Similar articles for PMID: 23722869

Year	Number of Results
1993	1
2000	1
2003	1
2004	3
2005	9
2006	14
2007	7
2008	5
2009	8
2010	8
2011	8
2012	3
2013	9
2014	8
2015	8
2016	2
2017	5
2018	9
2019	7
2020	14
2021	13
2022	14
2023	9
2024	0

1

Endoscopic evaluation of gastrointestinal tract in patients with hereditary hemorrhagic telangiectasia and correlation with their genotypes.

Canzonieri C, Centenara L, Ornati F, Pagella F, Matti E, Alvisi C, Danesino C, Perego M, Olivieri C. Canzonieri C, et al. Genet Med. 2014 Jan;16(1):3-10. doi: 10.1038/gim.2013.62. Epub 2013 May 30. Genet Med. 2014. PMID: 23722869 Free article.

2

Clinical features and mutations in the ENG, ACVRL1, and SMAD4 genes in Korean patients with hereditary hemorrhagic telangiectasia.

Lee ST, Kim JA, Jang SY, Kim DK, Do YS, Suh GY, Kim JW, Ki CS. Lee ST, et al. J Korean Med Sci. 2009 Feb;24(1):69-76. doi: 10.3346/jkms.2009.24.1.69. Epub 2009 Feb 28. J Korean Med Sci. 2009. PMID: 19270816 Free PMC article.

3

Mutations in the ENG, ACVRL1, and SMAD4 genes and clinical manifestations of hereditary haemorrhagic telangiectasia: experience from the Center for Osler's Disease, Uppsala University Hospital.

Karlsson T, Cherif H. Karlsson T, et al. Ups J Med Sci. 2018 Sep;123(3):153-157. doi: 10.1080/03009734.2018.1483452. Epub 2018 Sep 25. Ups J Med Sci. 2018. PMID: 30251589 Free PMC article.

4

The ACVRL1 c.314-35A>G polymorphism is associated with organ vascular malformations in hereditary hemorrhagic telangiectasia patients with ENG mutations, but not in patients with ACVRL1 mutations.

Pawlikowska L, Nelson J, Guo DE, McCulloch CE, Lawton MT, Young WL, Kim H, Faughnan ME; Brain Vascular Malformation Consortium HHT Investigator Group. Pawlikowska L, et al. Am J Med Genet A. 2015 Jun;167(6):1262-7. doi: 10.1002/ajmg.a.36936. Epub 2015 Apr 2. Am J Med Genet A. 2015. PMID: 25847705 Free PMC article.

5

SMAD4 mutations found in unselected HHT patients.

Gallione CJ, Richards JA, Letteboer TG, Rushlow D, Prigoda NL, Leedom TP, Ganguly A, Castells A, Ploos van Amstel JK, Westermann CJ, Pyeritz RE, Marchuk DA. Gallione CJ, et al. J Med Genet. 2006 Oct;43(10):793-7. doi: 10.1136/jmg.2006.041517. Epub 2006 Apr 13. J Med Genet. 2006. PMID: 16613914 Free PMC article.

6

Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.

Bossler AD, Richards J, George C, Godmilow L, Ganguly A. Bossler AD, et al. Hum Mutat. 2006 Jul;27(7):667-75. doi: 10.1002/humu.20342. Hum Mutat. 2006. PMID: 16752392

7

Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients.

Lesca G, Burnichon N, Raux G, Tosi M, Pinson S, Marion MJ, Babin E, Gilbert-Dussardier B, Rivière S, Goizet C, Faivre L, Plauchu H, Frébourg T, Calender A, Giraud S; French Rendu-Osler Network. Lesca G, et al. Hum Mutat. 2006 Jun;27(6):598. doi: 10.1002/humu.9421. Hum Mutat. 2006. PMID: 16705692

8

Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers.

Sabbà C, Pasculli G, Lenato GM, Suppressa P, Lastella P, Memeo M, Dicuonzo F, Guant G. Sabbà C, et al. J Thromb Haemost. 2007 Jun;5(6):1149-57. doi: 10.1111/j.1538-7836.2007.02531.x. J Thromb Haemost. 2007. PMID: 17388964 Free article.

9

Global gene expression profiling of telangiectasial tissue from patients with hereditary hemorrhagic telangiectasia.

Tørring PM, Larsen MJ, Kjeldsen AD, Ousager LB, Tan Q, Brusgaard K. Tørring PM, et al. Microvasc Res. 2015 May;99:118-26. doi: 10.1016/j.mvr.2015.04.002. Epub 2015 Apr 16. Microvasc Res. 2015. PMID: 25892364

10

Clinical and genetic analyses of three Korean families with hereditary hemorrhagic telangiectasia.

Kim MJ, Kim ST, Lee HD, Lee KY, Seo J, Lee JB, Lee YJ, Oh SP. Kim MJ, et al. BMC Med Genet. 2011 Oct 3;12:130. doi: 10.1186/1471-2350-12-130. BMC Med Genet. 2011. PMID: 21967607 Free PMC article.

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