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A Reuser

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

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Somatic Cell Genetics|September 1, 1982
Isolation of Chinese hamster ovary cells with reduced unscheduled DNA synthesis after UV irradiationM Stefanini, A Reuser, D Bootsma
Acta Neurologica Belgica|December 17, 2013
Rupture of the middle cerebral artery aneurysm as a presenting symptom of late-onset Pompe disease in an adult with a novel GAA gene mutationS Peric, K Fumic, K Bilic, et al.
Biochemical and Biophysical Research Communications|February 29, 1984
Cloning a cDNA for the lysosomal alpha-glucosidaseA Konings, P Hupkes, R Versteeg, et al.
Biochemical and Biophysical Research Communications|March 22, 1976
Intercellular exchange of lysosomal enzymes: enzyme assays in single human fibroblasts after co-cultivationA Reuser, D Halley, E de Wit, et al.
Enzyme|January 1, 1987
alpha-Glucosidase deficiency (Pompe's disease)J M Tager, R P Oude Elferink, A Reuser, et al.
Children (Basel, Switzerland)|October 27, 2022
The DUX-25 after Twenty-Five Years: New Analyses and Reference DataHendrik M Koopman, Benjamin S D Telkamp, Annelieke Hijkoop, et al.
BMC Pediatrics|December 19, 2021
Sex differences in children's health status as measured by the Pediatric Quality of Life Inventory (PedsQL)™: cross-sectional findings from a large school-based sample in the NetherlandsAnnelieke Hijkoop, Chantal A Ten Kate, Marlous J Madderom, et al.
Isozymes|January 1, 1983
Multiple molecular forms of human acid alpha-glucosidaseJ M Tager, R O Elferink, B Brouwer-Kelder, et al.
Journal of Inherited Metabolic Disease|July 14, 2006
Seven cases of Pompe disease from GreeceM Kroos, P Manta, I Mavridou, et al.
Human Molecular Genetics|June 13, 1998
Interaction between hamartin and tuberin, the TSC1 and TSC2 gene productsM van Slegtenhorst, M Nellist, B Nagelkerken, et al.
Pageof 2

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

Sort By:
Pageof 2
Somatic Cell Genetics|September 1, 1982
Isolation of Chinese hamster ovary cells with reduced unscheduled DNA synthesis after UV irradiationM Stefanini, A Reuser, D Bootsma
Acta Neurologica Belgica|December 17, 2013
Rupture of the middle cerebral artery aneurysm as a presenting symptom of late-onset Pompe disease in an adult with a novel GAA gene mutationS Peric, K Fumic, K Bilic, et al.
Biochemical and Biophysical Research Communications|February 29, 1984
Cloning a cDNA for the lysosomal alpha-glucosidaseA Konings, P Hupkes, R Versteeg, et al.
Biochemical and Biophysical Research Communications|March 22, 1976
Intercellular exchange of lysosomal enzymes: enzyme assays in single human fibroblasts after co-cultivationA Reuser, D Halley, E de Wit, et al.
Enzyme|January 1, 1987
alpha-Glucosidase deficiency (Pompe's disease)J M Tager, R P Oude Elferink, A Reuser, et al.
Children (Basel, Switzerland)|October 27, 2022
The DUX-25 after Twenty-Five Years: New Analyses and Reference DataHendrik M Koopman, Benjamin S D Telkamp, Annelieke Hijkoop, et al.
BMC Pediatrics|December 19, 2021
Sex differences in children's health status as measured by the Pediatric Quality of Life Inventory (PedsQL)™: cross-sectional findings from a large school-based sample in the NetherlandsAnnelieke Hijkoop, Chantal A Ten Kate, Marlous J Madderom, et al.
Isozymes|January 1, 1983
Multiple molecular forms of human acid alpha-glucosidaseJ M Tager, R O Elferink, B Brouwer-Kelder, et al.
Journal of Inherited Metabolic Disease|July 14, 2006
Seven cases of Pompe disease from GreeceM Kroos, P Manta, I Mavridou, et al.
Human Molecular Genetics|June 13, 1998
Interaction between hamartin and tuberin, the TSC1 and TSC2 gene productsM van Slegtenhorst, M Nellist, B Nagelkerken, et al.
Pageof 2