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A Wevers

Showing results (31-40 of 543) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|February 14, 1980
Mitochondrial CK (EC 2.7.3.2) in the human heartR A Wevers, M W Mul-Steinbusch, J B Soons
Annals of Clinical Biochemistry|January 25, 2003
Proton nuclear magnetic resonance spectroscopy of body fluids in the field of inborn errors of metabolismS H Moolenaar, U F H Engelke, R A Wevers
Journal of Inherited Metabolic Disease|September 14, 2002
Neurotransmitter metabolites in CSF: an external quality control schemeC Bräutigam, C Weykamp, G F Hoffmann, et al.
Neurology|October 7, 2009
Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debré typeE Morava, R A Wevers, M A Willemsen, et al.
Clinical Chemistry|February 25, 2006
Mechanisms in protein O-glycan biosynthesis and clinical and molecular aspects of protein O-glycan biosynthesis defects: a reviewSuzan Wopereis, Dirk J Lefeber, Eva Morava, et al.
Clinical Chemistry|June 1, 1994
HPLC analysis of oligosaccharides in urine from oligosaccharidosis patientsG O Peelen, J G de Jong, R A Wevers
Molecular Genetics and Metabolism Reports|December 25, 2018
Response to "Leigh-like syndrome with mild mtDNA depletion due to the SUCLG1 variant c.626C>A"Christos Chinopoulos, Ron A Wevers, Hans R Waterham, et al.
Future Microbiology|July 12, 2013
C-type lectin receptors orchestrate antifungal immunityBrigitte A Wevers, Teunis B H Geijtenbeek, Sonja I Gringhuis
Journal of the American Academy of Dermatology|September 1, 1991
Antiproliferative potential of zidovudine in human keratinocyte culturesB Bonnekoh, A Wevers, J Geisel, et al.
European Journal of Human Genetics : EJHG|April 30, 2009
Autosomal recessive cutis laxa syndrome revisitedEva Morava, Maïlys Guillard, Dirk J Lefeber, et al.
Pageof 55

Showing results (31-40 of 543) with videos related to

Sort By:
Pageof 55
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 14, 1980
Mitochondrial CK (EC 2.7.3.2) in the human heartR A Wevers, M W Mul-Steinbusch, J B Soons
Annals of Clinical Biochemistry|January 25, 2003
Proton nuclear magnetic resonance spectroscopy of body fluids in the field of inborn errors of metabolismS H Moolenaar, U F H Engelke, R A Wevers
Journal of Inherited Metabolic Disease|September 14, 2002
Neurotransmitter metabolites in CSF: an external quality control schemeC Bräutigam, C Weykamp, G F Hoffmann, et al.
Neurology|October 7, 2009
Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debré typeE Morava, R A Wevers, M A Willemsen, et al.
Clinical Chemistry|February 25, 2006
Mechanisms in protein O-glycan biosynthesis and clinical and molecular aspects of protein O-glycan biosynthesis defects: a reviewSuzan Wopereis, Dirk J Lefeber, Eva Morava, et al.
Clinical Chemistry|June 1, 1994
HPLC analysis of oligosaccharides in urine from oligosaccharidosis patientsG O Peelen, J G de Jong, R A Wevers
Molecular Genetics and Metabolism Reports|December 25, 2018
Response to "Leigh-like syndrome with mild mtDNA depletion due to the SUCLG1 variant c.626C>A"Christos Chinopoulos, Ron A Wevers, Hans R Waterham, et al.
Future Microbiology|July 12, 2013
C-type lectin receptors orchestrate antifungal immunityBrigitte A Wevers, Teunis B H Geijtenbeek, Sonja I Gringhuis
Journal of the American Academy of Dermatology|September 1, 1991
Antiproliferative potential of zidovudine in human keratinocyte culturesB Bonnekoh, A Wevers, J Geisel, et al.
European Journal of Human Genetics : EJHG|April 30, 2009
Autosomal recessive cutis laxa syndrome revisitedEva Morava, Maïlys Guillard, Dirk J Lefeber, et al.
Pageof 55