Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1990 1
1991 4
1993 3
1994 4
1995 6
1996 5
1997 5
1998 3
1999 4
2000 4
2001 9
2002 3
2003 1
2004 6
2005 4
2006 5
2007 4
2008 1
2009 3
2010 8
2011 4
2012 3
2013 6
2014 1
2015 6
2016 4
2017 2
2018 4
2019 2
2020 5
2021 7
2022 10
2023 13
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

133 results

Results by year

Filters applied: . Clear all
Page 1
Clinical Manifestations of 22q11.2 Deletion Syndrome.
Cirillo A, Lioncino M, Maratea A, Passariello A, Fusco A, Fratta F, Monda E, Caiazza M, Signore G, Esposito A, Baban A, Versacci P, Putotto C, Marino B, Pignata C, Cirillo E, Giardino G, Sarubbi B, Limongelli G, Russo MG. Cirillo A, et al. Heart Fail Clin. 2022 Jan;18(1):155-164. doi: 10.1016/j.hfc.2021.07.009. Epub 2021 Oct 25. Heart Fail Clin. 2022. PMID: 34776076 Review.
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 (tetralog …
Prenatal diagnosis of congenital heart disease: A review of current knowledge.
Bravo-Valenzuela NJ, Peixoto AB, Araujo Júnior E. Bravo-Valenzuela NJ, et al. Indian Heart J. 2018 Jan-Feb;70(1):150-164. doi: 10.1016/j.ihj.2017.12.005. Epub 2017 Dec 16. Indian Heart J. 2018. PMID: 29455772 Free PMC article. Review.
As low and high-risk pregnancies for CHD are subject to routine obstetric ultrasound, the diagnosis of structural heart defects represents a challenge that involves a team of specialists and subspecialists on fetal ultrasonography. In this review, the images highlight norm …
As low and high-risk pregnancies for CHD are subject to routine obstetric ultrasound, the diagnosis of structural heart defects repre …
Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach.
Szczawińska-Popłonyk A, Schwartzmann E, Chmara Z, Głukowska A, Krysa T, Majchrzycki M, Olejnicki M, Ostrowska P, Babik J. Szczawińska-Popłonyk A, et al. Int J Mol Sci. 2023 May 5;24(9):8317. doi: 10.3390/ijms24098317. Int J Mol Sci. 2023. PMID: 37176024 Free PMC article. Review.
The wide spectrum of clinical manifestations includes congenital heart defects-most frequently conotruncal cardiac anomalies-thymic hypoplasia and predominating cellular immune deficiency, laryngeal developmental defects, midline anomalies with cleft palate a …
The wide spectrum of clinical manifestations includes congenital heart defects-most frequently conotruncal cardiac anomalies-t …
Aortopathy in Congenital Heart Disease.
Cotts TB, Salciccioli KB, Swanson SK, Yetman AT. Cotts TB, et al. Cardiol Clin. 2020 Aug;38(3):325-336. doi: 10.1016/j.ccl.2020.04.002. Epub 2020 Jun 3. Cardiol Clin. 2020. PMID: 32622488 Review.
Aortic dilatation is common in patients with congenital heart disease and is seen in patients with bicuspid aortic valve and those with conotruncal congenital heart defects. It is important to identify patients with bicuspid aortic valve at high risk for aortic diss …
Aortic dilatation is common in patients with congenital heart disease and is seen in patients with bicuspid aortic valve and those with c
Aortopulmonary window.
Barnes ME, Mitchell ME, Tweddell JS. Barnes ME, et al. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2011;14(1):67-74. doi: 10.1053/j.pcsu.2011.01.017. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2011. PMID: 21444051 Review.
Aortopulmonary window is a rare defect caused by failure of fusion of the two opposing conotruncal ridges that are responsible for separating the truncus arteriosus into the aorta and pulmonary artery. Aortopulmonary window may occur as an isolated lesion or it can …
Aortopulmonary window is a rare defect caused by failure of fusion of the two opposing conotruncal ridges that are responsible …
Cardiovascular molecular genetics.
Anderson PA. Anderson PA. Curr Opin Cardiol. 1994 Jan;9(1):78-90. doi: 10.1097/00001573-199401000-00010. Curr Opin Cardiol. 1994. PMID: 7911041 Review.
This monograph reviews advances in understanding the genetic basis of heritable disorders of the heart and vasculature, including hypertrophic cardiomyopathy, Marfan syndrome, conotruncal malformations, atrioventricular septal defects, supravalvular aortic stenosis, …
This monograph reviews advances in understanding the genetic basis of heritable disorders of the heart and vasculature, including hypertroph …
DiGeorge syndrome: new insights.
Goldmuntz E. Goldmuntz E. Clin Perinatol. 2005 Dec;32(4):963-78, ix-x. doi: 10.1016/j.clp.2005.09.006. Clin Perinatol. 2005. PMID: 16325672 Review.
Most patients with the clinical features of DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes share a common genetic cause, namely, a deletion of chromosome 22q11, and define the most common deletion syndrome known at this time. ...A significant number of …
Most patients with the clinical features of DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes share a common genetic …
DiGeorge syndrome: an update.
Baldini A. Baldini A. Curr Opin Cardiol. 2004 May;19(3):201-4. doi: 10.1097/00001573-200405000-00002. Curr Opin Cardiol. 2004. PMID: 15096950 Review.
PURPOSE OF REVIEW: This article is an update on DiGeorge syndrome research focusing on the synergy of human and model systems genetics toward the understanding of conotruncal and aortic arch defects. RECENT FINDINGS: The identification of mutations of the human T-Bo …
PURPOSE OF REVIEW: This article is an update on DiGeorge syndrome research focusing on the synergy of human and model systems genetics towar …
The role of glucose in physiological and pathological heart formation.
Nakano H, Fajardo VM, Nakano A. Nakano H, et al. Dev Biol. 2021 Jul;475:222-233. doi: 10.1016/j.ydbio.2021.01.020. Epub 2021 Feb 10. Dev Biol. 2021. PMID: 33577830 Free PMC article. Review.
In utero hyperglycemia impacts the left-right axis establishment, migration of cardiac neural crest cells, conotruncal formation and mesenchymal formation of the cardiac cushion during early embryogenesis and causes cardiac hypertrophy in late fetal stages. ...
In utero hyperglycemia impacts the left-right axis establishment, migration of cardiac neural crest cells, conotruncal formation and …
133 results