نتایج جستجو برای: benign recurrent intrahepatic cholestasis

تعداد نتایج: 212837  

2005
Paloma Jara Pilar Martínez-Fernández Luis Alvarez

Cholestasis constitutes one of the most common and severe manifestations of acquired or inherited liver disease. When manifest in early infancy, it is often life-threatening and usually requires surgical management. In many cases, liver transplantation is the only effective therapy. Extensive knowledge about the molecular mechanisms underlying several pediatric cholestatic disorders has been ga...

Journal: :Transplantation 2000
S Emre K Kitibayashi M E Schwartz J Ahn A Birnbaum S N Thung C M Miller

BACKGROUND Sickle cell intrahepatic cholestasis is a potentially catastrophic complication of sickle cell anemia Once acute liver failure develops, transplantation is the only option. We describe a patient with sickle cell intrahepatic cholestasis who underwent liver transplantation. METHODS Data were obtained from the chart. Serial hemoglobin S levels were monitored, and measures were taken ...

2017
Linxi Yu Xiaoxin Liu Zihang Yuan Xiaojiaoyang Li Hang Yang Ziqiao Yuan Lixin Sun Luyong Zhang Zhengzhou Jiang

Intrahepatic cholestasis is a kind of clinical syndrome along with hepatotoxicity which caused by intrahepatic and systemic accumulations of bile acid. There are several crucial generating factors of the pathogenesis of cholestasis, such as inflammation, dysregulation of bile acid transporters and oxidative stress. SIRT1 is regarded as a class III histone deacetylase (HDAC). According to a set ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2001
R Wang M Salem I M Yousef B Tuchweber P Lam S J Childs C D Helgason C Ackerley M J Phillips V Ling

Mutations in the sister of P-glycoprotein (Spgp) or bile salt export pump (BSEP) are associated with Progressive Familial Intrahepatic Cholestasis (PFIC2). Spgp is predominantly expressed in the canalicular membranes of liver. Consistent with in vitro evidence demonstrating the involvement of Spgp in bile salt transport, PFIC2 patients secrete less than 1% of biliary bile salts compared with no...

2017
Jia-Sheng Wu Yi-Fei Li Yuan-Yuan Li Yan Dai Wen-Kai Li Min Zheng Zheng-Chun Shi Rong Shi Tian-Ming Wang Bing-Liang Ma Ping Liu Yue-Ming Ma

Intrahepatic cholestasis is a serious symptom of liver disorders with limited therapies. In this study, we investigated the efficacy of Huangqi decoction (HQD), a two-herb classic traditional Chinese medicine (TCM), in the treatment of alpha-naphthylisothiocyanate (ANIT)-induced intrahepatic cholestasis in mice. HQD treatment ameliorated impaired hepatic function and tissue damage. A metabolomi...

2014
GUORUI HU PING HE ZHIFENG LIU QIAN CHEN BIXIA ZHENG QIHUA ZHANG

Intrahepatic cholestasis represents a heterogeneous group of disorders that begin during childhood, most commonly manifesting as neonatal cholestasis, and lead to ongoing liver dysfunction in children and adults. For children, inherited pathogenic factors of cholestasis have gained increasing attention owing to the rapid development of molecular biology technology. However, these methods have t...

Journal: :Obstetrics and gynecology 2009
Richard H Lee Marc H Incerpi David A Miller Bhuvan Pathak T Murphy Goodwin

BACKGROUND Intrahepatic cholestasis of pregnancy is associated with an increased risk of fetal death. The mechanism of death is unknown. CASES The first case involved a young primipara with pruritus and a bile acid concentration of 79 mumol/dL. While undergoing fetal heart rate monitoring, the fetus had a prolonged deceleration resulting in intrauterine death. The second case involved a young...

Journal: :Clinical Obstetrics, Gynecology and Reproductive Medicine 2020

Journal: :Archives of Disease in Childhood 1968

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