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Aortopulmonary septal defect.

作者信息

Heilmann K

出版信息

Virchows Arch A Pathol Pathol Anat. 1971;354(1):99-104. doi: 10.1007/BF00544110.

DOI:10.1007/BF00544110
PMID:5315716
Abstract
摘要

相似文献

1
Aortopulmonary septal defect.主肺动脉间隔缺损
Virchows Arch A Pathol Pathol Anat. 1971;354(1):99-104. doi: 10.1007/BF00544110.
2
Isolation of the subclavian artery: 4 cases report and literature review.
Int J Cardiovasc Imaging. 2007 Aug;23(4):463-7. doi: 10.1007/s10554-006-9188-2. Epub 2006 Nov 22.
3
A coarctation on the wrong aortic arch side.主动脉缩窄位于错误的主动脉弓侧。
Rev Esp Cardiol (Engl Ed). 2013 Jun;66(6):497. doi: 10.1016/j.rec.2011.06.019. Epub 2011 Oct 12.
4
[Origin of the right pulmonary artery from the aorta. Tricuspid atresia and persistent ductus arteriosus].[右肺动脉起源于主动脉。三尖瓣闭锁和动脉导管未闭]
Arch Inst Cardiol Mex. 1973 Sep-Oct;43(5):787-92.
5
[On aorto-pulmonary defect].关于主-肺动脉缺损
Orv Hetil. 1968 Aug 4;109(31):1719-21.
6
Aortopulmonary window, aortic origin of the right pulmonary artery, and interrupted aortic arch: detection by two-dimensional and color Doppler echocardiography in an infant.主肺动脉窗、右肺动脉的主动脉起源及主动脉弓中断：二维及彩色多普勒超声心动图在一名婴儿中的检测
Pediatr Cardiol. 1986;7(1):49-52. doi: 10.1007/BF02315481.
7
Aortic arch and pulmonary artery anomalies in children.儿童主动脉弓及肺动脉异常
Semin Roentgenol. 1998 Jul;33(3):262-80. doi: 10.1016/s0037-198x(98)80008-4.
8
Neonatal correction of interrupted aortic arch, aortopulmonary window and ascending aortic origin of right pulmonary artery.新生儿期对主动脉弓中断、主肺动脉窗及右肺动脉起源于升主动脉的矫治。
Indian Heart J. 1996 Nov-Dec;48(6):717-20.
9
[Variation of the Bland, White and Garland syndrome. Isolated origin of the ramus interventricularis anterior from the pulmonary artery combined with extreme right-preponderance (author's transl)].[布兰德、怀特和加兰综合征的变异。室间前支单独起源于肺动脉并伴有极度右优势（作者译）]
Virchows Arch A Pathol Anat Histol. 1974 May 27;363(1):89-95. doi: 10.1007/BF00432207.
10
Tricuspid and pulmonary atresia with coarctation of the aorta: a rare combination possibly explained by persistence of the fifth aortic arch with a systemic-to-pulmonary arterial connection.三尖瓣和肺动脉闭锁合并主动脉缩窄：一种罕见的组合，可能是由于第五主动脉弓持续存在并伴有体循环至肺动脉连接所致。
Int J Cardiol. 1989 Aug;24(2):241-5. doi: 10.1016/0167-5273(89)90314-8.

引用本文的文献

1
The periods of determination of cardiac malformations.心脏畸形的确定时期。
Virchows Arch A Pathol Pathol Anat. 1972;356(2):95-110. doi: 10.1007/BF00549282.

本文引用的文献

1
COMMON AORTO-PULMONARY TRUNK: A RARE CONGENITAL DEFECT.共同主动脉-肺动脉干：一种罕见的先天性缺陷。
Br Heart J. 1943 Apr;5(2):97-100. doi: 10.1136/hrt.5.2.97.
2
Persistent truncus arteriosus; a classification according to anatomic types.永存动脉干；根据解剖类型的分类
Surg Clin North Am. 1949 Aug;29(4):1245-70. doi: 10.1016/s0039-6109(16)32803-1.
3
[A formal principle of combination of developmental abnormalities of the venous & arterial ventricular ostia].[静脉与动脉心室开口发育异常的一种形式上的组合原则]
Z Kreislaufforsch. 1952 Apr;41(7-8):269-84.
4
Hemodynamic research on the origin of malformations of the arterial cardiac end.关于心脏动脉端畸形起源的血流动力学研究
Virchows Arch Pathol Anat Physiol Klin Med. 1956;328(4):391-420. doi: 10.1007/BF00955163.
5
An ontogenetic theory for the explanation of congenital malformations involving the truncus and conus.一种用于解释涉及动脉干和圆锥的先天性畸形的个体发生学理论。
Am Heart J. 1956 May;51(5):782-805. doi: 10.1016/s0002-8703(56)80013-6.
6
[Effect of blood flow as a factor on the form of the heart during development].
Beitr Pathol Anat. 1955;115(1):33-56.
7
[Form development of important cardiovascular malformations; Eisenmenger, Fallot, Tassig-Bing complexes, transposition].
Beitr Pathol Anat. 1955;115(1):1-32.
8
The anatomy of common aorticopulmonary trunk (truncus arteriosus communis) and its embryologic implications. A study of 57 necropsy cases.共同主动脉肺动脉干（共同动脉干）的解剖结构及其胚胎学意义。对57例尸检病例的研究。
Am J Cardiol. 1965 Sep;16(3):406-25. doi: 10.1016/0002-9149(65)90732-0.
9
[The development of the interventricular syptum in the human heart, with special reference to bulbus-torsion].[人类心脏室间隔的发育，特别提及球室扭转]
Z Anat Entwicklungsgesch. 1969;128(1):1-17.