Similar articles for PMID: 19542084

Year	Number of Results
1991	1
1993	3
1997	1
1998	2
2001	1
2002	1
2003	4
2004	2
2005	3
2006	9
2007	8
2008	8
2009	11
2010	14
2011	17
2012	16
2013	21
2014	23
2015	12
2016	18
2017	9
2018	11
2019	10
2020	7
2021	11
2022	12
2023	8
2024	0

1

Analysis of multigenerational families with thoracic aortic aneurysms and dissections due to TGFBR1 or TGFBR2 mutations.

Tran-Fadulu V, Pannu H, Kim DH, Vick GW 3rd, Lonsford CM, Lafont AL, Boccalandro C, Smart S, Peterson KL, Hain JZ, Willing MC, Coselli JS, LeMaire SA, Ahn C, Byers PH, Milewicz DM. Tran-Fadulu V, et al. J Med Genet. 2009 Sep;46(9):607-13. doi: 10.1136/jmg.2008.062844. Epub 2009 Jun 18. J Med Genet. 2009. PMID: 19542084

2

Identification and in silico analyses of novel TGFBR1 and TGFBR2 mutations in Marfan syndrome-related disorders.

Mátyás G, Arnold E, Carrel T, Baumgartner D, Boileau C, Berger W, Steinmann B. Mátyás G, et al. Hum Mutat. 2006 Aug;27(8):760-9. doi: 10.1002/humu.20353. Hum Mutat. 2006. PMID: 16791849

3

Aneurysm syndromes caused by mutations in the TGF-beta receptor.

Loeys BL, Schwarze U, Holm T, Callewaert BL, Thomas GH, Pannu H, De Backer JF, Oswald GL, Symoens S, Manouvrier S, Roberts AE, Faravelli F, Greco MA, Pyeritz RE, Milewicz DM, Coucke PJ, Cameron DE, Braverman AC, Byers PH, De Paepe AM, Dietz HC. Loeys BL, et al. N Engl J Med. 2006 Aug 24;355(8):788-98. doi: 10.1056/NEJMoa055695. N Engl J Med. 2006. PMID: 16928994 Free article.

4

Exon 47 skipping of fibrillin-1 leads preferentially to cardiovascular defects in patients with thoracic aortic aneurysms and dissections.

Wang WJ, Han P, Zheng J, Hu FY, Zhu Y, Xie JS, Guo J, Zhang Z, Dong J, Zheng GY, Cao H, Liu TS, Fu Q, Sun L, Yang BB, Tian XL. Wang WJ, et al. J Mol Med (Berl). 2013 Jan;91(1):37-47. doi: 10.1007/s00109-012-0931-y. Epub 2012 Jul 8. J Mol Med (Berl). 2013. PMID: 22772377

5

Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients.

Drera B, Ritelli M, Zoppi N, Wischmeijer A, Gnoli M, Fattori R, Calzavara-Pinton PG, Barlati S, Colombi M. Drera B, et al. Orphanet J Rare Dis. 2009 Nov 2;4:24. doi: 10.1186/1750-1172-4-24. Orphanet J Rare Dis. 2009. PMID: 19883511 Free PMC article.

6

Mutations in transforming growth factor-beta receptor type II cause familial thoracic aortic aneurysms and dissections.

Pannu H, Fadulu VT, Chang J, Lafont A, Hasham SN, Sparks E, Giampietro PF, Zaleski C, Estrera AL, Safi HJ, Shete S, Willing MC, Raman CS, Milewicz DM. Pannu H, et al. Circulation. 2005 Jul 26;112(4):513-20. doi: 10.1161/CIRCULATIONAHA.105.537340. Epub 2005 Jul 18. Circulation. 2005. PMID: 16027248

7

Duplication of the TGFBR1 gene causes features of Loeys-Dietz syndrome.

Breckpot J, Budts W, De Zegher F, Vermeesch JR, Devriendt K. Breckpot J, et al. Eur J Med Genet. 2010 Nov-Dec;53(6):408-10. doi: 10.1016/j.ejmg.2010.08.004. Epub 2010 Sep 20. Eur J Med Genet. 2010. PMID: 20813212

8

Autosomal dominant inheritance of a predisposition to thoracic aortic aneurysms and dissections and intracranial saccular aneurysms.

Regalado E, Medrek S, Tran-Fadulu V, Guo DC, Pannu H, Golabbakhsh H, Smart S, Chen JH, Shete S, Kim DH, Stern R, Braverman AC, Milewicz DM. Regalado E, et al. Am J Med Genet A. 2011 Sep;155A(9):2125-30. doi: 10.1002/ajmg.a.34050. Epub 2011 Aug 3. Am J Med Genet A. 2011. PMID: 21815248 Free PMC article.

9

Clinical features and genetic analysis of Korean patients with Loeys-Dietz syndrome.

Yang JH, Ki CS, Han H, Song BG, Jang SY, Chung TY, Sung K, Lee HJ, Kim DK. Yang JH, et al. J Hum Genet. 2012 Jan;57(1):52-6. doi: 10.1038/jhg.2011.130. Epub 2011 Nov 24. J Hum Genet. 2012. PMID: 22113417

10

Three Novel Mutations in FBN1 and TGFBR2 in Patients with the Syndromic Form of Thoracic Aortic Aneurysms and Dissections.

Cao Y, Tan H, Li Z, Linpeng S, Long X, Liang D, Wu L. Cao Y, et al. Int Heart J. 2018 Sep 26;59(5):1059-1068. doi: 10.1536/ihj.18-046. Epub 2018 Aug 11. Int Heart J. 2018. PMID: 30101859 Free article.

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