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J E M Groener

Showing results (1-10 of 13) with videos related to

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Human Genetics|June 29, 2007
Gene symbol: GLACostel Spanu, R H Lekanne dit Deprez, J E M Groener, et al.
Molecular Genetics and Metabolism|October 3, 2002
L-Arabinosuria: a new defect in human pentose metabolismW Onkenhout, J E M Groener, N M Verhoeven, et al.
Biochimica Et Biophysica Acta|December 25, 2007
Plasma glucosylceramide and ceramide in type 1 Gaucher disease patients: correlations with disease severity and response to therapeutic interventionJ E M Groener, B J H M Poorthuis, S Kuiper, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|May 18, 2005
Identification and use of biomarkers in Gaucher disease and other lysosomal storage diseasesJ M F G Aerts, C E M Hollak, M van Breemen, et al.
Journal of Inherited Metabolic Disease|May 17, 2014
Value of plasma chitotriosidase to assess non-neuronopathic Gaucher disease severity and progression in the era of enzyme replacement therapyL van Dussen, E J Hendriks, J E M Groener, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
GLUT-1 deficiency without epilepsy--an exceptional caseW C G Overweg-Plandsoen, J E M Groener, D Wang, et al.
Molecular Genetics and Metabolism|June 13, 2006
Plasma chitotriosidase in male Fabry patients: a marker for monitoring lipid-laden macrophages and their correction by enzyme replacement therapyA C Vedder, J Cox-Brinkman, C E M Hollak, et al.
The Netherlands Journal of Medicine|April 9, 2015
Hypercholesterolaemia and hepatosplenomegaly: two manifestations of cholesteryl ester storage diseaseB Sjouke, J W J van der Stappen, J E M Groener, et al.
The Journal of Clinical Endocrinology and Metabolism|May 6, 2011
Markers of bone turnover in Gaucher disease: modeling the evolution of bone diseaseL van Dussen, P Lips, V E Everts, et al.
Journal of Inherited Metabolic Disease|January 9, 2007
The Dutch Fabry cohort: diversity of clinical manifestations and Gb3 levelsA C Vedder, G E Linthorst, M J van Breemen, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Human Genetics|June 29, 2007
Gene symbol: GLACostel Spanu, R H Lekanne dit Deprez, J E M Groener, et al.
Molecular Genetics and Metabolism|October 3, 2002
L-Arabinosuria: a new defect in human pentose metabolismW Onkenhout, J E M Groener, N M Verhoeven, et al.
Biochimica Et Biophysica Acta|December 25, 2007
Plasma glucosylceramide and ceramide in type 1 Gaucher disease patients: correlations with disease severity and response to therapeutic interventionJ E M Groener, B J H M Poorthuis, S Kuiper, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|May 18, 2005
Identification and use of biomarkers in Gaucher disease and other lysosomal storage diseasesJ M F G Aerts, C E M Hollak, M van Breemen, et al.
Journal of Inherited Metabolic Disease|May 17, 2014
Value of plasma chitotriosidase to assess non-neuronopathic Gaucher disease severity and progression in the era of enzyme replacement therapyL van Dussen, E J Hendriks, J E M Groener, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
GLUT-1 deficiency without epilepsy--an exceptional caseW C G Overweg-Plandsoen, J E M Groener, D Wang, et al.
Molecular Genetics and Metabolism|June 13, 2006
Plasma chitotriosidase in male Fabry patients: a marker for monitoring lipid-laden macrophages and their correction by enzyme replacement therapyA C Vedder, J Cox-Brinkman, C E M Hollak, et al.
The Netherlands Journal of Medicine|April 9, 2015
Hypercholesterolaemia and hepatosplenomegaly: two manifestations of cholesteryl ester storage diseaseB Sjouke, J W J van der Stappen, J E M Groener, et al.
The Journal of Clinical Endocrinology and Metabolism|May 6, 2011
Markers of bone turnover in Gaucher disease: modeling the evolution of bone diseaseL van Dussen, P Lips, V E Everts, et al.
Journal of Inherited Metabolic Disease|January 9, 2007
The Dutch Fabry cohort: diversity of clinical manifestations and Gb3 levelsA C Vedder, G E Linthorst, M J van Breemen, et al.
Pageof 2