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
1945 1
1946 2
1947 2
1948 3
1949 1
1950 1
1951 5
1952 9
1953 11
1954 12
1955 12
1956 5
1957 8
1958 9
1959 7
1960 3
1961 11
1962 10
1963 19
1964 29
1965 21
1966 15
1967 31
1968 29
1969 35
1970 18
1971 29
1972 27
1973 41
1974 23
1975 38
1976 30
1977 27
1978 28
1979 34
1980 28
1981 29
1982 34
1983 30
1984 31
1985 36
1986 40
1987 33
1988 32
1989 44
1990 42
1991 52
1992 38
1993 51
1994 70
1995 74
1996 60
1997 67
1998 72
1999 72
2000 59
2001 71
2002 63
2003 79
2004 84
2005 83
2006 109
2007 125
2008 132
2009 125
2010 143
2011 156
2012 150
2013 183
2014 185
2015 201
2016 170
2017 176
2018 180
2019 207
2020 202
2021 223
2022 197
2023 176
2024 86

Text availability

Article attribute

Article type

Publication date

Search Results

4,637 results

Results by year

Filters applied: . Clear all
Page 1
Should We Move Up the Clock on Preventive Intervention in Marfan's Disease?
Robicsek F. Robicsek F. Thorac Cardiovasc Surg. 2020 Jun;68(4):328-329. doi: 10.1055/s-0039-1678680. Epub 2019 Feb 28. Thorac Cardiovasc Surg. 2020. PMID: 30818410
Gradual dilatation of the ascending aorta is a common phenomenon in patients with Marfan's disease, which often leads to dissection and rupture. It is estimated that around two-thirds of the patients either die or require major surgery before the age of 42 ye …
Gradual dilatation of the ascending aorta is a common phenomenon in patients with Marfan's disease, which often leads t …
Aortic root disease in athletes: aortic root dilation, anomalous coronary artery, bicuspid aortic valve, and Marfan's syndrome.
Yim ES. Yim ES. Sports Med. 2013 Aug;43(8):721-32. doi: 10.1007/s40279-013-0057-6. Sports Med. 2013. PMID: 23674060 Review.
These cases have attracted attention in sports medicine to the importance of aortic root disease in athletes. In addition to aortic root dilation, other forms of aortic disease include anomalous coronary artery, bicuspid aortic valve, and Marfan's synd …
These cases have attracted attention in sports medicine to the importance of aortic root disease in athletes. In addition to aortic r …
Marfan's disease.
Olsen EG. Olsen EG. Pathol Microbiol (Basel). 1975;43(2-O):120-3. Pathol Microbiol (Basel). 1975. PMID: 1236714 No abstract available.
Cardiovascular disease in Marfan's syndrome.
MARVEL RJ, GENOVESE PD. MARVEL RJ, et al. Am Heart J. 1951 Dec;42(6):814-25. doi: 10.1016/0002-8703(51)90054-3. Am Heart J. 1951. PMID: 14885078 No abstract available.
Cardiovascular disease in pregnancy.
Oakley CM. Oakley CM. Can J Cardiol. 1990 May;6 Suppl B:3B-9B. Can J Cardiol. 1990. PMID: 2188716 Review.
The practical management of the pregnant patient with various concomitant heart conditions (congenital heart disease, pulmonary hypertension, rheumatic heart disease, anticoagulants and artificial valves, constrictive pericarditis, kyphoscoliosis, Marfan's …
The practical management of the pregnant patient with various concomitant heart conditions (congenital heart disease, pulmonary hyper …
[Respiratory manifestations of Marfan's syndrome].
Neuville M, Jondeau G, Crestani B, Taillé C. Neuville M, et al. Rev Mal Respir. 2015 Feb;32(2):173-81. doi: 10.1016/j.rmr.2014.06.030. Epub 2014 Nov 6. Rev Mal Respir. 2015. PMID: 25765122 Review. French.
Marfan's syndrome is a rare genetic disorder caused by a mutation of the gene FBN1, coding for the protein fibrillin-1. ...Surgery may be required (using the Nuss procedure) in case of cardiovascular or psychological symptoms. Marfan's syndrome is freq …
Marfan's syndrome is a rare genetic disorder caused by a mutation of the gene FBN1, coding for the protein fibrillin-1. ...Sur …
Marfan's syndrome.
ROSE D. ROSE D. Br J Ophthalmol. 1959 Apr;43(4):252. doi: 10.1136/bjo.43.4.252. Br J Ophthalmol. 1959. PMID: 13638521 Free PMC article. No abstract available.
Genetically Triggered Thoracic Aortic Disease: Who Should be Tested?
Duarte VE, Yousefzai R, Singh MN. Duarte VE, et al. Methodist Debakey Cardiovasc J. 2023 Mar 7;19(2):24-28. doi: 10.14797/mdcvj.1218. eCollection 2023. Methodist Debakey Cardiovasc J. 2023. PMID: 36910552 Free PMC article. Review.
Up to 25% of patients with thoracic aortic disease have an underlying Mendelian pathogenic variant. This is a heterogeneous group of disorders known as heritable thoracic aortic diseases (HTAD). ...Recently released 2022 American College of Cardiology/American Heart …
Up to 25% of patients with thoracic aortic disease have an underlying Mendelian pathogenic variant. This is a heterogeneous group of …
Oxidative Stress-Related Susceptibility to Aneurysm in Marfan's Syndrome.
Rysz J, Gluba-Brzózka A, Rokicki R, Franczyk B. Rysz J, et al. Biomedicines. 2021 Sep 6;9(9):1171. doi: 10.3390/biomedicines9091171. Biomedicines. 2021. PMID: 34572356 Free PMC article. Review.
The involvement of highly reactive oxygen-derived free radicals (ROS) in the genesis and progression of various cardiovascular diseases, including arrhythmias, aortic dilatation, aortic dissection, left ventricular hypertrophy, coronary arterial disease and congesti …
The involvement of highly reactive oxygen-derived free radicals (ROS) in the genesis and progression of various cardiovascular diseases …
Dupuytren's disease in Marfan's syndrome.
Rennie WJ, Rangan A. Rennie WJ, et al. J Hand Surg Br. 1999 Dec;24(6):752-3. doi: 10.1054/jhsb.1999.0247. J Hand Surg Br. 1999. PMID: 10672821
We report a case of histologically confirmed Dupuytren's disease of the hand in a young man with Marfan's syndrome....
We report a case of histologically confirmed Dupuytren's disease of the hand in a young man with Marfan's syndrome....
4,637 results