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A Wevers

Showing results (271-280 of 543) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|May 30, 1984
A study on post-synthetic modifications in alfa-alfa enolase (EC 4.2.1.11) brought about by a human serum proteinR A Wevers, J P Boegheim, O R Hommes, et al.
NMR in Biomedicine|July 14, 2009
N-acetyl resonances in in vivo and in vitro NMR spectroscopy of cystic ovarian tumorsEva Kolwijck, Udo F Engelke, Marinette van der Graaf, et al.
Annals of Human Genetics|April 3, 2001
A branch site mutation leading to aberrant splicing of the human tyrosine hydroxylase gene in a child with a severe extrapyramidal movement disorderR J Janssen, R A Wevers, M Häussler, et al.
Drugs Under Experimental and Clinical Research|May 10, 2001
Chitotriosidase as a new marker of macrophage stimulation in a tumor model treated with cyclophosphamide and UkrainT A Korolenko, S J Djanayeva, O V Falameyeva, et al.
Neurology|December 11, 2013
Child neurology: differential diagnosis of a low CSF glucose in children and young adultsWilhelmina G Leen, Cornelis J de Wit, Ron A Wevers, et al.
Metabolic Brain Disease|December 22, 2015
Expanding the phenotype in aminoacylase 1 (ACY1) deficiency: characterization of the molecular defect in a 63-year-old woman with generalized dystoniaJörn Oliver Sass, Jathana Vaithilingam, Corinne Gemperle-Britschgi, et al.
Neuropediatrics|April 25, 2000
I-cell disease presenting with severe hypophosphatemia and cardiomyopathyG Bocca, C Noordam, R A Wevers, et al.
Clinical Chemistry|April 2, 1999
1H-NMR spectroscopy of body fluids: inborn errors of purine and pyrimidine metabolismR A Wevers, U F Engelke, S H Moolenaar, et al.
Neurology|March 24, 2004
Mevalonate kinase deficiency: Evidence for a phenotypic continuumA Simon, H P H Kremer, R A Wevers, et al.
American Journal of Medical Genetics. Part A|October 19, 2010
MACS syndrome: A combined collagen and elastin disorder due to abnormal Golgi traffickingBeate Albrecht, Arjan P de Brouwer, Dirk J Lefeber, et al.
Pageof 55

Showing results (271-280 of 543) with videos related to

Sort By:
Pageof 55
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 30, 1984
A study on post-synthetic modifications in alfa-alfa enolase (EC 4.2.1.11) brought about by a human serum proteinR A Wevers, J P Boegheim, O R Hommes, et al.
NMR in Biomedicine|July 14, 2009
N-acetyl resonances in in vivo and in vitro NMR spectroscopy of cystic ovarian tumorsEva Kolwijck, Udo F Engelke, Marinette van der Graaf, et al.
Annals of Human Genetics|April 3, 2001
A branch site mutation leading to aberrant splicing of the human tyrosine hydroxylase gene in a child with a severe extrapyramidal movement disorderR J Janssen, R A Wevers, M Häussler, et al.
Drugs Under Experimental and Clinical Research|May 10, 2001
Chitotriosidase as a new marker of macrophage stimulation in a tumor model treated with cyclophosphamide and UkrainT A Korolenko, S J Djanayeva, O V Falameyeva, et al.
Neurology|December 11, 2013
Child neurology: differential diagnosis of a low CSF glucose in children and young adultsWilhelmina G Leen, Cornelis J de Wit, Ron A Wevers, et al.
Metabolic Brain Disease|December 22, 2015
Expanding the phenotype in aminoacylase 1 (ACY1) deficiency: characterization of the molecular defect in a 63-year-old woman with generalized dystoniaJörn Oliver Sass, Jathana Vaithilingam, Corinne Gemperle-Britschgi, et al.
Neuropediatrics|April 25, 2000
I-cell disease presenting with severe hypophosphatemia and cardiomyopathyG Bocca, C Noordam, R A Wevers, et al.
Clinical Chemistry|April 2, 1999
1H-NMR spectroscopy of body fluids: inborn errors of purine and pyrimidine metabolismR A Wevers, U F Engelke, S H Moolenaar, et al.
Neurology|March 24, 2004
Mevalonate kinase deficiency: Evidence for a phenotypic continuumA Simon, H P H Kremer, R A Wevers, et al.
American Journal of Medical Genetics. Part A|October 19, 2010
MACS syndrome: A combined collagen and elastin disorder due to abnormal Golgi traffickingBeate Albrecht, Arjan P de Brouwer, Dirk J Lefeber, et al.
Pageof 55