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扩张型心肌病的诊断与治疗 被引量:1

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作者 牛书华
出处 《中国伤残医学》 2010年第4期101-102,共2页 Chinese Journal of Trauma and Disability Medicine
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同被引文献16

  • 1黄榕翀,姚康,李延林,章轶琦,徐世坤,施鸿毓,潘翠珍,杨珊,张少衡,葛雷,牛玉宏,张峰,钱菊英,邹云增,葛均波.经冠状动脉骨髓单个核细胞移植治疗原发性扩张型心肌病的安全性与疗效近期观察[J].中华心血管病杂志,2006,34(2):111-113. 被引量:24
  • 2冯娟,董伟,全雄志,祝梅香,邸冉,高苒,马春梅,黄澜,刘亚莉,朱华,秦川,张连峰.cTnT^(R141W)转基因小鼠扩张型心肌病模型的建立[J].中国比较医学杂志,2007,17(10):563-567. 被引量:16
  • 3Yaney CW,Jessup M,Bozkurt B,et al.2013 ACCF/AHA guideline for the management of heart failure:a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines.J Am Coll Cardiol,2013,62(16):e 147-e239.
  • 4Fatkin D.Guidelines for the diagnosis and management of familial dilated cardiomyopathy.Heart Lung Cire,2011,20(11):691-693.
  • 5Petretta M,Pirozzi F,Sasso L,et al.Review and metaanalysis of the frequency of familial dilated cardiomyopathy.Am J Cardiol,2011,108(8):1171-1176.
  • 6Hershberger RE,Siegfried JD.Update 2011:clinical and genetic issues in familied dilated cardiomyopathy.Am J Cardiol,2011,57(16):1641-1649.
  • 7van Spaendonck-Zwarts K Y,van Rijsingen I A,van den Berg M P,et al.Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy:overview of 10 years" experience.European journal of heart failure 2013 Jun;15(6):628-636.
  • 8Lu QW,Morimoto S,Harada K,et al.Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca^2+ desensitization.J Mol Cell Cardiol,2003,35(12):1421-1427.
  • 9Memo M,Leung MC,Ward DG,et al.Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca^2+ sensitivity.Cardiovasc Res,2013,99(1):65-73.
  • 10Pugh TJ,Kelly MA,Gowrlsankar S,et al.The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing.Genet Med,2014,Epub ahead of print.

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