نتایج جستجو برای: chronic cholestasis

تعداد نتایج: 503138  

Journal: :Gut 1982
N M Bass A K Burroughs P J Scheuer D G James S Sherlock

Two West Indian patients with Kveim-biopsy proven sarcoidosis developed chronic cholestatic liver disease, clinically and biochemically similar to primary biliary cirrhosis. Liver histology revealed multiple granulomas with reduction in bile ducts and, in one patient, progression to biliary cirrhosis. Portal hypertension was present in both patients leading to severe variceal haemorrhage in one...

Journal: :Gut 1963
D V DATTA S SHERLOCK P J SCHEUER

Features of biliary obstruction were seen in 57 of 300 cases of post-necrotic cirrhosis but gave rise to real diagnostic difficulty in only 11 cases. The paper deals with the recognition and possible pathogenesis of this syndrome.

Journal: :The American journal of clinical nutrition 1988
O Amédée-Manesme M S Mourey J Therasse M Couturier F Alvarez A Hanck O Bernard

Newborns have limited reserve supplies of vitamin A. Infants with chronic cholestasis are in a precarious nutritional state because of their limited ability to build these stores even though the vitamin is present in their diet. In this study, we investigated liver concentrations of vitamin A in 30 children with extrahepatic biliary atresia. We demonstrate that correction of the deficiency occu...

Journal: : 2021

The aim: Improving the effects of pregnancy on fetus and newborn through early diagnosis timely comprehensive therapy pregnant women with intrahepatic cholestasis. Materials methods: We have conducted a complex examination 60 who got owing to assisted reproductive technologies, concomitant cholestasis, 20 practically healthy physiological course labor (reference group), aged between 18 42. rese...

Hassan Teheri, Javad Shokry- Shirvani, Naser Ghaemian, Yaser Taghavi,

Background: Cholangiocarcinoma is an invasive biliary malignancy with poor prognosis. Diagnostic accuracy of conventional methods is low which is mainly due to the specific anatomy of the disease. The aim of this study was to evaluate the diagnostic value of biochemical profile and tumor marker of the bile in patients with malignant cholestasis compared to that of choledocholithiasis. ...

2011
Hanno Ehlken Vangelis Kondylis Jan Heinrichsdorff Laura Ochoa-Callejero Tania Roskams Manolis Pasparakis

UNLABELLED Mice lacking the Abc4 protein encoded by the multidrug resistance-2 gene (Mdr2(-/-)) develop chronic periductular inflammation and cholestatic liver disease resulting in the development of hepatocellular carcinoma (HCC). Inhibition of NF-κB by expression of an IκBα super-repressor (IκBαSR) transgene in hepatocytes was shown to prevent HCC development in Mdr2(-/-) mice, suggesting tha...

Journal: :Canadian journal of surgery. Journal canadien de chirurgie 2008
Joachim Maier Jasna Rudez Andreas Huber

Twice in January 2003 we treated a 66-year-old man for recurrent severe bleeding from a duodenal ulcer by endoscopic injection of polidocanol. After the second intervention, he suffered acute but mild pancreatitis. One year later, he presented with abdominal pain in the right upper quadrant and intermittent cholestasis. The cholangio-MRI showed cholecystolithiasis and stenosis of the CBD and wa...

Journal: :Jornal de pediatria 2005
Regina Helena G da Motta Mattar Ramiro Anthero de Azevedo Patrícia G L Speridião Ulysses Fagundes Neto Mauro Batista de Morais

OBJECTIVE To evaluate food intake, occurrence of energy-protein malnutrition and anemia, and intestinal iron absorption in children with chronic liver disease. METHODS The study included 25 children with chronic liver disease, 14 with cholestasis and 11 without cholestasis. The age varied between 6.5 months and 12.1 years. Intestinal iron absorption was evaluated by the increment of serum iro...

2013
Sohela Shah Laura K. Conlin Luis Gomez Øystein Aagenaes Kristin Eiklid A. S. Knisely Michael T. Mennuti Randolph P. Matthews Nancy B. Spinner Laura N. Bull

BACKGROUND Lymphedema-cholestasis syndrome (LCS; Aagenaes syndrome) is a rare autosomal recessive disorder, characterized by 1) neonatal intrahepatic cholestasis, often lessening and becoming intermittent with age, and 2) severe chronic lymphedema, mainly lower limb. LCS was originally described in a Norwegian kindred in which a locus, LCS1, was mapped to a 6.6cM region on chromosome 15. Mutati...

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