ライフサイエンスコーパス: noncompaction

1 tricular cardiomyopathy, or left ventricular noncompaction.

2 atients with DCM met imaging criteria for LV noncompaction.

3 with findings overlapping myocarditis and LV noncompaction.

4 iomyopathy with features of left ventricular noncompaction.

5 omyopathy, and 23% for left ventricular (LV) noncompaction.

6 nt trabeculations to fulfill criteria for LV noncompaction.

7 oventricular block, and (3) left ventricular noncompaction.

8 ses to pregnancy and are not specific for LV noncompaction.

9 h may be compatible with the diagnosis of LV noncompaction.

10 e develop ventricular hypertrabeculation and noncompaction.

11 rtrophic cardiomyopathy and left ventricular noncompaction.

12 y and diagnosis of isolated left ventricular noncompaction.

13 diomyopathy (7%), 1 VF with left ventricular noncompaction (7%), and 1 catecholaminergic polymorphic

14 tudy, and those with a diagnosis of dilated, noncompaction, alcoholic, or toxic cardiomyopathy.

15 lar layer in the ventricular wall, so called noncompaction, along with diverse cardiac anomalies, inc

16 ycardia and his father with left ventricular noncompaction and catecholaminergic polymorphic ventricu

17 ne (ZASP) in a patient with left ventricular noncompaction and conduction disturbances.

18 veloped biventricular hypertrabeculation and noncompaction and died at birth.

19 e cell cycle withdrawal leads to ventricular noncompaction and heart failure.

20 sed to define trabeculae in left ventricular noncompaction and to identify normal racial variations.

21 opment led to heart defect including cardiac noncompaction and ventricular septal defect, which pheno

22 rt failure, her father with left ventricular noncompaction, and 2 fourth-degree relatives with hypert

23 ypertrophic cardiomyopathy, left ventricular noncompaction, and arrhythmogenic right ventricular dysp

24 myopathies are the most common; restrictive, noncompaction, and mixed cardiomyopathies occur infreque

25 ventricular septal defect (VSD), myocardium noncompaction, and ventricular hypertrabeculation.

26 ered cardiomyocyte cell cycling, ventricular noncompaction, and ventricular septal defects, while, in

27 may be the primary disease determinant, with noncompaction arising as a maladaptive remodelling respo

28 all children diagnosed with left ventricular noncompaction at Texas Children's Hospital from January

29 s hypertrophic, dilated and left ventricular noncompaction, but the molecular mechanisms involved in

30 Left ventricular noncompaction cardiomyopathy (LVNC) is associated with p

31 Left ventricular noncompaction cardiomyopathy (LVNC) was discovered half

32 ycardia in association with left ventricular noncompaction cardiomyopathy (LVNC), pointing to a share

33 ap in genetic causes and cardiac features in noncompaction cardiomyopathy (NCCM), hypertrophic cardio

34 eported for sinus node dysfunction (SND) and noncompaction cardiomyopathy (NCCM).

35 a PRDM16-Q187X variant with left ventricular noncompaction cardiomyopathy and demonstrated infant-ons

36 nect premature cardiomyocyte binucleation to noncompaction cardiomyopathy and highlight the role of R

37 cycle reentry, with relevance to ventricular noncompaction cardiomyopathy and regenerative medicine.

38 ntricular (LV) hypertrabeculation fulfilling noncompaction cardiomyopathy criteria has been detected

39 impairs myocardial development resulting in noncompaction cardiomyopathy in humans and mice associat

40 Noncompaction cardiomyopathy is a common congenital card

41 Noncompaction cardiomyopathy is characterized by the pre

42 The human genetics of left ventricular noncompaction cardiomyopathy suggest that cardiomyocyte

43 In this review, left ventricular noncompaction cardiomyopathy, which is often caused by m

44 DM16 variants and pediatric left ventricular noncompaction cardiomyopathy.

45 tures of autosomal dominant left ventricular noncompaction cardiomyopathy.

46 yonic day 10.5 leads to a severe ventricular noncompaction defect associated with reduced cardiomyocy

47 ical to understanding the pathophysiology of noncompaction disease.

48 tiple cardiac defects, including ventricular noncompaction, double outlet right ventricles and ventri

49 ascular Magnetic Resonance, Left Ventricular Noncompaction, Free-breathing Imaging Technique Suppleme

50 Left ventricular noncompaction has a heterogeneous clinical presentation

51 Left ventricular noncompaction has a high mortality rate and is strongly

52 , other genetic and metabolic syndromes with noncompaction have been described.

