Corinne C. De Laet

Brussels, BRU, Belgium

Last Updated: 09/26/2026

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Found 35 publications

Therapeutic Monitoring of Patients With Hereditary Tyrosinemia Type 1-A Belgian Monocentric Experience.

Therapeutic Monitoring of Patients With Hereditary Tyrosinemia Type 1-A Belgian Monocentric Experience.

Journal: JIMD reports
Published: June 21, 2025

Solute Carrier 45A1: A New Cerebral Glucose Transporter Brain Disorder with Focal Refractory Epilepsy Responsive to Ketogenic Diet and Acetazolamide.

Solute Carrier 45A1: A New Cerebral Glucose Transporter Brain Disorder with Focal Refractory Epilepsy Responsive to Ketogenic Diet and Acetazolamide.

Journal: Neuropediatrics
Published: June 20, 2025

Advancing Neonatal Screening for Pyridoxine-Dependent Epilepsy-ALDH7A1 Through Combined Analysis of 2-OPP, 6-Oxo-Pipecolate and Pipecolate in a Butylated FIA-MS/MS Workflow.

Advancing Neonatal Screening for Pyridoxine-Dependent Epilepsy-ALDH7A1 Through Combined Analysis of 2-OPP, 6-Oxo-Pipecolate and Pipecolate in a Butylated FIA-MS/MS Workflow.

Journal: International journal of neonatal screening
Published: May 08, 2025

Morphological abnormalities in the white blood cells of a baby with type VI mucopolysaccharidosis.

Morphological abnormalities in the white blood cells of a baby with type VI mucopolysaccharidosis.

Journal: Annales de biologie clinique
Published: November 29, 2024

Lactate and gastrointestinal complications during enteral nutrition in pediatric ECMO patients: a retrospective cohort study.

Lactate and gastrointestinal complications during enteral nutrition in pediatric ECMO patients: a retrospective cohort study.

Journal: European journal of pediatrics
Published: November 20, 2024

Empagliflozin for treating neutropenia and neutrophil dysfunction in 21 infants with glycogen storage disease 1b.

Empagliflozin for treating neutropenia and neutrophil dysfunction in 21 infants with glycogen storage disease 1b.

Journal: Molecular genetics and metabolism
Published: February 13, 2024

Severe rhabdomyolysis in an infant due to fatty acid oxidation disorder: a case report.

Severe rhabdomyolysis in an infant due to fatty acid oxidation disorder: a case report.

Journal: Journal of medical case reports
Published: September 18, 2023

Impact of the SARS-CoV-2 pandemic on the health of individuals with intoxication-type metabolic diseases-Data from the E-IMD consortium.

Impact of the SARS-CoV-2 pandemic on the health of individuals with intoxication-type metabolic diseases-Data from the E-IMD consortium.

Journal: Journal of inherited metabolic disease
Published: August 17, 2022

Carbamazepine efficacy in a severe electro-clinical presentation of SLC13A5-epilepsy.

Carbamazepine efficacy in a severe electro-clinical presentation of SLC13A5-epilepsy.

Journal: Annals of clinical and translational neurology
Published: March 18, 2022

Neurocognitive outcome and mental health in children with tyrosinemia type 1 and phenylketonuria: A comparison between two genetic disorders affecting the same metabolic pathway.

Neurocognitive outcome and mental health in children with tyrosinemia type 1 and phenylketonuria: A comparison between two genetic disorders affecting the same metabolic pathway.

Journal: Journal of inherited metabolic disease
Published: March 04, 2022

Ascites in infantile onset type II Sialidosis.

Ascites in infantile onset type II Sialidosis.

Journal: JIMD reports
Published: February 25, 2022

Acquired Zinc Deficiency Mimicking Acrodermatitis Enteropathica in a Breast-Fed Premature Infant.

Acquired Zinc Deficiency Mimicking Acrodermatitis Enteropathica in a Breast-Fed Premature Infant.

Journal: Pediatric reports
Published: June 29, 2021
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Last Updated: 09/26/2026