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Lancet (London, England)
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March 2, 1985
Possibilities for treatment and for early prenatal diagnosis of hereditary tyrosinaemia
E Holme, B Lindblad, S Lindstedt
Acta Paediatrica Scandinavica
|
November 1, 1985
Pyruvate-carboxylase deficiency with urea cycle impairment
J Greter, J Gustafsson, E Holme
Bioscience Reports
|
May 1, 1984
Uncoupling and isotope effects in gamma-butyrobetaine hydroxylation
E Holme, S Lindstedt, I Nordin
Biochemical and Biophysical Research Communications
|
July 30, 1982
Uncoupling in the gamma-butyrobetaine hydroxylase reaction by D- and L-carnitine
E Holme, S Linstedt, I Nordin
Archives of Disease in Childhood
|
July 1, 1989
Betaine for treatment of homocystinuria caused by methylenetetrahydrofolate reductase deficiency
E Holme, B Kjellman, E Ronge
Journal of Inherited Metabolic Disease
|
January 1, 1988
Biotin-responsive multiple carboxylase deficiency in an 8-year-old boy with normal serum biotinidase and fibroblast holocarboxylase-synthetase activities
E Holme, C E Jacobson, B Kristiansson
Circulation Research
|
November 1, 1992
Interferon-gamma and tumor necrosis factor synergize to induce nitric oxide production and inhibit mitochondrial respiration in vascular smooth muscle cells
Y Geng, G K Hansson, E Holme
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 24, 1982
Superoxide dismutase in extracellular fluids
S L Marklund, E Holme, L Hellner
British Journal of Anaesthesia
|
August 1, 1975
Proceedings: Mass spectrometric analysis of gas mixtures which include high oxygen concentrations
B Goodwin, A E Holme, J H Leck
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 28, 1980
A modification of the isotope assay method for determination of thymidylate synthetase in normal and malignant tissues
B Gustavsson, O Almersjö, E Holme, et al.
Page
of 12
Search research articles
Search
Showing results (11-20 of 111) with videos related to
Sort By:
Page
of 12
Lancet (London, England)
|
March 2, 1985
Possibilities for treatment and for early prenatal diagnosis of hereditary tyrosinaemia
E Holme, B Lindblad, S Lindstedt
Acta Paediatrica Scandinavica
|
November 1, 1985
Pyruvate-carboxylase deficiency with urea cycle impairment
J Greter, J Gustafsson, E Holme
Bioscience Reports
|
May 1, 1984
Uncoupling and isotope effects in gamma-butyrobetaine hydroxylation
E Holme, S Lindstedt, I Nordin
Biochemical and Biophysical Research Communications
|
July 30, 1982
Uncoupling in the gamma-butyrobetaine hydroxylase reaction by D- and L-carnitine
E Holme, S Linstedt, I Nordin
Archives of Disease in Childhood
|
July 1, 1989
Betaine for treatment of homocystinuria caused by methylenetetrahydrofolate reductase deficiency
E Holme, B Kjellman, E Ronge
Journal of Inherited Metabolic Disease
|
January 1, 1988
Biotin-responsive multiple carboxylase deficiency in an 8-year-old boy with normal serum biotinidase and fibroblast holocarboxylase-synthetase activities
E Holme, C E Jacobson, B Kristiansson
Circulation Research
|
November 1, 1992
Interferon-gamma and tumor necrosis factor synergize to induce nitric oxide production and inhibit mitochondrial respiration in vascular smooth muscle cells
Y Geng, G K Hansson, E Holme
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 24, 1982
Superoxide dismutase in extracellular fluids
S L Marklund, E Holme, L Hellner
British Journal of Anaesthesia
|
August 1, 1975
Proceedings: Mass spectrometric analysis of gas mixtures which include high oxygen concentrations
B Goodwin, A E Holme, J H Leck
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 28, 1980
A modification of the isotope assay method for determination of thymidylate synthetase in normal and malignant tissues
B Gustavsson, O Almersjö, E Holme, et al.
Page
of 12