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1 atresia, pulmonary stenosis, and persistent truncus arteriosus.
2 x1, whose inactivation results in persistent truncus arteriosus.
3 , valvular disease, tetralogy of Fallot, and truncus arteriosus.
4 uding interrupted aortic arch and persistent truncus arteriosus.
5 ral crest ingress, with resultant persistent truncus arteriosus.
6 notruncal heart defects including persistent truncus arteriosus.
7 cle, aorticopulmonary window, and persistent truncus arteriosus.
8 nic atresia or stenosis (7 patients, 11.5%), truncus arteriosus (6 patients, 10%), TGA (10 patients,
9 nificantly increased incidence of persistent truncus arteriosus, a phenotypic change characteristic o
10 embryos die at mid-gestation with persistent truncus arteriosus, a severe cardiac outflow tract defec
11 (mean 7.2+/-4.9); group B, 14 patients with truncus arteriosus, aged 27 to 50 years (mean 33.7+/-7.3
13 ular septal defects), aortic sac (persistent truncus arteriosus and aorticopulmonary window), and aor
15 neural crest ablation results in persistent truncus arteriosus and failure of addition of myocardium
16 derstand the embryonic defects of persistent truncus arteriosus and impaired semilunar valve formatio
17 ular disease, including tetralogy of Fallot, truncus arteriosus and interruption of the aortic arch.
20 cardiovascular defects, including persistent truncus arteriosus, and abnormal maturation of the aorti
21 have a cardiovascular malformation, one had truncus arteriosus, and another had a bicuspid aortic va
22 from ascending aorta, paracoarctation aorta, truncus arteriosus, and pulmonary trunk in 86 patients w
23 s in ascending aorta, paracoarctation aorta, truncus arteriosus, and pulmonary trunk were prevalent i
24 coarctation, atrioventricular septal defect, truncus arteriosus, aortopulmonary septal defect, and to
25 f 71 (4%) with a secundum ASD, one each with truncus arteriosus, double-outlet right ventricle, L-tra
26 developmental defects, including persistent truncus arteriosus, hypomorphic pulmonary arteries, inte
27 ow tract remodeling, resulting in persistent truncus arteriosus in the majority of mutant embryos.
28 work together to perturb the rotation of the truncus arteriosus, leading to OFT malalignment defects
31 atrioventricular septal defect, Fallot, and truncus arteriosus operations were 1.1%, 0.6%, 3.6%, 2.3
33 hese cardiac anomalies present as persistent truncus arteriosus (PTA) and interrupted aortic arch (IA
34 nct cardiovascular malformations--persistent truncus arteriosus (PTA) and interrupted aortic arch (IA
36 ial arch development and leads to persistent truncus arteriosus (PTA), indicative of neural crest dys
37 t mice lacking Smad4 in NCCs have persistent truncus arteriosus (PTA), severe OFT cushion hypoplasia,
39 ricle, ventricular septal defect, persistent truncus arteriosus, reduced myocardial proliferation, an
40 ed aortic arch (IAA), 34.5% of patients with truncus arteriosus (TA), and 15.9% with tetralogy of Fal
42 vere CHD was defined as tetralogy of Fallot, truncus arteriosus, transposition complexes, endocardial
44 --Sema3CL605P was associated with persistent truncus arteriosus with interrupted aortic arch, and the
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