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Volumn 19, Issue 4, 2013, Pages 233-239

Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathy

Author keywords

Dilated cardiomypathy; genetics

Indexed keywords

ADULT; AGED; ARTICLE; CARDIOMYOPATHY; CONTROLLED STUDY; ECG ABNORMALITY; FEMALE; GENE; GENE MUTATION; HEART LEFT VENTRICLE HYPERTROPHY; HEART SUPRAVENTRICULAR ARRHYTHMIA; HEART VENTRICLE CONDUCTION; HEART VENTRICLE FUNCTION; HUMAN; LMNA GENE; MAJOR CLINICAL STUDY; MALE; ONSET AGE; PEDIGREE; PRIORITY JOURNAL; SYSTOLIC DYSFUNCTION;

EID: 84876260987     PISSN: 10719164     EISSN: 15328414     Source Type: Journal    
DOI: 10.1016/j.cardfail.2013.03.001     Document Type: Article
Times cited : (46)

References (24)
  • 1
    • 15944403997 scopus 로고    scopus 로고
    • Clinical and genetic issues in familial dilated cardiomyopathy
    • E.L. Burkett, and R.E. Hershberger Clinical and genetic issues in familial dilated cardiomyopathy J Am Coll Cardiol 45 2005 969 981
    • (2005) J Am Coll Cardiol , vol.45 , pp. 969-981
    • Burkett, E.L.1    Hershberger, R.E.2
  • 2
    • 79953842000 scopus 로고    scopus 로고
    • State of the art review. Update 2011: Clinical and genetic issues in familial dilated cardiomyopathy
    • R.E. Hershberger, and J.D. Siegfried State of the art review. Update 2011: clinical and genetic issues in familial dilated cardiomyopathy J Am Coll Cardiol 57 2011 1641 1649
    • (2011) J Am Coll Cardiol , vol.57 , pp. 1641-1649
    • Hershberger, R.E.1    Siegfried, J.D.2
  • 6
    • 79957978324 scopus 로고    scopus 로고
    • Recommendations for the use of genetic testing in the clinical evaluation of inherited cardiac arrhythmias associated with sudden cardiac death: Canadian Cardiovascular Society/Canadian Heart Rhythm Society joint position paper
    • M.H. Gollob, L. Blier, R. Brugada, J. Champagne, V. Chauhan, and S. Connors Recommendations for the use of genetic testing in the clinical evaluation of inherited cardiac arrhythmias associated with sudden cardiac death: Canadian Cardiovascular Society/Canadian Heart Rhythm Society joint position paper Can J Cardiol 27 2011 232 245
    • (2011) Can J Cardiol , vol.27 , pp. 232-245
    • Gollob, M.H.1    Blier, L.2    Brugada, R.3    Champagne, J.4    Chauhan, V.5    Connors, S.6
  • 7
    • 79960867817 scopus 로고    scopus 로고
    • HRS/EHRA Expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies. Developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)
    • M.J. Ackerman, S.G. Priori, S. Willems, C. Berul, R. Brugada, and H. Calkins HRS/EHRA Expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies. Developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA) Heart Rhythm 8 2011 1308 1339
    • (2011) Heart Rhythm , vol.8 , pp. 1308-1339
    • Ackerman, M.J.1    Priori, S.G.2    Willems, S.3    Berul, C.4    Brugada, R.5    Calkins, H.6
  • 8
    • 78751632066 scopus 로고    scopus 로고
    • Mitogen-activated protein kinase inhibitors improve heart function and prevent fibrosis in cardiomyopathy caused by mutation in lamin A/C gene
    • W. Wu, A. Muchir, J. Shan, G. Bonne, and H.J. Worman Mitogen-activated protein kinase inhibitors improve heart function and prevent fibrosis in cardiomyopathy caused by mutation in lamin A/C gene Circulation 123 2011 53 61
    • (2011) Circulation , vol.123 , pp. 53-61
    • Wu, W.1    Muchir, A.2    Shan, J.3    Bonne, G.4    Worman, H.J.5
  • 9
    • 79959776029 scopus 로고    scopus 로고
    • Rapamycin reverses cellular phenotypes and enhances mutant protein clearance in Hutchinson-Gilford progeria syndrome cells
    • K. Cao, J.J. Graziotto, C.D. Blair, J.R. Mazzulli, M.R. Erdos, and D. Krainc Rapamycin reverses cellular phenotypes and enhances mutant protein clearance in Hutchinson-Gilford progeria syndrome cells Sci Transl Med 3 2011 89ra58
    • (2011) Sci Transl Med , vol.3
    • Cao, K.1    Graziotto, J.J.2    Blair, C.D.3    Mazzulli, J.R.4    Erdos, M.R.5    Krainc, D.6
  • 10
    • 0034820958 scopus 로고    scopus 로고
    • Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease
    • P.M. Jakobs, E. Hanson, K.A. Crispell, W. Toy, H. Keegan, and K. Schilling Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease J Card Fail 7 2001 249 256
    • (2001) J Card Fail , vol.7 , pp. 249-256
    • Jakobs, P.M.1    Hanson, E.2    Crispell, K.A.3    Toy, W.4    Keegan, H.5    Schilling, K.6
  • 11
    • 0036911038 scopus 로고    scopus 로고
    • A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation
    • R.E. Hershberger, E. Hanson, P.M. Jakobs, H. Keegan, K. Coates, and S. Bousman A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation Am Heart J 144 2002 1081 1086
    • (2002) Am Heart J , vol.144 , pp. 1081-1086
    • Hershberger, R.E.1    Hanson, E.2    Jakobs, P.M.3    Keegan, H.4    Coates, K.5    Bousman, S.6
  • 12
    • 45649083874 scopus 로고    scopus 로고
    • Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy
