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Showing results (31-40 of 93) with videos related to

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Molecular Genetics and Metabolism Reports|January 4, 2024
Combining angiotensin receptor blockade and enzyme replacement therapy for vascular disease in mucopolysaccharidosis type ISarah C Hurt, Moin U Vera, Steven Q Le, et al.
The American Journal of Cardiology|March 17, 2004
Normal right and left ventricular mass development during early infancyJames J Joyce, Patricia I Dickson, Ning Qi, et al.
Biotechnology and Applied Biochemistry|December 17, 2011
Biochemical characterization of fluorescent-labeled recombinant human alpha-L-iduronidase in vitroBrigette L Tippin, Larisa Troitskaya, Shih-hsin Kan, et al.
Molecular Therapy. Methods & Clinical Development|March 24, 2025
Antibodies to recombinant human alpha-L-iduronidase prevent disease correction in cortical bone in MPS I miceSarah C Hurt, Steven Q Le, Shih-Hsin Kan, et al.
Molecular Genetics and Metabolism|November 21, 2017
Treatment of brain disease in the mucopolysaccharidosesMaurizio Scarpa, Paul J Orchard, Angela Schulz, et al.
American Journal of Medical Genetics. Part A|September 24, 2004
Costello syndrome with pancreatic islet cell hyperplasiaPatricia I Dickson, Norman Y Briones, Barry G Baylen, et al.
The Biochemical Journal|May 25, 2021
Evaluation of artificial signal peptides for secretion of two lysosomal enzymes in CHO cellsKai-Wen Cheng, Feng Wang, George A Lopez, et al.
JIMD Reports|July 5, 2023
Postmortem diagnosis of very long chain acyl-CoA dehydrogenase (VLCAD) deficiency in a neonate with sudden cardiac deathPrapti Singh, Deirdre Amaro, Olugbemisola Obi, et al.
Behavioural Brain Research|June 25, 2016
Behavioral deficits and cholinergic pathway abnormalities in male Sanfilippo B miceShih-Hsin Kan, Steven Q Le, Quang D Bui, et al.
Journal of Inherited Metabolic Disease|June 30, 2009
Continuous infusion of enzyme replacement therapy is inferior to weekly infusions in MPS I dogsM B Passage, A W Krieger, M C Peinovich, et al.
Pageof 10

Showing results (31-40 of 93) with videos related to

Sort By:
Pageof 10
Molecular Genetics and Metabolism Reports|January 4, 2024
Combining angiotensin receptor blockade and enzyme replacement therapy for vascular disease in mucopolysaccharidosis type ISarah C Hurt, Moin U Vera, Steven Q Le, et al.
The American Journal of Cardiology|March 17, 2004
Normal right and left ventricular mass development during early infancyJames J Joyce, Patricia I Dickson, Ning Qi, et al.
Biotechnology and Applied Biochemistry|December 17, 2011
Biochemical characterization of fluorescent-labeled recombinant human alpha-L-iduronidase in vitroBrigette L Tippin, Larisa Troitskaya, Shih-hsin Kan, et al.
Molecular Therapy. Methods & Clinical Development|March 24, 2025
Antibodies to recombinant human alpha-L-iduronidase prevent disease correction in cortical bone in MPS I miceSarah C Hurt, Steven Q Le, Shih-Hsin Kan, et al.
Molecular Genetics and Metabolism|November 21, 2017
Treatment of brain disease in the mucopolysaccharidosesMaurizio Scarpa, Paul J Orchard, Angela Schulz, et al.
American Journal of Medical Genetics. Part A|September 24, 2004
Costello syndrome with pancreatic islet cell hyperplasiaPatricia I Dickson, Norman Y Briones, Barry G Baylen, et al.
The Biochemical Journal|May 25, 2021
Evaluation of artificial signal peptides for secretion of two lysosomal enzymes in CHO cellsKai-Wen Cheng, Feng Wang, George A Lopez, et al.
JIMD Reports|July 5, 2023
Postmortem diagnosis of very long chain acyl-CoA dehydrogenase (VLCAD) deficiency in a neonate with sudden cardiac deathPrapti Singh, Deirdre Amaro, Olugbemisola Obi, et al.
Behavioural Brain Research|June 25, 2016
Behavioral deficits and cholinergic pathway abnormalities in male Sanfilippo B miceShih-Hsin Kan, Steven Q Le, Quang D Bui, et al.
Journal of Inherited Metabolic Disease|June 30, 2009
Continuous infusion of enzyme replacement therapy is inferior to weekly infusions in MPS I dogsM B Passage, A W Krieger, M C Peinovich, et al.
Pageof 10