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

Year Number of Results
1990 1
1992 5
1993 4
1994 3
1995 3
1996 2
1997 4
1998 13
1999 10
2000 8
2001 6
2002 8
2003 10
2004 9
2005 7
2006 17
2007 14
2008 25
2009 26
2010 25
2011 32
2012 45
2013 54
2014 44
2015 47
2016 36
2017 23
2018 46
2019 46
2020 36
2021 30
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201 results
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Page 1
The Many Lives of a Complex Marfan Syndrome Patient: Staged Therapeutic Decisions.
Militaru C, Moldovan H, Fetecău B, Popescu BA, Pólos M, Szabolcs Z, Jurcuţ R. Militaru C, et al. Among authors: szabolcs z. JACC Case Rep. 2020 Dec 2;3(2):236-241. doi: 10.1016/j.jaccas.2020.09.041. eCollection 2021 Feb. JACC Case Rep. 2020. PMID: 34317509 Free PMC article.
We present a complex Marfan case, with previous type A aortic dissection, subsequent progressing aortic arch aneurysm, type B chronic aortic dissection, and Barlow disease with severe mitral regurgitation, all expressions of the same phenotype, all needing staged complex s …
We present a complex Marfan case, with previous type A aortic dissection, subsequent progressing aortic arch aneurysm, type B chronic …
[Marfan syndrome and related disorders].
Eliahou L, Milleron O, Jondeau G. Eliahou L, et al. Among authors: jondeau g. Rev Prat. 2020 Nov;70(9):1005-1009. Rev Prat. 2020. PMID: 33739763 French.
Marfan syndrome and related disorders. Marfan syndrome is an autosomal dominant disease, affecting about 1/5000 persons. ...
Marfan syndrome and related disorders. Marfan syndrome is an autosomal dominant disease, affecting about 1/5000 persons. ...
Staged hybrid repair of type II thoracoabdominal aneurysms.
Pellenc Q, Roussel A, Senemaud J, Cerceau P, Iquille J, Boitet A, Leclere JB, Milleron O, Jondeau G, Castier Y. Pellenc Q, et al. Among authors: jondeau g. J Vasc Surg. 2021 Jul;74(1):20-27. doi: 10.1016/j.jvs.2020.12.049. Epub 2020 Dec 16. J Vasc Surg. 2021. PMID: 33340705
RESULTS: The mean patient age was 48 15 years. Of the 14 patients, 5 had had Marfan syndrome (36%) and 6 had undergone previous aortic arch repair (43%). ...
RESULTS: The mean patient age was 48 15 years. Of the 14 patients, 5 had had Marfan syndrome (36%) and 6 had undergone previous aorti …
Myocardial disease and ventricular arrhythmia in Marfan syndrome: a prospective study.
Muiño-Mosquera L, De Wilde H, Devos D, Babin D, Jordaens L, Demolder A, De Groote K, De Wolf D, De Backer J. Muiño-Mosquera L, et al. Among authors: de backer j. Orphanet J Rare Dis. 2020 Oct 23;15(1):300. doi: 10.1186/s13023-020-01581-8. Orphanet J Rare Dis. 2020. PMID: 33097072 Free PMC article.
BACKGROUND: Aortic root dilatation and-dissection and mitral valve prolapse are established cardiovascular manifestations in Marfan syndrome (MFS). Heart failure and arrhythmic sudden cardiac death have emerged as additional causes of morbidity and mortality. ...RESULTS: C …
BACKGROUND: Aortic root dilatation and-dissection and mitral valve prolapse are established cardiovascular manifestations in Marfan s …
Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvement.
Stengl R, Bors A, Ágg B, Pólos M, Matyas G, Molnár MJ, Fekete B, Csabán D, Andrikovics H, Merkely B, Radovits T, Szabolcs Z, Benke K. Stengl R, et al. Among authors: szabolcs z. Orphanet J Rare Dis. 2020 Oct 15;15(1):290. doi: 10.1186/s13023-020-01569-4. Orphanet J Rare Dis. 2020. PMID: 33059708 Free PMC article.
BACKGROUND: Marfan syndrome (MFS) is a systemic connective tissue disorder with life-threatening manifestations affecting the ascending aorta. ...
