메뉴 건너뛰기




Volumn 8, Issue 8, 2006, Pages 816-825

Familial inflammatory dilated cardiomyopathy

Author keywords

Dilated cardiomyopathy; Familial dilated cardiomyopathy; Inflammatory DCM

Indexed keywords

ADULT; AGED; ARTICLE; AUTOIMMUNITY; AUTOSOMAL RECESSIVE DISORDER; CLINICAL FEATURE; CONGESTIVE CARDIOMYOPATHY; CONTROLLED STUDY; FEMALE; GENETICS; HEART MUSCLE CONDUCTION DISTURBANCE; HUMAN; INHERITANCE; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; PATHOPHYSIOLOGY; PRIORITY JOURNAL;

EID: 33751183060     PISSN: 13889842     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejheart.2006.02.010     Document Type: Article
Times cited : (16)

References (56)
  • 1
    • 0027193330 scopus 로고
    • X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus
    • Towbin J.A., Hejtmancik J.F., Brink P., et al. X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. Circulation 87 (1993) 1854-1865
    • (1993) Circulation , vol.87 , pp. 1854-1865
    • Towbin, J.A.1    Hejtmancik, J.F.2    Brink, P.3
  • 2
    • 17344373157 scopus 로고    scopus 로고
    • Missense mutations in desmin associated with familial cardiac and skeletal myopathy
    • Goldfarb L.G., Park K.-Y., Cervenáková L., et al. Missense mutations in desmin associated with familial cardiac and skeletal myopathy. Nat Genet 19 (1998) 402-403
    • (1998) Nat Genet , vol.19 , pp. 402-403
    • Goldfarb, L.G.1    Park, K.-Y.2    Cervenáková, L.3
  • 3
    • 0027985787 scopus 로고
    • Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy
    • Bione S., Maestrini E., Rivella S., et al. Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy. Nat Genet 8 (1994) 323-327
    • (1994) Nat Genet , vol.8 , pp. 323-327
    • Bione, S.1    Maestrini, E.2    Rivella, S.3
  • 4
    • 0343963762 scopus 로고    scopus 로고
    • Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathy
    • Franz W.M., Muller M., Muller O.J., et al. Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathy. Lancet 355 (2000) 1781-1785
    • (2000) Lancet , vol.355 , pp. 1781-1785
    • Franz, W.M.1    Muller, M.2    Muller, O.J.3
  • 5
    • 0033520037 scopus 로고    scopus 로고
    • Desmin mutation responsible for idiopathic dilated cardiomyopathy
    • Li D., Tapscoft T., Gonzalez O., et al. Desmin mutation responsible for idiopathic dilated cardiomyopathy. Circulation 100 (1999) 461-464
    • (1999) Circulation , vol.100 , pp. 461-464
    • Li, D.1    Tapscoft, T.2    Gonzalez, O.3
  • 6
    • 0033818186 scopus 로고    scopus 로고
    • Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy
    • Tsubata S., Bowles K.R., Vatta M., et al. Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy. J Clin Invest 106 (2000) 655-662
    • (2000) J Clin Invest , vol.106 , pp. 655-662
    • Tsubata, S.1    Bowles, K.R.2    Vatta, M.3
  • 7
    • 0034063935 scopus 로고    scopus 로고
    • Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by δ-sarcoglycan mutations
    • Barresi R., Di Blasi C., Negri T., et al. Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by δ-sarcoglycan mutations. J Med Genet 37 (2000) 102-107
    • (2000) J Med Genet , vol.37 , pp. 102-107
    • Barresi, R.1    Di Blasi, C.2    Negri, T.3
  • 8
    • 0032076955 scopus 로고    scopus 로고
