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Volumn 31, Issue 8, 2014, Pages 931-935

Double jeopardy in the echocardiography laboratory: Coexistence of two distinct cardiomyopathies?

Author keywords

Amyloid heart disease; Hypertrophic cardiomyopathy; Left ventricular noncompaction; Phenotypic variability

Indexed keywords

ADULT; AGED; CARDIAC PATIENT; CARDIOVASCULAR MAGNETIC RESONANCE; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE ASSOCIATION; FEMALE; GENETIC SCREENING; HEART AMYLOIDOSIS; HEART MUSCLE BIOPSY; HUMAN; HUMAN TISSUE; HYPERTROPHIC CARDIOMYOPATHY; LABORATORY DIAGNOSIS; MALE; MEDICAL RECORD REVIEW; MIDDLE AGED; NUCLEAR MAGNETIC RESONANCE SCANNER; PATIENT IDENTIFICATION; RARE DISEASE; SHORT SURVEY; TRANSTHORACIC ECHOCARDIOGRAPHY; ULTRASOUND SCANNER; VENTRICULAR NONCOMPACTION; AMYLOIDOSIS; CASE REPORT; COMPLICATION; CONGENITAL HEART MALFORMATION; DIFFERENTIAL DIAGNOSIS; ECHOCARDIOGRAPHY; ECHOGRAPHY; PROCEDURES;

EID: 84908068112     PISSN: 07422822     EISSN: 15408175     Source Type: Journal    
DOI: 10.1111/echo.12502     Document Type: Short Survey
Times cited : (1)

References (8)
  • 1
    • 83555176173 scopus 로고    scopus 로고
    • 2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: A report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines
    • Gersh BJ, Maron BJ, Bonow RO, et al: 2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: A report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Circulation 2011;124:e783-e831.
    • (2011) Circulation , vol.124 , pp. e783-e831
    • Gersh, B.J.1    Maron, B.J.2    Bonow, R.O.3
  • 3
    • 21344474382 scopus 로고    scopus 로고
    • Left ventricular non-compaction: Insights from cardiovascular magnetic resonance imaging
    • Petersen SE, Selvanayagam JB, Wiesmann F, et al: Left ventricular non-compaction: Insights from cardiovascular magnetic resonance imaging. J Am Coll Cardiol 2005;46:101-105.
    • (2005) J Am Coll Cardiol , vol.46 , pp. 101-105
    • Petersen, S.E.1    Selvanayagam, J.B.2    Wiesmann, F.3
  • 4
    • 78649958228 scopus 로고    scopus 로고
    • The R820W mutation in the MYBPC3 gene, associated with hypertrophic cardiomyopathy in cats, causes hypertrophic cardiomyopathy and left ventricular non-compaction in humans
    • Ripoll Vera T, Monserrat Iglesias L, Hermida Prieto M, et al: The R820W mutation in the MYBPC3 gene, associated with hypertrophic cardiomyopathy in cats, causes hypertrophic cardiomyopathy and left ventricular non-compaction in humans. Int J Cardiol 2010;145:405-407.
    • (2010) Int J Cardiol , vol.145 , pp. 405-407
    • Ripoll Vera, T.1    Monserrat Iglesias, L.2    Hermida Prieto, M.3
  • 5
    • 84856205285 scopus 로고    scopus 로고
    • Cardiac MRI in a patient with coincident left ventricular non-compaction and hypertrophic cardiomyopathy
    • Alizadeh-Sani Z, Madadi S, Sadeghpour A, et al: Cardiac MRI in a patient with coincident left ventricular non-compaction and hypertrophic cardiomyopathy. J Tehran Heart Cent 2011;6:214-216.
    • (2011) J Tehran Heart Cent , vol.6 , pp. 214-216
    • Alizadeh-Sani, Z.1    Madadi, S.2    Sadeghpour, A.3
  • 6
    • 84885587721 scopus 로고    scopus 로고
    • Cardiac myosin-binding protein C gene mutation expressed as hypertrophic cardiomyopathy and left ventricular noncompaction within two families: Insights from cardiac magnetic resonance in clinical screening: Camuglia MYBPC3 gene mutation and MRI
    • Camuglia AC, Younger JF, McGaughran J, et al: Cardiac myosin-binding protein C gene mutation expressed as hypertrophic cardiomyopathy and left ventricular noncompaction within two families: Insights from cardiac magnetic resonance in clinical screening: Camuglia MYBPC3 gene mutation and MRI. Int J Cardiol 2013;168:2950-2952.
    • (2013) Int J Cardiol , vol.168 , pp. 2950-2952
    • Camuglia, A.C.1    Younger, J.F.2    McGaughran, J.3
  • 7
    • 77952431044 scopus 로고    scopus 로고
    • Short communication: The cardiac myosin binding protein C Arg502Trp mutation: A common cause of hypertrophic cardiomyopathy
    • Saltzman AJ, Mancini-DiNardo D, Li C, et al: Short communication: The cardiac myosin binding protein C Arg502Trp mutation: A common cause of hypertrophic cardiomyopathy. Circ Res 2010;106:1549-1552.
    • (2010) Circ Res , vol.106 , pp. 1549-1552
    • Saltzman, A.J.1    Mancini-DiNardo, D.2    Li, C.3
  • 8
    • 44649118695 scopus 로고    scopus 로고
    • Mutations in sarcomere protein genes in left ventricular noncompaction
    • Klaassen S, Probst S, Oechslin E, et al: Mutations in sarcomere protein genes in left ventricular noncompaction. Circulation 2008;117:2893-2901.
    • (2008) Circulation , vol.117 , pp. 2893-2901
    • Klaassen, S.1    Probst, S.2    Oechslin, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.