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

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

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

3 ) age was 51.2 (13.8) years, and 7 (70%) had idiopathic dilated cardiomyopathy.

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

5 imited evidence is available specifically on idiopathic dilated cardiomyopathy.

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

7 nts with endstage ischemic cardiomyopathy or idiopathic dilated cardiomyopathy.

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

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

10 ing ventricular arrhythmias in patients with idiopathic dilated cardiomyopathy.

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

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

13 left ventricular efficiency in patients with idiopathic dilated cardiomyopathy.

14 1Met, was identified as the genetic cause of idiopathic dilated cardiomyopathy.

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

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

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

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

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

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

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

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

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

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

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

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

27 be present in the hearts of individuals with idiopathic dilated cardiomyopathy, as well as the hearts

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

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

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

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

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

33 Idiopathic dilated cardiomyopathy (DCM) aggregates in fa

34 n may act as a trigger in the development of idiopathic dilated cardiomyopathy (DCM) among individual

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

36 Idiopathic dilated cardiomyopathy (DCM) is a disease of

37 Idiopathic dilated cardiomyopathy (DCM) is responsible f

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

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

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

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

42 gene (TTNtvs) are common in individuals with idiopathic dilated cardiomyopathy (DCM).

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

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

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

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

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

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

49 eart failure programs included patients with idiopathic dilated cardiomyopathy defined as left ventri

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

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

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

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

54 In idiopathic dilated cardiomyopathy, functional improvemen

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

56 Idiopathic dilated cardiomyopathy had severe hypertrophy

57 Idiopathic dilated cardiomyopathy hearts were obtained a

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

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

60 Idiopathic dilated cardiomyopathy (IDC) is characterized

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

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

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

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

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

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

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

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

69 1 with X-linked cardiomyopathy, and 23 with idiopathic dilated cardiomyopathy (IDC).

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

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

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

73 VC) and postmyocarditis VT; in patients with idiopathic dilated cardiomyopathy (IDCM) and postmyocard

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

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

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

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

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

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

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

81 Initial diagnostic categories were idiopathic dilated cardiomyopathy in 67 children (47%),

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

83 Idiopathic dilated cardiomyopathy is a common cause of h

84 Although idiopathic dilated cardiomyopathy is often viewed as an

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

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

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

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

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

90 Idiopathic dilated cardiomyopathy occurring in families,

91 Idiopathic dilated cardiomyopathy, of which approximatel

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

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

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

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

96 137 children with myocarditis and 1249 with idiopathic dilated cardiomyopathy received HT.

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

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

99 Idiopathic dilated cardiomyopathy showed a doubling of c

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

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

102 In idiopathic dilated cardiomyopathy, there are scarce data

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

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

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

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

107 Sixty-nine patients with idiopathic dilated cardiomyopathy underwent implantable

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

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

110 Ten patients with idiopathic dilated cardiomyopathy were also analyzed to

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

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

113 221 children with myocarditis and 1583 with idiopathic dilated cardiomyopathy who were <18 years old