Similar articles for PMID: 22843229

Year	Number of Results
1963	1
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2000	2
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2023	3
2024	0

1

The clinical and genetic distinction between familial supravalvular aortic stenosis (Eisenberg syndrome) and Williams-Beuren syndrome.

Samanich JM, Levin TL, Berdon WE. Samanich JM, et al. Pediatr Radiol. 2012 Oct;42(10):1269. doi: 10.1007/s00247-012-2475-2. Epub 2012 Jul 29. Pediatr Radiol. 2012. PMID: 22843229 No abstract available.

2

Better late than never: diagnosis and successful treatment in late adulthood of supravalvular aortic stenosis secondary to Williams-Beuren syndrome.

Safa K, El Ghazal R. Safa K, et al. Conn Med. 2011 Jan;75(1):21-3. Conn Med. 2011. PMID: 21329288

3

Cardiovascular spectrum in Williams-Beuren syndrome: the Mexican experience in 40 patients.

De Rubens Figueroa J, Rodríguez LM, Hach JL, Del Castillo Ruíz V, Martínez HO. De Rubens Figueroa J, et al. Tex Heart Inst J. 2008;35(3):279-85. Tex Heart Inst J. 2008. PMID: 18941598 Free PMC article.

4

[Genetic analysis of a child with atypical Williams-Beuren syndrome presenting as supravalvular aortic stenosis].

Wu D, Zhang M, Gao Y, Huo X, Xiao H, Zhang Q, Kang B, Wang X, Liao S. Wu D, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Apr 10;37(4):475-478. doi: 10.3760/cma.j.issn.1003-9406.2020.04.028. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32219841 Chinese.

5

Review of referrals for the FISH detection of Williams syndrome highlights the importance of testing in supravalvular aortic stenosis/pulmonary stenosis.

St Heaps L, Robson L, Smith A. St Heaps L, et al. Am J Med Genet. 2001 Jan 1;98(1):109-11. doi: 10.1002/1096-8628(20010101)98:1<109::aid-ajmg1003>3.3.co;2-2. Am J Med Genet. 2001. PMID: 11428332 No abstract available.

6

De novo obstruction after supravalvular aortic stenosis repair in Williams-Beuren syndrome.

Nassar MS, Pushparajah K, Bell A, Austin CB. Nassar MS, et al. Ann Thorac Surg. 2015 May;99(5):1806-7. doi: 10.1016/j.athoracsur.2014.06.108. Ann Thorac Surg. 2015. PMID: 25952214

7

Supravalvular aortic stenosis in a case of Williams syndrome.

Gupte Y, Acharya S. Gupte Y, et al. Pan Afr Med J. 2022 Jul 1;42:170. doi: 10.11604/pamj.2022.42.170.35211. eCollection 2022. Pan Afr Med J. 2022. PMID: 36187037 Free PMC article. No abstract available.

8

An unusual combination of an atypical maternally inherited novel 0.3 Mb deletion in Williams-Beuren region and a de novo 22q11.21 microduplication in an infant with supravalvular aortic stenosis.

Evangelidou P, Kousoulidou L, Salameh N, Alexandrou A, Papaevripidou I, Alexandrou IM, Ketoni A, Ioannidou C, Christophidou-Anastasiadou V, Tanteles GA, Sismani C. Evangelidou P, et al. Eur J Med Genet. 2020 Dec;63(12):104084. doi: 10.1016/j.ejmg.2020.104084. Epub 2020 Oct 9. Eur J Med Genet. 2020. PMID: 33045407

9

Williams-Beuren syndrome in the Hong Kong Chinese population: retrospective study.

Yau EK, Lo IF, Lam ST. Yau EK, et al. Hong Kong Med J. 2004 Feb;10(1):22-7. Hong Kong Med J. 2004. PMID: 14967851 Free article.

10

Elastin-driven genetic diseases.

Duque Lasio ML, Kozel BA. Duque Lasio ML, et al. Matrix Biol. 2018 Oct;71-72:144-160. doi: 10.1016/j.matbio.2018.02.021. Epub 2018 Feb 28. Matrix Biol. 2018. PMID: 29501665 Free PMC article. Review.

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