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Stephen D Cederbaum

Showing results (1-10 of 50) with videos related to

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Molecular Genetics and Metabolism|February 8, 2005
Hyperargininemia due to liver arginase deficiencyEric A Crombez, Stephen D Cederbaum
Molecular Genetics and Metabolism|June 9, 2005
Clinical, pathological, and biochemical studies in a patient with propionic acidemia and fatal cardiomyopathyRebecca Mardach, M Anthony Verity, Stephen D Cederbaum
Journal of Inherited Metabolic Disease|September 29, 2022
The role and control of arginine levels in arginase 1 deficiencyGeorge A Diaz, Mark Bechter, Stephen D Cederbaum
American Journal of Medical Genetics. Part A|October 6, 2006
Diagnostic yield of chromosome analysis in patients with developmental delay or mental retardation who are otherwise nondysmorphicJoanne F Macayran, Stephen D Cederbaum, Michelle A Fox
Molecular Genetics and Metabolism|October 16, 2007
Contrasting features of urea cycle disorders in human patients and knockout mouse modelsJoshua L Deignan, Stephen D Cederbaum, Wayne W Grody
Molecular Genetics and Metabolism|March 12, 2011
Combined Hurler and Sanfilippo syndrome in a sibling pairAngela Sun, John J Hopwood, Jerry Thompson, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 1, 2017
Biopsy-proven Hepatocellular Carcinoma in a 53-year-old Woman With Arginase DeficiencyMatthew Koo, Gerald S Lipshutz, Stephen D Cederbaum, et al.
Molecular Genetics and Metabolism|June 30, 2017
Newborn screening for hyperargininemia due to arginase 1 deficiencyBradford L Therrell, Robert Currier, David Lapidus, et al.
Molecular Genetics and Metabolism|April 2, 2023
Taste-masked formulation of sodium phenylbutyrate (ACER-001) for the treatment of urea cycle disordersStephen D Cederbaum, Jeffrey Edwards, Terrie Kellmeyer, et al.
Molecular Genetics and Metabolism|March 27, 2002
Cloning and characterization of human agmatinaseRamaswamy K Iyer, Ho K Kim, Rosemarie W Tsoa, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Molecular Genetics and Metabolism|February 8, 2005
Hyperargininemia due to liver arginase deficiencyEric A Crombez, Stephen D Cederbaum
Molecular Genetics and Metabolism|June 9, 2005
Clinical, pathological, and biochemical studies in a patient with propionic acidemia and fatal cardiomyopathyRebecca Mardach, M Anthony Verity, Stephen D Cederbaum
Journal of Inherited Metabolic Disease|September 29, 2022
The role and control of arginine levels in arginase 1 deficiencyGeorge A Diaz, Mark Bechter, Stephen D Cederbaum
American Journal of Medical Genetics. Part A|October 6, 2006
Diagnostic yield of chromosome analysis in patients with developmental delay or mental retardation who are otherwise nondysmorphicJoanne F Macayran, Stephen D Cederbaum, Michelle A Fox
Molecular Genetics and Metabolism|October 16, 2007
Contrasting features of urea cycle disorders in human patients and knockout mouse modelsJoshua L Deignan, Stephen D Cederbaum, Wayne W Grody
Molecular Genetics and Metabolism|March 12, 2011
Combined Hurler and Sanfilippo syndrome in a sibling pairAngela Sun, John J Hopwood, Jerry Thompson, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 1, 2017
Biopsy-proven Hepatocellular Carcinoma in a 53-year-old Woman With Arginase DeficiencyMatthew Koo, Gerald S Lipshutz, Stephen D Cederbaum, et al.
Molecular Genetics and Metabolism|June 30, 2017
Newborn screening for hyperargininemia due to arginase 1 deficiencyBradford L Therrell, Robert Currier, David Lapidus, et al.
Molecular Genetics and Metabolism|April 2, 2023
Taste-masked formulation of sodium phenylbutyrate (ACER-001) for the treatment of urea cycle disordersStephen D Cederbaum, Jeffrey Edwards, Terrie Kellmeyer, et al.
Molecular Genetics and Metabolism|March 27, 2002
Cloning and characterization of human agmatinaseRamaswamy K Iyer, Ho K Kim, Rosemarie W Tsoa, et al.
Pageof 5