Child A[au] - Search Results

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	3

1

Irbesartan in Marfan syndrome (AIMS): a double-blind, placebo-controlled randomised trial.

Mullen M, Jin XY, Child A, Stuart AG, Dodd M, Aragon-Martin JA, Gaze D, Kiotsekoglou A, Yuan L, Hu J, Foley C, Van Dyck L, Knight R, Clayton T, Swan L, Thomson JDR, Erdem G, Crossman D, Flather M; AIMS Investigators. Mullen M, et al. Among authors: child a. Lancet. 2019 Dec 21;394(10216):2263-2270. doi: 10.1016/S0140-6736(19)32518-8. Epub 2019 Dec 10. Lancet. 2019. PMID: 31836196 Free PMC article. Clinical Trial.

2

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.

3

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.

4

Telehealth diagnosis of autism spectrum disorder through clinical cases.

Ludwig NN, Child AE, Jashar DT, Mostow AJ, Wodka EL. Ludwig NN, et al. Among authors: child ae. Clin Neuropsychol. 2021 Sep 2:1-21. doi: 10.1080/13854046.2021.1970228. Online ahead of print. Clin Neuropsychol. 2021. PMID: 34473008

5

Prevalence of POC5 Coding Variants in French-Canadian and British AIS Cohort.

Mathieu H, Spataru A, Aragon-Martin JA, Child A, Barchi S, Fortin C, Parent S, Moldovan F. Mathieu H, et al. Among authors: child a. Genes (Basel). 2021 Jul 1;12(7):1032. doi: 10.3390/genes12071032. Genes (Basel). 2021. PMID: 34356048 Free PMC article.

6

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.

7

Genetic variant of TTLL11 gene and subsequent ciliary defects are associated with idiopathic scoliosis in a 5-generation UK family.

Mathieu H, Patten SA, Aragon-Martin JA, Ocaka L, Simpson M, Child A, Moldovan F. Mathieu H, et al. Among authors: child a. Sci Rep. 2021 May 26;11(1):11026. doi: 10.1038/s41598-021-90155-0. Sci Rep. 2021. PMID: 34040021 Free PMC article.

8

Gastrointestinal Symptoms in Marfan Syndrome and Hypermobile Ehlers-Danlos Syndrome.

Inayet N, Hayat JO, Kaul A, Tome M, Child A, Poullis A. Inayet N, et al. Among authors: child a. Gastroenterol Res Pract. 2018 Jul 29;2018:4854701. doi: 10.1155/2018/4854701. eCollection 2018. Gastroenterol Res Pract. 2018. PMID: 30151001 Free PMC article.

9

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.

10

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

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