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
1968 1
1975 1
1977 1
1989 3
1996 1
1998 1
2000 1
2002 1
2003 1
2005 1
2006 1
2007 4
2008 3
2009 2
2011 3
2012 1
2013 1
2015 3
2018 2
2019 4
2020 2
2021 4
2022 5
2023 2
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

45 results

Results by year

Filters applied: . Clear all
Page 1
Recommendations for the Use of Echocardiography in the Evaluation of Rheumatic Heart Disease: A Report from the American Society of Echocardiography.
Pandian NG, Kim JK, Arias-Godinez JA, Marx GR, Michelena HI, Chander Mohan J, Ogunyankin KO, Ronderos RE, Sade LE, Sadeghpour A, Sengupta SP, Siegel RJ, Shu X, Soesanto AM, Sugeng L, Venkateshvaran A, Campos Vieira ML, Little SH. Pandian NG, et al. J Am Soc Echocardiogr. 2023 Jan;36(1):3-28. doi: 10.1016/j.echo.2022.10.009. Epub 2022 Nov 23. J Am Soc Echocardiogr. 2023. PMID: 36428195
Echocardiography is the most important diagnostic tool in recognizing this preventable and treatable disease and plays an invaluable role in detecting the presence of subclinical disease needing prompt therapy or follow-up assessment. ...The mitral val …
Echocardiography is the most important diagnostic tool in recognizing this preventable and treatable disease and plays an invaluable …
The MAP3K7 gene: Further delineation of clinical characteristics and genotype/phenotype correlations.
van Woerden GM, Senden R, de Konink C, Trezza RA, Baban A, Bassetti JA, van Bever Y, Bird LM, van Bon BW, Brooks AS, Guan Q, Klee EW, Marcelis C, Rosado JM, Schimmenti LA, Shikany AR, Terhal PA, Nicole Weaver K, Wessels MW, van Wieringen H, Hurst AC, Gooch CF, Steindl K, Joset P, Rauch A, Tartaglia M, Niceta M, Elgersma Y, Demirdas S. van Woerden GM, et al. Hum Mutat. 2022 Oct;43(10):1377-1395. doi: 10.1002/humu.24425. Epub 2022 Jul 29. Hum Mutat. 2022. PMID: 35730652 Free PMC article.
Mutationsin the MAP3K7 gene have been linked to two distinct disorders: frontometaphyseal dysplasia type 2 (FMD2) and cardiospondylocarpofacial syndrome (CSCF). ...Additionally, patients with pathogenic mutations in MAP3K7 are at risk for (severe) cardiac disease, h …
Mutationsin the MAP3K7 gene have been linked to two distinct disorders: frontometaphyseal dysplasia type 2 (FMD2) and cardiospondyloc …
Aortopathies: etiologies, genetics, differential diagnosis, prognosis and management.
Paterick TE, Humphries JA, Ammar KA, Jan MF, Loberg R, Bush M, Khandheria BK, Tajik AJ. Paterick TE, et al. Am J Med. 2013 Aug;126(8):670-8. doi: 10.1016/j.amjmed.2013.01.029. Epub 2013 Jun 22. Am J Med. 2013. PMID: 23800581 Review.
Aortic root and ascending aortic dimensions should be measured routinely with echocardiography. Pharmacologic therapy may reduce the rate of progression. Timing of surgical intervention is guided by indexed aortic size and rate of change of aortic root and ascending aorta …
Aortic root and ascending aortic dimensions should be measured routinely with echocardiography. Pharmacologic therapy may reduce the …
Stepwise approach for diagnosis and management of Takotsubo syndrome with cardiac imaging tools.
Santoro F, Mallardi A, Leopizzi A, Vitale E, Stiermaier T, Trambaiolo P, Di Biase M, Eitel I, Brunetti ND. Santoro F, et al. Heart Fail Rev. 2022 Mar;27(2):545-558. doi: 10.1007/s10741-021-10205-7. Epub 2022 Jan 18. Heart Fail Rev. 2022. PMID: 35040000 Review.
Takotsubo syndrome is featured by transient left ventricle dysfunction in the absence of significant coronary artery disease, mainly triggered by emotional or physical stress. Its clinical presentation is similar to acute coronary syndrome; therefore, cardiac imaging tools …
Takotsubo syndrome is featured by transient left ventricle dysfunction in the absence of significant coronary artery disease, mainly …
Secondary pulmonary hypertension--diagnosis and management.
Carbone R, Bossone E, Bottino G, Monselise A, Rubenfire M. Carbone R, et al. Eur Rev Med Pharmacol Sci. 2005 Nov-Dec;9(6):331-42. Eur Rev Med Pharmacol Sci. 2005. PMID: 16479737 Review.
