ライフサイエンスコーパス: Marfan's syndrome

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1 h atenolol in children and young adults with Marfan's syndrome.

2 in cause of premature death in patients with Marfan's syndrome.

3 on of severe periodontitis in a patient with Marfan's syndrome.

4 d aortic valves (n = 5) from 7 patients with Marfan's syndrome.

5 as well as fibrillin defects associated with Marfan's syndrome.

6 of the reasons why these mutations result in Marfan's syndrome.

7 dissection is the leading cause of death in Marfan's syndrome.

8 This report describes a case of Marfan's syndrome, an inherited disorder of connective t

9 ficiency, the main cardiovascular lesions in Marfan's syndrome, are associated with destruction of co

10 ular junction, which is prone to dilation in Marfan's syndrome as well, also showed a reduced rate of

11 ary causes of large-artery aneurysms such as Marfan's syndrome have long been recognized; recent year

12 t for nonrepairable abnormalities, including Marfan's syndrome in four, bicuspid aortic valve in four

13 Marfan's syndrome is a genetic disorder affecting connec

14 Marfan's syndrome is a systemic disorder of connective t

15 ypothesize that the defect in fibrillin-1 in Marfan's syndrome leads to (1) formation of elastin that

16 prosthetic graft and valve in patients with Marfan's syndrome may prevent premature death from ruptu

17 ted with connective tissue disorders such as Marfan's syndrome or skin fibrosis in the tight skin mou

18 Allografts were used for Marfan's syndrome patients or those with unusable pulmon

19 A 31-year-old woman with Marfan's syndrome presented with amblyopia and a history

20 udy, the use of ARB therapy in patients with Marfan's syndrome significantly slowed the rate of progr

21 Recent data from mouse models of Marfan's syndrome suggest that aortic-root enlargement i

22 A total of 675 patients with Marfan's syndrome underwent replacement of the aortic ro

23 a, which does not normally become dilated in Marfan's syndrome, was not affected by ARB therapy.

24 repair of aortic aneurysms in patients with Marfan's syndrome when the diameter of the aorta is well

25 The treatment of women with Marfan's syndrome who already have aortic root widening

26 We identified 18 pediatric patients with Marfan's syndrome who had been followed during 12 to 47

27 response to ARBs in pediatric patients with Marfan's syndrome who had severe aortic-root enlargement

28 Among children and young adults with Marfan's syndrome who were randomly assigned to losartan

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