Results 131 to 140 of about 116,093 (277)

Perbedaan Manifestasi Klinis dan Laboratorium Kolestasis Intrahepatal dengan Ekstrahepatal pada Bayi

Majalah Kedokteran Bandung, 2016
Physiological jaundice found in infants and most symptoms are often mild. Jaundice symptoms usually disappear within 2 weeks after birth. In conjugated jaundice defects in intra-hepatic production, transmembran transport from bile, i.e. cholestasis intra
Dwi Prasetyo, Yudith Setiati Ermaya, Iesje Martiza   +2 more
doaj  

Prolonged cholestasis in children secondary to acute hepatitis A

, 1987
Yong Poovorawan
openalex   +2 more sources

Cholestasis in Chronic Liver Disease and the Role of Ademetionine in its Treatment (Literature Review and Expert Panel Resolution)

Российский журнал гастроэнтерологии, гепатологии, колопроктологии
Aim: to analyse the principles of diagnosis and treatment of intrahepatic cholestasis in chronic liver diseases, to present data on the effectiveness of ademetionine in the treatment of chronic liver diseases with intrahepatic cholestasis and the ...
K. L. Raikhelson, A. O. Bueverov, E. A. Kondrashina, M. V. Maevskaya, I. B. Khlynov, E. N. Shirokova, V. T. Ivashkin   +6 more
doaj   +1 more source

Novel mutation in CCBE 1 as a cause of recurrent hydrops fetalis from Hennekam lymphangiectasia-lymphedema syndrome-1. [PDF]

, 2018
Whole exome sequencing (WES) was used to determine the etiology of recurrent hydrops fetalis in this case of Hennekam lymphangiectasia-lymphedema syndrome-1.
Andreasen, Tara S, Lamale-Smith, Leah M, Mao, Rong, Melber, Dora J, Miller, Christine E, Moore, Thomas R, Tvrdik, Tatiana, Woelkers, Douglas A   +7 more
core  

CHOLESTASIS SYNDROME IN CHILDREN WITH KAWASAKI DISEASE [PDF]

, 2006
Vaidotas Urbonas
openalex   +1 more source

Severe hepatopulmonary syndrome with end-stage liver cirrhosis associated with pan-hypopituitarism in a pediatric patient

Journal of Clinical and Translational Endocrinology Case Reports
Cholestasis in the neonatal period requires a prompt and thorough evaluation. Panhypopituitarism is an uncommon but known cause of cholestasis. Here we present a rare and late complication of liver disease secondary to congenital hypopituitarism ...
Shawn A. Haupt, Jessica C. Chang, Roya Zarpak, Arash R. Zandieh, Nada A. Yazigi, Udeme D. Ekong, Juan F. Guerra, Thomas M. Fishbein, Cal S. Matsumoto, Alexander H. Kroemer, Khalid M. Khan   +10 more
doaj   +1 more source

Glycochenodeoxycholate-Induced Apoptosis Is Not Reduced by Augmenter of Liver Regeneration in the Human Hepatoma Cell Line HuH-7 [PDF]

, 2010
Denk, Gerald Ulrich, Pusl, Thomas, Rust, Christian, Thasler, Wolfgang H., Vennegeerts, Timo, Wimmer, Ralf   +5 more
core   +1 more source

Novel Variant ATP8B1 mutation in a child with progressive familial intrahepatic cholestasis (type 1)

, 2020
Nida Mirza, Ravi Bharadwaj, Smita Malhotra, Anupam Sibal   +3 more
openalex   +1 more source

A Korean patient with Guillain-Barré syndrome following acute hepatitis E whose cholestasis resolved with steroid therapy [PDF]

, 2016
Sung Bok Ji, Sang Soo Lee, Hee Cheul Jung, Hong Jun Kim, Hyun‐Jin Kim, Tae Hyo Kim, Woon Tae Jung, Ok‐Jae Lee, Dae Hyun Song   +8 more
openalex   +1 more source

320 3.5-Diethoxycarbonyl-1.4-dihydrocollidine (DDC) feeding induces cholestasis, chronic inflammatory bile duct damage and biliary fibrosis in mice

, 2006
Ulrike Stöger, E. Fickert, Andrea Fuchsbichler, Tarek Moustafa, J. Gumhold, Dagmar Silbert, Kurt Zatloukal, Helmut Denk, Michael Trauner   +8 more
openalex   +1 more source