UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ‐glutamyltransferase cholestasis

Hepatology (Baltimore, Md.), 2017-05, Vol.65 (5), p.1655-1669

2017

Volltextzugriff (PDF)

Splicing Analysis of MYO5B Noncanonical Variants in Patients with Low Gamma-Glutamyltransferase Cholestasis

Human mutation, 2023-07, Vol.2023, p.1-12

2023

Volltextzugriff (PDF)

A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/Deletions

PloS one, 2016-10, Vol.11 (10), p.e0164058-e0164058

2016

Volltextzugriff (PDF)

Neonatal cholestasis is an early liver manifestation of children with acid sphingomyelinase deficiency

BMC gastroenterology, 2022-05, Vol.22 (1), p.227-227, Article 227

2022

Volltextzugriff (PDF)

Improving outpatient satisfaction by extending expected waiting time

BMC health services research, 2019-08, Vol.19 (1), p.565-565, Article 565

2019

Volltextzugriff (PDF)

The Features of GGT in Patients with ATP8B1 or ABCB11 Deficiency Improve the Diagnostic Efficiency

PloS one, 2016-04, Vol.11 (4), p.e0153114-e0153114

2016

Volltextzugriff (PDF)

Comprehensive bile acid profiling in hereditary intrahepatic cholestasis: Genetic and clinical correlations

Liver international, 2018-09, Vol.38 (9), p.1676-1685

2018

Volltextzugriff (PDF)

Molecular findings in children with inherited intrahepatic cholestasis

Pediatric research, 2020-01, Vol.87 (1), p.112-117

2020

Volltextzugriff (PDF)

Severe Neonatal Cholestasis in Cerebrotendinous Xanthomatosis: Genetics, Immunostaining, Mass Spectrometry

Journal of pediatric gastroenterology and nutrition, 2017-11, Vol.65 (5), p.561-568

2017

Volltextzugriff (PDF)

Splicing analysis of rare/novel synonymous or intronic variants identified in ABCB11 heterozygotes presenting as progressive intrahepatic cholestasis with low γ‐glutamyltransferase

Hepatology research, 2018-06, Vol.48 (7), p.574-584

2018

Volltextzugriff (PDF)

The Presence of Vacuolated Kupffer Cells Raises a Clinical Suspicion of Niemann-Pick Disease Type C in Neonatal Cholestasis

Frontiers in genetics, 2022-03, Vol.13, p.867413-867413

2022

Volltextzugriff (PDF)

Dynamic Hybrid Multiple Attribute Decision-Making Problem Based on Reference Point Adaptation

Mathematical problems in engineering, 2019, Vol.2019 (2019), p.1-8

2019

Volltextzugriff (PDF)

Fibrinogen storage disease in a Chinese boy with de novo fibrinogen Aguadilla mutation: Incomplete response to carbamazepine and ursodeoxycholic acid

BMC gastroenterology, 2016-08, Vol.16 (1), p.92-92, Article 92

2016

Volltextzugriff (PDF)

Wilson disease with hepatic presentation in an eight-month-old boy

World journal of gastroenterology : WJG, 2015-08, Vol.21 (29), p.8981-8984

2015

Volltextzugriff (PDF)

Non-invasive biomarkers for identification of vanishing bile duct syndrome among children with acute cholestatic hepatitis

Translational pediatrics, 2023-10, Vol.12 (10), p.1782-1790

2023

Volltextzugriff (PDF)

Pediatric Wilson disease presenting as acute liver failure: Prognostic indices

World journal of clinical cases, 2021-05, Vol.9 (14), p.3273-3286

2021

Volltextzugriff (PDF)

Severe Neonatal Cholestasis in Cerebrotendinous Xanthomatosis

Journal of pediatric gastroenterology and nutrition, 2017-11, Vol.65 (5), p.561-568

2017

Volltextzugriff (PDF)

A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/Deletions

PloS one, 2016-10, Vol.11 (10), p.e0164058

2016

Volltextzugriff (PDF)

Improved ultraviolet/visible rejection ratio using MgZnO/SiO 2/n-Si heterojunction photodetectors

Applied surface science, 2010-08, Vol.256 (21), p.6153-6156

2010

Volltextzugriff (PDF)

Tartaric acid-assisted co-precipitation synthesis of Er3+-doped Lu2O3 nanopowders

Chinese chemical letters, 2012-11, Vol.23 (11), p.1299-1302

2012

Volltextzugriff (PDF)

Synthesis and photoluminescence properties of LaPO 4 : Ce 3+ , Tb 3+ nanophosphors by microwave-assisted co-precipitation method at low temperature

Functional materials letters, 2015-12, Vol.8 (6), p.1550078

2015

Volltextzugriff (PDF)

Improved ultraviolet/visible rejection ratio using MgZnO/SiO2/n-Si heterojunction photodetectors

