Dilated Cardiomyopathy: Does Etiological Heterogeneity Portend Clinical Heterogeneity?

[1]  L. Mestroni,et al.  Molecular genetics of dilated cardiomyopathy. , 2014, Current opinion in cardiology.

[2]  Jason T. Su,et al.  Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy. , 1997, Circulation.

[3]  Y. Hayashizaki,et al.  Identification of the Syrian hamster cardiomyopathy gene. , 1997, Human molecular genetics.

[4]  B. Lowes,et al.  Dilated cardiomyopathy associated with deficiency of the cytoskeletal protein metavinculin. , 1996, Circulation.

[5]  L. Mestroni,et al.  Familial dilated cardiomyopathy with subclinical skeletal muscle involvement , 1996 .

[6]  J. Towbin,et al.  Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23. , 1996, The Journal of clinical investigation.

[7]  J. Ferguson,et al.  American College of Cardiology 45th Annual Scientific Session, Orlando, Florida, March 24 to 27, 1996. , 1996, Circulation.

[8]  L. Mestroni,et al.  Genetic factors in dilated cardiomyopathy. , 1996, Archives des maladies du coeur et des vaisseaux.

[9]  S. Dimauro,et al.  Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial tRNA(Lys) gene (G8363A). , 1996, American journal of human genetics.

[10]  B Maisch,et al.  Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies. , 1996, Circulation.

[11]  K. Campbell,et al.  Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathy. , 1996, The New England journal of medicine.

[12]  M. Keating,et al.  Mapping a cardiomyopathy locus to chromosome 3p22-p25. , 1996, The Journal of clinical investigation.

[13]  L. Mestroni,et al.  A point mutation in the 5' splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy. , 1996, Human molecular genetics.

[14]  J. Stark How to choose a cardiac surgeon , 1996 .

[15]  J. Towbin,et al.  Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32. , 1995, Circulation.

[16]  D. Schaid,et al.  Exclusion of a primary gene defect at the HLA locus in familial idiopathic dilated cardiomyopathy. , 1995, Journal of medical genetics.

[17]  L. Mestroni,et al.  Linkage of familial dilated cardiomyopathy to chromosome 9. Heart Muscle Disease Study Group. , 1995, American journal of human genetics.

[18]  L. Mestroni,et al.  A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart. , 1995, The Journal of clinical investigation.

[19]  W. McKenna,et al.  Familial dilated cardiomyopathy in the United Kingdom. , 1995, British heart journal.

[20]  A. Heim,et al.  Myocardial enterovirus infection with left ventricular dysfunction: a benign disease compared with idiopathic dilated cardiomyopathy. , 1995, Journal of the American College of Cardiology.

[21]  L. Mestroni,et al.  Low frequency of detection by nested polymerase chain reaction of enterovirus ribonucleic acid in endomyocardial tissue of patients with idiopathic dilated cardiomyopathy. , 1994, Journal of the American College of Cardiology.

[22]  L. Mestroni,et al.  Absence of linkage between idiopathic dilated cardiomyopathy and candidate genes involved in the immune function in a large Italian pedigree. , 1994, Journal of medical genetics.

[23]  L. Mestroni,et al.  Evidence from family studies for autoimmunity in dilated cardiomyopathy , 1994, The Lancet.

[24]  A. Kong,et al.  A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1–1q1 , 1994, Nature Genetics.

[25]  J. Towbin,et al.  Acute Myocarditis : Rapid Diagnosis by PCR in Children 331 TABLE 1 . Dallas Criteria * General definition : Myocardial cell injury with degeneration or necrosis with inflammatory infiltrate not due to ischemia , 2005 .

[26]  G. Wallukat,et al.  Autoimmunity in idiopathic dilated cardiomyopathy. Characterization of antibodies against the beta 1-adrenoceptor with positive chronotropic effect. , 1994, Circulation.

[27]  N. Bowles,et al.  Clinical and prognostic significance of detection of enteroviral RNA in the myocardium of patients with myocarditis or dilated cardiomyopathy. , 1994, Circulation.

[28]  L. Mestroni,et al.  Molecular genetics of dilated cardiomyopathy. , 1994, Herz.

[29]  G. Hutchins,et al.  The causes of dilated cardiomyopathy: a clinicopathologic review of 673 consecutive patients. , 1994, Journal of the American College of Cardiology.

