ライフサイエンスコーパス: secondary pulmonary hypertension

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1 lure, and treating it in those patients with secondary pulmonary hypertension.

2 t patients with congestive heart failure and secondary pulmonary hypertension.

3 reduction was also observed in patients with secondary pulmonary hypertension.

4 n PASMCs from PPH but not from patients with secondary pulmonary hypertension.

5 treatment of patients with certain types of secondary pulmonary hypertension.

6 tion of survival in children with primary or secondary pulmonary hypertension.

7 benefits of arginine therapy for primary and secondary pulmonary hypertension.

8 s detected in lung tissue from patients with secondary pulmonary hypertension, although one such pati

9 ese data indicate that ET contributes to the secondary pulmonary hypertension associated with HF.

10 n, pulmonary hypertension of the newborn, or secondary pulmonary hypertension attributable to a varie

11 pulmonary hypertension and 14 patients with secondary pulmonary hypertension for evidence of infecti

12 Treatment of patients with secondary pulmonary hypertension has been unsatisfactory

13 These findings suggest that secondary pulmonary hypertension may have different biol

14 or PPH (n=11, including 3 familial cases) or secondary pulmonary hypertension (n=6) and from unused d

15 ch higher than in those from normotensive or secondary pulmonary hypertension patients.

16 with systolic heart failure (HF) who develop secondary pulmonary hypertension (PH) have reduced exerc

17 om female PPH patients (n = 4) compared with secondary pulmonary hypertension (PH) patients (n = 4).

18 cise capacity were confined to patients with secondary pulmonary hypertension (rest pulmonary arteria

19 Although PPH and secondary pulmonary hypertension (SPH) share many clinic

20 splantation for advanced cardiomyopathy with secondary pulmonary hypertension who developed seemingly

21 ldenafil in carefully selected patients with secondary pulmonary hypertension who undergo implantatio

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