Applied surface science, 2010-08, Vol.256 (21), p.6153-6156

2010

Volltextzugriff (PDF)

Abnormal Bilirubin Metabolism in Patients With Sodium Taurocholate Cotransporting Polypeptide Deficiency

Journal of pediatric gastroenterology and nutrition, 2020-11, Vol.71 (5), p.e138-e141

2020

Volltextzugriff (PDF)

Fabrication and spectroscopic characterization of Er3+:Lu2O3 transparent ceramics

Materials letters, 2013-03, Vol.94, p.5-7

2013

Volltextzugriff (PDF)

Printed Three-dimensional Anatomic Templates for Virtual Preoperative Planning Before Reconstruction of Old Pelvic Injuries： Initial Results

Chinese medical journal, 2015-02, Vol.128 (4), p.477-482

2015

Volltextzugriff (PDF)

1 – 25 von 1.823

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.493)
Mit Volltextzugriff
(1.534)

Publikationsform

Artikel
(1.690)
Tagungsberichte
(110)
Buchkapitel
(17)
Berichte
(3)
Texte
(2)
Bücher
(1)

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Englisch
(1.605)
Chinesisch
(230)
Koreanisch
(2)
Deutsch
(1)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(1.194)
Life Sciences & Biomedicine
(575)
Physical Sciences
(414)
Technology
(389)
Humans
(326)
Chemistry
(267)
Male
(191)
Female
(188)
Engineering
(177)
Materials Science
(173)
Animals
(149)
Materials Science, Multidisciplinary
(139)
Physics
(128)
Science & Technology - Other Topics
(114)
Adult
(105)
Middle Aged
(100)
Chemistry, Multidisciplinary
(94)
Chemistry, Physical
(94)
Oncology
(83)
Biochemistry & Molecular Biology
(80)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

中国肺癌杂志
(22)
Plos One
(21)
Chinese Physics Letters
(17)
Ssrn Electronic Journal
(17)
Cheminform
(16)
Wuli Xuebao
(16)
Chinese Physics B
(14)
Journal Of Materials Chemistry. A, Materials For Energy And Sustainability
(13)
Acta Pharmacologica Sinica
(12)
Scientific Reports
(12)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(33)
... seit 30 Tagen
(7)

Menü

Weitere Dienste

Einstellungen

Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ‐glutamyltransferase cholestasis

Splicing Analysis of MYO5B Noncanonical Variants in Patients with Low Gamma-Glutamyltransferase Cholestasis

A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/Deletions

Neonatal cholestasis is an early liver manifestation of children with acid sphingomyelinase deficiency

Improving outpatient satisfaction by extending expected waiting time

The Features of GGT in Patients with ATP8B1 or ABCB11 Deficiency Improve the Diagnostic Efficiency

Comprehensive bile acid profiling in hereditary intrahepatic cholestasis: Genetic and clinical correlations

Molecular findings in children with inherited intrahepatic cholestasis

Severe Neonatal Cholestasis in Cerebrotendinous Xanthomatosis: Genetics, Immunostaining, Mass Spectrometry

Splicing analysis of rare/novel synonymous or intronic variants identified in ABCB11 heterozygotes presenting as progressive intrahepatic cholestasis with low γ‐glutamyltransferase

The Presence of Vacuolated Kupffer Cells Raises a Clinical Suspicion of Niemann-Pick Disease Type C in Neonatal Cholestasis

Dynamic Hybrid Multiple Attribute Decision-Making Problem Based on Reference Point Adaptation

Fibrinogen storage disease in a Chinese boy with de novo fibrinogen Aguadilla mutation: Incomplete response to carbamazepine and ursodeoxycholic acid

Wilson disease with hepatic presentation in an eight-month-old boy

Non-invasive biomarkers for identification of vanishing bile duct syndrome among children with acute cholestatic hepatitis

Pediatric Wilson disease presenting as acute liver failure: Prognostic indices

Severe Neonatal Cholestasis in Cerebrotendinous Xanthomatosis

A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/Deletions

Improved ultraviolet/visible rejection ratio using MgZnO/SiO 2/n-Si heterojunction photodetectors

Tartaric acid-assisted co-precipitation synthesis of Er3+-doped Lu2O3 nanopowders

Synthesis and photoluminescence properties of LaPO 4 : Ce 3+ , Tb 3+ nanophosphors by microwave-assisted co-precipitation method at low temperature

Improved ultraviolet/visible rejection ratio using MgZnO/SiO2/n-Si heterojunction photodetectors

Abnormal Bilirubin Metabolism in Patients With Sodium Taurocholate Cotransporting Polypeptide Deficiency

Fabrication and spectroscopic characterization of Er3+:Lu2O3 transparent ceramics

Printed Three-dimensional Anatomic Templates for Virtual Preoperative Planning Before Reconstruction of Old Pelvic Injuries： Initial Results

Suchergebnisse filtern