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The Journal of Nutrition
|
January 7, 2003
The H475Y polymorphism in the glutamate carboxypeptidase II gene increases plasma folate without affecting the risk for neural tube defects in humans
Lydia A Afman, Frans J M Trijbels, Henk J Blom
Biochemical Medicine
|
June 1, 1978
Measurement of cytochromes in human skeletal muscle mitochondria, isolated from fresh and frozen stored muscle specimens
H Bookelman, J M Trijbels, R C Sengers, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 30, 1983
A mutation of pyruvate carboxylase in fibroblasts from a patient with severe, chronic lactic acidaemia
T L Hansen, E Christensen, J L Willems, et al.
Tijdschrift Voor Kindergeneeskunde
|
August 1, 1984
[Mitochondrial myopathy associated with cytochrome oxidase deficiency]
R C Sengers, J M Trijbels, W Ruitenbeek, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
March 19, 1977
[Inborn errors of metabolism in muscle cells]
R C Sengers, A M Stadhouders, J M Trijbels, et al.
Dermatologica
|
January 1, 1970
The sweat gland as a mucous gland
E Seutter, J M Trijbels, A H Sutorius, et al.
European Journal of Pediatrics
|
April 1, 1992
3-Methylglutaconic aciduria in a patient with a disturbed mitochondrial energy metabolism
J A Bakkeren, R C Sengers, W Ruitenbeek, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 27, 1984
Serum very long chain fatty acid pattern in Zellweger syndrome
J A Bakkeren, L A Monnens, J M Trijbels, et al.
European Journal of Pediatrics
|
December 30, 1977
Organic aciduria in hypoxic premature newborns simulating an inborn error of metabolism
J A Bakkeren, R C Sengers, J M Trijbels, et al.
Infusionstherapie Und Klinische Ernahrung
|
June 1, 1980
Serum-free amino acid concentrations in low birth weight infants during the first 4 weeks of life
J M Boon, L A Monnens, J T Knuiman, et al.
Page
of 18
Search research articles
Search
Showing results (11-20 of 177) with videos related to
Sort By:
Page
of 18
The Journal of Nutrition
|
January 7, 2003
The H475Y polymorphism in the glutamate carboxypeptidase II gene increases plasma folate without affecting the risk for neural tube defects in humans
Lydia A Afman, Frans J M Trijbels, Henk J Blom
Biochemical Medicine
|
June 1, 1978
Measurement of cytochromes in human skeletal muscle mitochondria, isolated from fresh and frozen stored muscle specimens
H Bookelman, J M Trijbels, R C Sengers, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 30, 1983
A mutation of pyruvate carboxylase in fibroblasts from a patient with severe, chronic lactic acidaemia
T L Hansen, E Christensen, J L Willems, et al.
Tijdschrift Voor Kindergeneeskunde
|
August 1, 1984
[Mitochondrial myopathy associated with cytochrome oxidase deficiency]
R C Sengers, J M Trijbels, W Ruitenbeek, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
March 19, 1977
[Inborn errors of metabolism in muscle cells]
R C Sengers, A M Stadhouders, J M Trijbels, et al.
Dermatologica
|
January 1, 1970
The sweat gland as a mucous gland
E Seutter, J M Trijbels, A H Sutorius, et al.
European Journal of Pediatrics
|
April 1, 1992
3-Methylglutaconic aciduria in a patient with a disturbed mitochondrial energy metabolism
J A Bakkeren, R C Sengers, W Ruitenbeek, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 27, 1984
Serum very long chain fatty acid pattern in Zellweger syndrome
J A Bakkeren, L A Monnens, J M Trijbels, et al.
European Journal of Pediatrics
|
December 30, 1977
Organic aciduria in hypoxic premature newborns simulating an inborn error of metabolism
J A Bakkeren, R C Sengers, J M Trijbels, et al.
Infusionstherapie Und Klinische Ernahrung
|
June 1, 1980
Serum-free amino acid concentrations in low birth weight infants during the first 4 weeks of life
J M Boon, L A Monnens, J T Knuiman, et al.
Page
of 18