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Timothy M Cox

Showing results (111-120 of 117) with videos related to

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JIMD Reports|February 23, 2013
Recommendations on reintroduction of agalsidase Beta for patients with fabry disease in europe, following a period of shortageGabor E Linthorst, Alessandro P Burlina, Franco Cecchi, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 4, 2018
The Lysosomal Protein Arylsulfatase B Is a Key Enzyme Involved in Skeletal TurnoverSandra Pohl, Alexandra Angermann, Anke Jeschke, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 22, 2013
Therapeutic response in feline sandhoff disease despite immunity to intracranial gene therapyAllison M Bradbury, J Nicholas Cochran, Victoria J McCurdy, et al.
Blood Cells, Molecules & Diseases|April 28, 2019
Addendum to Letter to the Editor: Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1Pramod K Mistry, Manisha Balwani, Hagit N Baris, et al.
Blood Cells, Molecules & Diseases|April 23, 2018
Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1Pramod K Mistry, Manisha Balwani, Hagit N Baris, et al.
Journal of Lipid Research|January 3, 2016
Glucosylated cholesterol in mammalian cells and tissues: formation and degradation by multiple cellular β-glucosidasesAndré R A Marques, Mina Mirzaian, Hisako Akiyama, et al.
The Journal of Clinical Investigation|February 4, 2014
Relative acidic compartment volume as a lysosomal storage disorder-associated biomarkerDanielle te Vruchte, Anneliese O Speak, Kerri L Wallom, et al.
Pageof 12

Showing results (111-120 of 117) with videos related to

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Pageof 12
You have reached the last page of results.This site can display upto 117 results.
JIMD Reports|February 23, 2013
Recommendations on reintroduction of agalsidase Beta for patients with fabry disease in europe, following a period of shortageGabor E Linthorst, Alessandro P Burlina, Franco Cecchi, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 4, 2018
The Lysosomal Protein Arylsulfatase B Is a Key Enzyme Involved in Skeletal TurnoverSandra Pohl, Alexandra Angermann, Anke Jeschke, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 22, 2013
Therapeutic response in feline sandhoff disease despite immunity to intracranial gene therapyAllison M Bradbury, J Nicholas Cochran, Victoria J McCurdy, et al.
Blood Cells, Molecules & Diseases|April 28, 2019
Addendum to Letter to the Editor: Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1Pramod K Mistry, Manisha Balwani, Hagit N Baris, et al.
Blood Cells, Molecules & Diseases|April 23, 2018
Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1Pramod K Mistry, Manisha Balwani, Hagit N Baris, et al.
Journal of Lipid Research|January 3, 2016
Glucosylated cholesterol in mammalian cells and tissues: formation and degradation by multiple cellular β-glucosidasesAndré R A Marques, Mina Mirzaian, Hisako Akiyama, et al.
The Journal of Clinical Investigation|February 4, 2014
Relative acidic compartment volume as a lysosomal storage disorder-associated biomarkerDanielle te Vruchte, Anneliese O Speak, Kerri L Wallom, et al.
Pageof 12