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Biochemistry
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October 4, 1977
Ribonucleotide reductase from Escherichia coli. Identification of allosteric effector sites by chromatography on immobilized effectors
U von Döbeln
The Journal of Biological Chemistry
|
June 25, 1976
Binding of substrates to Escherichia coli ribonucleotide reductase
U von Döbeln, P Reichard
Journal of Inherited Metabolic Disease
|
August 13, 1998
Fatty acid oxidation in fibroblasts from patients with defects in beta-oxidation and in the respiratory chain
N Venizelos, U von Döbeln, L Hagenfeldt
Journal of Inherited Metabolic Disease
|
December 5, 2006
Pregnancy and lactation in a woman with classical galactosaemia heterozygous for p.Q188R and p.R333W
A Ohlsson, J Nasiell, U von Döbeln
Human Genetics
|
May 1, 1991
Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus and their relation to phenotype in Swedish phenylketonuria families
E Svensson, U von Döbeln, L Hagenfeldt
Journal of Inherited Metabolic Disease
|
January 1, 1990
Retrospective diagnosis of 3-hydroxydicarboxylic aciduria by analysis of filter paper blood samples
U von Döbeln, N Venizelos, L Hagenfeldt
Fertility and Sterility
|
January 1, 1989
Gonadal failure in young women and galactose-1-phosphate uridyl transferase activity
K Hagenfeldt, U von Döbeln, L Hagenfeldt
Journal of Inherited Metabolic Disease
|
January 1, 1994
Long-chain 3-hydroxyacyl-CoA dehydrogenase in chorionic villi, fetal liver and fibroblasts and prenatal diagnosis of 3-hydroxyacyl-CoA dehydrogenase deficiency
U von Döbeln, N Venizelos, M Westgren, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
July 1, 1996
Antiepileptic drug treatment during pregnancy and neonatal screening results
K Wide, B Winbladh, C Guthenberg, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
February 25, 1998
Carbohydrate-deficient transferrin in galactosaemia
H Stibler, U von Döbeln, B Kristiansson, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 31) with videos related to
Sort By:
Page
of 4
Biochemistry
|
October 4, 1977
Ribonucleotide reductase from Escherichia coli. Identification of allosteric effector sites by chromatography on immobilized effectors
U von Döbeln
The Journal of Biological Chemistry
|
June 25, 1976
Binding of substrates to Escherichia coli ribonucleotide reductase
U von Döbeln, P Reichard
Journal of Inherited Metabolic Disease
|
August 13, 1998
Fatty acid oxidation in fibroblasts from patients with defects in beta-oxidation and in the respiratory chain
N Venizelos, U von Döbeln, L Hagenfeldt
Journal of Inherited Metabolic Disease
|
December 5, 2006
Pregnancy and lactation in a woman with classical galactosaemia heterozygous for p.Q188R and p.R333W
A Ohlsson, J Nasiell, U von Döbeln
Human Genetics
|
May 1, 1991
Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus and their relation to phenotype in Swedish phenylketonuria families
E Svensson, U von Döbeln, L Hagenfeldt
Journal of Inherited Metabolic Disease
|
January 1, 1990
Retrospective diagnosis of 3-hydroxydicarboxylic aciduria by analysis of filter paper blood samples
U von Döbeln, N Venizelos, L Hagenfeldt
Fertility and Sterility
|
January 1, 1989
Gonadal failure in young women and galactose-1-phosphate uridyl transferase activity
K Hagenfeldt, U von Döbeln, L Hagenfeldt
Journal of Inherited Metabolic Disease
|
January 1, 1994
Long-chain 3-hydroxyacyl-CoA dehydrogenase in chorionic villi, fetal liver and fibroblasts and prenatal diagnosis of 3-hydroxyacyl-CoA dehydrogenase deficiency
U von Döbeln, N Venizelos, M Westgren, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
July 1, 1996
Antiepileptic drug treatment during pregnancy and neonatal screening results
K Wide, B Winbladh, C Guthenberg, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
February 25, 1998
Carbohydrate-deficient transferrin in galactosaemia
H Stibler, U von Döbeln, B Kristiansson, et al.
Page
of 4