dioxide and isolated ventricular septal defects (odds ratio = 2.16, 95% confi

130 in patients with acute mitral regurgitation, ventricular septal defect or poor left ventricular funct

131 s and cross-clamp times, and the presence of ventricular septal defects or abnormal coronary anatomy.

132 redictors of failure included moderate/large ventricular septal defect (OR=22, P=0.001), unicommissur

133 t defects (OR = 0.46; 95% Cl 0.24, 0.86) and ventricular septal defects (OR = 0.61; 95% Cl: 0.38, 0.9

134 abundant endocardial cushions accompanied by ventricular septal defects, outflow tract abnormalities

135 The cardiac defects include atrial and ventricular septal defects, overriding aorta, double-out

136 persistent left superior vena cava (P=0.85), ventricular septal defect (P=0.12), and bicuspid aortic

137 ying pulmonary homograft in 1, and overlying ventricular septal defect patch in 1.

138 to-tricuspid annulus, (1B) ventriculotomy-to-ventricular septal defect patch, (2) ventriculotomy-to-p

139 -pulmonary annulus, (3) pulmonary annulus-to-ventricular septal defect patch, and (4) ventricular sep

140 -to-ventricular septal defect patch, and (4) ventricular septal defect patch-to-tricuspid annulus.

141 ng the outlet septum and an appropriate-size ventricular septal defect patch.

142 ed in the outflow tract (99%) or the site of ventricular septal defect patching (98%) and in the infe

143 with intact ventricular septum and TGA with ventricular septal defect performed from 2010 to 2013.

144 ransposition of the great arteries, muscular ventricular septal defect, perimembranous ventricular se

145 rabeculation defects in the right ventricle, ventricular septal defect, persistent truncus arteriosus

146 One family with forelimb anomalies and ventricular septal defects, phenotypes similar to Holt-O

147 patients with a posterior malalignment type ventricular septal defect (PMVSD) and only 1 of 20 patie

148 ck) after operative repair of perimembranous ventricular septal defect (PMVSD) in a large multi-insti

149 s of transcatheter closure of perimembranous ventricular septal defects (PmVSDs) using the new Amplat

150 (relative risk = 10.2), followed by multiple ventricular septal defects (relative risk = 4.7).

151 o 1.93) or between the use of sertraline and ventricular septal defects (relative risk, 1.04; 95% CI,

152 ion of mXinbeta led to abnormal heart shape, ventricular septal defects, severe growth retardation, a

153 the neonatal period as well as for muscular ventricular septal defects should be the transcatheter a

154 lial-specific NSML SHP2 expression developed ventricular septal defects, suggesting that NSML-associa

155 veal that > or = 2 loci influence membranous ventricular septal defect susceptibility, whereas > or =

156 e (Cx40+/-) included bifid atrial appendage, ventricular septal defect, tetralogy of Fallot (TOF), an

157 eath after surgery for atrial septal defect, ventricular septal defect, tetralogy of Fallot, and tran

158 all patients with CHD (atrial septal defect, ventricular septal defect, tetralogy of Fallot, Ebstein

159 spectrum of cardiac malformations including ventricular septal defects, tetralogy of Fallot, and tri

160 ular septum (TGA/IVS, n = 79, 63%), TGA with ventricular septal defect (TGA/VSD, n = 37, 30%), and Ta

161 e but have severe dilated cardiomyopathy and ventricular septal defects that mimic a human congenital

162 ndromic patients with isolated atrial and/or ventricular septal defects, the predominant cardiac defe

163 Moderate/large ventricular septal defect, unicommissural aortic valve,

164 ate, cleft palate only, conotruncal defects, ventricular septal defects, urinary tract defects, limb

165 tflow tract and creation or enlargement of a ventricular septal defect using stents are potential the

166 results of device closure of perimembranous ventricular septal defects using the Amplatzer membranou

167 egrees and 0 degree), presence/location of a ventricular septal defect (VSD) (3-mm VSD; 2 and 6 mm fr

168 rmine the accuracy of expert examination for ventricular septal defect (VSD) among children with a he

169 ar to those in the human proband, as well as ventricular septal defect (VSD) and double-outlet right

