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

Year Number of Results
1968 1
1969 1
1970 1
1973 1
1976 2
1977 2
1980 2
1981 2
1982 3
1983 7
1984 4
1985 4
1986 5
1987 3
1988 5
1989 3
1990 8
1991 7
1992 8
1993 17
1994 11
1995 15
1996 12
1997 15
1998 19
1999 9
2000 16
2001 20
2002 19
2003 19
2004 21
2005 20
2006 25
2007 32
2008 29
2009 28
2010 42
2011 53
2012 45
2013 56
2014 58
2015 51
2016 60
2017 59
2018 46
2019 55
2020 61
2021 77
2022 47
2023 37
2024 24

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1,009 results

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Page 1
The revised Ghent nosology for the Marfan syndrome.
Loeys BL, Dietz HC, Braverman AC, Callewaert BL, De Backer J, Devereux RB, Hilhorst-Hofstee Y, Jondeau G, Faivre L, Milewicz DM, Pyeritz RE, Sponseller PD, Wordsworth P, De Paepe AM. Loeys BL, et al. J Med Genet. 2010 Jul;47(7):476-85. doi: 10.1136/jmg.2009.072785. J Med Genet. 2010. PMID: 20591885
The diagnosis of Marfan syndrome (MFS) relies on defined clinical criteria (Ghent nosology), outlined by international expert opinion to facilitate accurate recognition of this genetic aneurysm syndrome and to improve patient management and counselling. ...In absenc …
The diagnosis of Marfan syndrome (MFS) relies on defined clinical criteria (Ghent nosology), outlined by international expert …
The Musculoskeletal Manifestations of Marfan Syndrome: Diagnosis, Impact, and Management.
Pollock L, Ridout A, Teh J, Nnadi C, Stavroulias D, Pitcher A, Blair E, Wordsworth P, Vincent TL. Pollock L, et al. Curr Rheumatol Rep. 2021 Nov 26;23(11):81. doi: 10.1007/s11926-021-01045-3. Curr Rheumatol Rep. 2021. PMID: 34825999 Free PMC article. Review.
PURPOSE OF REVIEW: Marfan syndrome (MFS) is an autosomal dominant heritable disorder of fibrillin-1 (FBN1) with predominantly ocular, cardiovascular, and musculoskeletal manifestations that has a population prevalence of approximately 1 in 5-10,000 (Chiu et al. ...T …
PURPOSE OF REVIEW: Marfan syndrome (MFS) is an autosomal dominant heritable disorder of fibrillin-1 (FBN1) with predominantly …
Meester-Loeys Syndrome.
Meester JAN, De Kinderen P, Verstraeten A, Loeys B. Meester JAN, et al. Adv Exp Med Biol. 2021;1348:265-272. doi: 10.1007/978-3-030-80614-9_12. Adv Exp Med Biol. 2021. PMID: 34807424
More specifically, the cardiovascular, skeletal, craniofacial, cutaneous and neurological systems are affected. Clear clinical overlap with Marfan syndrome and Loeys-Dietz syndrome is observed. Aortic dissections occur typically at young ages and are most oft …
More specifically, the cardiovascular, skeletal, craniofacial, cutaneous and neurological systems are affected. Clear clinical overlap with …
Evaluating the quality of Marfan genotype-phenotype correlations in existing FBN1 databases.
Groth KA, Von Kodolitsch Y, Kutsche K, Gaustadnes M, Thorsen K, Andersen NH, Gravholt CH. Groth KA, et al. Genet Med. 2017 Jul;19(7):772-777. doi: 10.1038/gim.2016.181. Epub 2016 Dec 1. Genet Med. 2017. PMID: 27906200 Free article.
The Marfan score calculated for phenotype data from the records quantified variant associations with Marfan syndrome phenotype. We calculated a Marfan score for 1,283 variants, of which we confirmed the database diagnosis of Marfan syndrome …
The Marfan score calculated for phenotype data from the records quantified variant associations with Marfan syndrome ph …