Secondary pulmonary hypertension (SPHtn) is generally attributable to abnormalities in structure or function of the heart or lung parenchyma. ...We will review the pathophysiology, diagnostic tools, and treatment strategies in SPHtn with an emphasis on cor pulmonale associ …
Secondary pulmonary hypertension (SPHtn) is generally attributable to abnormalities in structure or function of the heart or lung par …
Floppy mitral valve/mitral valve prolapse: A complex entity with multiple genotypes and phenotypes.
Boudoulas KD, Pitsis AA, Mazzaferri EL, Gumina RJ, Triposkiadis F, Boudoulas H. Boudoulas KD, et al. Prog Cardiovasc Dis. 2020 May-Jun;63(3):308-326. doi: 10.1016/j.pcad.2020.03.004. Epub 2020 Mar 19. Prog Cardiovasc Dis. 2020. PMID: 32201287 Review.
Floppy mitral valve/mitral valve prolapse (FMV/MVP) is a common valvular abnormality affecting 2% to 3% of the general population. ...FMV/MVP can be familial or sporadic, isolated (called non-syndromic) or as a part of a well-defined syndrome of heritable connective …
Floppy mitral valve/mitral valve prolapse (FMV/MVP) is a common valvular abnormality affecting 2% to 3% of the general populat …
Pectus excavatum: historical background, clinical picture, preoperative evaluation and criteria for operation.
Kelly RE Jr. Kelly RE Jr. Semin Pediatr Surg. 2008 Aug;17(3):181-93. doi: 10.1053/j.sempedsurg.2008.03.002. Semin Pediatr Surg. 2008. PMID: 18582824 Review.
Indications for surgical treatment include two or more of the following: a severe, symptomatic deformity; progression of deformity; paradoxical respiratory chest wall motion; computer tomography scan with a pectus index greater than 3.25; cardiac compression/displacement and/or p …
Indications for surgical treatment include two or more of the following: a severe, symptomatic deformity; progression of deformity; paradoxi …
Genotype-cardiac phenotype correlations in a large single-center cohort of patients affected by RASopathies: Clinical implications and literature review.
Leoni C, Blandino R, Delogu AB, De Rosa G, Onesimo R, Verusio V, Marino MV, Lanza GA, Rigante D, Tartaglia M, Zampino G. Leoni C, et al. Am J Med Genet A. 2022 Feb;188(2):431-445. doi: 10.1002/ajmg.a.62529. Epub 2021 Oct 13. Am J Med Genet A. 2022. PMID: 34643321 Review.
Congenital heart disease (CHD) and hypertrophic cardiomyopathy (HCM) are common features in patients affected by RASopathies. ...Other cardiac anomalies less reported until recently in this population, such as isolated functional and structural mitral valve diseases …
Congenital heart disease (CHD) and hypertrophic cardiomyopathy (HCM) are common features in patients affected by RASopathies. ...Othe …
Neonatal cardiac distress. A practical approach to recognition, diagnosis, and management.
Cayler GG. Cayler GG. Calif Med. 1968 Mar;108(3):188-200. Calif Med. 1968. PMID: 4867629 Free PMC article. Review.
The death rate among neonates with cardiovascular disease is 50 percent during the first six months, with the majority dying during the first month. ...Lesions such as hypoplasia of the left heart, transposition of the great arteries, endocardial fibroelastosis, pulmonary …
The death rate among neonates with cardiovascular disease is 50 percent during the first six months, with the majority dying during t …
Cardiac disease in patients with mucopolysaccharidosis: presentation, diagnosis and management.
Braunlin EA, Harmatz PR, Scarpa M, Furlanetto B, Kampmann C, Loehr JP, Ponder KP, Roberts WC, Rosenfeld HM, Giugliani R. Braunlin EA, et al. J Inherit Metab Dis. 2011 Dec;34(6):1183-97. doi: 10.1007/s10545-011-9359-8. Epub 2011 Jul 9. J Inherit Metab Dis. 2011. PMID: 21744090 Free PMC article. Review.
The mucopolysaccharidoses (MPSs) are inherited lysosomal storage disorders caused by the absence of functional enzymes that contribute to the degradation of glycosaminoglycans (GAGs). ...The optimal technique for evaluation of coronary artery involvement remains unsettled. …
The mucopolysaccharidoses (MPSs) are inherited lysosomal storage disorders caused by the absence of functional enzymes that contribut …
45 results