    • Actin mutations in dilated cardiomyopathy, a heritable form of heart failure
    • Olson T.M., Michels V.V., Thibodeau S.N., Tai Y.S., and Keating M.T. Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science 280 (1998) 750-752
    • (1998) Science , vol.280 , pp. 750-752
    • Olson, T.M.1    Michels, V.V.2    Thibodeau, S.N.3    Tai, Y.S.4    Keating, M.T.5
  • 9
    • 0034267888 scopus 로고    scopus 로고
    • Genetic abnormalities responsible for dilated cardiomyopathy
    • Towbin J.A., and Bowles N.E. Genetic abnormalities responsible for dilated cardiomyopathy. Curr Cardiol Rep 2 (2000) 475-480
    • (2000) Curr Cardiol Rep , vol.2 , pp. 475-480
    • Towbin, J.A.1    Bowles, N.E.2
  • 10
    • 0842283230 scopus 로고    scopus 로고
    • Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy
    • Murphy R.T., Mogensen J., Shaw A., Kubo T., Hughes S., and McKenna W.J. Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy. Lancet 363 (2004) 371-372
    • (2004) Lancet , vol.363 , pp. 371-372
    • Murphy, R.T.1    Mogensen, J.2    Shaw, A.3    Kubo, T.4    Hughes, S.5    McKenna, W.J.6
  • 11
    • 0034971165 scopus 로고    scopus 로고
    • Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy
    • Olson T.M., Kishimoto N.Y., Whitby F.G., and Michels V.V. Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy. J Mol Cell Cardiol 33 (2001) 723-732
    • (2001) J Mol Cell Cardiol , vol.33 , pp. 723-732
    • Olson, T.M.1    Kishimoto, N.Y.2    Whitby, F.G.3    Michels, V.V.4
  • 12
    • 0034619996 scopus 로고    scopus 로고
    • Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy
    • Kamisago M., Sharma S.D., DePalma S.R., et al. Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy. N Engl J Med 343 (2000) 1688-1696
    • (2000) N Engl J Med , vol.343 , pp. 1688-1696
    • Kamisago, M.1    Sharma, S.D.2    DePalma, S.R.3
  • 13
    • 0033518282 scopus 로고    scopus 로고
    • Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease
    • Fatkin D., MacRae C., Sasaki T., et al. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. N Engl J Med 341 (1999) 1715-1724
    • (1999) N Engl J Med , vol.341 , pp. 1715-1724
    • Fatkin, D.1    MacRae, C.2    Sasaki, T.3
  • 14
    • 0035153087 scopus 로고    scopus 로고
    • Lamins in disease: why do ubiquitously expressed nuclear envelope proteins give rise to tissue-specific disease phenotypes?
    • Hutchison C.J., Alvarez-Reyes M., and Vaughan O.A. Lamins in disease: why do ubiquitously expressed nuclear envelope proteins give rise to tissue-specific disease phenotypes?. J Cell Sci 114 (2001) 9-19
    • (2001) J Cell Sci , vol.114 , pp. 9-19
    • Hutchison, C.J.1    Alvarez-Reyes, M.2    Vaughan, O.A.3
  • 15
    • 0042327845 scopus 로고    scopus 로고
    • Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations
    • Sebillon P., Bouchier C., Bidot L.D., et al. Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations. J Med Genet 40 (2003) 560-567
    • (2003) J Med Genet , vol.40 , pp. 560-567
    • Sebillon, P.1    Bouchier, C.2    Bidot, L.D.3
  • 16
    • 33751186847 scopus 로고    scopus 로고
    • Schönberger J, Zimmer M, Ertl G. Genetics in dilated cardiomyopathy. DÄ 2004;101:1099-1105 [available via www.aerzteblatt.de].