Pharmacologic Management of Aneurysms.
Lindeman JH, Matsumura JS. Lindeman JH, et al. Circ Res. 2019 Feb 15;124(4):631-646. doi: 10.1161/CIRCRESAHA.118.312439. Circ Res. 2019. PMID: 30763216 Free PMC article. Review.
Similarly, the concept of pharmaceutical aorta stabilization in Marfan syndrome is supported by a wealth of promising studies in the murine models of Marfan syndrome-related aortapathy. Although some clinical studies report successful medical stabiliza …
Similarly, the concept of pharmaceutical aorta stabilization in Marfan syndrome is supported by a wealth of promising studies …
Recent Clinical Drug Trials Evidence in Marfan Syndrome and Clinical Implications.
Singh MN, Lacro RV. Singh MN, et al. Can J Cardiol. 2016 Jan;32(1):66-77. doi: 10.1016/j.cjca.2015.11.003. Epub 2015 Nov 10. Can J Cardiol. 2016. PMID: 26724512 Review.
Marfan syndrome is a genetic disorder of connective tissue with principal manifestations in the cardiovascular, ocular, and skeletal systems. ...For patients with Marfan syndrome without aortic dilation, the available evidence is less clear. ...
Marfan syndrome is a genetic disorder of connective tissue with principal manifestations in the cardiovascular, ocular, and sk …
Neurovascular manifestations of connective-tissue diseases: A review.
Kim ST, Brinjikji W, Lanzino G, Kallmes DF. Kim ST, et al. Interv Neuroradiol. 2016 Dec;22(6):624-637. doi: 10.1177/1591019916659262. Epub 2016 Aug 10. Interv Neuroradiol. 2016. PMID: 27511817 Free PMC article. Review.
In this report, we aim to understand the prevalence and occurrences of such neurovascular manifestations in four heritable connective tissue disorders: Marfan syndrome, Ehlers-Danlos syndrome, Neurofibromatosis Type 1, and Loeys-Dietz syndrome. We discuss the fact t …
In this report, we aim to understand the prevalence and occurrences of such neurovascular manifestations in four heritable connective tissue …
A clinical scoring system for early onset (neonatal) Marfan syndrome.
Zarate YA, Morris SA, Blackshare A, Algaze CA, Connor BS, Kim AJ, Yutzey KE, Miller EM, Weaver KN, Collins RT 2nd. Zarate YA, et al. Genet Med. 2022 Jul;24(7):1503-1511. doi: 10.1016/j.gim.2022.03.016. Epub 2022 Apr 14. Genet Med. 2022. PMID: 35420547 Free article.
PURPOSE: This study aimed to develop objective diagnostic criteria for early onset Marfan syndrome (eoMFS) to facilitate early diagnosis and timely interventions. ...CONCLUSION: Distinct from classical Marfan syndrome in phenotype and morbidity, eoMFS …
PURPOSE: This study aimed to develop objective diagnostic criteria for early onset Marfan syndrome (eoMFS) to facilitate early …
Intrinsic left ventricular impairment in Marfan syndrome: A systematic review and meta-analysis.
Xu H, Ma N, Guo R, Luo H, Zhang L, Liu D, Zang S, Zhao L, Zhang X, Qiao C. Xu H, et al. J Card Surg. 2021 Dec;36(12):4715-4721. doi: 10.1111/jocs.16019. Epub 2021 Sep 25. J Card Surg. 2021. PMID: 34562283 Review.
BACKGROUND: Intrinsic cardiac impairment in Marfan syndrome (MFS) has been explored in many clinical studies; however, their results have been inconsistent. ...Furthermore, Marfan patients showed a lower left ventricular ejection fraction than healthy people (MD: -2 …
BACKGROUND: Intrinsic cardiac impairment in Marfan syndrome (MFS) has been explored in many clinical studies; however, their r …
1,009 results