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Titolo:
Cholestatic syndromes
Autore:
Trauner, M; Boyer, JL;
Indirizzi:
Karl Franzens Univ Graz, Sch Med, Dept Internal Med, Div Gastroenterol & Hepatol, Graz, Austria Karl Franzens Univ Graz Graz Austria roenterol & Hepatol, Graz, Austria
Titolo Testata:
CURRENT OPINION IN GASTROENTEROLOGY
fascicolo: 3, volume: 17, anno: 2001,
pagine: 242 - 256
SICI:
0267-1379(200105)17:3<242:CS>2.0.ZU;2-#
Fonte:
ISI
Lingua:
ENG
Soggetto:
PRIMARY BILIARY-CIRRHOSIS; PRIMARY SCLEROSING CHOLANGITIS; FAMILIAL INTRAHEPATIC CHOLESTASIS; BINDING CASSETTE TRANSPORTER-1; MULTIDRUG-RESISTANCE PROTEIN-2; URSODEOXYCHOLIC-ACID THERAPY; MAGNETIC-RESONANCE CHOLANGIOGRAPHY; IDIOPATHIC ADULTHOOD DUCTOPENIA; RANDOMIZED CONTROLLED TRIALS; HUMAN PDC-E2-163-176 PEPTIDE;
Tipo documento:
Review
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Citazioni:
220
Recensione:
Indirizzi per estratti:
Indirizzo: Boyer, JL Yale Univ, Sch Med, Yale Liver Ctr, POB 208019, New Haven, CT 06520 USA Yale Univ POB 208019 New Haven CT USA 06520 Haven, CT 06520 USA
Citazione:
M. Trauner e J.L. Boyer, "Cholestatic syndromes", CURR OPIN G, 17(3), 2001, pp. 242-256

Abstract

New insights into the regulation of hepatobiliary transport proteins have provided the basis for a better understanding of the pathogenesis of cholestatic liver diseases. Mutations of transporter genes can cause hereditary cholestatic syndromes, the study of which has shed much light on the basic mechanisms of bile secretion and cholestasis. Important new studies have been published about the pathogenesis, clinical features, and treatment of primary biliary cirrhosis, primary sclerosing cholangitis, cholestasis of pregnancy, total parenteral nutrition-induced cholestasis, and drug-induced cholestasis, Curr Opin Gastroenterol 2001, 17:242-256 (C) 2001 Lippincott Williams & Wilkins, Inc.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 02/12/20 alle ore 15:11:04