  • 17
    • 0037470512 scopus 로고    scopus 로고
    • Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban
    • Schmitt J.P., Kamisago M., Asahi M., et al. Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban. Science 299 (2003) 1410-1413
    • (2003) Science , vol.299 , pp. 1410-1413
    • Schmitt, J.P.1    Kamisago, M.2    Asahi, M.3
  • 18
    • 0037050022 scopus 로고    scopus 로고
    • The failing heart
    • Towbin J.A., and Bowles N.E. The failing heart. Nature 415 (2002) 227-233
    • (2002) Nature , vol.415 , pp. 227-233
    • Towbin, J.A.1    Bowles, N.E.2
  • 19
    • 0343183359 scopus 로고    scopus 로고
    • Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24
    • Schonberger J., Levy H., Grunig E., et al. Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24. Circulation 101 (2000) 1812-1818
    • (2000) Circulation , vol.101 , pp. 1812-1818
    • Schonberger, J.1    Levy, H.2    Grunig, E.3
  • 20
    • 0033165780 scopus 로고    scopus 로고
    • Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group
    • Mestroni L., Rocco C., Gregori D., et al. Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group. J Am Coll Cardiol 34 (1999) 181-190
    • (1999) J Am Coll Cardiol , vol.34 , pp. 181-190
    • Mestroni, L.1    Rocco, C.2    Gregori, D.3
  • 21
    • 0023181940 scopus 로고
    • Myocarditis: the Dallas criteria
    • Aretz H.T. Myocarditis: the Dallas criteria. Hum Pathol 18 (1987) 619-624
    • (1987) Hum Pathol , vol.18 , pp. 619-624
    • Aretz, H.T.1
  • 22
    • 0033931349 scopus 로고    scopus 로고
    • Definition of inflammatory cardiomyopathy (myocarditis): on the way to consensus. A status report
    • [available via www.springerlink.com]
    • Maisch B., Portig I., Ristic A., Hufnagel G., and Pankuweit S. Definition of inflammatory cardiomyopathy (myocarditis): on the way to consensus. A status report. Herz 25 (2000) 200-209. http://www.springerlink.com [available via www.springerlink.com]
    • (2000) Herz , vol.25 , pp. 200-209
    • Maisch, B.1    Portig, I.2    Ristic, A.3    Hufnagel, G.4    Pankuweit, S.5
  • 23
    • 1842633196 scopus 로고    scopus 로고
    • Task Force on the Diagnosis and Management of Pericardial Diseases of the European Society of Cardiology. Guidelines on the diagnosis and management of pericardial diseases executive summary
    • Maisch B., Seferovic P.M., Ristic A.D., et al. Task Force on the Diagnosis and Management of Pericardial Diseases of the European Society of Cardiology. Guidelines on the diagnosis and management of pericardial diseases executive summary. Eur Heart J 25 (2004) 587-610
    • (2004) Eur Heart J , vol.25 , pp. 587-610
    • Maisch, B.1    Seferovic, P.M.2    Ristic, A.D.3
  • 24
    • 0029864693 scopus 로고    scopus 로고
    • Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of Cardiomyopathies
    • Richardson P., McKenna W., Bristow M., et al. Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of Cardiomyopathies. Circulation 93 (1996) 841-842
    • (1996) Circulation , vol.93 , pp. 841-842
    • Richardson, P.1    McKenna, W.2    Bristow, M.3
  • 25
    • 0019165493 scopus 로고
    • Echocardiographic measurements in normal subjects from infancy to old age
    • Henry W.L., Gardin J.M., and Ware J.H. Echocardiographic measurements in normal subjects from infancy to old age. Circulation 62 (1980) 1054-1061
    • (1980) Circulation , vol.62 , pp. 1054-1061
    • Henry, W.L.1    Gardin, J.M.2    Ware, J.H.3
  • 26
