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Charles R Scriver

Showing results (11-20 of 28) with videos related to

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The American Journal of Medicine|October 7, 2004
The last day of the past is the first day of the future: Transitional care for genetic patientsCharles R Scriver, Philip J Lee
Molecular Genetics and Metabolism|June 27, 2018
Phenylalanine ammonia lyase (PAL): From discovery to enzyme substitution therapy for phenylketonuriaHarvey L Levy, Christineh N Sarkissian, Charles R Scriver
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 11, 2011
Phenylalanine hydroxylase deficiencyJohn J Mitchell, Yannis J Trakadis, Charles R Scriver
Journal of Mass Spectrometry : JMS|May 19, 2007
Quantitation of phenylalanine and its trans-cinnamic, benzoic and hippuric acid metabolites in biological fluids in a single GC-MS analysisChristineh N Sarkissian, Charles R Scriver, Orval A Mamer
Molecular Genetics and Metabolism|August 15, 2008
A 25-year longitudinal analysis of treatment efficacy in inborn errors of metabolismPhilippe M Campeau, Charles R Scriver, John J Mitchell
Molecular Genetics and Metabolism|August 2, 2011
Evaluation of orally administered PEGylated phenylalanine ammonia lyase in mice for the treatment of PhenylketonuriaChristineh N Sarkissian, Tse Siang Kang, Alejandra Gámez, et al.
Molecular Genetics and Metabolism|October 2, 2009
Converting an injectable protein therapeutic into an oral form: phenylalanine ammonia lyase for phenylketonuriaTse Siang Kang, Lin Wang, Christineh N Sarkissian, et al.
JIMD Reports|February 23, 2013
Chaperone-like therapy with tetrahydrobiopterin in clinical trials for phenylketonuria: is genotype a predictor of response?Christineh N Sarkissian, Alejandra Gamez, Patrick Scott, et al.
Molecular Genetics and Metabolism|June 15, 2007
Structure-based epitope and PEGylation sites mapping of phenylalanine ammonia-lyase for enzyme substitution treatment of phenylketonuriaAlejandra Gámez, Lin Wang, Christineh N Sarkissian, et al.
Nucleic Acids Research|December 1, 2006
FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwideSjozef van Baal, Polynikis Kaimakis, Manyphong Phommarinh, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
The American Journal of Medicine|October 7, 2004
The last day of the past is the first day of the future: Transitional care for genetic patientsCharles R Scriver, Philip J Lee
Molecular Genetics and Metabolism|June 27, 2018
Phenylalanine ammonia lyase (PAL): From discovery to enzyme substitution therapy for phenylketonuriaHarvey L Levy, Christineh N Sarkissian, Charles R Scriver
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 11, 2011
Phenylalanine hydroxylase deficiencyJohn J Mitchell, Yannis J Trakadis, Charles R Scriver
Journal of Mass Spectrometry : JMS|May 19, 2007
Quantitation of phenylalanine and its trans-cinnamic, benzoic and hippuric acid metabolites in biological fluids in a single GC-MS analysisChristineh N Sarkissian, Charles R Scriver, Orval A Mamer
Molecular Genetics and Metabolism|August 15, 2008
A 25-year longitudinal analysis of treatment efficacy in inborn errors of metabolismPhilippe M Campeau, Charles R Scriver, John J Mitchell
Molecular Genetics and Metabolism|August 2, 2011
Evaluation of orally administered PEGylated phenylalanine ammonia lyase in mice for the treatment of PhenylketonuriaChristineh N Sarkissian, Tse Siang Kang, Alejandra Gámez, et al.
Molecular Genetics and Metabolism|October 2, 2009
Converting an injectable protein therapeutic into an oral form: phenylalanine ammonia lyase for phenylketonuriaTse Siang Kang, Lin Wang, Christineh N Sarkissian, et al.
JIMD Reports|February 23, 2013
Chaperone-like therapy with tetrahydrobiopterin in clinical trials for phenylketonuria: is genotype a predictor of response?Christineh N Sarkissian, Alejandra Gamez, Patrick Scott, et al.
Molecular Genetics and Metabolism|June 15, 2007
Structure-based epitope and PEGylation sites mapping of phenylalanine ammonia-lyase for enzyme substitution treatment of phenylketonuriaAlejandra Gámez, Lin Wang, Christineh N Sarkissian, et al.
Nucleic Acids Research|December 1, 2006
FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwideSjozef van Baal, Polynikis Kaimakis, Manyphong Phommarinh, et al.
Pageof 3