UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 1.083

Sortiert nach

Progressive Familial Intrahepatic Cholestasis

Clinics in liver disease, 2018-11, Vol.22 (4), p.657

2018

Link zum Volltext

Verfügbarkeit prüfen

Mutations in DCDC2 (doublecortin domain containing protein 2) in neonatal sclerosing cholangitis

Journal of hepatology, 2016-12, Vol.65 (6), p.1179-1187

2016

Link zum Volltext

Verfügbarkeit prüfen

The human bile salt export pump: Characterization of substrate specificity and identification of inhibitors

Gastroenterology (New York, N.Y. 1943), 2002-11, Vol.123 (5), p.1649-1658

2002

Link zum Volltext

Verfügbarkeit prüfen

Genetic cholestasis in children and adults

Journal of hepatology, 2024-04, Vol.80 (4), p.670-672

2024

Link zum Volltext

Verfügbarkeit prüfen

Sequencing of transporter genes in cholestasis: We are still learning

Journal of hepatology, 2017-12, Vol.67 (6), p.1132-1133

Thompson, Richard J.

2017

Link zum Volltext

Verfügbarkeit prüfen

Genetics of liver disease: From pathophysiology to clinical practice

Journal of hepatology, 2015-04, Vol.62 (1), p.S6-S14

2015

Link zum Volltext

Verfügbarkeit prüfen

Challenges in understanding the consequences of variants in ABCB4 gene

Journal of hepatology, 2021-01, Vol.74 (1), p.242-243

2021

Link zum Volltext

Verfügbarkeit prüfen

ATP7B Genotype and Chronic Liver Disease Treatment Outcomes in Wilson Disease: Worse Survival With Loss-of-Function Variants

Clinical gastroenterology and hepatology, 2023-05, Vol.21 (5), p.1323-1329.e4

2023

Link zum Volltext

Verfügbarkeit prüfen

Reply to: Doublecortin domain containing protein 2 ( DCDC2 ) genetic variants in primary sclerosing cholangitis

Journal of hepatology, 2017-09, Vol.67 (3), p.652-653

2017

Link zum Volltext

Verfügbarkeit prüfen

Multiple β-catenin mutations in hepatocellular lesions arising in Abernethy malformation

Human pathology, 2016-07, Vol.53, p.153-158

2016

Link zum Volltext

Verfügbarkeit prüfen

A discontinuous wave-in-cell numerical scheme for hyperbolic conservation laws

Journal of computational physics, 2015-10, Vol.299, p.404-428

2015

Link zum Volltext

Verfügbarkeit prüfen

Study of Acute Liver Failure in Children Using Next Generation Sequencing Technology

The Journal of pediatrics, 2021-09, Vol.236, p.124-130

2021

Link zum Volltext

Verfügbarkeit prüfen

Reduced Hepatocellular Expression of Canalicular Transport Proteins in Infants with Neonatal Cholestasis and Congenital Hypopituitarism

The Journal of pediatrics, 2018-09, Vol.200, p.181-187

2018

Link zum Volltext

Verfügbarkeit prüfen

Effects of odevixibat on pruritus and bile acids in children with cholestatic liver disease: Phase 2 study

Clinics and research in hepatology and gastroenterology, 2021-09, Vol.45 (5), p.101751-101751, Article 101751

2021

Link zum Volltext

Verfügbarkeit prüfen

Severe Bile Salt Export Pump Deficiency: 82 Different ABCB11 Mutations in 109 Families

Gastroenterology (New York, N.Y. 1943), 2008-04, Vol.134 (4), p.1203-1214.e8

2008

Link zum Volltext

Verfügbarkeit prüfen

846 Mutations in Tight Junction Protein 2 Underlie a Spectrum of Cholestatic Liver Disease

Gastroenterology (New York, N.Y. 1943), 2014-05, Vol.146 (5), p.S-928-S-928

2014

Link zum Volltext

Verfügbarkeit prüfen

Progressive familial intrahepatic cholestasis, type 1, is associated with decreased farnesoid X receptor activity

Gastroenterology (New York, N.Y. 1943), 2004-03, Vol.126 (3), p.756-764

2004

Link zum Volltext

Verfügbarkeit prüfen

Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis

Gastroenterology (New York, N.Y. 1943), 1999-12, Vol.117 (6), p.1370-1379

1999

Link zum Volltext

Verfügbarkeit prüfen

Congenital bile duct anomalies (biliary atresia) and chromosome 22 aneuploidy

Journal of pediatric surgery, 2008-09, Vol.43 (9), p.1736-1740

2008

Link zum Volltext

Verfügbarkeit prüfen

Numerical simulations of high frequency transverse pulsed jet injection into a supersonic crossflow

Aerospace science and technology, 2020-08, Vol.103, p.105908, Article 105908

2020

Link zum Volltext

Verfügbarkeit prüfen

EP1230: EFFICACY AND SAFETY OF ODEVIXIBAT IN CHILDREN WITH PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS WITH PRIOR PARTIAL EXTERNAL BILIARY DIVERSION

