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Biochemia Medica|October 22, 2024
A case of alkaptonuria presenting with unexplained dark-stained diapers and spurious hyperoxaluria and proteinuria due to homogentisic acid interferenceThibault Vanhove, Margo Aertgeerts, Peter Witters, et al.BMC Pediatrics|May 3, 2022
Cystic fibrosis and alpha-1 antitrypsin deficiency: case report and review of literatureEvi Jaspers, Ine Van Dijck, Ilse Hoffman, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 30, 2012
Lung transplantation in cystic fibrosis normalizes essential fatty acid profilesPeter Witters, Lieven Dupont, François Vermeulen, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Revisiting mitochondrial diagnostic criteria in the new era of genomicsPeter Witters, Ann Saada, Tomas Honzik, et al.Genes|November 27, 2021
Genotype-Phenotype Correlations in PMM2-CDGLaurien Vaes, Daisy Rymen, David Cassiman, et al.Molecular Genetics and Metabolism|December 13, 2017
Renal involvement in PMM2-CDG, a mini-reviewRuqaiah Altassan, Peter Witters, Zubaida Saifudeen, et al.Journal of Inherited Metabolic Disease|October 6, 2017
Isolated sulfite oxidase deficiencyHelena Claerhout, Peter Witters, Luc Régal, et al.Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry|January 19, 2019
Hypophosphatasia in Adults: Clinical Spectrum and Its Association With Genetics and Metabolic SubstratesEveline Lefever, Peter Witters, Evelien Gielen, et al.European Journal of Gastroenterology & Hepatology|January 1, 2010
Wilson's disease: long-term follow-up of a cohort of 24 patients treated with D-penicillamineKlaartje F Lowette, Koen Desmet, Peter Witters, et al.Frontiers in Cardiovascular Medicine|July 28, 2022
Smartwatch-Based Blood Pressure Measurement Demonstrates Insufficient AccuracyMaarten Falter, Martijn Scherrenberg, Karen Driesen, et al.Pageof 8