A J Reuser - JoVE Visualize

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The Histochemical Journal|January 1, 1988

Ultrastructural localization of steroid sulphatase in cultured human fibroblasts by immunocytochemistry: a comparative study with lysosomal enzymes and the mannose 6-phosphate receptorR Willemsen, M Kroos, A T Hoogeveen, et al.

Lancet (London, England)|September 6, 2000

Recombinant human alpha-glucosidase from rabbit milk in Pompe patientsH Van den Hout, A J Reuser, A G Vulto, et al.

European Journal of Cell Biology|November 1, 1985

The subcellular localization of soluble and membrane-bound lysosomal enzymes in I-cell fibroblasts: a comparative immunocytochemical studyJ M van Dongen, R Willemsen, E I Ginns, et al.

Biochemical and Biophysical Research Communications|September 30, 1994

Deletion of exon 18 is a frequent mutation in glycogen storage disease type IIM Van der Kraan, M A Kroos, M Joosse, et al.

Human Molecular Genetics|September 16, 1998

Adenovirus-mediated transfer of the acid alpha-glucosidase gene into fibroblasts, myoblasts and myotubes from patients with glycogen storage disease type II leads to high level expression of enzyme and corrects glycogen accumulationM P Nicolino, J P Puech, E J Kremer, et al.

The Journal of Pathology|November 5, 1999

Pathological features of glycogen storage disease type II highlighted in the knockout mouse modelA G Bijvoet, H Van Hirtum, M Vermey, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 1983

Determination of Gaucher's disease phenotypes with monoclonal antibodyE I Ginns, F P Tegelaers, R Barneveld, et al.

Journal of Neurology|September 1, 1988

Prospect for enzyme therapy in glycogenosis II variants: a study on cultured muscle cellsA T van der Ploeg, P A Bolhuis, R A Wolterman, et al.

Journal of Inherited Metabolic Disease|June 19, 2001

Enzyme therapy for pompe disease with recombinant human alpha-glucosidase from rabbit milkJ M Van den Hout, A J Reuser, J B de Klerk, et al.

Journal of the Neurological Sciences|July 1, 1987

Breakdown of lysosomal glycogen in cultured fibroblasts from glycogenosis type II patients after uptake of acid alpha-glucosidaseA T van der Ploeg, M Kroos, J M van Dongen, et al.

Pageof 10

Showing results (61-70 of 98) with videos related to

Sort By:

Pageof 10

The Histochemical Journal|January 1, 1988

Ultrastructural localization of steroid sulphatase in cultured human fibroblasts by immunocytochemistry: a comparative study with lysosomal enzymes and the mannose 6-phosphate receptorR Willemsen, M Kroos, A T Hoogeveen, et al.

Lancet (London, England)|September 6, 2000

Recombinant human alpha-glucosidase from rabbit milk in Pompe patientsH Van den Hout, A J Reuser, A G Vulto, et al.

European Journal of Cell Biology|November 1, 1985

The subcellular localization of soluble and membrane-bound lysosomal enzymes in I-cell fibroblasts: a comparative immunocytochemical studyJ M van Dongen, R Willemsen, E I Ginns, et al.

Biochemical and Biophysical Research Communications|September 30, 1994

Deletion of exon 18 is a frequent mutation in glycogen storage disease type IIM Van der Kraan, M A Kroos, M Joosse, et al.

Human Molecular Genetics|September 16, 1998

Adenovirus-mediated transfer of the acid alpha-glucosidase gene into fibroblasts, myoblasts and myotubes from patients with glycogen storage disease type II leads to high level expression of enzyme and corrects glycogen accumulationM P Nicolino, J P Puech, E J Kremer, et al.

The Journal of Pathology|November 5, 1999

Pathological features of glycogen storage disease type II highlighted in the knockout mouse modelA G Bijvoet, H Van Hirtum, M Vermey, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 1983

Determination of Gaucher's disease phenotypes with monoclonal antibodyE I Ginns, F P Tegelaers, R Barneveld, et al.

Journal of Neurology|September 1, 1988

Prospect for enzyme therapy in glycogenosis II variants: a study on cultured muscle cellsA T van der Ploeg, P A Bolhuis, R A Wolterman, et al.

Journal of Inherited Metabolic Disease|June 19, 2001

Enzyme therapy for pompe disease with recombinant human alpha-glucosidase from rabbit milkJ M Van den Hout, A J Reuser, J B de Klerk, et al.

Journal of the Neurological Sciences|July 1, 1987

Breakdown of lysosomal glycogen in cultured fibroblasts from glycogenosis type II patients after uptake of acid alpha-glucosidaseA T van der Ploeg, M Kroos, J M van Dongen, et al.

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