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

Year Number of Results
1962 1
1964 1
1965 3
1966 1
1967 1
1968 5
1969 3
1970 2
1971 4
1972 4
1973 10
1974 2
1975 7
1976 4
1977 2
1978 6
1979 6
1980 5
1981 6
1982 6
1983 5
1984 5
1985 3
1986 4
1987 10
1988 12
1989 15
1990 10
1991 12
1992 11
1993 22
1994 23
1995 30
1996 30
1997 25
1998 28
1999 17
2000 26
2001 26
2002 25
2003 18
2004 25
2005 32
2006 30
2007 34
2008 40
2009 39
2010 36
2011 43
2012 40
2013 41
2014 50
2015 52
2016 60
2017 28
2018 22
2019 37
2020 40
2021 38
2022 35
2023 24
2024 14

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1,114 results

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Page 1
Pathophysiology and Pathogenesis of Marfan Syndrome.
Zeigler SM, Sloan B, Jones JA. Zeigler SM, et al. Adv Exp Med Biol. 2021;1348:185-206. doi: 10.1007/978-3-030-80614-9_8. Adv Exp Med Biol. 2021. PMID: 34807420 Free PMC article. Review.
Marfan syndrome (MFS) is a systemic connective tissue disorder that is inherited in an autosomal dominant pattern with variable penetrance. ...The present chapter will focus on the pathophysiology and clinical treatment of Marfan syndrome, providing an …
Marfan syndrome (MFS) is a systemic connective tissue disorder that is inherited in an autosomal dominant pattern with variabl …
Marfan syndrome.
Milewicz DM, Braverman AC, De Backer J, Morris SA, Boileau C, Maumenee IH, Jondeau G, Evangelista A, Pyeritz RE. Milewicz DM, et al. Nat Rev Dis Primers. 2021 Sep 2;7(1):64. doi: 10.1038/s41572-021-00298-7. Nat Rev Dis Primers. 2021. PMID: 34475413 Free PMC article. Review.
Marfan syndrome (MFS) is an autosomal dominant, age-related but highly penetrant condition with substantial intrafamilial and interfamilial variability. ...
Marfan syndrome (MFS) is an autosomal dominant, age-related but highly penetrant condition with substantial intrafamilial and …
Marfan's syndrome: an overview.
Yuan SM, Jing H. Yuan SM, et al. Sao Paulo Med J. 2010 Dec;128(6):360-6. doi: 10.1590/s1516-31802010000600009. Sao Paulo Med J. 2010. PMID: 21308160 Free PMC article. Review.
Marfan's syndrome is an autosomal dominant condition with an estimated prevalence of one in 10,000 to 20,000 individuals. ...Aortic root dilation and mitral valve prolapse are the main presentations among the cardiovascular malformations of Marfan's syndro …
Marfan's syndrome is an autosomal dominant condition with an estimated prevalence of one in 10,000 to 20,000 individuals. ...A …
Marfan's syndrome.
Judge DP, Dietz HC. Judge DP, et al. Lancet. 2005 Dec 3;366(9501):1965-76. doi: 10.1016/S0140-6736(05)67789-6. Lancet. 2005. PMID: 16325700 Free PMC article. Review.
Marfan's syndrome is a systemic disorder of connective tissue caused by mutations in the extracellular matrix protein fibrillin 1. ...Insights derived from studying this mendelian disorder are anticipated to have relevance for more common and non-syndromic presentat …
Marfan's syndrome is a systemic disorder of connective tissue caused by mutations in the extracellular matrix protein fibrilli …
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 …
FBN1: The disease-causing gene for Marfan syndrome and other genetic disorders.
Sakai LY, Keene DR, Renard M, De Backer J. Sakai LY, et al. Gene. 2016 Oct 10;591(1):279-291. doi: 10.1016/j.gene.2016.07.033. Epub 2016 Jul 18. Gene. 2016. PMID: 27437668 Free PMC article. Review.
Fibrillin microfibrils are morphologically distinctive fibrils, present in all connective tissues and assembled into tissue-specific architectural frameworks. FBN1 is the causative gene for Marfan syndrome, an inherited disorder of connective tissue whose major feat …
Fibrillin microfibrils are morphologically distinctive fibrils, present in all connective tissues and assembled into tissue-specific archite …
[Latest advances in the diagnosis and treatment of Marfan syndrome].
Yang ST, Luo F. Yang ST, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2022 Jul 15;24(7):826-831. doi: 10.7499/j.issn.1008-8830.2203099. Zhongguo Dang Dai Er Ke Za Zhi. 2022. PMID: 35894201 Free PMC article. Review. Chinese.
Marfan syndrome (MFS) is a multisystem connective tissue disease with autosomal dominant inheritance. ...
Marfan syndrome (MFS) is a multisystem connective tissue disease with autosomal dominant inheritance. ...
Marfan syndrome and aortic involvement: a narrative review.
Carbone RG, Monselise A, Puppo F. Carbone RG, et al. Eur Rev Med Pharmacol Sci. 2023 Sep;27(17):8218-8224. doi: 10.26355/eurrev_202309_33582. Eur Rev Med Pharmacol Sci. 2023. PMID: 37750650 Free article. Review.
Marfan syndrome (MFS) is a systemic connective tissue disease that commonly and most severely affects the ocular, skeletal, and cardiovascular systems. The aim of the manuscript is to review the aortic involvement and complications in MFS, including aortal dissectio …
Marfan syndrome (MFS) is a systemic connective tissue disease that commonly and most severely affects the ocular, skeletal, an …
Marfan syndrome.
Spencer M. Spencer M. Nursing. 2024 Apr 1;54(4):19-25. doi: 10.1097/01.NURSE.0001007604.09204.9a. Epub 2024 Mar 22. Nursing. 2024. PMID: 38517496 Review.
This article provides a comprehensive review of Marfan Syndrome (MFS), covering its epidemiology, etiology, clinical presentations, diagnostics, complications, and treatment modalities. ...
This article provides a comprehensive review of Marfan Syndrome (MFS), covering its epidemiology, etiology, clinical presentat …
Aortopathy in pregnancy.
Curtis SL, Swan L. Curtis SL, et al. Heart. 2022 Nov 10;108(23):1851-1857. doi: 10.1136/heartjnl-2021-319828. Heart. 2022. PMID: 35144984 Review.
1,114 results