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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 3
1994 3
1995 1
1996 2
1997 4
1998 13
1999 8
2000 8
2001 4
2002 6
2003 8
2004 9
2005 6
2006 15
2007 14
2008 18
2009 20
2010 22
2011 31
2012 43
2013 49
2014 42
2015 39
2016 31
2017 22
2018 39
2019 39
2020 5
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Article type
Publication date

Search Results

425 results
Results by year
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Page 1
Loeys-Dietz syndrome.
Van Laer L, Dietz H, Loeys B. Van Laer L, et al. Among authors: loeys b. Adv Exp Med Biol. 2014;802:95-105. doi: 10.1007/978-94-007-7893-1_7. Adv Exp Med Biol. 2014. PMID: 24443023 Review.
Loeys-Dietz syndrome: a primer for diagnosis and management.
MacCarrick G, Black JH 3rd, Bowdin S, El-Hamamsy I, Frischmeyer-Guerrerio PA, Guerrerio AL, Sponseller PD, Loeys B, Dietz HC 3rd. MacCarrick G, et al. Among authors: loeys b. Genet Med. 2014 Aug;16(8):576-87. doi: 10.1038/gim.2014.11. Epub 2014 Feb 27. Genet Med. 2014. PMID: 24577266 Free PMC article. Review.
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. Among authors: de backer j. 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.
Marfan Syndrome and Related Disorders: 25 Years of Gene Discovery.
Verstraeten A, Alaerts M, Van Laer L, Loeys B. Verstraeten A, et al. Among authors: loeys b. Hum Mutat. 2016 Jun;37(6):524-31. doi: 10.1002/humu.22977. Epub 2016 Mar 14. Hum Mutat. 2016. PMID: 26919284 Review.
A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/3.
Schepers D, Tortora G, Morisaki H, MacCarrick G, Lindsay M, Liang D, Mehta SG, Hague J, Verhagen J, van de Laar I, Wessels M, Detisch Y, van Haelst M, Baas A, Lichtenbelt K, Braun K, van der Linde D, Roos-Hesselink J, McGillivray G, Meester J, Maystadt I, Coucke P, El-Khoury E, Parkash S, Diness B, Risom L, Scurr I, Hilhorst-Hofstee Y, Morisaki T, Richer J, Désir J, Kempers M, Rideout AL, Horne G, Bennett C, Rahikkala E, Vandeweyer G, Alaerts M, Verstraeten A, Dietz H, Van Laer L, Loeys B. Schepers D, et al. Among authors: van de laar i, kempers m, loeys b. Hum Mutat. 2018 May;39(5):621-634. doi: 10.1002/humu.23407. Epub 2018 Mar 6. Hum Mutat. 2018. PMID: 29392890 Free PMC article.
Chronic type B aortic dissection: indications and strategies for treatment.
Rohlffs F, Tsilimparis N, Diener H, Larena-Avellaneda A, Von Kodolitsch Y, Wipper S, Debus ES, Kölbel T. Rohlffs F, et al. Among authors: von kodolitsch y. J Cardiovasc Surg (Torino). 2015 Apr;56(2):231-8. Epub 2015 Jan 21. J Cardiovasc Surg (Torino). 2015. PMID: 25604323 Review.
Features of Marfan syndrome not listed in the Ghent nosology - the dark side of the disease.
von Kodolitsch Y, Demolder A, Girdauskas E, Kaemmerer H, Kornhuber K, Muino Mosquera L, Morris S, Neptune E, Pyeritz R, Rand-Hendriksen S, Rahman A, Riise N, Robert L, Staufenbiel I, Szöcs K, Vanem TT, Linke SJ, Vogler M, Yetman A, De Backer J. von Kodolitsch Y, et al. Among authors: robert l, de backer j. Expert Rev Cardiovasc Ther. 2019 Dec;17(12):883-915. doi: 10.1080/14779072.2019.1704625. Expert Rev Cardiovasc Ther. 2019. PMID: 31829751 Review.
Cardiovascular Health in Turner Syndrome: A Scientific Statement From the American Heart Association.
Silberbach M, Roos-Hesselink JW, Andersen NH, Braverman AC, Brown N, Collins RT, De Backer J, Eagle KA, Hiratzka LF, Johnson WH Jr, Kadian-Dodov D, Lopez L, Mortensen KH, Prakash SK, Ratchford EV, Saidi A, van Hagen I, Young LT; American Heart Association Council on Cardiovascular Disease in the Young; Council on Genomic and Precision Medicine; and Council on Peripheral Vascular Disease. Silberbach M, et al. Among authors: de backer j. Circ Genom Precis Med. 2018 Oct;11(10):e000048. doi: 10.1161/HCG.0000000000000048. Circ Genom Precis Med. 2018. PMID: 30354301 Review.
Atenolol versus losartan in children and young adults with Marfan's syndrome.
Lacro RV, Dietz HC, Sleeper LA, Yetman AT, Bradley TJ, Colan SD, Pearson GD, Selamet Tierney ES, Levine JC, Atz AM, Benson DW, Braverman AC, Chen S, De Backer J, Gelb BD, Grossfeld PD, Klein GL, Lai WW, Liou A, Loeys BL, Markham LW, Olson AK, Paridon SM, Pemberton VL, Pierpont ME, Pyeritz RE, Radojewski E, Roman MJ, Sharkey AM, Stylianou MP, Wechsler SB, Young LT, Mahony L; Pediatric Heart Network Investigators. Lacro RV, et al. Among authors: de backer j, loeys bl. N Engl J Med. 2014 Nov 27;371(22):2061-71. doi: 10.1056/NEJMoa1404731. Epub 2014 Nov 18. N Engl J Med. 2014. PMID: 25405392 Free PMC article. Clinical Trial.
From genetics to response to injury: vascular smooth muscle cells in aneurysms and dissections of the ascending aorta.
Michel JB, Jondeau G, Milewicz DM. Michel JB, et al. Among authors: jondeau g. Cardiovasc Res. 2018 Mar 15;114(4):578-589. doi: 10.1093/cvr/cvy006. Cardiovasc Res. 2018. PMID: 29360940 Free PMC article. Review.
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