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

Year Number of Results
1964 1
1965 2
1967 1
1969 4
1970 10
1971 4
1972 6
1973 8
1974 6
1975 32
1976 31
1977 30
1978 36
1979 33
1980 25
1981 21
1982 31
1983 35
1984 51
1985 45
1986 45
1987 41
1988 66
1989 83
1990 64
1991 79
1992 84
1993 87
1994 81
1995 92
1996 99
1997 102
1998 128
1999 134
2000 144
2001 138
2002 150
2003 166
2004 147
2005 187
2006 197
2007 211
2008 248
2009 226
2010 238
2011 319
2012 399
2013 396
2014 382
2015 351
2016 349
2017 383
2018 397
2019 384
2020 334
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2022 279
2023 230
2024 69

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7,198 results

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Quoted phrase not found in phrase index: "Congenital malformation of the right heart"
Page 1
Cardiac imaging in Ebstein anomaly.
Qureshi MY, O'Leary PW, Connolly HM. Qureshi MY, et al. Trends Cardiovasc Med. 2018 Aug;28(6):403-409. doi: 10.1016/j.tcm.2018.01.002. Epub 2018 Jan 12. Trends Cardiovasc Med. 2018. PMID: 29409687 Review.
Ebstein anomaly is a congenital disorder of right ventricular myocardial development, which affects the tricuspid valve in addition to the right ventricular myocardium. ...
Ebstein anomaly is a congenital disorder of right ventricular myocardial development, which affects the tricuspid valve in add …
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.
Ebstein anomaly is a congenital malformation involving primarily the tricuspid valve, with failure of delamination from the underlying myocardium and right ventricular myopathy. Echocardiography is diagnostic in most patients and demonstrates apical displacem …
Ebstein anomaly is a congenital malformation involving primarily the tricuspid valve, with failure of delamination from the un …
Pregnancy loss in major fetal congenital heart disease: incidence, risk factors and timing.
Jepson BM, Metz TD, Miller TA, Son SL, Ou Z, Presson AP, Nance A, Pinto NM. Jepson BM, et al. Ultrasound Obstet Gynecol. 2023 Jul;62(1):75-87. doi: 10.1002/uog.26231. Ultrasound Obstet Gynecol. 2023. PMID: 37099500
OBJECTIVE: Fetuses with congenital heart disease (CHD) are at increased risk of pregnancy loss compared with the general population. ...Of study cases, 1848 (59.2%) had isolated CHD and 1272 (40.8%) had an additional fetal diagnosis, including 736 (57.9%) with a gen …
OBJECTIVE: Fetuses with congenital heart disease (CHD) are at increased risk of pregnancy loss compared with the general popul …
Isomerism of the atrial appendages: morphology and terminology.
Frescura C, Ho SY, Giordano M, Thiene G. Frescura C, et al. Cardiovasc Pathol. 2020 Jul-Aug;47:107205. doi: 10.1016/j.carpath.2020.107205. Epub 2020 Jan 16. Cardiovasc Pathol. 2020. PMID: 32179252
BACKGROUND: Our aim is to identify the pathognomonic anatomical markers and the best terminology to describe the cardiac malformations associated with absent or multiple spleens, which are known as asplenia or polysplenia syndromes or isomerism. MATERIALS AND METHODS: We have rev …
BACKGROUND: Our aim is to identify the pathognomonic anatomical markers and the best terminology to describe the cardiac malformations assoc …
Cat eye syndrome.
Sharma D, Murki S, Pratap T, Vasikarla M. Sharma D, et al. BMJ Case Rep. 2014 May 19;2014:bcr2014203923. doi: 10.1136/bcr-2014-203923. BMJ Case Rep. 2014. PMID: 24842361 Free PMC article.
A full-term female baby, a product of non-consanguineous marriage, was born at 37 weeks of gestation with a birth weight of 2.08 kg. Antenatal scan at 31 weeks revealed complex congenital heart disease with a hypoplastic right ventricle, pulmonary atresia and …
A full-term female baby, a product of non-consanguineous marriage, was born at 37 weeks of gestation with a birth weight of 2.08 kg. Antenat …
Echocardiographic evaluation of the single right ventricle in congenital heart disease: results of new techniques.
Cua CL, Feltes TF. Cua CL, et al. Circ J. 2012;76(1):22-31. doi: 10.1253/circj.cj-11-1267. Epub 2011 Dec 3. Circ J. 2012. PMID: 22139360 Free article. Review.
Right ventricular (RV) function is increasingly recognized as having prognostic significance in various disease processes. ...The evaluation of RV function almost certainly has no greater importance than in the congenital heart population, especially i …
Right ventricular (RV) function is increasingly recognized as having prognostic significance in various disease processes. ... …
Double-chambered Right Ventricle in Children.
Yuan SM. Yuan SM. J Coll Physicians Surg Pak. 2019 Dec;29(12):1193-1198. doi: 10.29271/jcpsp.2019.12.1193. J Coll Physicians Surg Pak. 2019. PMID: 31839094
A double-chambered right ventricle (DCRV) is a rare congenital heart defect. The clinical features of DCRV, especially in the pediatric population, have not been sufficiently elaborated. ...This systematic review showed a higher prevalence of symptomatic pati …
A double-chambered right ventricle (DCRV) is a rare congenital heart defect. The clinical features of DCRV, especially …
The hemi-Fontan operation.
Jacobs ML, Pourmoghadam KK. Jacobs ML, et al. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2003;6:90-7. doi: 10.1053/pcsu.2003.50007. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2003. PMID: 12740775 Review.
In hearts with a functional single ventricle, cavity volume and myocardial muscle mass increase as a consequence of the excessive volume load associated with parallel pulmonary and systemic circulations. ...The hemi-Fontan procedure includes association of the superior ven …
In hearts with a functional single ventricle, cavity volume and myocardial muscle mass increase as a consequence of the excessive vol …
Double-chambered right ventricle: a review.
Loukas M, Housman B, Blaak C, Kralovic S, Tubbs RS, Anderson RH. Loukas M, et al. Cardiovasc Pathol. 2013 Nov-Dec;22(6):417-23. doi: 10.1016/j.carpath.2013.03.004. Epub 2013 May 20. Cardiovasc Pathol. 2013. PMID: 23701985 Review.
A double-chambered right ventricle is a rare heart defect in which the right ventricle is separated into a high-pressure proximal and low-pressure distal chamber. ...It can be caused by the presence of anomalous muscle tissue, hypertrophy of the endogenous tr …
A double-chambered right ventricle is a rare heart defect in which the right ventricle is separated into a high-pressur …
Impact of Era, Type of Isomerism, and Ventricular Morphology on Survival in Heterotaxy: Implications for Therapeutic Management.
Loomba RS, Nijhawan K, Anderson R. Loomba RS, et al. World J Pediatr Congenit Heart Surg. 2016 Jan;7(1):54-62. doi: 10.1177/2150135115601831. World J Pediatr Congenit Heart Surg. 2016. PMID: 26714995 Review.
This was done for all patients, those born in a more recent era, those with right and left isomerism, and those with biventricular or functionally univentricular hearts. ...Those with left isomerism tended to have a survival benefit compared to those with right …
This was done for all patients, those born in a more recent era, those with right and left isomerism, and those with biventricular or …
7,198 results