Results 251 to 260 of about 105,725 (272)
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Progressive familial intrahepatic cholestasis.

Acta bio-medica : Atenei Parmensis, 2002
Progressive familial intrahepatic cholestasis (PFIC) is a heterogeneous group of autosomal recessive childhood cholestasis of hepatocellular origin. PFIC 1, also known as Byler disease, was first described in Amish kindred. It is characterized by cholestasis often arising in the neonatal period and it leads to death due to liver failure.
CAVESTRO GM   +7 more
openaire   +3 more sources

Acute Intrahepatic Cholestasis

Medical Clinics of North America, 1960
G H, JEFFRIES, M H, SLEISENGER
openaire   +2 more sources

Intrahepatic Cholestasis

Archives of Internal Medicine, 1979
openaire   +2 more sources

Intrahepatic cholestasis

The American Journal of Surgery, 1959
openaire   +2 more sources

Intrahepatic cholestasis of pregnancy as a risk factor for preeclampsia

Archives of Gynecology and Obstetrics, 2020
Matan Mor   +7 more
semanticscholar   +1 more source

Benign Recurrent Intrahepatic Cholestasis

Clinical Pediatrics, 1971
S, Ozsoylu, N, Koçak
openaire   +2 more sources

[Intrahepatic cholestasis].

Sovetskaia meditsina, 1977
Kh Kh, Mansurov   +2 more
openaire   +1 more source

Intrahepatic cholestasis after thiabendazole

Transactions of the Royal Society of Tropical Medicine and Hygiene, 1988
R N, Davidson   +3 more
openaire   +2 more sources

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