Gastroenterology (New York, N.Y. 1943), 2022-05, Vol.162 (7), p.S-1296

2022

Link zum Volltext

Verfügbarkeit prüfen

EP1233: LONG-TERM TREATMENT WITH ODEVIXIBAT IMPROVES MULTIPLE SLEEP PARAMETERS IN PATIENTS WITH PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS: A POOLED RESPONDER ANALYSIS FROM THE PHASE 3 PEDFIC STUDIES

Gastroenterology (New York, N.Y. 1943), 2022-05, Vol.162 (7), p.S-1297

2022

Link zum Volltext

Verfügbarkeit prüfen

EP1231: ODEVIXIBAT THERAPY IMPROVES CLINICALLY MEANINGFUL ENDPOINTS IN CHILDREN WITH PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS: DATA FROM THE PEDFIC 1 AND PEDFIC 2 TRIALS

Gastroenterology (New York, N.Y. 1943), 2022-05, Vol.162 (7), p.S-1296

2022

Link zum Volltext

Verfügbarkeit prüfen

Genotype correlates with the natural history of severe bile salt export pump deficiency

Journal of hepatology, 2020-07, Vol.73 (1), p.84-93

2020

Link zum Volltext

Verfügbarkeit prüfen

A strong conservative Riemann solver for the solution of the coupled Maxwell and Navier–Stokes equations

Journal of computational physics, 2014-02, Vol.258, p.431-450

2014

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 1.083

Suche als RSS-Feed

Aktive Filter

KollektionElsevier ScienceDirect Journals Complete

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.068)
Mit Volltextzugriff
(1.059)

Publikationsform

Sprache

Englisch
(1.082)
Japanisch
(158)
Russisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(781)
Life Sciences & Biomedicine
(713)
Humans
(490)
Male
(367)
Biological And Medical Sciences
(323)
Female
(292)
Animals
(214)
Medical Sciences
(187)
Middle Aged
(157)
Adult
(155)
Neurosciences & Neurology
(147)
Fundamental And Applied Biological Sciences. Psychology
(143)
Neurosciences
(132)
Aged
(124)
Physical Sciences
(106)
Psychology. Psychoanalysis. Psychiatry
(101)
Surgery
(85)
Behavioral Sciences
(75)
Cardiovascular System & Cardiology
(75)
Psychology. Psychophysiology
(75)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Behavioral Neuroscience
(67)
The Lancet
(33)
Bioorganic & Medicinal Chemistry Letters
(32)
Alzheimer's & Dementia
(30)
Gastroenterology
(29)
Journal Of The American College Of Cardiology
(26)
Neuroimage
(21)
American Journal Of Human Genetics
(20)
Brain Research
(18)
Journal Of Hepatology
(17)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(6)

Menü

Weitere Dienste

Einstellungen

Progressive Familial Intrahepatic Cholestasis

Mutations in DCDC2 (doublecortin domain containing protein 2) in neonatal sclerosing cholangitis

The human bile salt export pump: Characterization of substrate specificity and identification of inhibitors

Genetic cholestasis in children and adults

Sequencing of transporter genes in cholestasis: We are still learning

Genetics of liver disease: From pathophysiology to clinical practice

Challenges in understanding the consequences of variants in ABCB4 gene

ATP7B Genotype and Chronic Liver Disease Treatment Outcomes in Wilson Disease: Worse Survival With Loss-of-Function Variants

Reply to: Doublecortin domain containing protein 2 ( DCDC2 ) genetic variants in primary sclerosing cholangitis

Multiple β-catenin mutations in hepatocellular lesions arising in Abernethy malformation

A discontinuous wave-in-cell numerical scheme for hyperbolic conservation laws

Study of Acute Liver Failure in Children Using Next Generation Sequencing Technology

Reduced Hepatocellular Expression of Canalicular Transport Proteins in Infants with Neonatal Cholestasis and Congenital Hypopituitarism

Effects of odevixibat on pruritus and bile acids in children with cholestatic liver disease: Phase 2 study

Severe Bile Salt Export Pump Deficiency: 82 Different ABCB11 Mutations in 109 Families

846 Mutations in Tight Junction Protein 2 Underlie a Spectrum of Cholestatic Liver Disease

Progressive familial intrahepatic cholestasis, type 1, is associated with decreased farnesoid X receptor activity

Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis

Congenital bile duct anomalies (biliary atresia) and chromosome 22 aneuploidy

Numerical simulations of high frequency transverse pulsed jet injection into a supersonic crossflow

EP1230: EFFICACY AND SAFETY OF ODEVIXIBAT IN CHILDREN WITH PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS WITH PRIOR PARTIAL EXTERNAL BILIARY DIVERSION

EP1233: LONG-TERM TREATMENT WITH ODEVIXIBAT IMPROVES MULTIPLE SLEEP PARAMETERS IN PATIENTS WITH PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS: A POOLED RESPONDER ANALYSIS FROM THE PHASE 3 PEDFIC STUDIES

EP1231: ODEVIXIBAT THERAPY IMPROVES CLINICALLY MEANINGFUL ENDPOINTS IN CHILDREN WITH PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS: DATA FROM THE PEDFIC 1 AND PEDFIC 2 TRIALS

Genotype correlates with the natural history of severe bile salt export pump deficiency

A strong conservative Riemann solver for the solution of the coupled Maxwell and Navier–Stokes equations

Aktive Filter

Suchergebnisse filtern