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C E Hollak

Showing results (11-20 of 21) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|January 6, 2001
[Fabry's disease; towards a treatment]G E Linthorst, C E Hollak, D K Bosman, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1995
Increased basal glucose production in type 1 Gaucher's diseaseE P Corssmit, C E Hollak, E Endert, et al.
The American Journal of Medicine|October 8, 1997
Differential effects of enzyme supplementation therapy on manifestations of type 1 Gaucher diseaseC E Hollak, E P Corssmit, J M Aerts, et al.
Biochimica Et Biophysica Acta|December 16, 1996
Plasma tumor necrosis factor-a (TNF-a) levels in Gaucher diseaseH Michelakakis, C Spanou, A Kondyli, et al.
Journal of Inherited Metabolic Disease|February 11, 2005
Plasma chitotriosidase and CCL18: early biochemical surrogate markers in type B Niemann-Pick diseaseJ Brinkman, F A Wijburg, C E Hollak, et al.
JIMD Reports|August 13, 2016
Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency and Perioperative Management in Adult PatientsM M Welsink-Karssies, J A W Polderman, E J Nieveen van Dijkum, et al.
Lancet (London, England)|June 10, 1995
Individualised low-dose alglucerase therapy for type 1 Gaucher's diseaseC E Hollak, J M Aerts, R Goudsmit, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Oligosaccharide excretion in adult Gaucher diseaseJ G de Jong, J M Aerts, S van Weely, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Elevated plasma chitotriosidase activity in various lysosomal storage disordersY Guo, W He, A M Boer, et al.
Human Mutation|January 1, 1997
Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic valueR G Boot, C E Hollak, M Verhoek, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Nederlands Tijdschrift Voor Geneeskunde|January 6, 2001
[Fabry's disease; towards a treatment]G E Linthorst, C E Hollak, D K Bosman, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1995
Increased basal glucose production in type 1 Gaucher's diseaseE P Corssmit, C E Hollak, E Endert, et al.
The American Journal of Medicine|October 8, 1997
Differential effects of enzyme supplementation therapy on manifestations of type 1 Gaucher diseaseC E Hollak, E P Corssmit, J M Aerts, et al.
Biochimica Et Biophysica Acta|December 16, 1996
Plasma tumor necrosis factor-a (TNF-a) levels in Gaucher diseaseH Michelakakis, C Spanou, A Kondyli, et al.
Journal of Inherited Metabolic Disease|February 11, 2005
Plasma chitotriosidase and CCL18: early biochemical surrogate markers in type B Niemann-Pick diseaseJ Brinkman, F A Wijburg, C E Hollak, et al.
JIMD Reports|August 13, 2016
Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency and Perioperative Management in Adult PatientsM M Welsink-Karssies, J A W Polderman, E J Nieveen van Dijkum, et al.
Lancet (London, England)|June 10, 1995
Individualised low-dose alglucerase therapy for type 1 Gaucher's diseaseC E Hollak, J M Aerts, R Goudsmit, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Oligosaccharide excretion in adult Gaucher diseaseJ G de Jong, J M Aerts, S van Weely, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Elevated plasma chitotriosidase activity in various lysosomal storage disordersY Guo, W He, A M Boer, et al.
Human Mutation|January 1, 1997
Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic valueR G Boot, C E Hollak, M Verhoek, et al.
Pageof 3