نتایج جستجو برای: benign recurrent intrahepatic cholestasis

تعداد نتایج: 212837  

Journal: :Hepatology 1998
P Sörös J Böttcher H Maschek O Selberg M J Müller

Lipoprotein-X (Lp-X) is an abnormal low-density lipoprotein frequently found in liver disease. It is regarded as the most sensitive and specific biochemical parameter for the diagnosis of intra- and extrahepatic cholestasis. Moreover, Lp-X is supposed to contribute to the development of hypercholesterolemia in cholestatic liver disease, because it fails to inhibit de novo cholesterol synthesis....

Journal: :Clinical medicine 2006
Nick Murphy

heterogeneity in intrahepatic cholestasis of pregnancy. Gut 2003;52:1025–9. 24 Mullenbach R, Bennett A, Tetlow N, Patel N et al. ATP8B1 mutations in British cases with intrahepatic cholestasis of pregnancy. Gut 2005;54:829–34. 25 Ch’ng CL, Morgan M, Kingham JG. Obstetric cholestasis in South Wales. Gut 2002;50(Suppl II):A114. 26 Williamson C, Hems LM, Goulis DG, Walker I et al. Clinical outcome...

Journal: :Archives of Disease in Childhood 1973

Journal: :Archives of disease in childhood 1996
B Bourke N Goggin D Walsh S Kennedy K D Setchell B Drumm

Progressive familial intrahepatic cholestasis (PFIC) occurs in many communities and races. A form of PFIC in five children from two consanguineous marriages in an Irish kindred is described. In addition, a review of clinical information from the records of three deceased members of the kindred strongly implies that they also suffered from PFIC. The children had a history of neonatal diarrhoea, ...

2017
Ahmad Mohamed Sira Mostafa Mohamed Sira

2006
Tom Hargreaves

SYNOPSIS Oral contraceptives can cause liver damage and jaundice but this is very rare in women in the United Kingdom. The drugs are contraindicated where there is a history of recurrent intrahepatic cholestasis of pregnancy and acute or chronic disturbance of liver function which can be congenital or acquired. It is not yet known whether the oestrogenic or progestogenic components of oral cont...

Journal: :Journal of Clinical and Experimental Hepatology 2014

Journal: :Orphanet Journal of Rare Diseases 1999
Anne Davit-Spraul Emmanuel Gonzales Christiane Baussan Emmanuel Jacquemin

Progressive familial intrahepatic cholestasis (PFIC) refers to a heterogeneous group of autosomal-recessive disorders of childhood that disrupt bile formation and present with cholestasis of hepatocellular origin. The exact prevalence remains unknown, but the estimated incidence varies between 1/50,000 and 1/100,000 births. Three types of PFIC have been identified and associated with mutations ...

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