53 Isolated left ventricular noncompaction (ILVNC) is a cardiomyopathy caused by intr

54 Isolated left ventricular noncompaction (ILVNC) is a cardiomyopathy that was first

55 Left ventricular noncompaction is a cardiomyopathy characterized by exces

56 Left ventricular noncompaction is also observed in families with hypertro

57 tructural cardiac diseases, left ventricular noncompaction (LVNC) and bicuspid aortic valve, can be c

58 lthough an association with left ventricular noncompaction (LVNC) and DCM has been proposed, it is st

59 onsiderable overlap between left ventricular noncompaction (LVNC) and other cardiomyopathies.

60 Left ventricular noncompaction (LVNC) can occur in isolation or can co-oc

61 linked to gene mutations is left ventricular noncompaction (LVNC) characterized by a typical diffuse

62 Left ventricular noncompaction (LVNC) describes a ventricular wall anatom

63 Although left ventricular noncompaction (LVNC) has been associated with an increas

64 Whether left ventricular noncompaction (LVNC) is a distinct cardiomyopathy or a m

65 Left ventricular noncompaction (LVNC) is a genetically and phenotypically

66 Left ventricular noncompaction (LVNC) is a heterogeneous entity with unce

67 Isolated left ventricular noncompaction (LVNC) is a myocardial disorder characteri

68 Left ventricular noncompaction (LVNC) is a prevalent cardiomyopathy assoc

69 Left ventricular noncompaction (LVNC) is a reportedly uncommon genetic di

70 Left ventricular noncompaction (LVNC) is an autosomal-dominant, genetical

71 Left ventricular noncompaction (LVNC) is characterized by excessive trabe

72 Left ventricular noncompaction (LVNC) is the third most common pediatric

73 ion satisfying criteria for left ventricular noncompaction (LVNC) on routine cardiac magnetic resonan

74 However, the association between LV noncompaction (LVNC) phenotype and vigorous physical act

75 crease our understanding of left ventricular noncompaction (LVNC), a cardiomyopathy characterized by

76 useful for the diagnosis of left ventricular noncompaction (LVNC).

77 ociated with a diagnosis of left ventricular noncompaction (LVNC).

78 ent cardiac MR criteria for left ventricular noncompaction may be necessary.

79 Left ventricular noncompaction may be sporadic or familial and is linked

80 of myocardial dysfunction, left ventricular noncompaction may represent a secondary consequence of a

81 ophic cardiomyopathy (n=2), left ventricular noncompaction (n=1), or long-QT syndrome (n=2).

82 ricular fibrillation (n=4), left ventricular noncompaction (n=2), hypertrophic cardiomyopathy (n=1),

83 diomyopathy (n=26, 29%) and left ventricular noncompaction (n=3, 25%).

84 lated the ventricular hypertrabeculation and noncompaction observed in Fkbp1a systemically deficient

85 Right ventricular noncompaction occurred in 12 subjects (22.2%).

86 hat mimic a human congenital heart disorder, noncompaction of left ventricular myocardium.

87 Noncompaction of the left ventricle is a descriptive ana

88 al relevance and management of patients with noncompaction of the left ventricle will remain elusive.

89 -linked cardiomyopathy described as isolated noncompaction of the left ventricular myocardium (INVM).

90 ody mutants including hypertrabeculation and noncompaction of the ventricle.

91 null mutation was cardiac failure because of noncompaction of the ventricular myocardium and resultan

92 ations, including ventricular septal defect, noncompaction of the ventricular wall, double-outlet rig

93 ac defects including hypertrabeculation with noncompaction of the ventricular wall.

94 ction, mimicking the pathological changes of noncompaction of ventricular myocardium.

95 of cardiomyopathy and 1 had left ventricular noncompaction on echocardiogram.

96 FG+/phenotype-negative relatives, and 9 with noncompaction or dilated cardiomyopathy.

97 ere diagnosed with isolated left ventricular noncompaction over the study period.

98 All individuals with a noncompaction ratio of >/=2 underwent short axis systoli

99 Long axis noncompaction ratios were the least specific, with curre

100 ETS1 in endothelial cells causes ventricular noncompaction, reproducing the phenotype arising from gl

101 cardiomyopathies, including left ventricular noncompaction, restrictive cardiomyopathy, and arrhythmo

102 The left ventricular noncompaction-specific ZASP1 mutation can cause loss of

103 ric remodeling can occur in left ventricular noncompaction subject because of a direct effect of muta

104 yocyte proliferation resulted in ventricular noncompaction that was markedly rescued by heterozygous

105 sed LV trabeculations and the presence of LV noncompaction were based on established criteria.

106 Common sites of noncompaction were the apical (100%), midinferior (74.1%

107 on and dysfunction, as well as biventricular noncompaction, which fully recapitulated LVNC in patient

108 tectural proteins can cause left ventricular noncompaction, which is often associated with conduction

109 other 14-3-3 isoforms but led to ventricular noncompaction, with features similar to LVNC, resulting