Supravalvular aortic stenosis as a non-syndromic familial disease. Relevance of familial screening.

María Martín; Sandra Secades; Ana M Plasencia; María Luisa Rodríguez; Cecilia Corros; Ana García-Campos; José Manuel García-Ruiz; Jesús M de la Hera; Carlos Morales

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Supravalvular aortic stenosis as a non-syndromic familial disease. Relevance of familial screening.

机译：瓣膜上主动脉瓣狭窄是一种非综合征性家族性疾病。家族筛查的相关性。

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HEx reduced office BPs and 24-hour ABPM levels in resistant hypertensive patients. These effects suggest that HEx may be a potential new therapeutic approach in these patients.

机译：HEx降低了耐药性高血压患者的办公室血压和24小时ABPM水平。这些效应表明，HEx可能是这些患者中潜在的新治疗方法。

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《International Journal of Cardiology》 |2014年第2期|共2页
作者
María Martín; Sandra Secades; Ana M Plasencia; María Luisa Rodríguez; Cecilia Corros; Ana García-Campos; José Manuel García-Ruiz; Jesús M de la Hera; Carlos Morales;
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正文语种 eng
中图分类心脏、血管（循环系）疾病;
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1. Supravalvular aortic stenosis as a non-syndromic familial disease. Relevance of familial screening. [J] . María Martín, Sandra Secades, Ana M Plasencia, International Journal of Cardiology . 2014,第2期

机译：瓣膜上主动脉瓣狭窄是一种非综合征性家族性疾病。家族筛查的相关性。
2. Frequent intragenic microdeletions of elastin in familial supravalvular aortic stenosis [J] . Hayano Satoshi, Okuno Yusuke, Tsutsumi Makiko, International Journal of Cardiology . 2019,第期

机译：家族性急性主动脉狭窄频繁的Elastin缺血性微缺
3. Corrigendum to "Frequent intragenic microdeletions of elastin in familial supravalvular aortic stenosis." [Int. J. Cardiol., 274 290-295] [J] . Satoshi Hayano, Yusuke Okuno, Makiko Tsutsumi, International Journal of Cardiology . 2019,第期

机译：“家族性上颌狭窄的常见肝硬化常见的腺体微缺乏术”。 [int。 J. Cardiol。，274 290-295]
4. Surgery for Aortic Stenosis and Mitral Regurgitation: The Impact of Concomitant Coronary Disease. [C] . Silberman S, Ofir S, Butnaru A, International Congress on Coronary Artery Disease . 2011

机译：主动脉狭窄和二尖瓣反流的手术：伴随冠心病的影响。
5. Frequent intragenic microdeletions of elastin in familial supravalvular aortic stenosis [D] . Hayano Satoshi, 早野聡 2019

机译：家族性上瓣主动脉狭窄中弹性蛋白的频繁基因内微缺失
6. Supravalvular Aortic Stenosis Caused by a Familial Chromosome 7 Inversion Disrupting the ELN Gene Uncovered by Whole-Genome Sequencing [O] . Linda Pons, Patrice Bouvagnet, Mohamed Bakloul, 2019

机译：由家族染色体7倒位引起的瓣膜上主动脉瓣狭窄破坏了全基因组测序发现的ELN基因
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Supravalvular aortic stenosis as a non-syndromic familial disease. Relevance of familial screening.

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