List of works - Peter Witters

A coffee bean in an infant: Call the endoscopist

scientific article published on 01 May 2017

A rare cause of persisting anaemia in a patient with a failing Fontan circulation

scientific article

ADP-degrading enzymes inhibit platelet activation in bile duct-ligated rats

scientific article published on 6 November 2009

ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

scientific article published on 10 June 2016

Alpers syndrome presenting with anatomopathological features of fulminant autoimmune hepatitis

Autism in patients with propionic acidemia.

scientific article published on 31 October 2016

Beyond pancreatic insufficiency and liver disease in cystic fibrosis

scientific article published on 7 April 2016

Central nervous involvement is common in PGM1-CDG

scientific article published on 21 August 2018

Clinical and biochemical improvement with galactose supplementation in SLC35A2-CDG

scientific article published on 27 February 2020

Congenital veno-venous malformations of the liver: widely variable clinical presentations.

scientific article published on 14 September 2007

Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

scientific article published on 8 August 2016

Evaluation of electrocardiographic algorithms in the assessment of the infarct-related artery in acute myocardial infarction

scientific article published in August 2006

Expanding the phenotype of metabolic cutis laxa with an additional disorder of N-linked protein glycosylation

scientific article published on 30 November 2017

Galactose Supplementation in Patients With TMEM165-CDG Rescues the Glycosylation Defects.

scientific article published on 9 January 2017

Human T cell activation by costimulatory signal-deficient allogeneic cells induces inducible costimulator-expressing anergic T cells with regulatory cell activity.

scientific article published in May 2004

Hypophosphatasia in Adults: Clinical Spectrum and Its Association With Genetics and Metabolic Substrates

scientific article published on 21 December 2018

Intrauterine thrombosis of the ductus venosus leading to neonatal demise

scientific article published on 08 June 2011

King's Variceal Prediction Score: A Novel Noninvasive Marker of Portal Hypertension in Pediatric Chronic Liver Disease

scientific article published on 4 October 2016

Liver disease in cystic fibrosis presents as non-cirrhotic portal hypertension.

scientific article

Liver involvement in congenital disorders of glycosylation (CDG). A systematic review of the literature.

scientific article published on 20 January 2017

Liver involvement in kidney disease and vice versa.

scientific article

Lung transplantation in cystic fibrosis normalizes essential fatty acid profiles

scientific article published on 25 October 2012

Non-invasive liver elastography (Fibroscan) for detection of cystic fibrosis-associated liver disease

scientific article

Noncirrhotic presinusoidal portal hypertension is common in cystic fibrosis-associated liver disease

scientific article published on 01 March 2011

Normal cognitive outcome in a PEX6 deficient girl despite neonatal multisystem presentation

scientific article published on 23 March 2016

Nutritional Therapies in Congenital Disorders of Glycosylation (CDG).

scientific article published on 7 November 2017

Nutritional status, nutrient intake and use of enzyme supplements in paediatric patients with Cystic Fibrosis; a European multicentre study with reference to current guidelines.

scientific article published on 17 March 2017

Oxygraphy Versus Enzymology for the Biochemical Diagnosis of Primary Mitochondrial Disease

scientific article published on 10 October 2019

Renal involvement in PMM2-CDG, a mini-review.

scientific article published on 28 November 2017

Review article: blood platelet number and function in chronic liver disease and cirrhosis.

scientific article

The role of endothelial cells in cystic fibrosis

scientific article published on 07 August 2019

Therapeutic approaches in Congenital Disorders of Glycosylation (CDG) involving N-linked glycosylation: an update

scientific article published on 19 September 2019

Wilson's disease: long-term follow-up of a cohort of 24 patients treated with D-penicillamine.

scientific article published in May 2010

List of works by Peter Witters

A coffee bean in an infant: Call the endoscopist

A rare cause of persisting anaemia in a patient with a failing Fontan circulation

ADP-degrading enzymes inhibit platelet activation in bile duct-ligated rats

ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

Alpers syndrome presenting with anatomopathological features of fulminant autoimmune hepatitis

Autism in patients with propionic acidemia.

Beyond pancreatic insufficiency and liver disease in cystic fibrosis

Central nervous involvement is common in PGM1-CDG

Clinical and biochemical improvement with galactose supplementation in SLC35A2-CDG

Congenital veno-venous malformations of the liver: widely variable clinical presentations.

Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

Evaluation of electrocardiographic algorithms in the assessment of the infarct-related artery in acute myocardial infarction

Expanding the phenotype of metabolic cutis laxa with an additional disorder of N-linked protein glycosylation

Galactose Supplementation in Patients With TMEM165-CDG Rescues the Glycosylation Defects.

Human T cell activation by costimulatory signal-deficient allogeneic cells induces inducible costimulator-expressing anergic T cells with regulatory cell activity.

Hypophosphatasia in Adults: Clinical Spectrum and Its Association With Genetics and Metabolic Substrates

Intrauterine thrombosis of the ductus venosus leading to neonatal demise

King's Variceal Prediction Score: A Novel Noninvasive Marker of Portal Hypertension in Pediatric Chronic Liver Disease

Liver disease in cystic fibrosis presents as non-cirrhotic portal hypertension.

Liver involvement in congenital disorders of glycosylation (CDG). A systematic review of the literature.

Liver involvement in kidney disease and vice versa.

Lung transplantation in cystic fibrosis normalizes essential fatty acid profiles

Non-invasive liver elastography (Fibroscan) for detection of cystic fibrosis-associated liver disease

Noncirrhotic presinusoidal portal hypertension is common in cystic fibrosis-associated liver disease

Normal cognitive outcome in a PEX6 deficient girl despite neonatal multisystem presentation

Nutritional Therapies in Congenital Disorders of Glycosylation (CDG).

Nutritional status, nutrient intake and use of enzyme supplements in paediatric patients with Cystic Fibrosis; a European multicentre study with reference to current guidelines.

Oxygraphy Versus Enzymology for the Biochemical Diagnosis of Primary Mitochondrial Disease

Renal involvement in PMM2-CDG, a mini-review.

Review article: blood platelet number and function in chronic liver disease and cirrhosis.

The role of endothelial cells in cystic fibrosis

Therapeutic approaches in Congenital Disorders of Glycosylation (CDG) involving N-linked glycosylation: an update

Wilson's disease: long-term follow-up of a cohort of 24 patients treated with D-penicillamine.