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Sandra D K Kingma

Showing results (1-10 of 19) with videos related to

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Neuropediatrics|January 6, 2022
Recurrent Isolated Sixth Nerve Palsy in Childhood-Review on a Rare PhenomenonSandra D K Kingma, Berten Ceulemans
Journal of Inherited Metabolic Disease|September 4, 2021
MPS I: Early diagnosis, bone disease and treatment, where are we now?Sandra D K Kingma, An I Jonckheere
The Journal of Pediatrics|January 18, 2011
Ischemia-reperfusion and neonatal intestinal injuryChristopher M Young, Sandra D K Kingma, Josef Neu
Best Practice & Research. Clinical Endocrinology & Metabolism|May 20, 2015
Epidemiology and diagnosis of lysosomal storage disorders; challenges of screeningSandra D K Kingma, Olaf A Bodamer, Frits A Wijburg
Endocrinology and Metabolism Clinics of North America|August 21, 2010
The intestinal microbiome: relationship to type 1 diabetesJosef Neu, Graciela Lorca, Sandra D K Kingma, et al.
Clinics and Practice|April 26, 2014
Small atrial septal defect associated with heart failure in an infant with a marginal left ventricleSandra D K Kingma, Lukas A Rammeloo, Vladimir Sojak, et al.
JIMD Reports|May 12, 2021
Are GMI gangliosidosis and Morquio type B two different disorders or part of one phenotypic spectrum?Sandra D K Kingma, Berten Ceulemans, Sandra Kenis, et al.
Journal of Inherited Metabolic Disease|April 5, 2014
Genistein increases glycosaminoglycan levels in mucopolysaccharidosis type I cell modelsSandra D K Kingma, Tom Wagemans, Lodewijk IJlst, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 24, 2023
Metachromatic leukodystrophy: To screen or not to screen?An I Jonckheere, Sandra D K Kingma, François Eyskens, et al.
Orphanet Journal of Rare Diseases|September 14, 2023
Imerslund-Gräsbeck syndrome: a comprehensive review of reported casesSandra D K Kingma, Julie Neven, An Bael, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Neuropediatrics|January 6, 2022
Recurrent Isolated Sixth Nerve Palsy in Childhood-Review on a Rare PhenomenonSandra D K Kingma, Berten Ceulemans
Journal of Inherited Metabolic Disease|September 4, 2021
MPS I: Early diagnosis, bone disease and treatment, where are we now?Sandra D K Kingma, An I Jonckheere
The Journal of Pediatrics|January 18, 2011
Ischemia-reperfusion and neonatal intestinal injuryChristopher M Young, Sandra D K Kingma, Josef Neu
Best Practice & Research. Clinical Endocrinology & Metabolism|May 20, 2015
Epidemiology and diagnosis of lysosomal storage disorders; challenges of screeningSandra D K Kingma, Olaf A Bodamer, Frits A Wijburg
Endocrinology and Metabolism Clinics of North America|August 21, 2010
The intestinal microbiome: relationship to type 1 diabetesJosef Neu, Graciela Lorca, Sandra D K Kingma, et al.
Clinics and Practice|April 26, 2014
Small atrial septal defect associated with heart failure in an infant with a marginal left ventricleSandra D K Kingma, Lukas A Rammeloo, Vladimir Sojak, et al.
JIMD Reports|May 12, 2021
Are GMI gangliosidosis and Morquio type B two different disorders or part of one phenotypic spectrum?Sandra D K Kingma, Berten Ceulemans, Sandra Kenis, et al.
Journal of Inherited Metabolic Disease|April 5, 2014
Genistein increases glycosaminoglycan levels in mucopolysaccharidosis type I cell modelsSandra D K Kingma, Tom Wagemans, Lodewijk IJlst, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 24, 2023
Metachromatic leukodystrophy: To screen or not to screen?An I Jonckheere, Sandra D K Kingma, François Eyskens, et al.
Orphanet Journal of Rare Diseases|September 14, 2023
Imerslund-Gräsbeck syndrome: a comprehensive review of reported casesSandra D K Kingma, Julie Neven, An Bael, et al.
Pageof 2