BACKGROUND: Marfan syndrome (MFS) is a systemic connective tissue disorder with life-threatening manifestations affecting the ascendi …
Effects of fibrillin mutations on the behavior of heart muscle cells in Marfan syndrome.
Aalders J, Léger L, Van der Meeren L, Van den Vreken N, Skirtach AG, Sinha S, De Backer J, van Hengel J. Aalders J, et al. Among authors: de backer j. Sci Rep. 2020 Oct 7;10(1):16756. doi: 10.1038/s41598-020-73802-w. Sci Rep. 2020. PMID: 33028885 Free PMC article.
Marfan syndrome (MFS) is a systemic disorder of connective tissue caused by pathogenic variants in the fibrillin-1 (FBN1) gene. ...
Marfan syndrome (MFS) is a systemic disorder of connective tissue caused by pathogenic variants in the fibrillin-1 (FBN1) gene. ...
Myocardial Function, Heart Failure and Arrhythmia in Marfan Syndrome: A Systematic Literature Review.
Demolder A, von Kodolitsch Y, Muiño-Mosquera L, De Backer J. Demolder A, et al. Among authors: von kodolitsch y, de backer j. Diagnostics (Basel). 2020 Sep 25;10(10):751. doi: 10.3390/diagnostics10100751. Diagnostics (Basel). 2020. PMID: 32992882 Free PMC article. Review.
Marfan syndrome (MFS) is a heritable systemic connective tissue disease with important cardiovascular involvement, including aortic root dilatation and mitral valve prolapse. ...
Marfan syndrome (MFS) is a heritable systemic connective tissue disease with important cardiovascular involvement, including aortic r
A genotype-first approach to exploring Mendelian cardiovascular traits with clear external manifestations.
Wenger BM, Patel N, Lui M, Moscati A, Do R, Stewart DR, Tartaglia M, Muiño-Mosquera L, De Backer J, Kontorovich AR, Gelb BD. Wenger BM, et al. Among authors: de backer j. Genet Med. 2021 Jan;23(1):94-102. doi: 10.1038/s41436-020-00973-2. Epub 2020 Sep 29. Genet Med. 2021. PMID: 32989268 Free PMC article.
PURPOSE: The purpose of this study is to use a genotype-first approach to explore highly penetrant, autosomal dominant cardiovascular diseases with external features, the RASopathies and Marfan syndrome (MFS), using biobank data. METHODS: This study uses exome sequencing a …
PURPOSE: The purpose of this study is to use a genotype-first approach to explore highly penetrant, autosomal dominant cardiovascular diseas …
Spontaneous Right Ventricular Pseudoaneurysms and Increased Arrhythmogenicity in a Mouse Model of Marfan Syndrome.
Steijns F, Renard M, Vanhomwegen M, Vermassen P, Desloovere J, Raedt R, Larsen LE, Tóth MI, De Backer J, Sips P. Steijns F, et al. Among authors: de backer j. Int J Mol Sci. 2020 Sep 24;21(19):7024. doi: 10.3390/ijms21197024. Int J Mol Sci. 2020. PMID: 32987703 Free PMC article.
Patients with Marfan syndrome (MFS), a connective tissue disorder caused by pathogenic variants in the gene encoding the extracellular matrix protein fibrillin-1, have an increased prevalence of primary cardiomyopathy, arrhythmias, and sudden cardiac death. ...
Patients with Marfan syndrome (MFS), a connective tissue disorder caused by pathogenic variants in the gene encoding the extracellula …
When should a rare inherited connective tissue disorder be suspected in bicuspid aortic valve by primary-care internists and cardiologists? Proposal of a score.
Pepe G, Giusti B, Colonna S, Fugazzaro MP, Sticchi E, De Cario R, Kura A, Pratelli E, Melchiorre D, Nistri S. Pepe G, et al. Intern Emerg Med. 2021 Apr;16(3):609-615. doi: 10.1007/s11739-020-02458-1. Epub 2020 Sep 19. Intern Emerg Med. 2021. PMID: 32949381 Free PMC article.
Ninety-eight BAVs without ectopia lentis or personal/family history of aortic dissection were studied at the Marfan syndrome Tuscany Referral Center. Findings were compared with those detected in 84 Marfan patients matched for sex and age. ...Clustering of 3 of thes …
Ninety-eight BAVs without ectopia lentis or personal/family history of aortic dissection were studied at the Marfan syndrome Tuscany …
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