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
1967 2
1968 1
1969 1
1970 3
1971 4
1972 1
1973 4
1975 8
1976 6
1977 3
1978 2
1979 6
1980 4
1981 6
1982 6
1983 6
1984 9
1985 8
1986 10
1987 10
1988 3
1989 10
1990 14
1991 14
1992 13
1993 18
1994 27
1995 29
1996 24
1997 36
1998 37
1999 32
2000 31
2001 27
2002 44
2003 43
2004 41
2005 48
2006 57
2007 63
2008 67
2009 74
2010 76
2011 76
2012 93
2013 113
2014 99
2015 106
2016 110
2017 99
2018 106
2019 132
2020 127
2021 137
2022 104
2023 73
2024 37

Text availability

Article attribute

Article type

Publication date

Search Results

2,037 results

Results by year

Filters applied: . Clear all
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. ...
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 …
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 …
Connective Tissue Disorders in Pregnancy.
Ryan SL, Bhattacharyya S. Ryan SL, et al. Neurol Clin. 2019 Feb;37(1):121-129. doi: 10.1016/j.ncl.2018.09.006. Neurol Clin. 2019. PMID: 30470271 Review.
We review the neurologic complications and changes with pregnancy for systemic lupus erythematosus, Sjogren syndrome, idiopathic inflammatory myopathy, and Marfan syndrome....
We review the neurologic complications and changes with pregnancy for systemic lupus erythematosus, Sjogren syndrome, idiopathic inflammator …
Orthopaedic Conditions Associated with Aneurysms.
Marrache M, Byers PH, Sponseller PD. Marrache M, et al. JBJS Rev. 2020 Jun;8(6):e0122. doi: 10.2106/JBJS.RVW.19.00122. JBJS Rev. 2020. PMID: 33006458 Review.
Early recognition of the conditions associated with aneurysms can lead to effective treatment and minimize risks of morbidity and death. Marfan syndrome is characterized by abnormal fibrillin-1 protein and has a broad range of skeletal manifestations, including scol …
Early recognition of the conditions associated with aneurysms can lead to effective treatment and minimize risks of morbidity and death. …
Genotype-phenotype spectrum and prognosis of early-onset Marfan syndrome.
Kemezyte A, Gegieckiene R, Burnyte B. Kemezyte A, et al. BMC Pediatr. 2023 Oct 28;23(1):539. doi: 10.1186/s12887-023-04357-8. BMC Pediatr. 2023. PMID: 37891508 Free PMC article.
BACKGROUND: Marfan syndrome is a genetic connective tissue disorder affecting skeletal, ocular, and cardiovascular organ systems. ...METHODS: We analyzed clinical and genetic data of a new patient with early-onset Marfan syndrome together with 51 previ …
BACKGROUND: Marfan syndrome is a genetic connective tissue disorder affecting skeletal, ocular, and cardiovascular organ syste …
Thoracic and Thoracoabdominal Aneurysms: Etiology, Epidemiology, and Natural History.
Downey RT, Aron RA. Downey RT, et al. Anesthesiol Clin. 2022 Dec;40(4):671-683. doi: 10.1016/j.anclin.2022.08.011. Epub 2022 Oct 8. Anesthesiol Clin. 2022. PMID: 36328622 Review.
Most thoracic aneurysms grow slowly over time and factors that accelerate growth rate include dissection, aneurysm size, bicuspid valve disease, and Marfan syndrome. Size cutoffs where complications occur determine when surgery or intervention should be considered.. …
Most thoracic aneurysms grow slowly over time and factors that accelerate growth rate include dissection, aneurysm size, bicuspid valve dise …
Sudden death due to aortic pathology.
Papagiannis J. Papagiannis J. Cardiol Young. 2017 Jan;27(S1):S36-S42. doi: 10.1017/S1047951116002213. Cardiol Young. 2017. PMID: 28084959 Review.
Individuals at risk include those having any of a variety of conditions in which structural weakness of the ascending aorta predisposes to pathological dilation under prolonged periods of increased wall stress. These conditions include Marfan syndrome, Loeys-Dietz s …
Individuals at risk include those having any of a variety of conditions in which structural weakness of the ascending aorta predisposes to p …
Molecular pathogenesis of Marfan syndrome.
Ramachandra CJ, Mehta A, Guo KW, Wong P, Tan JL, Shim W. Ramachandra CJ, et al. Int J Cardiol. 2015;187:585-91. doi: 10.1016/j.ijcard.2015.03.423. Epub 2015 Mar 31. Int J Cardiol. 2015. PMID: 25863307 Review.
Marfan syndrome (MFS) is a genetic disorder that affects multiple organs. ...
Marfan syndrome (MFS) is a genetic disorder that affects multiple organs. ...
The corneoscleral shape in Marfan syndrome.
Vanhonsebrouck E, Consejo A, Coucke PJ, Leroy BP, Kreps EO. Vanhonsebrouck E, et al. Acta Ophthalmol. 2021 Jun;99(4):405-410. doi: 10.1111/aos.14636. Epub 2020 Sep 30. Acta Ophthalmol. 2021. PMID: 32996688 Free article.
PURPOSE: To investigate the corneoscleral shape in Marfan syndrome (MFS) patients. METHODS: Thirty eyes of 15 participants with molecularly proven MFS were included in this prospective, cross-sectional study. ...In MFS eyes, scleral asymmetry was not found to be cor …
PURPOSE: To investigate the corneoscleral shape in Marfan syndrome (MFS) patients. METHODS: Thirty eyes of 15 participants wit …
2,037 results