Isabelle Adant
Leuven, VLG, Belgium
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
The complexome contextualizes proteomics data to fingerprint biological states and highlight perturbed functional modules in disease.
Journal: NPJ systems biology and applications
Published: September 07, 2025
Complex Metabolomic Changes in a Combined Defect of Glycosylation and Oxidative Phosphorylation in a Patient with Pathogenic Variants in PGM1 and NDUFA13.
Journal: Cells
Published: March 20, 2025
Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy.
Journal: Brain : a journal of neurology
Published: October 27, 2024
Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy.
Journal: medRxiv : the preprint server for health sciences
Published: July 15, 2024
Pyruvate and uridine rescue the metabolic profile of OXPHOS dysfunction.
Journal: Molecular metabolism
Published: April 11, 2022
Two cases of non-alcoholic fatty liver disease caused by biallelic ABHD5 mutations.
Journal: Journal of hepatology
Published: November 29, 2019
Oxygraphy Versus Enzymology for the Biochemical Diagnosis of Primary Mitochondrial Disease.
Journal: Metabolites
Published: August 28, 2019
Long-term outcomes of very low birth weight infants with spontaneous intestinal perforation: A retrospective case-matched cohort study.
Journal: Journal of pediatric surgery
Published: September 11, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026