UB Paderborn / Katalog / Suche / in CDI

Percutaneous transhepatic or endoscopic ultrasound-guided biliary drainage in malignant distal bile duct obstruction using a self-expanding metal stent: Study protocol for a prospective European multicenter trial (PUMa trial)

PloS one, 2022-10, Vol.17 (10), p.e0275029-e0275029

2022

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Gaucher disease and malignancy: a model for cancer pathogenesis in an inborn error of metabolism

Critical reviews in oncogenesis, 2013, Vol.18 (3), p.235

2013

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Evaluation of acoustic radiation force impulse imaging for determination of liver stiffness using transient elastography as a reference

World journal of gastroenterology : WJG, 2012-03, Vol.18 (10), p.1077-1084

2012

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Seltene und genetisch bedingte Lebererkrankungen

Die Gastroenterologie, 2023-08, Vol.18 (5), p.345-348

2023

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Swelling-induced upregulation of miR-141-3p inhibits hepatocyte proliferation

JHEP reports, 2022-04, Vol.4 (4), p.100440-100440, Article 100440

2022

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Low Incidence of Esophageal Lesions After Pulmonary Vein Isolation Using Contact-Force Sensing Catheter Without Esophageal Temperature Probe

International Heart Journal, 2017/11/01, Vol.58(6), pp.880-884

2017

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obligatory requirement for the heterotrimeric G protein Gi₃ in the antiautophagic action of insulin in the liver

Proceedings of the National Academy of Sciences - PNAS, 2007-02, Vol.104 (8), p.3003-3008

2007

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Evidence-based recommendations for monitoring bone disease and the response to enzyme replacement therapy in Gaucher patients

Current medical research and opinion, 2006-06, Vol.22 (6), p.1045-1064

2006

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Hydrophobic Bile Salts Induce Hepatocyte Shrinkage via NADPH Oxidase Activation

Cellular physiology and biochemistry, 2007-01, Vol.19 (1-4), p.89-98

2007

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Involvement of Integrins in Osmosensing and Signaling toward Autophagic Proteolysis in Rat Liver

The Journal of biological chemistry, 2003-07, Vol.278 (29), p.27088-27095

2003

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Understanding the natural history of Gaucher disease

American journal of hematology, 2015-07, Vol.90 (S1), p.S6-S11

2015

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Long-term clinical outcomes in type 1 Gaucher disease following 10 years of imiglucerase treatment

Journal of inherited metabolic disease, 2013-05, Vol.36 (3), p.543-553

2013

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In yeast, loss of Hog1 leads to osmosensitivity of autophagy

Biochemical journal, 2006-02, Vol.394 (Pt 1), p.153-161

2006

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Hepatocellular carcinoma in Gaucher disease: an international case series

Journal of inherited metabolic disease, 2018-09, Vol.41 (5), p.819-827

2018

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Management and monitoring recommendations for the use of eliglustat in adults with type 1 Gaucher disease in Europe

European journal of internal medicine, 2017-01, Vol.37, p.25-32

2017

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Transition seltener Leberkrankheiten im Kindesalter – was kommt auf die Hepatologie zu?

Die Gastroenterologie, 2023-08, Vol.18 (5), p.385-396

2023

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Presenting signs and patient co‐variables in Gaucher disease: outcome of the Gaucher Earlier Diagnosis Consensus (GED‐C) Delphi initiative

Internal medicine journal, 2019-05, Vol.49 (5), p.578-591

2019

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Reply to Letter to the Editor: “The added benefit of contrast-enhanced CT in the evaluation of incidental FDG-avid colon lesions”

European journal of nuclear medicine and molecular imaging, 2020-09, Vol.47 (10), p.2245-2246

2020

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Cardiometabolic risk factor clustering in patients with deficient branched‐chain amino acid catabolism: A case‐control study

Journal of inherited metabolic disease, 2020-09, Vol.43 (5), p.981-993

2020

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Hepatic encephalopathy in chronic liver disease: a clinical manifestation of astrocyte swelling and low-grade cerebral edema?

Journal of Hepatology, 2000-06, Vol.32 (6), p.1035-1038

2000

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Deletion of HOG1 Leads to Osmosensitivity in Starvation-Induced, but not Rapamycin-Dependent Atg8 Degradation and Proteolysis: Further Evidence for Different Regulatory Mechanisms in Yeast Autophagy

Autophagy, 2006-07, Vol.2 (3), p.241-243

2006

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Lysosomal storage diseases as differential diagnosis of hepatosplenomegaly

Baillière's best practice & research. Clinical gastroenterology, 2010-10, Vol.24 (5), p.619-628

2010

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Percutaneous transhepatic or endoscopic ultrasound-guided biliary drainage in malignant distal bile duct obstruction using a self-expanding metal stent: Study protocol for a prospective European multicenter trial (PUMa trial)

Gaucher disease and malignancy: a model for cancer pathogenesis in an inborn error of metabolism

Evaluation of acoustic radiation force impulse imaging for determination of liver stiffness using transient elastography as a reference

Seltene und genetisch bedingte Lebererkrankungen

Swelling-induced upregulation of miR-141-3p inhibits hepatocyte proliferation

Low Incidence of Esophageal Lesions After Pulmonary Vein Isolation Using Contact-Force Sensing Catheter Without Esophageal Temperature Probe

Hepatorenal Tyrosinaemia: Impact of a Simplified Diet on Metabolic Control and Clinical Outcome

obligatory requirement for the heterotrimeric G protein Gi₃ in the antiautophagic action of insulin in the liver

Evidence-based recommendations for monitoring bone disease and the response to enzyme replacement therapy in Gaucher patients

Hydrophobic Bile Salts Induce Hepatocyte Shrinkage via NADPH Oxidase Activation

Involvement of Integrins in Osmosensing and Signaling toward Autophagic Proteolysis in Rat Liver

Understanding the natural history of Gaucher disease

Long-term clinical outcomes in type 1 Gaucher disease following 10 years of imiglucerase treatment

In yeast, loss of Hog1 leads to osmosensitivity of autophagy

Recommendations for diagnosing and managing individuals with glutaric aciduria type 1: Third revision

Hepatocellular carcinoma in Gaucher disease: an international case series

Management and monitoring recommendations for the use of eliglustat in adults with type 1 Gaucher disease in Europe

Transition seltener Leberkrankheiten im Kindesalter – was kommt auf die Hepatologie zu?

Impact of pregnancy planning and preconceptual dietary training on metabolic control and offspring's outcome in phenylketonuria

Presenting signs and patient co‐variables in Gaucher disease: outcome of the Gaucher Earlier Diagnosis Consensus (GED‐C) Delphi initiative

Reply to Letter to the Editor: “The added benefit of contrast-enhanced CT in the evaluation of incidental FDG-avid colon lesions”

Cardiometabolic risk factor clustering in patients with deficient branched‐chain amino acid catabolism: A case‐control study

Hepatic encephalopathy in chronic liver disease: a clinical manifestation of astrocyte swelling and low-grade cerebral edema?

Deletion of HOG1 Leads to Osmosensitivity in Starvation-Induced, but not Rapamycin-Dependent Atg8 Degradation and Proteolysis: Further Evidence for Different Regulatory Mechanisms in Yeast Autophagy

Lysosomal storage diseases as differential diagnosis of hepatosplenomegaly

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