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1 es in diagnosis, treatment and management of portopulmonary hypertension.
2 liver disease was not related to the risk of portopulmonary hypertension.
3 therefore be integral to the development of portopulmonary hypertension.
4 confidence interval 0.09-0.65, P = 0.005) of portopulmonary hypertension.
5 d aerosolized epoprostenol in a patient with portopulmonary hypertension.
10 atients were receiving ongoing treatment for portopulmonary hypertension at the time of transplant.
11 rtal hypertension (hepatopulmonary syndrome, portopulmonary hypertension, cardiac dysfunction), and h
13 increased pulmonary vascular resistance from portopulmonary hypertension, has been associated with in
15 t to determine the clinical risk factors for portopulmonary hypertension in patients with advanced li
17 ng of portal hypertension is referred to as "portopulmonary hypertension." Intravenous epoprostenol (
19 criteria; II. Hepatopulmonary syndrome; III. Portopulmonary hypertension; IV. Implications for liver
21 c shunts in patients with moderate or severe portopulmonary hypertension (POPH) and determined the as
24 isorders, hepatopulmonary syndrome (HPS) and portopulmonary hypertension (POPH) may occur as a conseq
25 clinical research: hepatopulmonary syndrome, portopulmonary hypertension (POPH), and hepatic hydrotho
26 aracterized: hepatopulmonary syndrome (HPS), portopulmonary hypertension (POPH), and hepatic hydrotho
27 ase (MELD) exception points to patients with portopulmonary hypertension (POPH), but potentially impo
28 of the liver transplant (OLT) candidate with portopulmonary hypertension (PPHTN) has dramatically cha
29 ension with portal hypertension, also called portopulmonary hypertension (PPHTN), is a known complica
30 g/min, for a 4-month period, after which the portopulmonary hypertension resolved and the patient und
31 and now report the first patient with severe portopulmonary hypertension successfully treated with ep
32 ale sex was associated with a higher risk of portopulmonary hypertension than male sex (adjusted odds
34 cular disease, congenital heart disease, and portopulmonary hypertension were analyzed with other pat
35 high risk of death in those with significant portopulmonary hypertension, where targeted medical ther
36 is were associated with an increased risk of portopulmonary hypertension, whereas hepatitis C infecti
37 irectly linked estrogen to increased risk of portopulmonary hypertension, whereas others implicate in
38 ecently reported the successful treatment of portopulmonary hypertension with chronic intravenous epo
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