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P Burgard

Showing results (31-40 of 50) with videos related to

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Pediatrics|March 1, 1997
Psychiatric disorders in adult patients with early-treated phenylketonuriaJ Pietz, B Fätkenheuer, P Burgard, et al.
Journal of Inherited Metabolic Disease|June 20, 2008
Newborn screening for methylmalonic acidurias--optimization by statistical parameter combinationM Lindner, S Ho, S Kölker, et al.
Journal of Clinical and Experimental Neuropsychology|October 1, 1994
Sustained attention in adult phenylketonuria: the influence of the concurrent phenylalanine-blood-levelE Schmidt, A Rupp, P Burgard, et al.
Industrial & Engineering Chemistry Research|January 15, 2024
Design and Multiobjective Dynamic Optimization of Superheaters for Load-Following Operation in Pulverized Coal Power PlantsQuang Minh Le, Jinliang Ma, Debangsu Bhattacharyya, et al.
European Journal of Pediatrics|July 1, 1992
Psychological and social findings in adolescents with phenylketonuriaJ Weglage, B Fünders, B Wilken, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Relation between phenylalanine hydroxylase genotypes and phenotypic parameters of diagnosis and treatment of hyperphenylalaninaemic disorders. German Collaborative Study of PKUU Lichter-Konecki, A Rupp, D S Konecki, et al.
European Journal of Pediatrics|July 1, 1996
Phenylalanine hydroxylase genotypes, predicted residual enzyme activity and phenotypic parameters of diagnosis and treatment of phenylketonuriaP Burgard, A Rupp, D S Konecki, et al.
BMC Bioinformatics|January 26, 2008
Predicting biological system objectives de novo from internal state measurementsErwin P Gianchandani, Matthew A Oberhardt, Anthony P Burgard, et al.
Acta Paediatrica (Oslo, Norway : 1992)|May 1, 1994
Growth and skeletal maturation in children with phenylketonuriaF Schaefer, P Burgard, U Batzler, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Looking forward--an evidence-based approach to glutaryl-CoA dehydrogenase deficiencyS Kölker, P Burgard, J G Okun, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Pediatrics|March 1, 1997
Psychiatric disorders in adult patients with early-treated phenylketonuriaJ Pietz, B Fätkenheuer, P Burgard, et al.
Journal of Inherited Metabolic Disease|June 20, 2008
Newborn screening for methylmalonic acidurias--optimization by statistical parameter combinationM Lindner, S Ho, S Kölker, et al.
Journal of Clinical and Experimental Neuropsychology|October 1, 1994
Sustained attention in adult phenylketonuria: the influence of the concurrent phenylalanine-blood-levelE Schmidt, A Rupp, P Burgard, et al.
Industrial & Engineering Chemistry Research|January 15, 2024
Design and Multiobjective Dynamic Optimization of Superheaters for Load-Following Operation in Pulverized Coal Power PlantsQuang Minh Le, Jinliang Ma, Debangsu Bhattacharyya, et al.
European Journal of Pediatrics|July 1, 1992
Psychological and social findings in adolescents with phenylketonuriaJ Weglage, B Fünders, B Wilken, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Relation between phenylalanine hydroxylase genotypes and phenotypic parameters of diagnosis and treatment of hyperphenylalaninaemic disorders. German Collaborative Study of PKUU Lichter-Konecki, A Rupp, D S Konecki, et al.
European Journal of Pediatrics|July 1, 1996
Phenylalanine hydroxylase genotypes, predicted residual enzyme activity and phenotypic parameters of diagnosis and treatment of phenylketonuriaP Burgard, A Rupp, D S Konecki, et al.
BMC Bioinformatics|January 26, 2008
Predicting biological system objectives de novo from internal state measurementsErwin P Gianchandani, Matthew A Oberhardt, Anthony P Burgard, et al.
Acta Paediatrica (Oslo, Norway : 1992)|May 1, 1994
Growth and skeletal maturation in children with phenylketonuriaF Schaefer, P Burgard, U Batzler, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Looking forward--an evidence-based approach to glutaryl-CoA dehydrogenase deficiencyS Kölker, P Burgard, J G Okun, et al.
Pageof 5