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Molecular Genetics and Metabolism
|
December 27, 2011
Lysosomal Disease Network's WORLD Symposium™ 2012
Chester B Whitley
Molecular Genetics and Metabolism
|
December 28, 2023
Two Decades of WORLDSymposium™
Chester B Whitley
Molecular Genetics and Metabolism
|
August 31, 2010
Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI): a single dose of galsulfase further reduces urine glycosaminoglycans after hematopoietic stem cell transplantation
Chester B Whitley, Jeanine R Jarnes Utz
The Journal of Gene Medicine
|
November 13, 2004
Improved gene transfer and normalized enzyme levels in primitive hematopoietic progenitors from patients with mucopolysaccharidosis type I using a bioreactor
Dao Pan, David F Stroncek, Chester B Whitley
Orphanet Journal of Rare Diseases
|
July 6, 2017
Phenotype prediction for mucopolysaccharidosis type I by in silico analysis
Li Ou, Michael J Przybilla, Chester B Whitley
Molecular Genetics and Metabolism
|
October 16, 2016
Proteomic analysis of mucopolysaccharidosis I mouse brain with two-dimensional polyacrylamide gel electrophoresis
Li Ou, Michael J Przybilla, Chester B Whitley
Molecular Genetics and Metabolism
|
September 22, 2018
Metabolomics profiling reveals profound metabolic impairments in mice and patients with Sandhoff disease
Li Ou, Michael J Przybilla, Chester B Whitley
Molecular Genetics and Metabolism Reports
|
October 14, 2021
Chitotriosidase as a biomarker for gangliosidoses
Sarah Kim, Chester B Whitley, Jeanine R Jarnes
Psychopharmacology
|
March 17, 2004
A preliminary report on dopamine system reactivity in PKU: acute effects of haloperidol on neuropsychological, physiological, and neuroendocrine functions
Monica Luciana, Karen L Hanson, Chester B Whitley
Orphanet Journal of Rare Diseases
|
May 13, 2018
Beneath the floor: re-analysis of neurodevelopmental outcomes in untreated Hurler syndrome
Elsa G Shapiro, Chester B Whitley, Julie B Eisengart
Page
of 12
Search research articles
Search
Showing results (1-10 of 116) with videos related to
Sort By:
Page
of 12
Molecular Genetics and Metabolism
|
December 27, 2011
Lysosomal Disease Network's WORLD Symposium™ 2012
Chester B Whitley
Molecular Genetics and Metabolism
|
December 28, 2023
Two Decades of WORLDSymposium™
Chester B Whitley
Molecular Genetics and Metabolism
|
August 31, 2010
Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI): a single dose of galsulfase further reduces urine glycosaminoglycans after hematopoietic stem cell transplantation
Chester B Whitley, Jeanine R Jarnes Utz
The Journal of Gene Medicine
|
November 13, 2004
Improved gene transfer and normalized enzyme levels in primitive hematopoietic progenitors from patients with mucopolysaccharidosis type I using a bioreactor
Dao Pan, David F Stroncek, Chester B Whitley
Orphanet Journal of Rare Diseases
|
July 6, 2017
Phenotype prediction for mucopolysaccharidosis type I by in silico analysis
Li Ou, Michael J Przybilla, Chester B Whitley
Molecular Genetics and Metabolism
|
October 16, 2016
Proteomic analysis of mucopolysaccharidosis I mouse brain with two-dimensional polyacrylamide gel electrophoresis
Li Ou, Michael J Przybilla, Chester B Whitley
Molecular Genetics and Metabolism
|
September 22, 2018
Metabolomics profiling reveals profound metabolic impairments in mice and patients with Sandhoff disease
Li Ou, Michael J Przybilla, Chester B Whitley
Molecular Genetics and Metabolism Reports
|
October 14, 2021
Chitotriosidase as a biomarker for gangliosidoses
Sarah Kim, Chester B Whitley, Jeanine R Jarnes
Psychopharmacology
|
March 17, 2004
A preliminary report on dopamine system reactivity in PKU: acute effects of haloperidol on neuropsychological, physiological, and neuroendocrine functions
Monica Luciana, Karen L Hanson, Chester B Whitley
Orphanet Journal of Rare Diseases
|
May 13, 2018
Beneath the floor: re-analysis of neurodevelopmental outcomes in untreated Hurler syndrome
Elsa G Shapiro, Chester B Whitley, Julie B Eisengart
Page
of 12