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Current Opinion in Pediatrics
|
November 19, 2002
Phenylketonuria: an update
Stephen Cederbaum
The Journal of Pediatrics
|
October 30, 2010
Tetrahydrobiopterin and PKU: into the future
Stephen Cederbaum
The Journal of Pediatrics
|
July 24, 2007
Newborn screening: the spigot is open and threatens to become a flood
Stephen Cederbaum
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 6, 2015
Interpreting sequence variants in a clinical context
Stephen Cederbaum
Molecular Genetics and Metabolism
|
March 24, 2010
"Overcoming barriers: new developments and future directions for urea cycle disorders.". Introduction
Stephen Cederbaum
Molecular Genetics and Metabolism Reports
|
October 24, 2019
Myopathy, lactic acidosis and sideroblastic anemia 1 (MLASA1): A 25-year follow-up
Jeremy Woods, Stephen Cederbaum
The Journal of Pediatrics
|
January 15, 2013
Is melatonin synthesis a new biomarker for the pathogenesis and treatment of phenylketonuria?
Stephen Cederbaum, Harvey L Levy
The Journal of Pediatrics
|
July 20, 2005
Pitfalls in newborn screening
Eric Crombez, Richard Koch, Stephen Cederbaum
Molecular Genetics and Metabolism
|
May 14, 2010
Alternative pathway or diversion therapy for urea cycle disorders now and in the future
Stephen Cederbaum, Cynthia Lemons, Mark L Batshaw
Molecular Genetics and Metabolism
|
November 27, 2007
Recommendations for evaluation of responsiveness to tetrahydrobiopterin (BH(4)) in phenylketonuria and its use in treatment
Harvey Levy, Barbara Burton, Stephen Cederbaum, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 38) with videos related to
Sort By:
Page
of 4
Current Opinion in Pediatrics
|
November 19, 2002
Phenylketonuria: an update
Stephen Cederbaum
The Journal of Pediatrics
|
October 30, 2010
Tetrahydrobiopterin and PKU: into the future
Stephen Cederbaum
The Journal of Pediatrics
|
July 24, 2007
Newborn screening: the spigot is open and threatens to become a flood
Stephen Cederbaum
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 6, 2015
Interpreting sequence variants in a clinical context
Stephen Cederbaum
Molecular Genetics and Metabolism
|
March 24, 2010
"Overcoming barriers: new developments and future directions for urea cycle disorders.". Introduction
Stephen Cederbaum
Molecular Genetics and Metabolism Reports
|
October 24, 2019
Myopathy, lactic acidosis and sideroblastic anemia 1 (MLASA1): A 25-year follow-up
Jeremy Woods, Stephen Cederbaum
The Journal of Pediatrics
|
January 15, 2013
Is melatonin synthesis a new biomarker for the pathogenesis and treatment of phenylketonuria?
Stephen Cederbaum, Harvey L Levy
The Journal of Pediatrics
|
July 20, 2005
Pitfalls in newborn screening
Eric Crombez, Richard Koch, Stephen Cederbaum
Molecular Genetics and Metabolism
|
May 14, 2010
Alternative pathway or diversion therapy for urea cycle disorders now and in the future
Stephen Cederbaum, Cynthia Lemons, Mark L Batshaw
Molecular Genetics and Metabolism
|
November 27, 2007
Recommendations for evaluation of responsiveness to tetrahydrobiopterin (BH(4)) in phenylketonuria and its use in treatment
Harvey Levy, Barbara Burton, Stephen Cederbaum, et al.
Page
of 4