    • S.B. Parks, J.D. Kushner, D. Nauman, D. Burgess, S. Ludwigsen, and A. Peterson Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy Am Heart J 156 2008 161 169
    • (2008) Am Heart J , vol.156 , pp. 161-169
    • Parks, S.B.1    Kushner, J.D.2    Nauman, D.3    Burgess, D.4    Ludwigsen, S.5    Peterson, A.6
  • 15
    • 55149117580 scopus 로고    scopus 로고
    • Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy
    • R.E. Hershberger, S.B. Parks, J.D. Kushner, D. Li, S. Ludwigsen, and P. Jakobs Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy Clin Translational Science 1 2008 21 26
    • (2008) Clin Translational Science , vol.1 , pp. 21-26
    • Hershberger, R.E.1    Parks, S.B.2    Kushner, J.D.3    Li, D.4    Ludwigsen, S.5    Jakobs, P.6
  • 16
    • 0030768395 scopus 로고    scopus 로고
    • Distribution and categorization of echocardiographic measurements in relation to reference limits. The Framingham Heart Study: Formulation of a height- and sex-specific classification and its prospective validation
    • R. Vasan, M. Larson, D. Levy, J. Evans, and E. Benjamin Distribution and categorization of echocardiographic measurements in relation to reference limits. The Framingham Heart Study: formulation of a height- and sex-specific classification and its prospective validation Circ 96 1997 1863 1873
    • (1997) Circ , vol.96 , pp. 1863-1873
    • Vasan, R.1    Larson, M.2    Levy, D.3    Evans, J.4    Benjamin, E.5
  • 17
    • 0032852339 scopus 로고    scopus 로고
    • Clinical profiles of four large pedigrees with familial dilated cardiomyopathy: Preliminary recommendations for clinical practice
    • K.A. Crispell, A. Wray, H. Ni, D.J. Nauman, and R.E. Hershberger Clinical profiles of four large pedigrees with familial dilated cardiomyopathy: preliminary recommendations for clinical practice J Am Coll Cardiol 34 1999 837 847
    • (1999) J Am Coll Cardiol , vol.34 , pp. 837-847
    • Crispell, K.A.1    Wray, A.2    Ni, H.3    Nauman, D.J.4    Hershberger, R.E.5
  • 19
    • 77952509742 scopus 로고    scopus 로고
    • Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy
    • J. Cowan, D. Li, J. Gonzalez-Quintana, A. Morales, and R.E. Hershberger Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy Circ Cardiovasc Genet 3 2010 6 14
    • (2010) Circ Cardiovasc Genet , vol.3 , pp. 6-14
    • Cowan, J.1    Li, D.2    Gonzalez-Quintana, J.3    Morales, A.4    Hershberger, R.E.5
  • 20
    • 79955929421 scopus 로고    scopus 로고
    • Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy
    • N. Norton, D. Li, M.J. Reider, J.D. Siegfried, E. Rampersaud, and S. Zuchner Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy Am J Hum Genet 88 2011 273 282
    • (2011) Am J Hum Genet , vol.88 , pp. 273-282
    • Norton, N.1    Li, D.2    Reider, M.J.3    Siegfried, J.D.4    Rampersaud, E.5    Zuchner, S.6
  • 21
    • 77953023261 scopus 로고    scopus 로고
    • Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy
    • R.E. Hershberger, N. Norton, A. Morales, D. Li, J.D. Siegfried, and J. Gonzalez-Quintana Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy Circ Cardiovasc Genet 3 2010 155 161
    • (2010) Circ Cardiovasc Genet , vol.3 , pp. 155-161
    • Hershberger, R.E.1    Norton, N.2    Morales, A.3    Li, D.4    Siegfried, J.D.5    Gonzalez-Quintana, J.6
  • 22
    • 85047692354 scopus 로고    scopus 로고
    • How do mutations in lamins A and C cause disease?
    • H.J. Worman, and J.C. Courvalin How do mutations in lamins A and C cause disease? J Clin Invest 113 2004 349 351
    • (2004) J Clin Invest , vol.113 , pp. 349-351
    • Worman, H.J.1    Courvalin, J.C.2
  • 23
    • 63849177462 scopus 로고    scopus 로고
    • 2009 focused update incorporated into the ACC/AHA 2005 guidelines for the diagnosis and management of heart failure in adults: A report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines developed in collaboration with the International Society for Heart and Lung Transplantation
    • S.A. Hunt, W.T. Abraham, M.H. Chin, A.M. Feldman, G.S. Francis, and T.G. Ganiats 2009 focused update incorporated into the ACC/AHA 2005 guidelines for the diagnosis and management of heart failure in adults: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines developed in collaboration with the International Society for Heart and Lung Transplantation J Am Coll Cardiol 53 2009 e1 90
    • (2009) J Am Coll Cardiol , vol.53 , pp. 1-90
    • Hunt, S.A.1    Abraham, W.T.2    Chin, M.H.3    Feldman, A.M.4    Francis, G.S.5    Ganiats, T.G.6
  • 24
    • 78649631986 scopus 로고    scopus 로고
    • Clinical and genetic issues in dilated cardiomyopathy: A review for genetics professionals
    • R.E. Hershberger, A. Morales, and J.D. Siegfried Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionals Genetics in Medicine 12 2010 655 667
    • (2010) Genetics in Medicine , vol.12 , pp. 655-667
    • Hershberger, R.E.1    Morales, A.2    Siegfried, J.D.3


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