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1 flow obstruction, which presents as an acute Budd-Chiari syndrome.
2 e patient died at 1 month from tumor-related Budd-Chiari syndrome.
3 arcoidosis, congenital hepatic fibrosis, and Budd-Chiari syndrome.
4 e frequently the venous system, typically as Budd-Chiari syndrome.
5 atichydrothorax, portal vein thrombosis, and Budd-Chiari syndrome.
9 s in patients with hepatic vein obstruction (Budd-Chiari Syndrome) and in those with portal vein thro
10 e described in the context of heart disease, Budd-Chiari syndrome, and the sinusoidal obstruction syn
11 dical records of all patients diagnosed with Budd-Chiari syndrome at the Johns Hopkins Hospital durin
12 an lead to hepatic congestion, cirrhosis and Budd-Chiari syndrome (BCS) and can predispose to develop
13 eoplasms (MPNs) are the most common cause of Budd-Chiari syndrome (BCS) and nonmalignant, noncirrhoti
19 the outcome of liver transplantation (LT) in Budd-Chiari Syndrome (BCS) patients who are listed as st
21 o orthotopic liver transplantation (OLT) for Budd-Chiari syndrome (BCS) traditionally have been antic
23 ic shunt (TIPS) in a series of patients with Budd-Chiari syndrome (BCS), and to determine the predict
24 ive disorders (MPDs) are a frequent cause of Budd-Chiari syndrome (BCS), treatment directed toward al
26 ngs included hepatofugal portal venous flow, Budd-Chiari syndrome, cavernous transformation of the po
27 d with autoimmune hepatitis, Wilson disease, Budd-Chiari syndrome, hepatitis B virus reactivation, in