Literature DB >> 6542602

Seventeen year follow-up of a patient with hypertrophic cardiomyopathy which progressed to dilated cardiomyopathy.

M Funakoshi, M Imamura, J Sasaki, M Fujino, T Kawano, Y Sasaki, Y Nakashima, T Motooka, K Fukuda, M Imagawa.   

Abstract

The progression of hypertrophic cardiomyopathy (HCM) to dilated cardiomyopathy (DCM) has been rarely reported. We report a patient with HCM who had been followed for 17 years and in whom DCM became evident.

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Year:  1984        PMID： 6542602     DOI： 10.1536/ihj.25.805

Source DB:  PubMed          Journal:  Jpn Heart J        ISSN： 0021-4868


  6 in total

1.  Cardiomyopathy.

Authors: 
Journal:  J Natl Med Assoc       Date:  1990-08       Impact factor: 1.798

2.  Cardiac troponin T Arg92Trp mutation and progression from hypertrophic to dilated cardiomyopathy.

Authors:  N Fujino; M Shimizu; H Ino; K Okeie; M Yamaguchi; T Yasuda; H Kokado; H Mabuchi
Journal:  Clin Cardiol       Date:  2001-05       Impact factor: 2.882

3.  Long-term course and cardiac sympathetic nerve activity in patients with hypertrophic cardiomyopathy.

Authors:  M Shimizu; N Sugihara; Y Kita; K Shimizu; Y Horita; K Nakajima; J Taki; R Takeda
Journal:  Br Heart J       Date:  1992-02

4.  Progression from hypertrophic cardiomyopathy to dilated cardiomyopathy.

Authors:  L L Cregler
Journal:  J Natl Med Assoc       Date:  1989-07       Impact factor: 1.798

5.  CMR assessment and clinical outcomes of hypertrophic cardiomyopathy with or without ventricular remodeling in the end-stage phase.

Authors:  Sainan Cheng; Yeon Hyeon Choe; Hideki Ota; Chen Cui; Gang Yin; Minjie Lu; Lu Li; Xiuyu Chen; Sanjay K Prasad; Shihua Zhao
Journal:  Int J Cardiovasc Imaging       Date:  2017-10-25       Impact factor: 2.357

6.  Left ventricular chamber dilatation in hypertrophic cardiomyopathy: related variables and prognosis in patients with medical and surgical therapy.

Authors:  C Seiler; R Jenni; G Vassalli; M Turina; O M Hess
Journal:  Br Heart J       Date:  1995-11
  6 in total

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