Search research articles
Contact Us
Filters
Showing results (11-20 of 30) with videos related to
Page
of 3
Sort By:
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 development
M 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 phenylketonuria
D N Donker, D Reits, F J Van Sprang, et al.
Clinical Genetics
|
August 1, 1985
The cerebro-costo-mandibular syndrome: third report of familial occurrence
R 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 phenylketonuria
J 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 supplementation
M 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 URINE
S 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-dependent
H 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 treatment
M Duran, R J Wanders, J P de Jager, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 30) with videos related to
Sort By:
Page
of 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 development
M 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 phenylketonuria
D N Donker, D Reits, F J Van Sprang, et al.
Clinical Genetics
|
August 1, 1985
The cerebro-costo-mandibular syndrome: third report of familial occurrence
R 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 phenylketonuria
J 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 supplementation
M 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 URINE
S 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-dependent
H 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 treatment
M Duran, R J Wanders, J P de Jager, et al.
Page
of 3