Results 201 to 210 of about 28,186 (243)
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Revista espanola de las enfermedades del aparato digestivo, 1976
Intrahepatic cholestasis has become a very important aspect of liver disease. The author, in the light of electron microscopy and the theory of filtration-reabsorption of bile secretion proposes that the disease may be explained by obstructions situated at various levels of the inter-cellular spaces of the liver. This obstruction is functional at first,
L, Yuguero del Moral +4 more
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Intrahepatic cholestasis has become a very important aspect of liver disease. The author, in the light of electron microscopy and the theory of filtration-reabsorption of bile secretion proposes that the disease may be explained by obstructions situated at various levels of the inter-cellular spaces of the liver. This obstruction is functional at first,
L, Yuguero del Moral +4 more
+6 more sources
Intrahepatic cholestasis of pregnancy
Seminars in Perinatology, 1998Intrahepatic cholestasis of pregnancy (ICP) is a disease of the third trimester of pregnancy involving pruritus and elevated bile acid levels. Its pathogenesis likely involves a genetic hypersensitivity to estrogen. Once thought to be benign for both mother and fetus, ICP has been associated with increased rates of fetal morbidity and mortality and an ...
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Estrogens in Intrahepatic Cholestasis of Pregnancy
Obstetrics & Gynecology, 2000To determine whether estrogen production and excretion are impaired in gravidas with intrahepatic cholestasis.Plasma and urine samples were collected from 13 women from the United States and Chile at 35-38 weeks' gestation with mild (n = 9) or severe (n = 4) intrahepatic cholestasis of pregnancy.
K K, Leslie +5 more
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BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS
Clinics in Liver Disease, 1999Benign recurrent intrahepatic cholestasis is a rare autosomal recessive disorder characterized by repeated episodes of intense pruritus and jaundice. Each attack lasts from several weeks to months before resolving spontaneously. Patients are completely asymptomatic for months to years between symptomatic periods.
Velimir A, Luketic, Mitchell L, Shiffman
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Pregnancy Outcome With Intrahepatic Cholestasis
Obstetrics & Gynecology, 1999To determine the risk of adverse pregnancy outcomes resulting from intrahepatic cholestasis.We analyzed 91 women with singleton pregnancies complicated by cholestasis who gave birth at Kuopio University Hospital from January 1990 to December 1996.
S, Heinonen, P, Kirkinen
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La Clinica terapeutica, 1997
The intrahepatic cholestasis is not an common syndrome, in particular way in people between 50 and 60 years of age. It is often unknown or confused, because of itching, with allergic or dermatologic diseases. The most frequent causes of intrahepatic cholestasis are primary sclerosing cholestasis, primary biliary cirrhosis and hepatic cirrhosis.
F, Stazi, P, Farello, C, Stazi
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The intrahepatic cholestasis is not an common syndrome, in particular way in people between 50 and 60 years of age. It is often unknown or confused, because of itching, with allergic or dermatologic diseases. The most frequent causes of intrahepatic cholestasis are primary sclerosing cholestasis, primary biliary cirrhosis and hepatic cirrhosis.
F, Stazi, P, Farello, C, Stazi
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PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS
Clinics in Liver Disease, 1999Abstract Progressive familial intrahepatic cholestasis (PFIC), also known as Byler disease, is an inherited disorder of childhood in which cholestasis of hepatocellular origin often presents in the neonatal period and leads to death from liver failure before adolescence. The pattern of appearance of affected children within families is consistent with
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