Peter Witters

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 9

Top Topics

Peritoneal Dialysis

Top Venues

Genetics in medicine : official journal of the American College of Medical Genetics

Orphanet journal of rare diseases

This page only lists publications with an associated author ORCID identifier.

Publications

Karen Driesen, Peter Witters
Understanding Inborn Errors of Metabolism through Metabolomics. Metabolites 12 (5) (2022)
Peter Witters, Hans Andersson, Jaak Jaeken, Laura Tseng, Clara D M van Karnebeek, Dirk J Lefeber, David Cassiman, Eva Morava
D-galactose supplementation in individuals with PMM2-CDG: results of a multicenter, open label, prospective pilot clinical trial. Orphanet journal of rare diseases 16 (1) (2021)
Laurien Vaes, Daisy Rymen, David Cassiman, Anna N Ligezka, Nele Vanhoutvin, Dulce Quelhas, Eva Morava, Peter Witters
Genotype-Phenotype Correlations in PMM2-CDG. Genes 12 (11) (2021)
Peter Witters, Andrew C Edmondson, Christina Lam, Christin Johnsen, Marc C Patterson, Kimiyo M Raymond, Miao He, Hudson H Freeze, Eva Morava
Spontaneous improvement of carbohydrate-deficient transferrin in PMM2-CDG without mannose observed in CDG natural history study. Orphanet journal of rare diseases 16 (1) (2021)
Peter Witters, Shawn Tahata, Rita Barone, Katrin Õunap, Ramona Salvarinova, Sabine Grønborg, George Hoganson, Fernando Scaglia, Andrea Margaret Lewis, Mari Mori, Jolanta Sykut-Cegielska, Andrew Edmondson, Miao He, Eva Morava
Clinical and biochemical improvement with galactose supplementation in SLC35A2-CDG. Genetics in medicine : official journal of the American College of Medical Genetics 22 (6) (2020)
Jan Verheijen, Shawn Tahata, Tamas Kozicz, Peter Witters, Eva Morava
Therapeutic approaches in Congenital Disorders of Glycosylation (CDG) involving N-linked glycosylation: an update. Genetics in medicine : official journal of the American College of Medical Genetics 22 (2) (2019)
Matthew J Bird, Isabelle Adant, Petra Windmolders, Ingrid Vander Elst, Catarina Felgueira, Ruqaiah Altassan, Sarah C Gruenert, Bart Ghesquière, Peter Witters, David Cassiman, Pieter Vermeersch
Oxygraphy Versus Enzymology for the Biochemical Diagnosis of Primary Mitochondrial Disease. Metabolites 9 (10) (2019)
Peter Witters, David Cassiman, Eva Morava
Nutritional Therapies in Congenital Disorders of Glycosylation (CDG). Nutrients 9 (11) (2017)
Peter Witters, Jeroen Breckpot, François Foulquier, Graem Preston, Jaak Jaeken, Eva Morava
Expanding the phenotype of metabolic cutis laxa with an additional disorder of N-linked protein glycosylation. European journal of human genetics : EJHG 26 (5) (2017)