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Volumn 17, Issue 10, 2001, Pages 1061-1069

Cardiac involvement in myotonic dystrophy, Becker muscular dystrophy and mitochondrial myopathy: A five-year follow-up

Author keywords

Echocardiography; Electrocardiography; Mitochondria

Indexed keywords

ADULT; AGED; AMBULATORY MONITORING; ANAMNESIS; ARTICLE; AUSTRALIA; BECKER MUSCULAR DYSTROPHY; CLINICAL ARTICLE; CLINICAL EXAMINATION; CLINICAL OBSERVATION; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DIAGNOSTIC PROCEDURE; DISEASE COURSE; DISEASE DURATION; DISEASE SEVERITY; ELECTROCARDIOGRAPHY; ELECTROCARDIOGRAPHY MONITORING; FATALITY; FEMALE; FOLLOW UP; HEART ARRHYTHMIA; HEART DISEASE; HOSPITAL DEPARTMENT; HUMAN; MALE; MITOCHONDRIAL MYOPATHY; MOTOR DYSFUNCTION; MYOTONIC DYSTROPHY; NEUROLOGIC EXAMINATION; OUTCOMES RESEARCH; PATIENT ATTITUDE; REFERENCE VALUE; SCORING SYSTEM; SYMPTOM; TRANSTHORACIC ECHOCARDIOGRAPHY;

EID: 0035204038     PISSN: 0828282X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (27)

References (43)
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    • Mitochondrial encephalomyopathies: Back to Mendelian genetics
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    • DiMauro, S.1
  • 17
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    • Mitochondrial defects in cardiomyopathy and neuromuscular disease
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    • Wallace, D.C.1
  • 23
  • 42
    • 15644384508 scopus 로고    scopus 로고
    • Coexistence of mitochondrial DNA and β-myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure
    • (1998) Heart , vol.80 , pp. 548-558
    • Arbustini, E.1    Fasani, R.2    Morbini, P.3
  • 43
    • 0033133413 scopus 로고    scopus 로고
    • Maternally inherited cardiomyopathy: Clinical and molecular characterization of a large kindred harboring the A4300G point mutation in mitochondrial deoxyribonucleic acid
    • (1999) J Am Coll Cardiol , vol.33 , pp. 1584-1589
    • Casali, C.1    D'Amati, G.2    Bernucci, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.