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F J van Sprang

Showing results (11-20 of 30) with videos related to

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Revue D'Electroencephalographie Et De Neurophysiologie Clinique|January 1, 1978
[Computer analysis of the EEG as an aid in terminating diet therapy in phenylketonuria]D N Donker, D Reits, W Storm van Leeuwen, et al.
European Journal of Pediatrics|June 28, 1979
Two sisters with isovaleric acidaemia, multiple attacks of ketoacidosis and normal developmentM Duran, F J van Sprang, J G Drewes, et al.
Electroencephalography and Clinical Neurophysiology|February 1, 1979
Computer analysis of the EEG as an aid in the evaluation of dietetic treatment in phenylketonuriaD N Donker, D Reits, F J Van Sprang, et al.
Clinical Genetics|August 1, 1985
The cerebro-costo-mandibular syndrome: third report of familial occurrenceR C Hennekam, F A Beemer, W A Huijbers, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 20, 1978
[Methylmalonic acidemia. Diagnosis and treatment in various patients]H D Bakker, M Duran, A H van Gennip, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 28, 1980
Chromatographic determination and mass spectrometric identification of gamma-glutamylphenylalanine, a urinary constituent in phenylketonuriaJ P Kamerling, G J Aarsen, M Duran, et al.
Pediatric Research|January 1, 1992
Diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in lymphocytes and liver by a gas chromatographic method: the effect of oral riboflavin supplementationM Duran, C B Cleutjens, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 24, 1975
N-EPSILON-(CARBOXYMETHYL)LYSINE, A CONSTITUENT OF HUMAN URINES K Wadman, P K De Bree, F J Van Sprang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 15, 1975
Tyrosinemia and tyrosyluria in healthy prematures: time courses not vitamin C-dependentH D Bakker, S K Wadman, F J Van Sprang, et al.
European Journal of Pediatrics|January 1, 1991
3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatmentM Duran, R J Wanders, J P de Jager, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Revue D'Electroencephalographie Et De Neurophysiologie Clinique|January 1, 1978
[Computer analysis of the EEG as an aid in terminating diet therapy in phenylketonuria]D N Donker, D Reits, W Storm van Leeuwen, et al.
European Journal of Pediatrics|June 28, 1979
Two sisters with isovaleric acidaemia, multiple attacks of ketoacidosis and normal developmentM Duran, F J van Sprang, J G Drewes, et al.
Electroencephalography and Clinical Neurophysiology|February 1, 1979
Computer analysis of the EEG as an aid in the evaluation of dietetic treatment in phenylketonuriaD N Donker, D Reits, F J Van Sprang, et al.
Clinical Genetics|August 1, 1985
The cerebro-costo-mandibular syndrome: third report of familial occurrenceR C Hennekam, F A Beemer, W A Huijbers, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 20, 1978
[Methylmalonic acidemia. Diagnosis and treatment in various patients]H D Bakker, M Duran, A H van Gennip, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 28, 1980
Chromatographic determination and mass spectrometric identification of gamma-glutamylphenylalanine, a urinary constituent in phenylketonuriaJ P Kamerling, G J Aarsen, M Duran, et al.
Pediatric Research|January 1, 1992
Diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in lymphocytes and liver by a gas chromatographic method: the effect of oral riboflavin supplementationM Duran, C B Cleutjens, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 24, 1975
N-EPSILON-(CARBOXYMETHYL)LYSINE, A CONSTITUENT OF HUMAN URINES K Wadman, P K De Bree, F J Van Sprang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 15, 1975
Tyrosinemia and tyrosyluria in healthy prematures: time courses not vitamin C-dependentH D Bakker, S K Wadman, F J Van Sprang, et al.
European Journal of Pediatrics|January 1, 1991
3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatmentM Duran, R J Wanders, J P de Jager, et al.
Pageof 3