Dimitri Schlemmer
Paris, France
Last Updated: 09/26/2026
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Found 14 publications
Analytical feasibility of linezolid quantification by LC-MS/MS using dried plasma spot microsampling.
Journal: International journal of antimicrobial agents
Published: November 03, 2025
Simultaneous quantification of four hormone therapy drugs by LC-MS/MS: Clinical applications in breast cancer patients.
Journal: Journal of pharmaceutical and biomedical analysis
Published: January 05, 2024
Determination of plasma concentration of Belimumab by LC-MS/MS: Method development, validation, and clinical application.
Journal: Journal of pharmaceutical and biomedical analysis
Published: June 01, 2023
Plasma lysosphingolipids in GRN-related diseases: Monitoring lysosomal dysfunction to track disease progression.
Journal: Neurobiology of disease
Published: February 21, 2023
Plasma GM2 ganglioside potential biomarker for diagnosis, prognosis and disease monitoring of GM2-Gangliosidosis.
Journal: Molecular genetics and metabolism
Published: September 22, 2022
Efficacy and pharmacokinetics of betaine in CBS and cblC deficiencies: a cross-over randomized controlled trial.
Journal: Orphanet journal of rare diseases
Published: July 01, 2022
LC-MS/MS Identification of Prolidase Deficiency: A Rare Cause of Infantile Hepatosplenomegaly.
Journal: Clinical chemistry
Published: April 23, 2021
Simple and accurate quantitative analysis of cefiderocol and ceftobiprole in human plasma using liquid chromatography-isotope dilution tandem mass spectrometry: interest for their therapeutic drug monitoring and pharmacokinetic studies.
Journal: Clinical chemistry and laboratory medicine
Published: April 08, 2021
ShiF acts as an auxiliary factor of aerobactin secretion in meningitis Escherichia coli strain S88.
Journal: BMC microbiology
Published: April 29, 2019
Mitochondrial trifunctional protein deficiency in human cultured fibroblasts: effects of bezafibrate.
Journal: Journal of inherited metabolic disease
Published: March 25, 2015
Stilbenes and resveratrol metabolites improve mitochondrial fatty acid oxidation defects in human fibroblasts.
Journal: Orphanet journal of rare diseases
Published: February 20, 2014
Last Updated: 09/26/2026