    • 0032934453 scopus 로고    scopus 로고
    • Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy
    • Mestroni L., Maisch B., McKenna W.J., et al. Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy. Eur Heart J 20 (1999) 10-93
    • (1999) Eur Heart J , vol.20 , pp. 10-93
    • Mestroni, L.1    Maisch, B.2    McKenna, W.J.3
  • 27
    • 0025289255 scopus 로고
    • Phenotyping of macrophages with monoclonal antibodies in endomyocardial biopsies as a new approach to diagnosis of myocarditis
    • Mues B., Brisse B., Zwadlo G., Themann H., Bender P., and Sorg C. Phenotyping of macrophages with monoclonal antibodies in endomyocardial biopsies as a new approach to diagnosis of myocarditis. Eur Heart J 11 (1990) 619-627
    • (1990) Eur Heart J , vol.11 , pp. 619-627
    • Mues, B.1    Brisse, B.2    Zwadlo, G.3    Themann, H.4    Bender, P.5    Sorg, C.6
  • 28
    • 0033935852 scopus 로고    scopus 로고
    • Prevalence of viral genome in endomyocardial biopsies from patients with inflammatory heart muscle disease
    • [available via www.springerlink.com]
    • Pankuweit S., Portig I., Eckhardt H., Crombach M., Hufnagel G., and Maisch B. Prevalence of viral genome in endomyocardial biopsies from patients with inflammatory heart muscle disease. Herz 25 (2000) 221-226. http://www.springerlink.com [available via www.springerlink.com]
    • (2000) Herz , vol.25 , pp. 221-226
    • Pankuweit, S.1    Portig, I.2    Eckhardt, H.3    Crombach, M.4    Hufnagel, G.5    Maisch, B.6
  • 29
    • 2142649184 scopus 로고    scopus 로고
    • Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome
    • Ruppert V., Nolte D., Aschenbrenner T., Pankuweit S., Funck R., and Maisch B. Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome. Biochem Biophys Res Commun 318 (2004) 535-543
    • (2004) Biochem Biophys Res Commun , vol.318 , pp. 535-543
    • Ruppert, V.1    Nolte, D.2    Aschenbrenner, T.3    Pankuweit, S.4    Funck, R.5    Maisch, B.6
  • 30
    • 22244436280 scopus 로고    scopus 로고
    • Echocardiographic evaluation in asymptomatic relatives of patients with dilated cardiomyopathy reveals preclinical disease
    • Mahon N.G., Murphy R.T., MacRae C.A., Caforio A.L., Elliott P.M., and McKenna W.J. Echocardiographic evaluation in asymptomatic relatives of patients with dilated cardiomyopathy reveals preclinical disease. Ann Intern Med 143 (2005) 108-115
    • (2005) Ann Intern Med , vol.143 , pp. 108-115
    • Mahon, N.G.1    Murphy, R.T.2    MacRae, C.A.3    Caforio, A.L.4    Elliott, P.M.5    McKenna, W.J.6
  • 31
    • 0028145745 scopus 로고
    • A genetic defect that causes conduction system disease and dilated cardiomyopathy maps to 1p1-1q21
    • Kass S., MacRae C., Graber H.L., et al. A genetic defect that causes conduction system disease and dilated cardiomyopathy maps to 1p1-1q21. Nat Genet 7 (1994) 546-551
    • (1994) Nat Genet , vol.7 , pp. 546-551
    • Kass, S.1    MacRae, C.2    Graber, H.L.3
  • 32
    • 0033358083 scopus 로고    scopus 로고
    • Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-2q22
    • Jung M., Poepping I., Perrot A., et al. Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-2q22. Am J Hum Genet 65 (1999) 1068-1077
    • (1999) Am J Hum Genet , vol.65 , pp. 1068-1077
    • Jung, M.1    Poepping, I.2    Perrot, A.3
  • 33
    • 0030031004 scopus 로고    scopus 로고
    • Mapping a cardiomyopathy locus to chromosome 3p22-p25
    • Olson T.M., and Keating M.T. Mapping a cardiomyopathy locus to chromosome 3p22-p25. J Clin Invest 97 (1996) 528-532
