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Pediatrics
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March 1, 1997
Psychiatric disorders in adult patients with early-treated phenylketonuria
J Pietz, B Fätkenheuer, P Burgard, et al.
Journal of Inherited Metabolic Disease
|
June 20, 2008
Newborn screening for methylmalonic acidurias--optimization by statistical parameter combination
M 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-level
E 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 Plants
Quang Minh Le, Jinliang Ma, Debangsu Bhattacharyya, et al.
European Journal of Pediatrics
|
July 1, 1992
Psychological and social findings in adolescents with phenylketonuria
J 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 PKU
U 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 phenylketonuria
P Burgard, A Rupp, D S Konecki, et al.
BMC Bioinformatics
|
January 26, 2008
Predicting biological system objectives de novo from internal state measurements
Erwin 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 phenylketonuria
F 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 deficiency
S Kölker, P Burgard, J G Okun, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 50) with videos related to
Sort By:
Page
of 5
Pediatrics
|
March 1, 1997
Psychiatric disorders in adult patients with early-treated phenylketonuria
J Pietz, B Fätkenheuer, P Burgard, et al.
Journal of Inherited Metabolic Disease
|
June 20, 2008
Newborn screening for methylmalonic acidurias--optimization by statistical parameter combination
M 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-level
E 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 Plants
Quang Minh Le, Jinliang Ma, Debangsu Bhattacharyya, et al.
European Journal of Pediatrics
|
July 1, 1992
Psychological and social findings in adolescents with phenylketonuria
J 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 PKU
U 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 phenylketonuria
P Burgard, A Rupp, D S Konecki, et al.
BMC Bioinformatics
|
January 26, 2008
Predicting biological system objectives de novo from internal state measurements
Erwin 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 phenylketonuria
F 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 deficiency
S Kölker, P Burgard, J G Okun, et al.
Page
of 5