[30]  G. Danieli,et al.  Cardiac involvement in Becker muscular dystrophy. , 1993, Journal of the American College of Cardiology.

[31]  N. Yanagisawa,et al.  Molecular analysis of the duchenne muscular dystrophy gene in patients with becker muscular dystrophy presenting with dilated cardiomyopathy , 1993, Muscle & nerve.

[32]  F. Muntoni,et al.  Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy. , 1993, The New England journal of medicine.

[33]  F. Waagstein,et al.  Localization of a functional autoimmune epitope on the muscarinic acetylcholine receptor-2 in patients with idiopathic dilated cardiomyopathy. , 1993, The Journal of clinical investigation.

[34]  L. Kunkel,et al.  The structural and functional diversity of dystrophin , 1993, Nature Genetics.

[35]  J. Towbin,et al.  X‐Linked Dilated Cardiomyopathy Molecular Genetic Evidence of Linkage to the Duchenne Muscular Dystrophy (Dystrophin) Gene at the Xp21 Locus , 1993, Circulation.

[36]  L. Peltonen,et al.  Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA , 1992, The Lancet.

[37]  K. Chang,et al.  Detection of enteroviral RNA in idiopathic dilated cardiomyopathy and other human cardiac tissues. , 1992, The Journal of clinical investigation.

[38]  W. Mckenna,et al.  Identification of alpha- and beta-cardiac myosin heavy chain isoforms as major autoantigens in dilated cardiomyopathy. , 1992, Circulation.

[39]  E. Arbustini,et al.  Search for Coxsackievirus B3 RNA in idiopathic dilated cardiomyopathy using gene amplification by polymerase chain reaction. , 1992, The American journal of cardiology.

[40]  A. Tajik,et al.  The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy. , 1992, The New England journal of medicine.

[41]  V. Tiranti,et al.  Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR) , 1991, The Lancet.

[42]  J. Carlquist,et al.  HLA class II (DR and DQ) antigen associations in idiopathic dilated cardiomyopathy. Validation study and meta-analysis of published HLA association studies. , 1991, Circulation.

[43]  F. Camerini,et al.  Advances in Cardiomyopathies , 1990, Springer Berlin Heidelberg.

[44]  P. McLaughlin,et al.  Detection of enterovirus RNA in myocardial biopsies from patients with myocarditis and cardiomyopathy using gene amplification by polymerase chain reaction. , 1990, Circulation.

[45]  L. Mestroni,et al.  Clinical and pathologic study of familial dilated cardiomyopathy. , 1990, The American journal of cardiology.

[46]  E. Bonifacio,et al.  Novel organ-specific circulating cardiac autoantibodies in dilated cardiomyopathy. , 1990, Journal of the American College of Cardiology.

[47]  H. Schultheiss,et al.  Antibodies to ADP-ATP carrier--an autoantigen in myocarditis and dilated cardiomyopathy--impair cardiac function. , 1990, Circulation.

[48]  M. Herzum,et al.  Humoral and Cell-Mediated Immunity: Pathogenetic Mechanisms in Dilated Cardiomyopathy , 1990 .

[49]  M. Yacoub,et al.  End-stage dilated cardiomyopathy. Persistence of enterovirus RNA in myocardium at cardiac transplantation and lack of immune response. , 1989, Circulation.

[50]  J. Towbin,et al.  X-linked dilated cardiomyopathy. , 1987, The New England journal of medicine.

[51]  W. Edwards,et al.  Myocarditis. A histopathologic definition and classification. , 1987, The American journal of cardiovascular pathology.

[52]  J. Ryan,et al.  Evolution of a hereditary cardiac conduction and muscle disorder: a study involving a family with six generations affected. , 1986, Circulation.

[53]  J. Carlquist,et al.  Quantitation of lymphocyte subsets by immunofluorescence flow cytometry in idiopathic dilated cardiomyopathy. , 1985, The American journal of cardiology.

[54]  R. Eckstein,et al.  Reduced Suppressor Cell Activity in Congestive Cardiomyopathy and in Myocarditis , 1982, Circulation.

[55]  E. Stinson,et al.  Defective In Vitro Suppressor Cell Function in Idiopathic Congestive Cardiomyopathy , 1979, Circulation.