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Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1987
Urinary excretion of 2-methyl-2,3-butanediol and 2,3-pentanediol in patients with disorders of propionate and methylmalonate metabolism
M Duran, D Ketting, L Bruinvis, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 10, 1982
The absolute configuration of urinary 5-hydroxyhexanoic acid - a product of fatty acid (omega-1)-oxidation - in patients with non-ketotic dicarboxylic aciduria
J P Kamerling, M Duran, L Bruinvis, et al.
The Journal of Pediatrics
|
October 1, 1982
Inherited 3-methylglutaconic aciduria in two brothers--another defect of leucine metabolism
M Duran, F A Beemer, A S Tibosch, et al.
Progress in Clinical and Biological Research
|
January 1, 1990
The fate of orally ingested 3-phenylpropionic acid
M Duran, R van Vossen, L Bruinvis, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 30, 1973
Gas chromatographic analysis of urinary volatile phenols in patients with gastro-intestinal disorders and normals
M Duran, D Ketting, P K de Bree, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1988
A patient with mevalonic aciduria presenting with hepatosplenomegaly, congenital anaemia, thrombocytopenia and leukocytosis
J B de Klerk, M Duran, L Dorland, et al.
Biomedical Mass Spectrometry
|
January 1, 1982
The identification of (E)-2-methylglutaconic acid, a new isoleucine metabolite, in the urine of patients with beta-ketothiolase deficiency, propionic acidaemia and methylmalonic acidaemia
M Duran, L Bruinvis, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 30, 1973
Beta-p-hydroxyphenylhydracrylic acid as a urinary constituent in a patient with gastrointestinal disease
S K Wadman, C van der Heiden, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 1, 1978
Organic acid excretion in a patient with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency: facts and artefacts
M Duran, D Ketting, S K Wadman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 31, 1991
Gas chromatography method for the separation of amino acids enantiomers in plasma and urine. Application in a case of short bowel syndrome
D Ketting, S K Wadman, L J Spaapen, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 55) with videos related to
Sort By:
Page
of 6
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1987
Urinary excretion of 2-methyl-2,3-butanediol and 2,3-pentanediol in patients with disorders of propionate and methylmalonate metabolism
M Duran, D Ketting, L Bruinvis, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 10, 1982
The absolute configuration of urinary 5-hydroxyhexanoic acid - a product of fatty acid (omega-1)-oxidation - in patients with non-ketotic dicarboxylic aciduria
J P Kamerling, M Duran, L Bruinvis, et al.
The Journal of Pediatrics
|
October 1, 1982
Inherited 3-methylglutaconic aciduria in two brothers--another defect of leucine metabolism
M Duran, F A Beemer, A S Tibosch, et al.
Progress in Clinical and Biological Research
|
January 1, 1990
The fate of orally ingested 3-phenylpropionic acid
M Duran, R van Vossen, L Bruinvis, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 30, 1973
Gas chromatographic analysis of urinary volatile phenols in patients with gastro-intestinal disorders and normals
M Duran, D Ketting, P K de Bree, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1988
A patient with mevalonic aciduria presenting with hepatosplenomegaly, congenital anaemia, thrombocytopenia and leukocytosis
J B de Klerk, M Duran, L Dorland, et al.
Biomedical Mass Spectrometry
|
January 1, 1982
The identification of (E)-2-methylglutaconic acid, a new isoleucine metabolite, in the urine of patients with beta-ketothiolase deficiency, propionic acidaemia and methylmalonic acidaemia
M Duran, L Bruinvis, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 30, 1973
Beta-p-hydroxyphenylhydracrylic acid as a urinary constituent in a patient with gastrointestinal disease
S K Wadman, C van der Heiden, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 1, 1978
Organic acid excretion in a patient with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency: facts and artefacts
M Duran, D Ketting, S K Wadman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 31, 1991
Gas chromatography method for the separation of amino acids enantiomers in plasma and urine. Application in a case of short bowel syndrome
D Ketting, S K Wadman, L J Spaapen, et al.
Page
of 6