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

Year Number of Results
1972 1
1976 1
1977 1
1978 1
1980 1
1981 1
1982 1
1985 2
1986 2
1989 1
1990 3
1993 1
1995 1
1998 1
2002 1
2003 2
2006 3
2007 2
2008 1
2009 4
2010 6
2011 5
2012 2
2013 7
2014 11
2015 11
2016 7
2017 9
2018 7
2019 6
2020 0
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Article type
Publication date

Similar Articles for PMID: 31792044

95 results
Results by year
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Page 1
Dysmorphology.
Kim AY, Bodurtha JN. Kim AY, et al. Pediatr Rev. 2019 Dec;40(12):609-618. doi: 10.1542/pir.2018-0331. Pediatr Rev. 2019. PMID: 31792044 Review. No abstract available.
Valve-sparing aortic root replacement in Loeys-Dietz syndrome and a novel mutation in TGFBR2.
Kasar T, Gezdirici A, Ayyıldız P, Haydin S, Güzeltaş A. Kasar T, et al. Anatol J Cardiol. 2018 Jan;19(1):74-77. doi: 10.14744/AnatolJCardiol.2017.7911. Anatol J Cardiol. 2018. PMID: 29339704 Free PMC article. No abstract available.
Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes.
Arslan-Kirchner M, Epplen JT, Faivre L, Jondeau G, Schmidtke J, De Paepe A, Loeys B. Arslan-Kirchner M, et al. Eur J Hum Genet. 2011 Oct;19(10). doi: 10.1038/ejhg.2011.68. Epub 2011 Apr 27. Eur J Hum Genet. 2011. PMID: 21522183 Free PMC article. No abstract available.
FEVR findings in patients with Loeys-Dietz syndrome type II.
Solinski MA, Blair MP, Dietz H, Mittelman D, Shapiro MJ. Solinski MA, et al. Ophthalmic Genet. 2018 Dec;39(6):754-758. doi: 10.1080/13816810.2018.1532526. Epub 2018 Nov 8. Ophthalmic Genet. 2018. PMID: 30406707
A new sporadic case of early-onset Loeys-Dietz syndrome due to the recurrent mutation p.R528C in the TGFBR2 gene substantiates interindividual clinical variability.
Jamsheer A, Henggeler C, Wierzba J, Loeys B, De Paepe A, Stheneur Ch, Badziag N, Matuszewska K, Matyas G, Latos-Bielenska A. Jamsheer A, et al. J Appl Genet. 2009;50(4):405-10. doi: 10.1007/BF03195701. J Appl Genet. 2009. PMID: 19875893 Review.
Ocular findings in Loeys-Dietz syndrome.
Busch C, Voitl R, Goergen B, Zemojtel T, Gehle P, Salchow DJ. Busch C, et al. Br J Ophthalmol. 2018 Aug;102(8):1036-1040. doi: 10.1136/bjophthalmol-2017-311254. Epub 2017 Nov 16. Br J Ophthalmol. 2018. PMID: 29146755
Genotypic Categorization of Loeys-Dietz Syndrome Based on 24 Novel Families and Literature Data.
Camerota L, Ritelli M, Wischmeijer A, Majore S, Cinquina V, Fortugno P, Monetta R, Gigante L, Marfan Syndrome Study Group Tor Vergata University Hospital, Sangiuolo FC, Novelli G, Colombi M, Brancati F. Camerota L, et al. Genes (Basel). 2019 Sep 28;10(10):764. doi: 10.3390/genes10100764. Genes (Basel). 2019. PMID: 31569402 Free PMC article. Review.
Spontaneous pneumothorax can be associated with TGFBR2 mutation.
Chambers JE, Dalton LE, Subramanian DN, Gooptu B, Balan A, Park SM, Holden S, Marciniak SJ. Chambers JE, et al. Eur Respir J. 2015 Dec;46(6):1832-5. doi: 10.1183/13993003.00952-2015. Epub 2015 Oct 22. Eur Respir J. 2015. PMID: 26493799 Free article. No abstract available.
Annuloaortic ectasia in a 16 year-old boy with Loeys-Dietz syndrome.
Ma BO, Song BG, Yang HJ, Jeon GJ, Lee JU, Kim TH, Kang GH, Park YH, Chun WJ, Oh JH. Ma BO, et al. Heart Lung Circ. 2012 Apr;21(4):215-7. doi: 10.1016/j.hlc.2012.01.001. Epub 2012 Feb 9. Heart Lung Circ. 2012. PMID: 22325833
Genetic testing of 10 patients with features of Loeys-Dietz syndrome.
Luo M, Yang H, Yin K, Chen Q, Zhang J, Fan Y, Zhou Z, Chang Q. Luo M, et al. Clin Chim Acta. 2016 May 1;456:144-148. doi: 10.1016/j.cca.2016.02.005. Epub 2016 Feb 11. Clin Chim Acta. 2016. PMID: 26877057
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