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

Year Number of Results
1962 1
1963 27
1964 51
1965 19
1966 29
1967 47
1968 68
1969 54
1970 73
1971 79
1972 106
1973 110
1974 92
1975 91
1976 74
1977 69
1978 92
1979 78
1980 91
1981 123
1982 79
1983 96
1984 127
1985 114
1986 111
1987 143
1988 240
1989 311
1990 310
1991 325
1992 390
1993 475
1994 431
1995 443
1996 532
1997 421
1998 518
1999 503
2000 576
2001 639
2002 652
2003 632
2004 734
2005 863
2006 874
2007 879
2008 859
2009 852
2010 937
2011 966
2012 1001
2013 1074
2014 1090
2015 1164
2016 1171
2017 1211
2018 1103
2019 1043
2020 1128
2021 1058
2022 1109
2023 626

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26,875 results

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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.
In the last decades, the introduction of fluorescence in situ hybridization assays, and in selected cases the use of multiplex ligation-dependent probe amplification, has allowed the detection of chromosomal microdeletions that could not be previously identified using standard ka …
In the last decades, the introduction of fluorescence in situ hybridization assays, and in selected cases the use of multiplex ligation-depe …
Ebstein's Anomaly.
Holst KA, Connolly HM, Dearani JA. Holst KA, et al. Methodist Debakey Cardiovasc J. 2019 Apr-Jun;15(2):138-144. doi: 10.14797/mdcj-15-2-138. Methodist Debakey Cardiovasc J. 2019. PMID: 31384377 Free PMC article. Review.
Congenital vascular ring.
Yoshimura N, Fukahara K, Yamashita A, Doi T, Yamashita S, Homma T, Yokoyama S, Aoki M, Higashida A, Shimada Y, Toritsuka D, Nagao K, Ikeno Y. Yoshimura N, et al. Surg Today. 2020 Oct;50(10):1151-1158. doi: 10.1007/s00595-019-01907-5. Epub 2019 Nov 1. Surg Today. 2020. PMID: 31676999 Review.
A vascular ring is a rare congenital cardiovascular anomaly, which encircles and compresses the trachea or esophagus, or both. ...The development of a vascular ring begins with the embryonic aortic arch system. The persistence, involution, or regression of the arche …
A vascular ring is a rare congenital cardiovascular anomaly, which encircles and compresses the trachea or esophagus, or both. ...The …
The heart in RASopathies.
Delogu AB, Limongelli G, Versacci P, Adorisio R, Kaski JP, Blandino R, Maiolo S, Monda E, Putotto C, De Rosa G, Chatfield KC, Gelb BD, Calcagni G. Delogu AB, et al. Am J Med Genet C Semin Med Genet. 2022 Dec;190(4):440-451. doi: 10.1002/ajmg.c.32014. Epub 2022 Nov 21. Am J Med Genet C Semin Med Genet. 2022. PMID: 36408797 Review.
The cardiovascular phenotype associated with RASopathies has expanded far beyond the original descriptions of pulmonary valve stenosis by Dr Jaqueline Noonan in 1968 and hypertrophic cardiomyopathy by Hirsch et al. in 1975. ...Characterization and understanding of genotype …
The cardiovascular phenotype associated with RASopathies has expanded far beyond the original descriptions of pulmonary valve stenosi …
Sudden cardiac death.
Kuriachan VP, Sumner GL, Mitchell LB. Kuriachan VP, et al. Curr Probl Cardiol. 2015 Apr;40(4):133-200. doi: 10.1016/j.cpcardiol.2015.01.002. Epub 2015 Feb 7. Curr Probl Cardiol. 2015. PMID: 25813838 Review.
Nonischemic cardiomyopathy and other structural abnormalities such as arrhythmogenic ventricular dysplasia and hypertrophic cardiomyopathy may also be causative. ...In other conditions, other markers for structural heart disease and electrical abnormalities need to …
Nonischemic cardiomyopathy and other structural abnormalities such as arrhythmogenic ventricular dysplasia and hypertrophic cardiomyo …
Complementary Role of Oxytocin and Vasopressin in Cardiovascular Regulation.
Szczepanska-Sadowska E, Wsol A, Cudnoch-Jedrzejewska A, Żera T. Szczepanska-Sadowska E, et al. Int J Mol Sci. 2021 Oct 24;22(21):11465. doi: 10.3390/ijms222111465. Int J Mol Sci. 2021. PMID: 34768894 Free PMC article. Review.
The synthesis and action of OXY and AVP in the peripheral organs (eye, heart, gastrointestinal system) is being investigated. The secretion of OXY and AVP is influenced by changes in body fluid osmolality, blood volume, blood pressure, hypoxia, and stress. ...The inappropr …
The synthesis and action of OXY and AVP in the peripheral organs (eye, heart, gastrointestinal system) is being investigated. The sec …
Congenital heart defects in Noonan syndrome: Diagnosis, management, and treatment.
Linglart L, Gelb BD. Linglart L, et al. Am J Med Genet C Semin Med Genet. 2020 Mar;184(1):73-80. doi: 10.1002/ajmg.c.31765. Epub 2020 Feb 5. Am J Med Genet C Semin Med Genet. 2020. PMID: 32022400 Free PMC article. Review.
Noonan syndrome is a pleomorphic genetic disorder, in which a high percentage of affected individuals have cardiovascular involvement, most prevalently various forms of congenital heart disease (i.e., pulmonary valve stenosis, septal defects, left-sided lesions, and comple …
Noonan syndrome is a pleomorphic genetic disorder, in which a high percentage of affected individuals have cardiovascular involvement …
Contemporary management and outcomes in congenitally corrected transposition of the great arteries.
Kutty S, Danford DA, Diller GP, Tutarel O. Kutty S, et al. Heart. 2018 Jul;104(14):1148-1155. doi: 10.1136/heartjnl-2016-311032. Epub 2018 Jan 11. Heart. 2018. PMID: 29326110 Review.
Occasionally, the anatomic peculiarities of ccTGA do not allow straightforward biventricular repair, and Fontan palliation is a reasonable option. Regardless of the approach selected, late cardiovascular complications are relatively common, so ongoing outpatient surveillan …
Occasionally, the anatomic peculiarities of ccTGA do not allow straightforward biventricular repair, and Fontan palliation is a reasonable o …
Ebstein Anomaly in the Adult Patient.
Fuchs MM, Connolly HM. Fuchs MM, et al. Cardiol Clin. 2020 Aug;38(3):353-363. doi: 10.1016/j.ccl.2020.04.004. Epub 2020 Jun 6. Cardiol Clin. 2020. PMID: 32622490 Review.
26,875 results
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