Results 141 to 150 of about 4,248 (155)
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[Recurrent benign familial intrahepatic cholestasis].

G.E.N, 1992
Benign recurrent intrahepatic cholestasis is a disorder described 3 decades ago. The literature describes at least 60 cases. This syndrome is characterized by attacks of jaundice with obstructive features recurring over a number of years. Though the etiology remains, obscure the coincidence in members of a family or brothers suggests that this may be a
M, Ortíz de Soto   +5 more
openaire   +1 more source

[Recurrent benign intrahepatic cholestasis syndrome].

Polskie Archiwum Medycyny Wewnetrznej, 1992
Up to now about 100 cases of benign recurrent intrahepatic cholestasis have been reported. In this case we give a description of familial form of this disease, in which cholestasis was associated with inflammatory liver response. A brief review of this rare condition and differential diagnosis have been presented.
M, Hartleb   +3 more
openaire   +1 more source

Benign recurrent intrahepatic cholestasis

Gastroenterology, 1987
G.Y. Minuk, E.A. Shaffer
openaire   +1 more source

Progressive familial intrahepatic cholestasis and benign recurrent intrahepatic cholestasis: a review.

Acta gastro-enterologica Belgica, 2013
Progressive familial intrahepatic cholestasis (PFIC) and benign recurrent intrahepatic cholestasis (BRIC) are two rare autosomal recessive disorders, characterized by cholestasis. They are related to mutations in hepatocellular transport system genes involved in bile formation.
B, Strubbe   +3 more
openaire   +1 more source

Benign Recurrent Intrahepatic Cholestasis

2009
Alexander K. C. Leung   +62 more
openaire   +1 more source

[Recurrent benign intrahepatic cholestasis].

Revue medicale de Liege, 1991
C, Drèze   +5 more
openaire   +1 more source

Cholestasis, Benign Recurrent Intrahepatic Type 1

2009
Nils Peters   +199 more
openaire   +1 more source

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