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Volumn 59, Issue 10, 2006, Pages 994-996

Hypertrophic cardiomyopathy: Never-ending complexity;Miocardiopatía hipertrófica: La complejidad que no cesa

Author keywords

[No Author keywords available]

Indexed keywords

EDITORIAL; GENE MUTATION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; PATHOPHYSIOLOGY; PREVALENCE; PROGNOSIS;

EID: 37849185591     PISSN: 03008932     EISSN: None     Source Type: Journal    
DOI: 10.1157/13093974     Document Type: Editorial
Times cited : (4)

References (14)
  • 1
    • 0025040392 scopus 로고
    • A molecular basis for familial hypertrophic cardiomyopathy: A beta cardiac myosin heavy chain gene missense mutation
    • Geisterfer-Lowrance AA, Kass S, Tanigawa G, Vosberg HP, McKenna W, Seidman CE, et al. A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation. Cell. 1990;62:999-1006.
    • (1990) Cell , vol.62 , pp. 999-1006
    • Geisterfer-Lowrance, A.A.1    Kass, S.2    Tanigawa, G.3    Vosberg, H.P.4    McKenna, W.5    Seidman, C.E.6
  • 2
    • 0035940383 scopus 로고    scopus 로고
    • New concepts in hypertrophic cardiomyopathy, part I
    • Roberts R, Sigwart U. New concepts in hypertrophic cardiomyopathy, part I. Circulation. 2001;104:2113-6.
    • (2001) Circulation , vol.104 , pp. 2113-2116
    • Roberts, R.1    Sigwart, U.2
  • 3
    • 0036796263 scopus 로고    scopus 로고
    • Phenotypic diversity in hypertrophic cardiomyopathy
    • Arad M, Seidman JG, Seidman CE. Phenotypic diversity in hypertrophic cardiomyopathy. Hum Mol Genet. 2002;11:2499-506.
    • (2002) Hum Mol Genet. , vol.11 , pp. 2499-2506
    • Arad, M.1    Seidman, J.G.2    Seidman, C.E.3
  • 4
    • 34247848939 scopus 로고    scopus 로고
    • Miocardiopatía hipertrófica. Bases genéticas e implicaciones clínicas
    • Navarro-López F. Miocardiopatía hipertrófica. Bases genéticas e implicaciones clínicas. Rev Esp Cardiol. 2004; 57 Supl 1:22-32.
    • (2004) Rev Esp Cardiol. , vol.57 , Issue.SUPPL. 1 , pp. 22-32
    • Navarro-López, F.1
  • 5
    • 37849187787 scopus 로고    scopus 로고
    • Mutaciones en el gen de la cadena pesada de la betamiosina en pacientes con miocardiopatía hipertrófica
    • Laredo R, Monserrat L, Hermida-Prieto M, Fernández X, Rodríguez I, Cazón L, et al. Mutaciones en el gen de la cadena pesada de la betamiosina en pacientes con miocardiopatía hipertrófica. Rev Esp Cardiol. 2006;59:1008-18.
    • (2006) Rev Esp Cardiol. , vol.59 , pp. 1008-1018
    • Laredo, R.1    Monserrat, L.2    Hermida-Prieto, M.3    Fernández, X.4    Rodríguez, I.5    Cazón, L.6
  • 6
    • 0037630018 scopus 로고    scopus 로고
    • Hypertrophic cardiomyopathy. Distribution of disease genes, spectrum of mutations, and implications for molecular diagnosis estrategy
    • 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 molecular diagnosis estrategy. 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
  • 7
    • 4043081356 scopus 로고    scopus 로고
    • Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy
    • Van Driest SL, Jaeger MA, Ommen SR, Hill ML, Gersh BJ, Tajik AJ. Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy. J Am Coll Cardiol. 2004;44:602-10.
    • (2004) J Am Coll Cardiol. , vol.44 , pp. 602-610
    • Van Driest, S.L.1    Jaeger, M.A.2    Ommen, S.R.3    Hill, M.L.4    Gersh, B.J.5    Tajik, A.J.6
  • 8
    • 10744228388 scopus 로고    scopus 로고
    • Genetics of hypertrophic cardiomyopathy in easter Finland: Few founder mutations with benign or intermediate phenotypes
    • Jaaskelainen P, Miettinen R, Karkkainen P, Toivonen L, Laakso M, Kuusisto J. Genetics of hypertrophic cardiomyopathy in easter Finland: few founder mutations with benign or intermediate phenotypes. Ann Med. 2004;36:23-32.
    • (2004) Ann Med. , vol.36 , pp. 23-32
    • Jaaskelainen, P.1    Miettinen, R.2    Karkkainen, P.3    Toivonen, L.4    Laakso, M.5    Kuusisto, J.6
  • 9
    • 9444255079 scopus 로고    scopus 로고
    • Mutations profile in Chinese patients with hypertrophic cardiomyopathy
    • Song L, Zou Y, Wang J, Wang Z, Zhen Y, Lou K, et al. Mutations profile in Chinese patients with hypertrophic cardiomyopathy. Clin Chim Acta. 2005;351:209-16.
    • (2005) Clin Chim Acta , vol.351 , pp. 209-216
    • Song, L.1    Zou, Y.2    Wang, J.3    Wang, Z.4    Zhen, Y.5    Lou, K.6
  • 10
    • 0041866796 scopus 로고    scopus 로고
    • Hypertrophic cardiomyopathy: Low frequency of mutations in the beta-myosin heavy chain (MYC7) and cardiac troponin T (TNNT2) genes among Spanish patients
    • García-Castro M, Reguero JR, Batalla A, Diaz-Molina B, González P, Álvarez V, et al. Hypertrophic cardiomyopathy: low frequency of mutations in the beta-myosin heavy chain (MYC7) and cardiac troponin T (TNNT2) genes among Spanish patients. Clin Chem. 2003; 49:1279-85.
    • (2003) Clin Chem. , vol.49 , pp. 1279-1285
    • García-Castro, M.1    Reguero, J.R.2    Batalla, A.3    Diaz-Molina, B.4    González, P.5    Álvarez, V.6
  • 13
    • 13944269529 scopus 로고    scopus 로고
    • Hypertrophic cardiomyopathy-related beta-myosin mutations cause highly variable calcum sensitivity with functional imbalances among individual muscle cells
    • Kirshner SE, Becker E, Antognozzi M, Kubis H-P, Francino A, Navarro-López F, et al. Hypertrophic cardiomyopathy-related beta-myosin mutations cause highly variable calcum sensitivity with functional imbalances among individual muscle cells. Am J Physiol Heart Circ Physiol. 2005;288:1242-51.
    • (2005) Am J Physiol Heart Circ Physiol. , vol.288 , pp. 1242-1251
    • Kirshner, S.E.1    Becker, E.2    Antognozzi, M.3    Kubis, H.-P.4    Francino, A.5    Navarro-López, F.6
  • 14
    • 33749584344 scopus 로고    scopus 로고
    • Miocardiopatía hipertrófica: Baja frecuencia de mutaciones en el gen de la cadena pesada de la betamiosina cardiaca
    • Mora R, Merino JL, Peinado R, Olias F, García-Guereta L, Del Cerro MJ, et al. Miocardiopatía hipertrófica: baja frecuencia de mutaciones en el gen de la cadena pesada de la betamiosina cardiaca. Rev Esp Cardiol. 2006;59:846-9.
    • (2006) Rev Esp Cardiol. , vol.59 , pp. 846-849
    • Mora, R.1    Merino, J.L.2    Peinado, R.3    Olias, F.4    García-Guereta, L.5    Del Cerro, M.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.