ライフサイエンスコーパス: idiopathic dilated cardiomyopathy

1 more severe heart failure than children with idiopathic dilated cardiomyopathy.

2 imited evidence is available specifically on idiopathic dilated cardiomyopathy.

3 oppose the negative effects of ischemic and idiopathic dilated cardiomyopathy.

4 ing ventricular arrhythmias in patients with idiopathic dilated cardiomyopathy.

5 nts with endstage ischemic cardiomyopathy or idiopathic dilated cardiomyopathy.

6 domain (MVt) and correlates with hereditary idiopathic dilated cardiomyopathy.

7 rdial biopsy samples, 180 were identified as idiopathic dilated cardiomyopathy.

8 HF and from patients with HF attributable to idiopathic dilated cardiomyopathy.

9 ay improve cardiac function in patients with idiopathic dilated cardiomyopathy.

10 left ventricular efficiency in patients with idiopathic dilated cardiomyopathy.

11 1Met, was identified as the genetic cause of idiopathic dilated cardiomyopathy.

12 pared with children who are transplanted for idiopathic dilated cardiomyopathy.

13 elderly persons who are at increased risk of idiopathic dilated cardiomyopathy.

14 ies had chronic heart failure resulting from idiopathic dilated cardiomyopathy.

15 B viruses are detected in about one-third of idiopathic dilated cardiomyopathies.

16 rt disease (152 myocytes per million) and in idiopathic dilated cardiomyopathy (131 myocytes per mill

17 ), of black ethnicity (18% vs. 2%), and have idiopathic-dilated cardiomyopathy (62% vs. 9%) (all p <

18 The molecular basis of idiopathic dilated cardiomyopathy, a primary myocardial

19 age 42+/-15.5 years; 64 patients (65.9%) had idiopathic dilated cardiomyopathy and 21 patients (21.6%

20 e studied 11 patients with LV failure due to idiopathic dilated cardiomyopathy and 7 control subjects

21 tion patients with ischemic heart disease or idiopathic dilated cardiomyopathy and compared with samp

22 Hearts from all four patients with idiopathic dilated cardiomyopathy and from one of the th

23 ng in approximately 25% of familial cases of idiopathic dilated cardiomyopathy and in 18% of sporadic

24 s had severe chronic heart failure: four had idiopathic dilated cardiomyopathy, and three had ischemi

25 r in patients with ischemic heart disease or idiopathic dilated cardiomyopathy as the cause of heart

26 lation in patients with heart failure due to idiopathic dilated cardiomyopathy but not in control sub

27 It shares many clinical characteristics with idiopathic dilated cardiomyopathy but occurs at a younge

28 sis of data from two case-control studies of idiopathic dilated cardiomyopathy carried out in Baltimo

29 hus examined changes in prognosis of a large idiopathic dilated cardiomyopathy cohort systematically

30 differentially upregulated in patients with idiopathic dilated cardiomyopathy compared with other fo

31 function exists in patients with acute-onset idiopathic dilated cardiomyopathy (DCM) and to explore i

32 Idiopathic dilated cardiomyopathy (DCM) is a disease of

33 Idiopathic dilated cardiomyopathy (DCM) is responsible f

34 The cause of idiopathic dilated cardiomyopathy (DCM) is unknown by de

35 re obtained at transplant from patients with idiopathic dilated cardiomyopathy (DCM) not requiring LV

36 Abs) against cardiac myosin (CM) in clinical idiopathic dilated cardiomyopathy (DCM) remains controve

37 ta-adrenergic contractility in patients with idiopathic dilated cardiomyopathy (DCM) through nitric o

38 hocardiographic function among children with idiopathic dilated cardiomyopathy (DCM).

39 ted in a substantial number of patients with idiopathic dilated cardiomyopathy (DCM).

40 r experimental pedigree used in the study of idiopathic dilated cardiomyopathy (DCM).

41 o chronic hypertension (LVH-HTN), and 9 with idiopathic dilated cardiomyopathy (DCM).

42 with ischemic cardiomyopathy (ICM, n=16) or idiopathic dilated cardiomyopathy (DCM, n=15) and nonfai

43 d by ischemic cardiomyopathy (ICM-MR) and by idiopathic dilated cardiomyopathy (DCM-MR) by use of rea

44 to dramatic improvement in the prognosis of idiopathic dilated cardiomyopathy during the past 3 deca

45 njury and in heart tissue from patients with idiopathic dilated cardiomyopathy, focal areas of intens

46 ssed genes in lymphocytic myocarditis versus idiopathic dilated cardiomyopathy (fold change >1.2; fal

47 Main etiologies of HF in LA are idiopathic dilated cardiomyopathy (from 1.3% to 37%), C'

48 In idiopathic dilated cardiomyopathy, functional improvemen

49 All of the cases of idiopathic dilated cardiomyopathy had evidence of ventri

50 Idiopathic dilated cardiomyopathy had severe hypertrophy

51 Idiopathic dilated cardiomyopathy hearts were obtained a

52 four index patients initially diagnosed with idiopathic dilated cardiomyopathy (IDC) and to provide c

53 may underlie from one-quarter to one-half of idiopathic dilated cardiomyopathy (IDC) diagnoses.

