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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 heart
R 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 metabolism
S 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 scheme
C Bräutigam, C Weykamp, G F Hoffmann, et al.
Neurology
|
October 7, 2009
Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debré type
E 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 review
Suzan Wopereis, Dirk J Lefeber, Eva Morava, et al.
Clinical Chemistry
|
June 1, 1994
HPLC analysis of oligosaccharides in urine from oligosaccharidosis patients
G 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 immunity
Brigitte 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 cultures
B Bonnekoh, A Wevers, J Geisel, et al.
European Journal of Human Genetics : EJHG
|
April 30, 2009
Autosomal recessive cutis laxa syndrome revisited
Eva Morava, Maïlys Guillard, Dirk J Lefeber, et al.
Page
of 55
Search research articles
Search
Showing results (31-40 of 543) with videos related to
Sort By:
Page
of 55
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 14, 1980
Mitochondrial CK (EC 2.7.3.2) in the human heart
R 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 metabolism
S 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 scheme
C Bräutigam, C Weykamp, G F Hoffmann, et al.
Neurology
|
October 7, 2009
Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debré type
E 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 review
Suzan Wopereis, Dirk J Lefeber, Eva Morava, et al.
Clinical Chemistry
|
June 1, 1994
HPLC analysis of oligosaccharides in urine from oligosaccharidosis patients
G 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 immunity
Brigitte 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 cultures
B Bonnekoh, A Wevers, J Geisel, et al.
European Journal of Human Genetics : EJHG
|
April 30, 2009
Autosomal recessive cutis laxa syndrome revisited
Eva Morava, Maïlys Guillard, Dirk J Lefeber, et al.
Page
of 55