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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)

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.235-246

2013

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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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Sekundäre Ursachen der Fettleber – Neues zur Pathogenese, rationalen Diagnostik und Therapie

Deutsche medizinische Wochenschrift, 2020-02, Vol.145 (3), p.140-145

2020

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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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Understanding the natural history of Gaucher disease

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

2015

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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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Radiofrequency Pulmonary Vein Isolation without Esophageal Temperature Monitoring: Contact-Force Characteristics and Incidence of Esophageal Thermal Damage

Journal of clinical medicine, 2022-11, Vol.11 (23), p.6917

2022

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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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Digital single-operator cholangioscopy with EHL as salvage therapy of an internalized and stone-impacted biliary stent 13 years after implantation

Endoscopy International Open, 2022-03, Vol.10 (3), p.E269-E272

2022

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Neurological outcome in long‐chain hydroxy fatty acid oxidation disorders

Annals of clinical and translational neurology, 2024-04, Vol.11 (4), p.883-898

2024

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Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision

Journal of inherited metabolic disease, 2017, Vol.40 (1), p.75-101

2017

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Marketing Communications

Second edition., 2021

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Therapy of adult Gaucher disease

Haematologica (Roma), 2007-02, Vol.92 (2), p.148-152

2007

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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

Seltene und genetisch bedingte Lebererkrankungen

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

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

Sekundäre Ursachen der Fettleber – Neues zur Pathogenese, rationalen Diagnostik und Therapie

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

Understanding the natural history of Gaucher disease

In yeast, loss of Hog1 leads to osmosensitivity of autophagy

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

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

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

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?

Radiofrequency Pulmonary Vein Isolation without Esophageal Temperature Monitoring: Contact-Force Characteristics and Incidence of Esophageal Thermal Damage

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

Digital single-operator cholangioscopy with EHL as salvage therapy of an internalized and stone-impacted biliary stent 13 years after implantation

Neurological outcome in long‐chain hydroxy fatty acid oxidation disorders

Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision

Marketing Communications

Therapy of adult Gaucher disease

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