Skip Navigation

European Heart Journal 2002 23(24):1972-1974; doi:10.1053/euhj.2002.3388
Copyright © 2002 by the European Society of Cardiology.
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (1)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Arbustini, E.
Right arrow Articles by Tendera, M.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Arbustini, E.
Right arrow Articles by Tendera, M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Letters to the Editor

The need for European Registries in inherited cardiomyopathies

E. Arbustinia, F. Cecchib, O. Dubourgc, M. Frenneauxd, A. Kerene, U. Khulf, B. Maischg, P. Richardsonh, P. Seferovici and M. Tenderaj

a Molecular Diagnostic, Cardiovascular and Transplant Pathology Lab., Transplant Research Area, IRCCS Policlinico San Matteo, Pavia, Italy
b Cardiology, Careggi Hospital, Firenze, Italy
c Cardiology, Hospital St Lapitriere, Paris, France
d University of Wales College of Medicine, Cardiff, U.K.
e Bikur Cholim Hospital and Hebrew University Hadassah Medical School, Jerusalem, Israel
f Department of Cardiology and Pneumonology, University Hospital - Free University of Berlin, Berlin, Germany
g Universitz of Marburg, Department of Internal Medicine and Cardiology, Marburg, Germany
h King's College Hospital, University of London, London, U.K.
i Institute for Cardiovascular Diseases, University Medical Center, Belgrade, Yugoslavia
j 3rd Department of Cardiology, Silesian Medical Academy, Katowice, Poland

References

  1. Richardson P, McKenna WJ, Bristow M. Report of the 1995 World Organization/International Society and Federation of Cardiology Task Force on the definition and classification of cardiomyopathies. Circulation. 1996;93:841–842[Free Full Text]
  2. Codd MB, Sugrue DD, Gersh BJ, Melton LJ. Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975–84. Circulation. 1989;80:564[Abstract/Free Full Text]
  3. Bozkurt B, Mann DL. Dilated cardiomyopathy. Willerson JT, Cohn JN. Cardiovascular Medicine. : Churchill Livingstone; 2000. p. 1034–1053
  4. Maron BJ, Gardin JM, Flack JM. Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA study. Circulation. 1995;92:785[Abstract/Free Full Text]
  5. Fuster V, Gersh BJ, Giuliani ER, Tajik AJ, Brandenburg RO, Frye RL. The natural history of idiopathic dilated cardiomyopathy. Am J Cardiol. 1981;47:525–531[CrossRef][Web of Science][Medline]
  6. Maron BJ, Olivotto I, Spirito P. Epidemiology of hypertrophic cardiomyopathy-related death: revisited in a large non-referral-based patient population. Circulation. 2000;22:858–864
  7. Maron BJ. Hypertrophic cardiomyopathy. Lancet. 1997;12:127–133
  8. Shah PM, Adelman AG, Wigle ED. The natural (an unnatural) history of hypertrophic obstructive cardiomyopathy. Circ Res. 1973;34:II179–95
  9. Maron BJ, Casey SA, Poliac L, Gohman TE, Almquist AK, Aeppli DM. Clinical course of hypertrophic cardiomyopathy in a Regional United States Cohort. JAMA. 1999;281:650–655[Abstract/Free Full Text]
  10. Maron BJ, Mathenge R, Casey SA, Poliac LC. Clinical profile of hypertrophic cardiomyopathy identified de novo in rural communities. J Am Coll Cardiol. 1999;33:1590–1595[Abstract/Free Full Text]
  11. Spirito P, Maron BJ, Bonow RO, Epstein SE. Occurrence and significance of progressive left ventricular wall thinning and relative cavity dilatation in patients with hypertrophic cardiomyopathy. Am J Cardiol. 1987;60:123–129[CrossRef][Web of Science][Medline]
  12. Maron BJ, McKenna WJ, Elliott P. Hypertrophic cardiomyopathy. JAMA. 1999;282:2302–2303[Free Full Text]
  13. Gavazzi A, Repetto A, Scelsi L. Evidence-based diagnosis of familial non-X-linked dilated cardiomyopathy. Prevalence, inheritance and characteristics. Eur Heart J. 2001;1:73–81
  14. Michels VV, Moll PP, Miller FA. The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy. N Engl J Med. 1992;326:77–82[Abstract]
  15. Grunig E, Tasman JA, Kucherer H, Franz W, Kubler W, Katus HA. Frequency and phenotypes of familial dilated cardiomyopathy. J Am Coll Cardiol. 1998;31:186–194[Abstract/Free Full Text]
  16. Mestroni L, Rocco C, Gregori D. Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. J Am Coll Cardiol. 1999;34:181–190[Abstract/Free Full Text]
  17. Michels VV, Driscoll DJ, Miller FA. Familial aggregation of idiopathic dilated cardiomyopathy. Am J Cardiol. 1985;55:1232–1233[CrossRef][Web of Science][Medline]
  18. Fragola PV, Autore A, Picelli A, Sommariva L, Cannata D, Sangiorgi M. Familial dilated cardiomyopathy. Am Heart J. 1998;115:912–914
  19. Charron P, Dubourg O, Desnos M. Familial hypertrophic cardiomyopathy: cardiac ultrasonic abnormalities in genetically affected subjects without echocardiographic evidence of left ventricular hypertrophy. Eur Heart J. 1998;19:490–499[Abstract/Free Full Text]
  20. Arbustine E, Pilotto A, Repetto A. Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease. J Am Coll Cardiol. 2002;39:981–990[Abstract/Free Full Text]
  21. Kamisago M, Sharma SD, DePalma SR. Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy. N Engl J Med. 2000;343:1688–1696[Abstract/Free Full Text]
  22. Olson TM, Michels VV, Thibodean SN, Tai YS, Keating MT. Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science. 1998;280:750–752[Abstract/Free Full Text]
  23. Mogensen J, Klausen IC, Pedersen AK. Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy. J Clin Invest. 1999;103:R39–43[Medline]
  24. Keren A, Meiner V, Potekhin M. Phenotypic-genotypic findings in hypertrophic cardiomyopathy in the ISAAC National Database. J Am Coll Cardiol. 2000;35:202A

Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?



This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (1)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Arbustini, E.
Right arrow Articles by Tendera, M.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Arbustini, E.
Right arrow Articles by Tendera, M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?