ライフサイエンスコーパス: fibromuscular

1 asal epithelial, luminal epithelial, stromal fibromuscular, and endothelial - and for prostate precur

2 , more lipid accumulates and is covered by a fibromuscular cap to form a fibrous plaque.

3 In addition, stromal fibromuscular cells associated with primary prostate can

4 The rectus extraocular muscles pass through fibromuscular connective tissue pulleys that stabilize m

5 extracoronary vascular anomalies, especially fibromuscular dysplasia (FMD) and a low prevalence of co

6 rteriography in diagnosing renal artery (RA) fibromuscular dysplasia (FMD) and correlating with the h

7 y dissection (SCAD) has been associated with fibromuscular dysplasia (FMD) and other extracoronary ar

8 ously described a strong association between fibromuscular dysplasia (FMD) and spontaneous coronary a

9 Multifocal fibromuscular dysplasia (FMD) and spontaneous coronary a

10 Fibromuscular dysplasia (FMD) involving the coronary art

11 Fibromuscular dysplasia (FMD) is a heterogeneous group o

12 Fibromuscular dysplasia (FMD) is a nonatheromatous, noni

13 Fibromuscular dysplasia (FMD) is a noninflammatory arter

14 Fibromuscular dysplasia (FMD) is a rare, nonatherosclero

15 Fibromuscular dysplasia (FMD) is an arteriopathy associa

16 Fibromuscular dysplasia (FMD) is found in 6 to 14% of pa

17 on histology, the diagnosis of renal artery fibromuscular dysplasia (FMD) is now based mostly on ang

18 ce of intracranial aneurysm in patients with fibromuscular dysplasia (FMD) is uncertain.

19 Fibromuscular dysplasia (FMD), a noninflammatory disease

20 oderate to severe arterial changes caused by fibromuscular dysplasia (FMD), mild and distal moderate

21 ily members of individuals having multifocal fibromuscular dysplasia (FMD).

22 (1) higher risk of SCAD in individuals with fibromuscular dysplasia (P = 0.021, OR = 1.82 [95% CI: 1

23 ed with extracoronary vasculopathy including fibromuscular dysplasia (P<0.05 for both).

24 rticipants who completed neuroimaging, 1 had fibromuscular dysplasia (this patient also experienced h

25 The most common causes were fibromuscular dysplasia and atherosclerosis.

26 , P-SCAD was less likely with a diagnosis of fibromuscular dysplasia and extracoronary vascular abnor

27 anial aneurysms, cervical artery dissection, fibromuscular dysplasia and moyamoya disease.

28 An association of CeAD with fibromuscular dysplasia and reversible cerebral vasocons

29 Majority of patients with NA-SCAD had fibromuscular dysplasia and type 2 angiographic SCAD.

30 dissections, aneurysms, atherosclerosis, and fibromuscular dysplasia can be identified on both MR ima

31 igorous program of prospective screening for fibromuscular dysplasia combined with intervention signi

32 Some patients may be asymptomatic and fibromuscular dysplasia could only be discovered by imag

33 Predisposing conditions included fibromuscular dysplasia in 42.9% (56.4% in those with co

34 been little new information published about fibromuscular dysplasia in the past 30 years.

35 Fibromuscular dysplasia is a noninflammatory, nonatheros

36 Fibromuscular dysplasia is a novel association and poten

37 Fibromuscular dysplasia is a pathologic diagnosis, but t

38 Fibromuscular dysplasia is an uncommon angiopathy that o

39 Fibromuscular dysplasia is an underdiagnosed and misunde

40 Fibromuscular dysplasia of the iliac artery was identifi

41 of primary RA repair correlated with complex fibromuscular dysplasia requiring branch ex vivo reconst

42 Fibromuscular dysplasia screening of renal, iliac, and c

43 Fibromuscular dysplasia was defined as either a history

44 Fibromuscular dysplasia was diagnosed in 72.0%.

45 Fibromuscular dysplasia was present in 62.7%, connective

46 isorders, peripartum SCAD, and extracoronary fibromuscular dysplasia were independent predictors of 3

47 of arterialized saphenous venous graft, and fibromuscular dysplasia) revealed a distinct increase in

48 ssues and a female-specific association with fibromuscular dysplasia, a female-biased vascular diseas

49 al imaging registered in the US Registry for Fibromuscular Dysplasia, an observational disease-based

50 graine headache, cervical artery dissection, fibromuscular dysplasia, and hypertension.

51 Genetic disorders, extracoronary fibromuscular dysplasia, and peripartum SCAD were indepe

52 isorders: coronary artery disease, migraine, fibromuscular dysplasia, cervical artery dissection and

53 s the most likely causal variant in LRP1 for fibromuscular dysplasia, migraine, pulse pressure, and s

54 cy and systemic arteriopathies, particularly fibromuscular dysplasia.

55 d with extracoronary vasculopathy, including fibromuscular dysplasia.

56 It is pathologically defined as intimal fibromuscular dysplasia.

57 or aneurysm may also occur in patients with fibromuscular dysplasia.

58 erial disease, is fundamentally a variant of fibromuscular dysplasia.

59 s and discrete, nonostial stenoses caused by fibromuscular dysplasia.

60 mplantation, reconstructed tissues displayed fibromuscular fatty structures typical of the alar lobul

61 pletely, the skin biopsy did show arteriolar fibromuscular intimal proliferation, which is usually se

62 infiltrated with macrophages than the stable fibromuscular lesion.

63 IVUS, lipid-laden lesions appear hypoechoic, fibromuscular lesions generate low-intensity echoes, and

64 focally into, and frequently compromise, the fibromuscular sheath.

65 ared with 8.6 for prazosin), 6.9 in anterior fibromuscular stroma (prazosin, 8.9), and 7.1 in bladder

66 Positive staining was seen in the fibromuscular stroma in normal prostates but not in the

67 Moreover, the fibromuscular stroma surrounding prostatic glands was re

68 ing, remodeling, and hypercellularity of the fibromuscular stroma.

69 on zone, apical peripheral zone and anterior fibromuscular stroma.

70 inal secretory epithelial, basal epithelial, fibromuscular stromal, nerve sheath, and endothelial cel