    • (1996) J Clin Invest , vol.97 , pp. 528-532
    • Olson, T.M.1    Keating, M.T.2
  • 34
    • 0030882270 scopus 로고    scopus 로고
    • Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23
    • Messina D.N., Speer M.C., Pericak-Vance A., and McNally E.M. Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23. Am J Hum Genet 61 (1997) 909-917
    • (1997) Am J Hum Genet , vol.61 , pp. 909-917
    • Messina, D.N.1    Speer, M.C.2    Pericak-Vance, A.3    McNally, E.M.4
  • 35
    • 0037323583 scopus 로고    scopus 로고
    • New phenotype of familial dilated cardiomyopathy and conduction disorders
    • Oropeza E.S., and Cadena C.N. New phenotype of familial dilated cardiomyopathy and conduction disorders. Am Heart J 145 (2003) 317-323
    • (2003) Am Heart J , vol.145 , pp. 317-323
    • Oropeza, E.S.1    Cadena, C.N.2
  • 36
    • 0034620567 scopus 로고    scopus 로고
    • Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement
    • Brodsky G.L., Muntoni F., Miocic S., Sinagra G., Sewry C., and Mestroni L. Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement. Circulation 101 (2000) 473-476
    • (2000) Circulation , vol.101 , pp. 473-476
    • Brodsky, G.L.1    Muntoni, F.2    Miocic, S.3    Sinagra, G.4    Sewry, C.5    Mestroni, L.6
  • 37
    • 0032977685 scopus 로고    scopus 로고
    • Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
    • Bonne G., Di Barletta M.R., Varnous S., et al. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nat Genet 21 (1999) 285-288
    • (1999) Nat Genet , vol.21 , pp. 285-288
    • Bonne, G.1    Di Barletta, M.R.2    Varnous, S.3
  • 39
    • 0033793971 scopus 로고    scopus 로고
    • Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genes
    • Zatz M., Vainzof M., and Passos-Bueno M.R. Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genes. Curr Opin Neurol 13 (2000) 511-517
    • (2000) Curr Opin Neurol , vol.13 , pp. 511-517
    • Zatz, M.1    Vainzof, M.2    Passos-Bueno, M.R.3
  • 40
    • 0037066427 scopus 로고    scopus 로고
    • The danger model: a renewed sense of self
    • Matzinger P. The danger model: a renewed sense of self. Science 296 (2002) 301-305
    • (2002) Science , vol.296 , pp. 301-305
    • Matzinger, P.1
  • 42
    • 0345491504 scopus 로고    scopus 로고
    • Asthma as a paradigm for autoimmune disease
    • Rottem M., and Shoenfeld Y. Asthma as a paradigm for autoimmune disease. Int Arch Allergy Immunol 123 (2003) 210-214
    • (2003) Int Arch Allergy Immunol , vol.123 , pp. 210-214
    • Rottem, M.1    Shoenfeld, Y.2
  • 43
    • 0036234468 scopus 로고    scopus 로고
    • Pathways of apoptosis in lymphocyte development, homeostasis, and disease
    • [Suppl.]
    • Rathmell J.C., and Thompson C.B. Pathways of apoptosis in lymphocyte development, homeostasis, and disease. Cell 109 (2002) S97-S107 [Suppl.]
    • (2002) Cell , vol.109
    • Rathmell, J.C.1    Thompson, C.B.2
  • 44
    • 0035555025 scopus 로고    scopus 로고
    • Autoimmunity and lymphoma: tribulations of B cells
    • Mackay I.R., and Rose N.R. Autoimmunity and lymphoma: tribulations of B cells. Nat Immunol 2 (2001) 793-795
    • (2001) Nat Immunol , vol.2 , pp. 793-795
    • Mackay, I.R.1    Rose, N.R.2
  • 45
    • 0036693720 scopus 로고    scopus 로고
    • Myelodysplastic and myeloproliferative syndromes associated with giant cell arteritis and polymyalgia rheumatica: a coincidental coexistence or a causal relationship?
