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Dimitri Schlemmer

Showing results (11-20 of 21) with videos related to

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Clinical Chemistry and Laboratory Medicine|July 9, 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 studiesBenoit Llopis, Alexandre Bleibtreu, Dimitri Schlemmer, et al.
Journal of Pharmaceutical and Biomedical Analysis|February 17, 2024
Simultaneous quantification of four hormone therapy drugs by LC-MS/MS: Clinical applications in breast cancer patientsBochra Mansour, Clarice Ngo, Dimitri Schlemmer, et al.
Analytical Chemistry|August 30, 2002
Development of a direct assay for measuring intracellular AZT triphosphate in humans peripheral blood mononuclear cellsFrançois Becher, Dimitri Schlemmer, Alain Pruvost, et al.
Journal of Pharmaceutical and Biomedical Analysis|September 21, 2023
Determination of plasma concentration of Belimumab by LC-MS/MS: Method development, validation, and clinical applicationClémence Marin, Gaëlle Noé, Dimitri Schlemmer, et al.
American Journal of Human Genetics|March 6, 2008
CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizuresJulie Mollet, Agnès Delahodde, Valérie Serre, et al.
Human Molecular Genetics|July 15, 2018
A new AMPK activator, GSK773, corrects fatty acid oxidation and differentiation defect in CPT2-deficient myotubesFatima-Zohra Boufroura, Carole Le Bachelier, Céline Tomkiewicz-Raulet, et al.
Journal of Lipid Research|April 5, 2005
Monolysocardiolipins accumulate in Barth syndrome but do not lead to enhanced apoptosisFredoen Valianpour, Voula Mitsakos, Dimitri Schlemmer, et al.
Molecular Genetics and Metabolism|January 29, 2023
Plasma G<sub>M2</sub> ganglioside potential biomarker for diagnosis, prognosis and disease monitoring of GM2-GangliosidosisAmélie Blondel, Ichraf Kraoua, Chloé Marcelino, et al.
Orphanet Journal of Rare Diseases|November 15, 2022
Efficacy and pharmacokinetics of betaine in CBS and cblC deficiencies: a cross-over randomized controlled trialApolline Imbard, Artemis Toumazi, Sophie Magréault, et al.
Journal of Inherited Metabolic Disease|June 26, 2015
Mitochondrial trifunctional protein deficiency in human cultured fibroblasts: effects of bezafibrateFatima Djouadi, Florence Habarou, Carole Le Bachelier, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Clinical Chemistry and Laboratory Medicine|July 9, 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 studiesBenoit Llopis, Alexandre Bleibtreu, Dimitri Schlemmer, et al.
Journal of Pharmaceutical and Biomedical Analysis|February 17, 2024
Simultaneous quantification of four hormone therapy drugs by LC-MS/MS: Clinical applications in breast cancer patientsBochra Mansour, Clarice Ngo, Dimitri Schlemmer, et al.
Analytical Chemistry|August 30, 2002
Development of a direct assay for measuring intracellular AZT triphosphate in humans peripheral blood mononuclear cellsFrançois Becher, Dimitri Schlemmer, Alain Pruvost, et al.
Journal of Pharmaceutical and Biomedical Analysis|September 21, 2023
Determination of plasma concentration of Belimumab by LC-MS/MS: Method development, validation, and clinical applicationClémence Marin, Gaëlle Noé, Dimitri Schlemmer, et al.
American Journal of Human Genetics|March 6, 2008
CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizuresJulie Mollet, Agnès Delahodde, Valérie Serre, et al.
Human Molecular Genetics|July 15, 2018
A new AMPK activator, GSK773, corrects fatty acid oxidation and differentiation defect in CPT2-deficient myotubesFatima-Zohra Boufroura, Carole Le Bachelier, Céline Tomkiewicz-Raulet, et al.
Journal of Lipid Research|April 5, 2005
Monolysocardiolipins accumulate in Barth syndrome but do not lead to enhanced apoptosisFredoen Valianpour, Voula Mitsakos, Dimitri Schlemmer, et al.
Molecular Genetics and Metabolism|January 29, 2023
Plasma G<sub>M2</sub> ganglioside potential biomarker for diagnosis, prognosis and disease monitoring of GM2-GangliosidosisAmélie Blondel, Ichraf Kraoua, Chloé Marcelino, et al.
Orphanet Journal of Rare Diseases|November 15, 2022
Efficacy and pharmacokinetics of betaine in CBS and cblC deficiencies: a cross-over randomized controlled trialApolline Imbard, Artemis Toumazi, Sophie Magréault, et al.
Journal of Inherited Metabolic Disease|June 26, 2015
Mitochondrial trifunctional protein deficiency in human cultured fibroblasts: effects of bezafibrateFatima Djouadi, Florence Habarou, Carole Le Bachelier, et al.
Pageof 3