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Ron A Wevers

Showing results (1-10 of 266) with videos related to

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Journal of Inherited Metabolic Disease|March 16, 2018
Think big - think omicsRon A Wevers, Nenad Blau
Neurology. Clinical Practice|February 15, 2018
Neurometabolic disorders: Five new thingsMichèl A Willemsen, Inga Harting, Ron A Wevers
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.
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.
European Journal of Human Genetics : EJHG|April 30, 2009
Autosomal recessive cutis laxa syndrome revisitedEva Morava, Maïlys Guillard, Dirk J Lefeber, et al.
Annals of Clinical Biochemistry|January 25, 2003
Reversal of clinical symptoms and radiographic abnormalities with protein restriction and ascorbic acid in alkaptonuriaEva Morava, György Kosztolányi, Udo F H Engelke, et al.
Magnetic Resonance in Chemistry : MRC|October 29, 2009
High-resolution 1H NMR spectroscopic investigation of a chick embryo model of neural tube developmentMuireann Coen, Ron A Wevers, John C Lindon, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 21, 2015
Lactate and its many facesMarjan Taher, Wilhelmina G Leen, Ron A Wevers, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 21, 2009
[The right medicine for cerebrotendinous xanthomatosis]Aad Verrips, Ron A Wevers, Francjan J van Spronsen, et al.
American Journal of Medical Genetics. Part A|August 12, 2011
Recognizable phenotype with common occurrence of microcephaly, psychomotor retardation, but no spontaneous bone fractures in autosomal recessive cutis laxa type IIB due to PYCR1 mutationsDorus Kouwenberg, Thatjana Gardeitchik, Ron A Wevers, et al.
Pageof 27

Showing results (1-10 of 266) with videos related to

Sort By:
Pageof 27
Journal of Inherited Metabolic Disease|March 16, 2018
Think big - think omicsRon A Wevers, Nenad Blau
Neurology. Clinical Practice|February 15, 2018
Neurometabolic disorders: Five new thingsMichèl A Willemsen, Inga Harting, Ron A Wevers
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.
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.
European Journal of Human Genetics : EJHG|April 30, 2009
Autosomal recessive cutis laxa syndrome revisitedEva Morava, Maïlys Guillard, Dirk J Lefeber, et al.
Annals of Clinical Biochemistry|January 25, 2003
Reversal of clinical symptoms and radiographic abnormalities with protein restriction and ascorbic acid in alkaptonuriaEva Morava, György Kosztolányi, Udo F H Engelke, et al.
Magnetic Resonance in Chemistry : MRC|October 29, 2009
High-resolution 1H NMR spectroscopic investigation of a chick embryo model of neural tube developmentMuireann Coen, Ron A Wevers, John C Lindon, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 21, 2015
Lactate and its many facesMarjan Taher, Wilhelmina G Leen, Ron A Wevers, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 21, 2009
[The right medicine for cerebrotendinous xanthomatosis]Aad Verrips, Ron A Wevers, Francjan J van Spronsen, et al.
American Journal of Medical Genetics. Part A|August 12, 2011
Recognizable phenotype with common occurrence of microcephaly, psychomotor retardation, but no spontaneous bone fractures in autosomal recessive cutis laxa type IIB due to PYCR1 mutationsDorus Kouwenberg, Thatjana Gardeitchik, Ron A Wevers, et al.
Pageof 27