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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1989 2
1990 1
1991 3
1993 1
2000 2
2002 1
2003 1
2005 1
2006 1
2010 2
2011 2
2018 1
2020 1
2023 1
2024 0

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20 results

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Page 1
22q11.2 deletion syndrome and congenital heart disease.
Goldmuntz E. Goldmuntz E. Am J Med Genet C Semin Med Genet. 2020 Mar;184(1):64-72. doi: 10.1002/ajmg.c.31774. Epub 2020 Feb 12. Am J Med Genet C Semin Med Genet. 2020. PMID: 32049433 Review.
Approximately 60-80% of patients have a cardiac malformation most commonly including a subset of conotruncal defects (tetralogy of Fallot, truncus arteriosus, interrupted aortic arch type B), conoventricular and/or atrial septal defects, and aortic arch anoma …
Approximately 60-80% of patients have a cardiac malformation most commonly including a subset of conotruncal defects (tetralogy of Fallot, …
Truncus arteriosus communis: report of three cases and review of literature.
Poaty H, Pelluard F, André G, Maugey-Laulom B, Carles D. Poaty H, et al. Afr Health Sci. 2018 Mar;18(1):147-156. doi: 10.4314/ahs.v18i1.19. Afr Health Sci. 2018. PMID: 29977268 Free PMC article. Review.
BACKGROUND: Truncus arteriosus communis (TAC) is a congenital heart defect in which the physiologic arterial common trunk was not divided into aorta and pulmonary artery trunk. ...The karyotype analysis performed in two cases was normal. CONCLUSION: Truncus
BACKGROUND: Truncus arteriosus communis (TAC) is a congenital heart defect in which the physiologic arterial common trunk was …
Truncus solitarius pulmonalis.
Sennari E, Nishiguchi T, Okishima T, Koono M, Matsuoka Y, Sato Y, Hayakawa K. Sennari E, et al. Pediatr Cardiol. 1990 Jan;11(1):50-3. doi: 10.1007/BF02239549. Pediatr Cardiol. 1990. PMID: 2406708 Review.
The case of a female neonate with truncus solitarius pulmonalis (TSP), a rare congenital heart anomaly, is reported. ...A single right ventricle with common atrioventricular (AV) valve was associated with (Collet & Edwards type II) truncus arteriosus
The case of a female neonate with truncus solitarius pulmonalis (TSP), a rare congenital heart anomaly, is reported. ...A single righ …
Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome.
Momma K. Momma K. Am J Cardiol. 2010 Jun 1;105(11):1617-24. doi: 10.1016/j.amjcard.2010.01.333. Am J Cardiol. 2010. PMID: 20494672 Review.
The most common diseases are conotruncal anomalies, which include tetralogy of Fallot (TF), TF with pulmonary atresia, truncus arteriosus, and interrupted aortic arch. A high prevalence of the deletion is noted in patients with TF with absent pulmonary valve, TF ass …
The most common diseases are conotruncal anomalies, which include tetralogy of Fallot (TF), TF with pulmonary atresia, truncus art
Congenital Heart Surgery Nomenclature and Database Project: truncus arteriosus.
Jacobs ML. Jacobs ML. Ann Thorac Surg. 2000 Apr;69(4 Suppl):S50-5. doi: 10.1016/s0003-4975(99)01320-x. Ann Thorac Surg. 2000. PMID: 10798416 Review.
The extant nomenclature for truncus arteriosus (TA) is reviewed for the purpose of establishing a unified reporting system. ...A modified Van Praagh (VP) classification is proposed involving three main categories of TA: TA with confluent or near confluent pulmonary …
The extant nomenclature for truncus arteriosus (TA) is reviewed for the purpose of establishing a unified reporting system. .. …
Outcomes of truncal valve replacement in neonates and infants: a meta-analysis.
Hardy WA, Kang L, Turek JW, Rajab TK. Hardy WA, et al. Cardiol Young. 2023 May;33(5):673-680. doi: 10.1017/S1047951123000604. Epub 2023 Mar 27. Cardiol Young. 2023. PMID: 36970855 Review.
BACKGROUND: Infants with truncus arteriosus typically undergo repair by repurposing the truncal valve as the neo-aortic valve and using a valved conduit homograft for the neo-pulmonary valve. ...Here, we conduct a meta-analysis to better understand the outcomes of i …
BACKGROUND: Infants with truncus arteriosus typically undergo repair by repurposing the truncal valve as the neo-aortic valve …
The DiGeorge anomaly.
Hong R. Hong R. Immunodefic Rev. 1991;3(1):1-14. Immunodefic Rev. 1991. PMID: 1931005 Review.
As a result, the facies and cardiovascular defects which occur are very characteristic. Two rare conotruncal anomalies, type B interrupted aortic arch and truncus arteriosus account for over half of the cardiac lesions seen in DGA. ...
As a result, the facies and cardiovascular defects which occur are very characteristic. Two rare conotruncal anomalies, type B interr …
Neural crest and cardiovascular development: a 20-year perspective.
Hutson MR, Kirby ML. Hutson MR, et al. Birth Defects Res C Embryo Today. 2003 Feb;69(1):2-13. doi: 10.1002/bdrc.10002. Birth Defects Res C Embryo Today. 2003. PMID: 12768653 Review.
BACKGROUND: Twenty years ago this year was the first publication describing a region of neural crest cells necessary for normal cardiovascular development. Ablation of this region in chick resulted in persistent truncus arteriosus, mispatterning of the great vessels …
BACKGROUND: Twenty years ago this year was the first publication describing a region of neural crest cells necessary for normal cardiovascul …
Repair of persistent truncus arteriosus with interrupted aortic arch.
Tlaskal T, Hucin B, Kucera V, Vojtovic P, Gebauer R, Chaloupecky V, Skovranek J. Tlaskal T, et al. Eur J Cardiothorac Surg. 2005 Nov;28(5):736-41. doi: 10.1016/j.ejcts.2005.08.014. Epub 2005 Sep 27. Eur J Cardiothorac Surg. 2005. PMID: 16194613 Review.
OBJECTIVE: The aim of our study was to analyse experience with repair of truncus arteriosus with interrupted aortic arch. METHODS: Between 1993 and 2004, eight consecutive patients underwent repair of truncus arteriosus with interrupted aortic arch. .. …
OBJECTIVE: The aim of our study was to analyse experience with repair of truncus arteriosus with interrupted aortic arch. METH …
Hyperammonemia and neonatal cardiac failure.
Adamovic T, Jouvet P, Vobecky S, Garel L, Rougemont AL, Alvarez F. Adamovic T, et al. Minerva Anestesiol. 2011 May;77(5):554-7. Epub 2011 Mar 2. Minerva Anestesiol. 2011. PMID: 21540812 Free article. Review.
We report a case of a 2470-g female infant born at the week 37 of gestation with complex congenital heart disease (truncus arteriosus type III, interrupted aortic arch and tricuspid valve insufficiency) and hemodynamically non-significant intrahepatic arterio …
We report a case of a 2470-g female infant born at the week 37 of gestation with complex congenital heart disease (truncus arterio
20 results