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Albert H Bootsma

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Journal of Inherited Metabolic Disease|November 21, 2014
Principles and practice of lipidomicsFrédéric M Vaz, Mia Pras-Raves, Albert H Bootsma, et al.
The Biochemical Journal|November 13, 2004
Characterization of carnitine and fatty acid metabolism in the long-chain acyl-CoA dehydrogenase-deficient mouseNaomi van Vlies, Liqun Tian, Henk Overmars, et al.
Journal of Lipid Research|March 19, 2017
A newborn screening method for cerebrotendinous xanthomatosis using bile alcohol glucuronides and metabolite ratiosFrédéric M Vaz, Albert H Bootsma, Willem Kulik, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 12, 2020
Toward newborn screening of cerebrotendinous xanthomatosis: results of a biomarker research study using 32,000 newborn dried blood spotsXinying Hong, Jessica Daiker, Martin Sadilek, et al.
The Biochemical Journal|March 7, 2002
Complete beta-oxidation of valproate: cleavage of 3-oxovalproyl-CoA by a mitochondrial 3-oxoacyl-CoA thiolaseMargarida F B Silva, Jos P N Ruiter, Henk Overmars, et al.
Hepatology (Baltimore, Md.)|May 29, 2014
Sodium taurocholate cotransporting polypeptide (SLC10A1) deficiency: conjugated hypercholanemia without a clear clinical phenotypeFrédéric M Vaz, Coen C Paulusma, Hidde Huidekoper, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 18, 2022
Newborn screening for Cerebrotendinous Xanthomatosis: A retrospective biomarker study using both flow-injection and UPLC-MS/MS analysis in 20,000 newbornsFrédéric M Vaz, Youssra Jamal, Rob Barto, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|December 6, 2024
Challenges in the identification and quantification of an unknown impurity in chenodeoxycholic acid drug substanceNatalja Bouwhuis, Yasmin Polak, Anneliene M Schimmel, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Journal of Inherited Metabolic Disease|November 21, 2014
Principles and practice of lipidomicsFrédéric M Vaz, Mia Pras-Raves, Albert H Bootsma, et al.
The Biochemical Journal|November 13, 2004
Characterization of carnitine and fatty acid metabolism in the long-chain acyl-CoA dehydrogenase-deficient mouseNaomi van Vlies, Liqun Tian, Henk Overmars, et al.
Journal of Lipid Research|March 19, 2017
A newborn screening method for cerebrotendinous xanthomatosis using bile alcohol glucuronides and metabolite ratiosFrédéric M Vaz, Albert H Bootsma, Willem Kulik, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 12, 2020
Toward newborn screening of cerebrotendinous xanthomatosis: results of a biomarker research study using 32,000 newborn dried blood spotsXinying Hong, Jessica Daiker, Martin Sadilek, et al.
The Biochemical Journal|March 7, 2002
Complete beta-oxidation of valproate: cleavage of 3-oxovalproyl-CoA by a mitochondrial 3-oxoacyl-CoA thiolaseMargarida F B Silva, Jos P N Ruiter, Henk Overmars, et al.
Hepatology (Baltimore, Md.)|May 29, 2014
Sodium taurocholate cotransporting polypeptide (SLC10A1) deficiency: conjugated hypercholanemia without a clear clinical phenotypeFrédéric M Vaz, Coen C Paulusma, Hidde Huidekoper, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 18, 2022
Newborn screening for Cerebrotendinous Xanthomatosis: A retrospective biomarker study using both flow-injection and UPLC-MS/MS analysis in 20,000 newbornsFrédéric M Vaz, Youssra Jamal, Rob Barto, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|December 6, 2024
Challenges in the identification and quantification of an unknown impurity in chenodeoxycholic acid drug substanceNatalja Bouwhuis, Yasmin Polak, Anneliene M Schimmel, et al.
Pageof 1