Literature DB >> 20031583

Multiple mutations in genetic cardiovascular disease: a marker of disease severity?

Matthew Kelly1, Christopher Semsarian.   

Abstract

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Year:  2009        PMID： 20031583     DOI： 10.1161/CIRCGENETICS.108.836478

Source DB:  PubMed          Journal:  Circ Cardiovasc Genet        ISSN： 1942-3268


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  53 in total

Review 1.  Role of animal models in HCM research.

Authors:  Rhian Shephard; Christopher Semsarian
Journal:  J Cardiovasc Transl Res       Date:  2009-08-07       Impact factor: 4.132

Review 2.  Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.

Authors:  Ray E Hershberger; Jill D Siegfried
Journal:  J Am Coll Cardiol       Date:  2011-04-19       Impact factor: 24.094

Review 3.  Genetics of age-related macular degeneration: current concepts, future directions.

Authors:  Margaret M Deangelis; Alexandra C Silveira; Elizabeth A Carr; Ivana K Kim
Journal:  Semin Ophthalmol       Date:  2011-05       Impact factor: 1.975

Review 4.  Linking myofilaments to sudden cardiac death: recent advances.

Authors:  Sabine Huke
Journal:  J Physiol       Date:  2017-03-16       Impact factor: 5.182

5.  An Investigation of the Molecular Mechanism of Double cMyBP-C Mutation in a Patient with End-Stage Hypertrophic Cardiomyopathy.

Authors:  Poornima Gajendrarao; Navaneethakrishnan Krishnamoorthy; Senthil Selvaraj; Francesca Girolami; Franco Cecchi; Iacopo Olivotto; Magdi Yacoub
Journal:  J Cardiovasc Transl Res       Date:  2015-05-14       Impact factor: 4.132

Review 6.  The Muscle-Bound Heart.

Authors:  Marwan M Refaat; Akl C Fahed; Sylvana Hassanieh; Mostafa Hotait; Mariam Arabi; Hadi Skouri; Jonathan G Seidman; Christine E Seidman; Fadi F Bitar; Georges Nemer
Journal:  Card Electrophysiol Clin       Date:  2016-03

7.  [Clinical and genetic aspects of hypertrophic and dilated cardiomyopathy].

Authors:  B Meder; H A Katus
Journal:  Internist (Berl)       Date:  2012-04       Impact factor: 0.743

8.  Intrafamilial variability for novel TAZ gene mutation: Barth syndrome with dilated cardiomyopathy and heart failure in an infant and left ventricular noncompaction in his great-uncle.

Authors:  Diti Ronvelia; Jaclyn Greenwood; Julia Platt; Simin Hakim; Michael V Zaragoza
Journal:  Mol Genet Metab       Date:  2012-09-18       Impact factor: 4.797

Review 9.  A clinical approach to inherited hypertrophy: the use of family history in diagnosis, risk assessment, and management.

Authors:  Kyla E Dunn; Colleen Caleshu; Allison L Cirino; Carolyn Y Ho; Euan A Ashley
Journal:  Circ Cardiovasc Genet       Date:  2013-02

10.  Synonymous ABCA3 variants do not increase risk for neonatal respiratory distress syndrome.

Authors:  Jennifer A Wambach; Daniel J Wegner; Hillary B Heins; Todd E Druley; Robi D Mitra; Aaron Hamvas; F Sessions Cole
Journal:  J Pediatr       Date:  2014-03-20       Impact factor: 4.406
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