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Volumn 15, Issue 4, 2007, Pages 161-163

Structural abnormalities of the left ventricle in hypertrophic cardiomyopathy mutation carriers detectable before the development of hypertrophy

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN; TROPOMYOSIN;

EID: 34547864988     PISSN: 15685888     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF03085974     Document Type: Article
Times cited : (7)

References (14)
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  • 2
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    • (2004) Am J Cardiol , vol.93 , pp. 1510-1514
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  • 3
    • 0037070514 scopus 로고    scopus 로고
    • Hypertrophic cardiomyopathy: A systematic review
    • Maron BJ. Hypertrophic cardiomyopathy: a systematic review. JAMA 2002;287:1308-20.
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    • Maron, B.J.1
  • 4
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    • Molecular mechanisms of inherited cardiomyopathies
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    • Fatkin, D.1    Graham, R.M.2
  • 5
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    • NHLBI Program for Genomic Applications HMS. Genomics of Cardiovascular Development, Adaptation, and Remodeling. URL: http://www.cardiogenomics.org, accessed 01-2007.
    • NHLBI Program for Genomic Applications HMS. Genomics of Cardiovascular Development, Adaptation, and Remodeling. URL: http://www.cardiogenomics.org, accessed 01-2007.
  • 7
    • 0037630018 scopus 로고    scopus 로고
    • Hypertrophic cardiomyopathy: Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy
    • Richard P, Charron P, Carrier L, Ledeuil C, Cheav T, Pichereau C, et al. Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation 2003;107:2227-32.
    • (2003) Circulation , vol.107 , pp. 2227-2232
    • Richard, P.1    Charron, P.2    Carrier, L.3    Ledeuil, C.4    Cheav, T.5    Pichereau, C.6
  • 8
    • 0031049263 scopus 로고    scopus 로고
    • Experience from clinical genetics in hypertrophic cardiomyopathy: Proposal for new diagnostic criteria in adult members of affected families
    • McKenna WJ, Spirito P, Desnos M, Dubourg O, Komajda M. Experience from clinical genetics in hypertrophic cardiomyopathy: proposal for new diagnostic criteria in adult members of affected families. Heart 1997;77:130-2.
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  • 9
    • 0041663643 scopus 로고    scopus 로고
    • Tissue Doppler imaging predicts the development of hypertrophic cardiomyopathy in subjects with subclinical disease
    • Nagueh SF, McFalls J, Meyer D, Hill R, Zoghbi WA, Tam JW, et al. Tissue Doppler imaging predicts the development of hypertrophic cardiomyopathy in subjects with subclinical disease. Circulation 2003;108:395-8.
    • (2003) Circulation , vol.108 , pp. 395-398
    • Nagueh, S.F.1    McFalls, J.2    Meyer, D.3    Hill, R.4    Zoghbi, W.A.5    Tam, J.W.6
  • 10
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    • Structural abnormalities of the inferoseptal left ventricular wall detected by cardiac magnetic resonance imaging in carriers of hypertrophic cardiomyopathy mutations
    • Germans T, Wilde AA, Dijkmans PA, Chai W, Kamp O, Pinto YM, et al. Structural abnormalities of the inferoseptal left ventricular wall detected by cardiac magnetic resonance imaging in carriers of hypertrophic cardiomyopathy mutations. J Am Coll Cardiol 2006;48:2518-23.
    • (2006) J Am Coll Cardiol , vol.48 , pp. 2518-2523
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  • 11
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    • The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands
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    • Alders, M.1    Jongbloed, R.2    Deelen, W.3    van den, W.A.4    Doevendans, P.A.5    Ten Cate, F.J.6
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.