    • Espinosa G., Font J., Munoz-Rodriguez F.J., Cervera R., and Ingelmo M. Myelodysplastic and myeloproliferative syndromes associated with giant cell arteritis and polymyalgia rheumatica: a coincidental coexistence or a causal relationship?. Clin Rheumatol 21 (2002) 309-313
    • (2002) Clin Rheumatol , vol.21 , pp. 309-313
    • Espinosa, G.1    Font, J.2    Munoz-Rodriguez, F.J.3    Cervera, R.4    Ingelmo, M.5
  • 46
    • 0020529334 scopus 로고
    • Familial autoimmunity: twenty years later
    • Olanoff L.S., and Fundenberg H.H. Familial autoimmunity: twenty years later. J Clin Lab Immunol 11 (1983) 105-111
    • (1983) J Clin Lab Immunol , vol.11 , pp. 105-111
    • Olanoff, L.S.1    Fundenberg, H.H.2
  • 47
    • 0346599403 scopus 로고    scopus 로고
    • An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains
    • Finnish-German APECED Consortium. An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains. Nat Genet 17 (1997) 399-403
    • (1997) Nat Genet , vol.17 , pp. 399-403
    • Finnish-German APECED Consortium1
  • 48
    • 0029006893 scopus 로고
    • Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunity
    • Rieux-Laucat F., Le Deist F., Hivroz C., et al. Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunity. Science 268 (1995) 1347-1349
    • (1995) Science , vol.268 , pp. 1347-1349
    • Rieux-Laucat, F.1    Le Deist, F.2    Hivroz, C.3
  • 49
    • 0029737324 scopus 로고    scopus 로고
    • Fas ligand mutation in a patient with systemic lupus erythematosus and lymphoproliferative disease
    • Wu J., Wilson J., He J., Xiang L., Schur P.H., and Mountz J.D. Fas ligand mutation in a patient with systemic lupus erythematosus and lymphoproliferative disease. J Clin Invest 98 (1996) 1107-1113
    • (1996) J Clin Invest , vol.98 , pp. 1107-1113
    • Wu, J.1    Wilson, J.2    He, J.3    Xiang, L.4    Schur, P.H.5    Mountz, J.D.6
  • 50
    • 0024466925 scopus 로고
    • Idiopathic dilated cardiomyopathy and atopic disease: epidemiologic evidence for an association with asthma
    • Coughlin S.S., Szklo M., Baughman K., and Pearson T.A. Idiopathic dilated cardiomyopathy and atopic disease: epidemiologic evidence for an association with asthma. Am Heart J 118 (1989) 768-774
    • (1989) Am Heart J , vol.118 , pp. 768-774
    • Coughlin, S.S.1    Szklo, M.2    Baughman, K.3    Pearson, T.A.4
  • 51
    • 0027233367 scopus 로고
    • Recent advances in pulmonary medicine
    • Weinberger S.E. Recent advances in pulmonary medicine. N Engl J Med 328 (1993) 1389-1397
    • (1993) N Engl J Med , vol.328 , pp. 1389-1397
    • Weinberger, S.E.1
  • 52
    • 0037972477 scopus 로고    scopus 로고
    • Doppler echocardiographic evaluation of ventricular function in patients with rheumatoid arthritis
    • Alpaslan M., Onrat E., and Evcik D. Doppler echocardiographic evaluation of ventricular function in patients with rheumatoid arthritis. Clin Rheumatol 22 (2003) 84-87
    • (2003) Clin Rheumatol , vol.22 , pp. 84-87
    • Alpaslan, M.1    Onrat, E.2    Evcik, D.3
  • 53
    • 0035985090 scopus 로고    scopus 로고
    • Genetic control of autoimmunity in Type I diabetes and associated disorders
    • Redondo M.J., and Eisenbarth G.S. Genetic control of autoimmunity in Type I diabetes and associated disorders. Diabetologia 45 (2002) 605-622
    • (2002) Diabetologia , vol.45 , pp. 605-622
    • Redondo, M.J.1    Eisenbarth, G.S.2
  • 54
    • 0034892128 scopus 로고    scopus 로고
    • Autoimmune disease: why and where it occurs
    • Marrack P., Kappler J., and Kotzin B.L. Autoimmune disease: why and where it occurs. Nat Med 7 (2001) 899-905
    • (2001) Nat Med , vol.7 , pp. 899-905
    • Marrack, P.1    Kappler, J.2    Kotzin, B.L.3
  • 55
    • 0036676656 scopus 로고    scopus 로고
    • An update on genetic studies of systemic lupus erythematosus
    • Tsao B.P. An update on genetic studies of systemic lupus erythematosus. Curr Rheumatol Rep 4 (2002) 359-367
    • (2002) Curr Rheumatol Rep , vol.4 , pp. 359-367
    • Tsao, B.P.1
  • 56
    • 0035555022 scopus 로고    scopus 로고
    • The genetics of complex autoimmune diseases: non-MHC susceptibility genes
    • Wandstrat A., and Wakeland E. The genetics of complex autoimmune diseases: non-MHC susceptibility genes. Nat Immunol 2 (2001) 802-809
    • (2001) Nat Immunol , vol.2 , pp. 802-809
    • Wandstrat, A.1    Wakeland, E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.