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R A Wevers

Showing results (121-130 of 222) with videos related to

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Molecular Genetics and Metabolism|August 30, 2008
Technical and biochemical factors affecting cerebrospinal fluid 5-MTHF, biopterin and neopterin concentrationsM M Verbeek, A M Blom, R A Wevers, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1985
The concentration of blood components related to fuel metabolism during prolonged fasting in childrenK J Lamers, W H Doesburg, F J Gabreëls, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 10, 2004
[Hydrops fetalis as an indication for a systematic investigation into the presence of lysosomal storage diseases]P M W Janssens, A N de Groot, J G de Jong, et al.
Analytica Chimica Acta|November 9, 2015
Regularized MANOVA (rMANOVA) in untargeted metabolomicsJ Engel, L Blanchet, B Bloemen, et al.
Translational Psychiatry|July 9, 2014
Early life adversity and serotonin transporter gene variation interact at the level of the adrenal gland to affect the adult hypothalamo-pituitary-adrenal axisR H A van der Doelen, W Deschamps, C D'Annibale, et al.
Human Genetics|December 1, 1996
Two new mutations in the sterol 27-hydroxylase gene in two families lead to cerebrotendinous xanthomatosisA Verrips, G C Steenbergen-Spanjers, J A Luyten, et al.
Neuromuscular Disorders : NMD|July 19, 2000
Cerebrotendinous xanthomatosis. Controversies about nerve and muscle: observations in ten patientsA Verrips, B G van Engelen, H ter Laak, et al.
Journal of Inherited Metabolic Disease|April 26, 2007
Transferrin hypoglycosylation in hereditary fructose intolerance: using the clues and avoiding the pitfallsM Adamowicz, R Płoski, D Rokicki, et al.
The Biochemical Journal|July 1, 1993
Deficiency of Na+/K(+)-ATPase and sarcoplasmic reticulum Ca(2+)-ATPase in skeletal muscle and cultured muscle cells of myotonic dystrophy patientsA A Benders, J A Timmermans, A Oosterhof, et al.
Clinical Science (London, England : 1979)|May 1, 2002
Muscle function during repetitive moderate-intensity muscle contractions in myoadenylate deaminase-deficient Dutch subjectsC J De Ruiter, A M May, B G M van Engelen, et al.
Pageof 23

Showing results (121-130 of 222) with videos related to

Sort By:
Pageof 23
Molecular Genetics and Metabolism|August 30, 2008
Technical and biochemical factors affecting cerebrospinal fluid 5-MTHF, biopterin and neopterin concentrationsM M Verbeek, A M Blom, R A Wevers, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1985
The concentration of blood components related to fuel metabolism during prolonged fasting in childrenK J Lamers, W H Doesburg, F J Gabreëls, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 10, 2004
[Hydrops fetalis as an indication for a systematic investigation into the presence of lysosomal storage diseases]P M W Janssens, A N de Groot, J G de Jong, et al.
Analytica Chimica Acta|November 9, 2015
Regularized MANOVA (rMANOVA) in untargeted metabolomicsJ Engel, L Blanchet, B Bloemen, et al.
Translational Psychiatry|July 9, 2014
Early life adversity and serotonin transporter gene variation interact at the level of the adrenal gland to affect the adult hypothalamo-pituitary-adrenal axisR H A van der Doelen, W Deschamps, C D'Annibale, et al.
Human Genetics|December 1, 1996
Two new mutations in the sterol 27-hydroxylase gene in two families lead to cerebrotendinous xanthomatosisA Verrips, G C Steenbergen-Spanjers, J A Luyten, et al.
Neuromuscular Disorders : NMD|July 19, 2000
Cerebrotendinous xanthomatosis. Controversies about nerve and muscle: observations in ten patientsA Verrips, B G van Engelen, H ter Laak, et al.
Journal of Inherited Metabolic Disease|April 26, 2007
Transferrin hypoglycosylation in hereditary fructose intolerance: using the clues and avoiding the pitfallsM Adamowicz, R Płoski, D Rokicki, et al.
The Biochemical Journal|July 1, 1993
Deficiency of Na+/K(+)-ATPase and sarcoplasmic reticulum Ca(2+)-ATPase in skeletal muscle and cultured muscle cells of myotonic dystrophy patientsA A Benders, J A Timmermans, A Oosterhof, et al.
Clinical Science (London, England : 1979)|May 1, 2002
Muscle function during repetitive moderate-intensity muscle contractions in myoadenylate deaminase-deficient Dutch subjectsC J De Ruiter, A M May, B G M van Engelen, et al.
Pageof 23