54 Idiopathic dilated cardiomyopathy (IDC) is characterized

55 Many cases of idiopathic dilated cardiomyopathy (IDC) result from an i

56 s to heart failure, patients with hereditary idiopathic dilated cardiomyopathy (IDC) were examined fo

57 left and right ventricular membranes from 14 idiopathic dilated cardiomyopathy (IDC), 8 primary pulmo

58 ons of hearts obtained from 36 subjects with idiopathic dilated cardiomyopathy (IDC), 8 subjects with

59 ult heart failure therapies to children with idiopathic dilated cardiomyopathy (IDC), prognosis remai

60 sus has emerged that with a new diagnosis of idiopathic dilated cardiomyopathy (IDC), the clinical sc

61 from primary pulmonary hypertension (PPH) or idiopathic dilated cardiomyopathy (IDC), we measured exp

62 ring follow-up in patients with recent onset idiopathic dilated cardiomyopathy (IDC).

63 1 with X-linked cardiomyopathy, and 23 with idiopathic dilated cardiomyopathy (IDC).

64 al human left ventricle and in patients with idiopathic dilated cardiomyopathy (IDC).

65 = 19) and failing human left ventricles with idiopathic dilated cardiomyopathy (IDC; n = 31) or ische

66 Idiopathic-dilated cardiomyopathy (IDC) is a common prim

67 study was to determine whether patients with idiopathic dilated cardiomyopathy (IDCM) exhibit alterat

68 rdiomyopathy (FDCM) to that of children with idiopathic dilated cardiomyopathy (IDCM) has produced co

69 thyroid function and myocardial injuries in idiopathic dilated cardiomyopathy (IDCM) using cardiac m

70 rvival is worse for patients with ACM versus idiopathic dilated cardiomyopathy (IDCM) with continued

71 In a subset of cases, clustered as idiopathic dilated cardiomyopathy (iDCM), the origin of

72 ance and insulin resistance in patients with idiopathic dilated cardiomyopathy (IDCM).

73 heart failure and rhythm disturbances due to idiopathic dilated cardiomyopathy identified two mutatio

74 lling World Health Organization criteria for idiopathic dilated cardiomyopathy, including negative co

75 Idiopathic dilated cardiomyopathy is a common cause of h

76 Although idiopathic dilated cardiomyopathy is often viewed as an

77 Forty-seven patients with idiopathic dilated cardiomyopathy (left ventricular ejec

78 in HF rabbit myocytes (P<0.05) and in human idiopathic dilated cardiomyopathy LV (P<0.05).

79 This study explores the possibility that idiopathic dilated cardiomyopathy may involve extensive

80 yocardium were obtained from 9 patients with idiopathic dilated cardiomyopathy (mean duration of LVAD

81 ly proven lymphocytic myocarditis (n=16) and idiopathic dilated cardiomyopathy (n=32) to develop accu

82 Idiopathic dilated cardiomyopathy occurring in families,

83 Idiopathic dilated cardiomyopathy, of which approximatel

84 ths after the procedure in two patients with idiopathic dilated cardiomyopathy, one of whom had a pac

85 duration, and an evaluation consistent with idiopathic dilated cardiomyopathy or myocarditis were en

86 action (LVEF) in adults with recent onset of idiopathic dilated cardiomyopathy or myocarditis.

87 ary prevention of sudden cardiac death in an idiopathic dilated cardiomyopathy population.

88 137 children with myocarditis and 1249 with idiopathic dilated cardiomyopathy received HT.

89 l hearts and hearts affected by ischemic and idiopathic dilated cardiomyopathy, respectively.

90 d adults, morbidity and mortality rates from idiopathic dilated cardiomyopathy rise sharply with age

91 Idiopathic dilated cardiomyopathy showed a doubling of c

92 were isolated from a patient suffering from idiopathic dilated cardiomyopathy, suggesting that such

93 In patients with idiopathic dilated cardiomyopathy, the absence of LGE at

94 In idiopathic dilated cardiomyopathy, there are scarce data

95 beta-blockers produce reverse-remodeling in idiopathic dilated cardiomyopathy, they partially revers

96 We randomly assigned 53 patients with idiopathic dilated cardiomyopathy to treatment with a be

97 mural sites was performed in 6 patients with idiopathic dilated cardiomyopathy undergoing cardiac tra

98 Fifty-eight consecutive patients with idiopathic dilated cardiomyopathy underwent baseline cli

99 Sixty-nine patients with idiopathic dilated cardiomyopathy underwent implantable

100 One hundred fifty-eight patients with idiopathic dilated cardiomyopathy underwent programmed v

101 In a patient diagnosed with idiopathic dilated cardiomyopathy, we identified two nov

102 Ten patients with idiopathic dilated cardiomyopathy were also analyzed to

103 inase activity falls to negligible levels in idiopathic dilated cardiomyopathy, whereas alpha 2-macro

104 METHOD AND In 104 patients with idiopathic dilated cardiomyopathy who underwent annulopl

105 221 children with myocarditis and 1583 with idiopathic dilated cardiomyopathy who were <18 years old