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1966
2025

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

Year Number of Results
1966 1
1967 1
1968 5
1969 1
1970 7
1971 9
1972 14
1973 11
1974 9
1975 10
1976 8
1977 9
1978 6
1979 10
1980 5
1981 8
1982 6
1983 9
1984 8
1985 9
1986 5
1987 11
1988 8
1989 17
1990 13
1991 13
1992 18
1993 19
1994 11
1995 19
1996 26
1997 21
1998 20
1999 18
2000 19
2001 20
2002 15
2003 18
2004 38
2005 39
2006 34
2007 32
2008 36
2009 28
2010 28
2011 48
2012 55
2013 41
2014 53
2015 56
2016 50
2017 49
2018 43
2019 65
2020 47
2021 30
2022 33
2023 15
2024 38
2025 4

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1,207 results

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Page 1
Calcific aortic valve disease: mechanisms, prevention and treatment.
Moncla LM, Briend M, Bossé Y, Mathieu P. Moncla LM, et al. Nat Rev Cardiol. 2023 Aug;20(8):546-559. doi: 10.1038/s41569-023-00845-7. Epub 2023 Feb 24. Nat Rev Cardiol. 2023. PMID: 36829083 Review.
Calcific aortic valve disease (CAVD) is the most common disorder affecting heart valves and is characterized by thickening, fibrosis and mineralization of the aortic valve leaflets. Analyses of surgically explanted aortic valve leaflets have sho …
Calcific aortic valve disease (CAVD) is the most common disorder affecting heart valves and is characterized by thicken …
Anatomy and Physiology of the Tricuspid Valve.
Dahou A, Levin D, Reisman M, Hahn RT. Dahou A, et al. JACC Cardiovasc Imaging. 2019 Mar;12(3):458-468. doi: 10.1016/j.jcmg.2018.07.032. JACC Cardiovasc Imaging. 2019. PMID: 30846121 Free article. Review.
An appreciation of the complex and variable anatomy of the tricuspid valve is essential to unraveling the pathophysiology of tricuspid regurgitation. A greater appreciation of normal and abnormal anatomy is important as new methods of treating the tricuspid regurgit …
An appreciation of the complex and variable anatomy of the tricuspid valve is essential to unraveling the pathophysiology of tricuspi …
Congenital Heart Disease: Causes, Diagnosis, Symptoms, and Treatments.
Sun R, Liu M, Lu L, Zheng Y, Zhang P. Sun R, et al. Cell Biochem Biophys. 2015 Jul;72(3):857-60. doi: 10.1007/s12013-015-0551-6. Cell Biochem Biophys. 2015. PMID: 25638345 Review.
The congenital heart disease includes abnormalities in heart structure that occur before birth. ...These are heart valves defects, atrial and ventricular septa defects, stenosis, the heart muscle abnormalities, and a hole in …
The congenital heart disease includes abnormalities in heart structure that occur before birth. ...These are …
Calcific aortic stenosis.
Lindman BR, Clavel MA, Mathieu P, Iung B, Lancellotti P, Otto CM, Pibarot P. Lindman BR, et al. Nat Rev Dis Primers. 2016 Mar 3;2:16006. doi: 10.1038/nrdp.2016.6. Nat Rev Dis Primers. 2016. PMID: 27188578 Free PMC article. Review.
Calcific aortic stenosis (AS) is the most prevalent heart valve disorder in developed countries. It is characterized by progressive fibro-calcific remodelling and thickening of the aortic valve leaflets that, over years, evolve to cause severe obstruction to …
Calcific aortic stenosis (AS) is the most prevalent heart valve disorder in developed countries. It is characterized by progre …
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.
Ebstein's anomaly is a malformation of the tricuspid valve with myopathy of the right ventricle (RV) that presents with variable anatomic and pathophysiologic characteristics, leading to equally variable clinical scenarios. ...Postoperative functional assessments generally …
Ebstein's anomaly is a malformation of the tricuspid valve with myopathy of the right ventricle (RV) that presents with variable anat …
Development of the human heart.
Buijtendijk MFJ, Barnett P, van den Hoff MJB. Buijtendijk MFJ, et al. Am J Med Genet C Semin Med Genet. 2020 Mar;184(1):7-22. doi: 10.1002/ajmg.c.31778. Epub 2020 Feb 12. Am J Med Genet C Semin Med Genet. 2020. PMID: 32048790 Free PMC article. Review.
Molecular genetic lineage analyses have since furthered our insight in the developmental origin of the various component parts of the heart, which currently can be unambiguously identified by their unique molecular phenotype. ...Despite the enormous advances in our knowled …
Molecular genetic lineage analyses have since furthered our insight in the developmental origin of the various component parts of the hea
Exercise recommendations in patients with valvular heart disease.
Gati S, Malhotra A, Sharma S. Gati S, et al. Heart. 2019 Jan;105(2):106-110. doi: 10.1136/heartjnl-2018-313372. Epub 2018 Sep 27. Heart. 2019. PMID: 30262455 Review.
Valvular heart disease affects 1%-2% of young individuals, many of whom aspire to partake in competitive sport or high intensity recreational exercise. ...Individuals anticoagulated for mechanical bioprosthetic valves should avoid contact or collision sport to minim …
Valvular heart disease affects 1%-2% of young individuals, many of whom aspire to partake in competitive sport or high intensity recr …
Acute aortic dissection: pathogenesis, risk factors and diagnosis.
Gawinecka J, Schönrath F, von Eckardstein A. Gawinecka J, et al. Swiss Med Wkly. 2017 Aug 25;147:w14489. doi: 10.4414/smw.2017.14489. eCollection 2017. Swiss Med Wkly. 2017. PMID: 28871571 Free article. Review.
However, patients with genetic connective tissue disorders such as Marfan, Loeys Dietz or Ehlers Danlos syndrome, and patients with bicuspid aortic valves are at the increased risk of aortic dissection at a much younger age. Imaging provides a robust foundation for diagnos …
However, patients with genetic connective tissue disorders such as Marfan, Loeys Dietz or Ehlers Danlos syndrome, and patients with bicuspid …
Morphologic Types of Tricuspid Regurgitation: Characteristics and Prognostic Implications.
Prihadi EA, Delgado V, Leon MB, Enriquez-Sarano M, Topilsky Y, Bax JJ. Prihadi EA, et al. JACC Cardiovasc Imaging. 2019 Mar;12(3):491-499. doi: 10.1016/j.jcmg.2018.09.027. JACC Cardiovasc Imaging. 2019. PMID: 30846123 Free article. Review.
Primary TR is caused by an anatomical abnormality of the tricuspid valve apparatus. Secondary TR is caused by dilation of the tricuspid valve annulus, related to right ventricular (RV), or right atrial remodeling and increased RV pressures (often secondary to …
Primary TR is caused by an anatomical abnormality of the tricuspid valve apparatus. Secondary TR is caused by dilation of the …
Turner syndrome: diagnosis and management.
Morgan T. Morgan T. Am Fam Physician. 2007 Aug 1;76(3):405-10. Am Fam Physician. 2007. PMID: 17708142 Free article. Review.
Patients with Turner syndrome are at risk of congenital heart defects (e.g., coarctation of aorta, bicuspid aortic valve) and may have progressive aortic root dilatation or dissection. These patients also are at risk of congenital lymphedema, renal mal …
Patients with Turner syndrome are at risk of congenital heart defects (e.g., coarctation of aorta, bicuspid aortic valve
1,207 results