Peter Ott

Cerebral metabolic disturbances in the brain during acute liver failure: from hyperammonemia to energy failure and proteolysis.

Brain metabolism of 13N-ammonia during acute hepatic encephalopathy in cirrhosis measured by positron emission tomography.

Quantitative liver functions in Turner syndrome with and without hormone replacement therapy.

Low cerebral oxygen consumption and blood flow in patients with cirrhosis and an acute episode of hepatic encephalopathy.

[Screening for hepatocellular carcinoma?].

A 15-year-old girl with severe hemolytic Wilson's crisis recovered without transplantation after extracorporeal circulation with the Prometheus system.

The galactose elimination capacity and mortality in 781 Danish patients with newly-diagnosed liver cirrhosis: a cohort study.

Clinical course of alcoholic liver cirrhosis: a Danish population-based cohort study.

Synthesis of neurotransmitter GABA via the neuronal tricarboxylic acid cycle is elevated in rats with liver cirrhosis consistent with a high GABAergic tone in chronic hepatic encephalopathy.

Vitamin D deficiency in cirrhosis relates to liver dysfunction rather than aetiology.

Validation of prognostic scores for clinical use in patients with alcoholic hepatitis.

Clinical presentation and mutations in Danish patients with Wilson disease.

Branched-chain amino acids increase arterial blood ammonia in spite of enhanced intrinsic muscle ammonia metabolism in patients with cirrhosis and healthy subjects.

Transjugular intrahepatic portosystemic shunt does not alter cerebral blood flow.

The effect of a single oral megadose of vitamin D provided as either ergocalciferol (D₂) or cholecalciferol (D₃) in alcoholic liver cirrhosis.

[N-methyl-11C]cholylsarcosine, a novel bile acid tracer for PET/CT of hepatic excretory function: radiosynthesis and proof-of-concept studies in pigs.

Risk for hepatocellular carcinoma in patients with alcoholic cirrhosis: a Danish nationwide cohort study.

Hepatic encephalopathy is associated with decreased cerebral oxygen metabolism and blood flow, not increased ammonia uptake.

The clinical course of alcoholic cirrhosis: effects of hepatic metabolic capacity, alcohol consumption, and hyponatremia--a historical cohort study.

Branched-chain amino acids and muscle ammonia detoxification in cirrhosis.

Brain alanine formation as an ammonia-scavenging pathway during hyperammonemia: effects of glutamine synthetase inhibition in rats and astrocyte-neuron co-cultures.

Chemoembolization of intermediate stage hepatocellular carcinomas: results from a Nordic tertiary liver cancer center.

Effect of glutamine synthetase inhibition on brain and interorgan ammonia metabolism in bile duct ligated rats.

Cerebral effects of ammonia in liver disease: current hypotheses.

Oxidative metabolism of astrocytes is not reduced in hepatic encephalopathy: a PET study with [(11)C]acetate in humans.

Muscle metabolism and whole blood amino acid profile in patients with liver disease.

Hepatobiliary Secretion Kinetics of Conjugated Bile Acids Measured in Pigs by 11C-Cholylsarcosine PET.

Detection of Kayser-Fleischer ring using Scheimpflug imaging.

Time-trends in incidence and prognosis of hepatocellular carcinoma in Denmark: A nationwide register-based cohort study.

Hepatobiliary transport kinetics of the conjugated bile acid tracer C-CSar quantified in healthy humans and patients by positron emission tomography.

Comment on Advantages of Anterior Segment Optical Coherence Tomography Evaluation of the Kayser-Fleischer Ring in Wilson Disease.

Isolated congenital hepatic fibrosis associated with mutations: report of a new genotype-phenotype relationship.

Functional assessment of hepatobiliary secretion by C-cholylsarcosine positron emission tomography.

Unexplained cholestasis in adults and adolescents: diagnostic benefit of genetic examination.

Obeticholic acid for severe bile acid diarrhea with intestinal failure: A case report and review of the literature.

High hepatic macrophage activation and low liver function in stable Wilson patients - a Danish cross-sectional study.

Terlipressin for variceal bleeding induces large plasma sodium fluctuations in patients without cirrhosis.

Ischemic Damage Represents the Main Risk Factor for Biliary Stricture After Liver Transplantation: A Follow-Up Study in a Danish Population.

Effects of implementation of a national fast track clinical pathway for hepatocellular carcinoma in Western Denmark.

Scheimpflug Imaging of the Danish Cohort of Patients With Wilson Disease.

The Prevalence of Wilson's Disease: An Update.

Computing the Pathogenicity of Wilson's Disease ATP7B Mutations: Implications for Disease Prevalence.

Spontaneous bacterial peritonitis - a shift in bacteria and resistance pattern.

New tight junction protein 2 variant causing progressive familial intrahepatic cholestasis type 4 in adults: A case report.

Intravenous and oral copper kinetics, biodistribution and dosimetry in healthy humans studied by [Cu]copper PET/CT.

The macrophage activation marker soluble CD163 is elevated and associated with liver disease phenotype in patients with Wilson's disease.

Compensated Cirrhosis and 20 mm Hg: A Point of No Return?

A placebo-controlled randomised trial of budesonide for PBC following an insufficient response to UDCA.

Recovery of Moderate Coronavirus Disease 2019 in a Liver Transplant Recipient on Continued Immunosuppression: A Case Report.

Hepatic bile acid transport increases in the postprandial state: A functional C-CSar PET/CT study in healthy humans.

Glutamate Dehydrogenase Is Important for Ammonia Fixation and Amino Acid Homeostasis in Brain During Hyperammonemia.

Cognitive impairment in stable Wilson disease across phenotype.

The pathophysiology of Wilson's disease visualized: A human Cu PET study.

The galactose elimination capacity test to monitor liver disease course in patients with Wilson's disease.

Low cerebral energy metabolism in hepatic encephalopathy reflects low neuronal energy demand. Role of ammonia-induced increased GABAergic tone.

Effect of oral zinc regimens on human hepatic copper content: a randomized intervention study.

Case report: Huppke-Brendel syndrome in an adult, mistaken for and treated as Wilson disease for 25 years.

Trientine tetrahydrochloride versus penicillamine for maintenance therapy in Wilson disease (CHELATE): a randomised, open-label, non-inferiority, phase 3 trial.

Outcome of elexacaftor/tezacaftor/ivacaftor therapy in patients with cystic fibrosis and solid organ transplantation.

The association between soluble CD163, disease severity, and ursodiol treatment in patients with primary biliary cholangitis.

Clearance and production of ammonia quantified in humans by constant ammonia infusion - the effects of cirrhosis and ammonia targeting treatments.