FIC1 and BSEP defects in Taiwanese patients with chronic intrahepatic cholestasis with low γ-glutamyltranspeptidase levels

2002 ◽  
Vol 140 (1) ◽  
pp. 119-124 ◽  
Author(s):  
Huey-Ling Chen ◽  
Pei-Shin Chang ◽  
Hey-Chi Hsu ◽  
Yen-Hsuan Ni ◽  
Hong-Yuan Hsu ◽  
...  
1993 ◽  
Vol 18 (3) ◽  
pp. 379-380 ◽  
Author(s):  
Juan Carlos Mayor ◽  
Juan Cabrera ◽  
Jesús Garcia ◽  
Teresa Romero

2014 ◽  
Vol 2014 ◽  
pp. 1-3 ◽  
Author(s):  
Efthymia Vlachaki ◽  
Panagiotis Andreadis ◽  
Nikolaos Neokleous ◽  
Aleka Agapidou ◽  
Evaggelia Vetsiou ◽  
...  

Sickle cell/β+thalassemia (Hb S/β+thal) is considered as a variant form of sickle cell disease. Acute episodes of vasoocclusive pain crisis are characteristic for sickle cell disorders and may be complicated by an acute or chronic life-threatening organ dysfunction. Chronic intrahepatic cholestasis is a rare and severe complication in sickle cell disease, characterized by marked hyperbilirubinemia and acute hepatic failure with an often fatal course. Despite the fact that patients with Hb S/β+thal usually have a mild type of disease, herein we describe an interesting case of chronic intrahepatic cholestasis with successful outcome in an adult patient with Hb S/β+thal.


1975 ◽  
Vol 59 (3) ◽  
pp. 373-387 ◽  
Author(s):  
Cesar Rudzki ◽  
Kamal G. Ishak ◽  
Hyman J. Zimmerman

2012 ◽  
Vol 55 (2) ◽  
pp. 150-156 ◽  
Author(s):  
Ling-Juan Fang ◽  
Xiao-Hong Wang ◽  
A.S. Knisely ◽  
Hui Yu ◽  
Yi Lu ◽  
...  

Hepatology ◽  
2007 ◽  
Vol 3 (3) ◽  
pp. 391-398 ◽  
Author(s):  
Sten Eriksson ◽  
Christer Larsson

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