170 Pulmonary atresia with ventricular septal defect (VSD) and major aortopulmonary

171 Ventricular septal defect (VSD) complicating acute myoca

172 enmenger syndrome when two ventricles with a ventricular septal defect (VSD) joined two great arterie

173 Prior ventricular septal defect (VSD) repair predicted neo-AI

174 tive data for atrial septal defect (ASD) and ventricular septal defect (VSD) surgeries in children 2

175 etrical and a moderate-sized apical muscular ventricular septal defect (VSD) was diagnosed after birt

176 efects in cardiac morphogenesis, including a ventricular septal defect (VSD), abnormal formation of t

177 odel, we observed an increased risk of CHDs, ventricular septal defect (VSD), and tetralogy of fallot

178 cts including double-outlet right ventricle, ventricular septal defect (VSD), atrioventricular (AV) c

179 which 6 were thought to have a subpulmonary ventricular septal defect (VSD), had incorrect prenatal

180 O for dTGA with intact ventricular septum or ventricular septal defect (VSD), including double-outlet

181 e types of congenital heart disease, such as ventricular septal defect (VSD), myocardium noncompactio

182 as double outlet right ventricle (DORV) and ventricular septal defect (VSD), similar to defects obse

183 and both an atrial septal defect (ASD) and a ventricular septal defect (VSD).

184 e aneurysm was identified with no associated ventricular septal defect (VSD).

185 ng-term outcomes after surgical closure of a ventricular septal defect (VSD).

186 rection and magnitude of shunting across the ventricular septal defect (VSD).

187 ted heart abnormalities, including PTA and a ventricular septal defect (VSD).

188 of double outlet right ventricle (DORV) and ventricular septal defects (VSD).

189 Intramural ventricular septal defects (VSDs) are interventricular c

190 The positions, sizes, and shapes of ventricular septal defects (VSDs) can be difficult to as

191 nd environmental factors on the incidence of ventricular septal defects (VSDs) caused by a heterozygo

192 heter or surgical closure of apical muscular ventricular septal defects (VSDs) requires accurate deli

193 try of device closure of congenital muscular ventricular septal defects (VSDs) using the new Amplatze

194 Ventricular septal defects (VSDs) were associated with t

195 ncation and kinking with 100% penetrance and ventricular septal defects (VSDs) with ~15% penetrance;

196 Defects within it, termed muscular ventricular septal defects (VSDs), are common, yet less

197 CHD was related to the relative frequency of ventricular septal defects (VSDs), the most common type

198 epaired congenital or postoperative residual ventricular septal defects (VSDs).

199 Ventricular septal defect was associated with tetralogy

200 n patients with CoA compared with those with ventricular septal defect was determined.

201 A large ventricular septal defect was present in all six nonsurv

202 Closure of a residual ventricular septal defect was required in 13 patients, a

203 Ventricular septal defect was the most common CHD observ

204 By multivariate analysis, noncommitted ventricular septal defect was the strongest independent

205 isk of specific birth defects, only that for ventricular septal defects was significantly elevated, w

206 Major ventricular septal defects were associated with larger H

207 exception of a single baby with an isolated ventricular septal defect, which closed spontaneously, n

208 t defect including cardiac noncompaction and ventricular septal defect, which phenocopies 1p36 deleti

209 cell cycling, ventricular noncompaction, and ventricular septal defects, while, in the postnatal card

210 compared patients with CoA and those with a ventricular septal defect, who are not known to be at in

211 sted cardiac disease, including classic ToF, ventricular septal defect with aortic dextroposition and

212 tation and on the left-ventricular side of a ventricular septal defect with left-to-right shunting.

213 MRI demonstrated a ventricular septal defect with over-riding aorta.

214 =3), functionally single ventricle (n=3) and ventricular septal defect with pulmonary outflow obstruc

215 36), or transposition of the great arteries, ventricular septal defect with pulmonary stenosis (n=8).

216 xhibit cardiac ventricular wall thinning and ventricular septal defects with double outlet right vent

217 ew strains model a specific subtype of atrio-ventricular septal defects with exclusive ventricular sh