Search research articles
Contact Us
Filters
Showing results (61-70 of 93) with videos related to
Page
of 10
Sort By:
Lancet (London, England)
|
October 3, 1992
Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase
S Lindstedt, E Holme, E A Lock, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Treatment of two children with hereditary tyrosinaemia type I and long-standing renal disease with a 4-hydroxyphenylpyruvate dioxygenase inhibitor (NTBC)
E Pronicka, E Rowinska, Z Bentkowski, et al.
European Journal of Biochemistry
|
May 1, 1993
Human 4-hydroxyphenylpyruvate dioxygenase. Primary structure and chromosomal localization of the gene
U Rüetschi, A Dellsén, P Sahlin, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
August 12, 2004
Glycerol kinase deficiency: follow-up during 20 years, genetics, biochemistry and prognosis
C Hellerud, N Wramner, A Erikson, et al.
FEBS Letters
|
February 1, 1979
gamma-Butyrobetaine hydroxylase activity in human and ovine liver and skeletal muscle tissue
G Cederblad, J Holm, G Lindstedt, et al.
Journal of Toxicology. Clinical Toxicology
|
July 1, 1983
Thallium poisoning--toxin elimination and therapy in three cases
A Heath, J Ahlmén, B Branegård, et al.
Cytogenetics and Cell Genetics
|
January 1, 1995
Regional assignment of the human 4-hydroxyphenylpyruvate dioxygenase gene (HPD) to 12q24-->qter by fluorescence in situ hybridization
G Stenman, E Röijer, U Rüetschi, et al.
Clinical Chemistry
|
July 1, 1979
Urinary excretion of thymine and uracil in a two-year-old child with a malignant tumor of the brain
G Berglund, J Greter, S Lindstedt, et al.
Journal of Inherited Metabolic Disease
|
July 10, 1999
NTBC as palliative treatment in chronic tyrosinaemia type I
J Ros, M A Vilaseca, N Lambruschini, et al.
Metabolism: Clinical and Experimental
|
December 1, 1996
Pivalic acid-induced carnitine deficiency and physical exercise in humans
K Abrahamsson, B O Eriksson, E Holme, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 93) with videos related to
Sort By:
Page
of 10
Lancet (London, England)
|
October 3, 1992
Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase
S Lindstedt, E Holme, E A Lock, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Treatment of two children with hereditary tyrosinaemia type I and long-standing renal disease with a 4-hydroxyphenylpyruvate dioxygenase inhibitor (NTBC)
E Pronicka, E Rowinska, Z Bentkowski, et al.
European Journal of Biochemistry
|
May 1, 1993
Human 4-hydroxyphenylpyruvate dioxygenase. Primary structure and chromosomal localization of the gene
U Rüetschi, A Dellsén, P Sahlin, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
August 12, 2004
Glycerol kinase deficiency: follow-up during 20 years, genetics, biochemistry and prognosis
C Hellerud, N Wramner, A Erikson, et al.
FEBS Letters
|
February 1, 1979
gamma-Butyrobetaine hydroxylase activity in human and ovine liver and skeletal muscle tissue
G Cederblad, J Holm, G Lindstedt, et al.
Journal of Toxicology. Clinical Toxicology
|
July 1, 1983
Thallium poisoning--toxin elimination and therapy in three cases
A Heath, J Ahlmén, B Branegård, et al.
Cytogenetics and Cell Genetics
|
January 1, 1995
Regional assignment of the human 4-hydroxyphenylpyruvate dioxygenase gene (HPD) to 12q24-->qter by fluorescence in situ hybridization
G Stenman, E Röijer, U Rüetschi, et al.
Clinical Chemistry
|
July 1, 1979
Urinary excretion of thymine and uracil in a two-year-old child with a malignant tumor of the brain
G Berglund, J Greter, S Lindstedt, et al.
Journal of Inherited Metabolic Disease
|
July 10, 1999
NTBC as palliative treatment in chronic tyrosinaemia type I
J Ros, M A Vilaseca, N Lambruschini, et al.
Metabolism: Clinical and Experimental
|
December 1, 1996
Pivalic acid-induced carnitine deficiency and physical exercise in humans
K Abrahamsson, B O Eriksson, E Holme, et al.
Page
of 10