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Pediatric Research
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October 1, 1977
Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles
J P Van Biervliet, L Bruinvis, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 2, 1979
Urinary excretion of orotic acid, orotidine and other pyrimidines in a patient with purine nucleoside phosphorylase deficiency
A H van Gennip, J Grift, P K de Bree, 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 1, 1990
O-phosphohydroxylysinuria: a new inborn error of metabolism?
L Dorland, M Duran, P K de Bree, 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.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 19, 1981
2-Mercaptoethanesulfonate-cysteine disulfide excretion following the administration of 2-mercaptoethanesulfonate--a pitfall in the diagnosis of sulfite oxidase deficiency
M Duran, G Aarsen, R H Fokkens, et al.
Journal of Chromatography
|
October 14, 1983
Azetidine-2-carboxylic acid contaminated dietary proline as a cause of urinary excretion of 4-amino-2-(S-cysteinyl)butyric acid in patients on oral treatment with a synthetic diet
J P Kamerling, S K Wadman, M Duran, et al.
European Journal of Pediatrics
|
July 1, 1981
A case of formiminoglutamic aciduria. Clinical and biochemical studies
M Duran, D Ketting, P K de Bree, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1978
Combined deficiency of xanthine oxidase and sulphite oxidase: a defect of molybdenum metabolism or transport?
M Duran, F A Beemer, C van de Heiden, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1978
Familial hyperlysinaemia due to L-lysine alpha-ketoglutarate reductase deficiency: results of attempted treatment
C vd Heiden, M Brink, P K de Bree, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
Pediatric Research
|
October 1, 1977
Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles
J P Van Biervliet, L Bruinvis, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 2, 1979
Urinary excretion of orotic acid, orotidine and other pyrimidines in a patient with purine nucleoside phosphorylase deficiency
A H van Gennip, J Grift, P K de Bree, 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 1, 1990
O-phosphohydroxylysinuria: a new inborn error of metabolism?
L Dorland, M Duran, P K de Bree, 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.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 19, 1981
2-Mercaptoethanesulfonate-cysteine disulfide excretion following the administration of 2-mercaptoethanesulfonate--a pitfall in the diagnosis of sulfite oxidase deficiency
M Duran, G Aarsen, R H Fokkens, et al.
Journal of Chromatography
|
October 14, 1983
Azetidine-2-carboxylic acid contaminated dietary proline as a cause of urinary excretion of 4-amino-2-(S-cysteinyl)butyric acid in patients on oral treatment with a synthetic diet
J P Kamerling, S K Wadman, M Duran, et al.
European Journal of Pediatrics
|
July 1, 1981
A case of formiminoglutamic aciduria. Clinical and biochemical studies
M Duran, D Ketting, P K de Bree, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1978
Combined deficiency of xanthine oxidase and sulphite oxidase: a defect of molybdenum metabolism or transport?
M Duran, F A Beemer, C van de Heiden, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1978
Familial hyperlysinaemia due to L-lysine alpha-ketoglutarate reductase deficiency: results of attempted treatment
C vd Heiden, M Brink, P K de Bree, et al.
Page
of 3