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

Year Number of Results
1885 1
1887 1
1929 1
1950 1
1971 1
1974 1
1977 1
1980 3
1983 2
1984 3
1985 3
1986 3
1987 3
1988 2
1989 3
1990 4
1991 3
1992 5
1993 1
1994 6
1995 5
1996 8
1997 5
1998 8
1999 8
2000 10
2001 6
2002 9
2003 6
2004 3
2005 5
2006 4
2007 8
2008 10
2009 7
2010 8
2011 10
2012 8
2013 7
2014 3
2015 5
2016 6
2017 6
2018 11
2019 6
2021 4
2022 6
2023 4
2024 1

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Article type

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214 results

Results by year

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Page 1
Non-cardiac manifestations of Marfan syndrome.
Child AH. Child AH. Ann Cardiothorac Surg. 2017 Nov;6(6):599-609. doi: 10.21037/acs.2017.10.02. Ann Cardiothorac Surg. 2017. PMID: 29270372 Free PMC article. Review.
Genetic testing in Marfan syndrome.
Child AH, Aragon-Martin JA, Sage K. Child AH, et al. Br J Hosp Med (Lond). 2016 Jan;77(1):38-41. doi: 10.12968/hmed.2016.77.1.38. Br J Hosp Med (Lond). 2016. PMID: 26903455 Review.
Cardiovascular Management of Adults with Marfan Syndrome.
Isekame Y, Gati S, Aragon-Martin JA, Bastiaenen R, Kondapally Seshasai SR, Child A. Isekame Y, et al. Among authors: child a. Eur Cardiol. 2016 Dec;11(2):102-110. doi: 10.15420/ecr/2016:19:2. Eur Cardiol. 2016. PMID: 30310455 Free PMC article. Review.
Milroy disease and the VEGFR-3 mutation phenotype.
Brice G, Child AH, Evans A, Bell R, Mansour S, Burnand K, Sarfarazi M, Jeffery S, Mortimer P. Brice G, et al. Among authors: child ah. J Med Genet. 2005 Feb;42(2):98-102. doi: 10.1136/jmg.2004.024802. J Med Genet. 2005. PMID: 15689446 Free PMC article. Review.
Diagnosing Marfan's syndrome.
Child AH. Child AH. Br Med J (Clin Res Ed). 1988 Jun 11;296(6637):1673-4. doi: 10.1136/bmj.296.6637.1673-b. Br Med J (Clin Res Ed). 1988. PMID: 3135075 Free PMC article. No abstract available.
Understanding Marfan's syndrome.
Child AH. Child AH. BMJ. 1992 Jan 11;304(6819):121. doi: 10.1136/bmj.304.6819.121. BMJ. 1992. PMID: 1737128 Free PMC article. No abstract available.
Angiotensin receptor blockers and β blockers in Marfan syndrome: an individual patient data meta-analysis of randomised trials.
Pitcher A, Spata E, Emberson J, Davies K, Halls H, Holland L, Wilson K, Reith C, Child AH, Clayton T, Dodd M, Flather M, Jin XY, Sandor G, Groenink M, Mulder B, De Backer J, Evangelista A, Forteza A, Teixido-Turà G, Boileau C, Jondeau G, Milleron O, Lacro RV, Sleeper LA, Chiu HH, Wu MH, Neubauer S, Watkins H, Dietz H, Baigent C; Marfan Treatment Trialists’ Collaboration. Pitcher A, et al. Among authors: child ah. Lancet. 2022 Sep 10;400(10355):822-831. doi: 10.1016/S0140-6736(22)01534-3. Epub 2022 Aug 29. Lancet. 2022. PMID: 36049495 Free PMC article.
Lipedema: an inherited condition.
Child AH, Gordon KD, Sharpe P, Brice G, Ostergaard P, Jeffery S, Mortimer PS. Child AH, et al. Am J Med Genet A. 2010 Apr;152A(4):970-6. doi: 10.1002/ajmg.a.33313. Am J Med Genet A. 2010. PMID: 20358611
Update of the UMD-FBN1 mutation database and creation of an FBN1 polymorphism database.
Collod-Béroud G, Le Bourdelles S, Ades L, Ala-Kokko L, Booms P, Boxer M, Child A, Comeglio P, De Paepe A, Hyland JC, Holman K, Kaitila I, Loeys B, Matyas G, Nuytinck L, Peltonen L, Rantamaki T, Robinson P, Steinmann B, Junien C, Béroud C, Boileau C. Collod-Béroud G, et al. Among authors: child a. Hum Mutat. 2003 Sep;22(3):199-208. doi: 10.1002/humu.10249. Hum Mutat. 2003. PMID: 12938084 Review.
Evidence for Marfan cardiomyopathy.
Alpendurada F, Wong J, Kiotsekoglou A, Banya W, Child A, Prasad SK, Pennell DJ, Mohiaddin RH. Alpendurada F, et al. Among authors: child a. Eur J Heart Fail. 2010 Oct;12(10):1085-91. doi: 10.1093/eurjhf/hfq127. Eur J Heart Fail. 2010. PMID: 20861133 Free article.
214 results