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

Year Number of Results
1974 1
1977 1
1980 1
1983 2
1984 1
1986 1
1987 1
1988 2
1989 1
1990 2
1992 3
1994 1
1995 2
1997 1
1998 2
1999 2
2000 3
2001 4
2002 4
2003 5
2004 1
2005 4
2006 2
2007 2
2008 6
2009 5
2010 5
2011 7
2012 4
2013 2
2014 1
2015 3
2016 2
2017 2
2019 1
2022 1
2024 0

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77 results

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Page 1
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.
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.
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.
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.
Letter to the editor.
Arno G, Comeglio P, Child AH. Arno G, et al. Among authors: child ah. Int J Angiol. 2010 Summer;19(2):e94. doi: 10.1055/s-0031-1278369. Int J Angiol. 2010. PMID: 22477598 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
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.
77 results