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European Journal of Pediatrics
|
January 1, 1993
Long-term outcome in 134 patients with galactosaemia
S Schweitzer, Y Shin, C Jakobs, et al.
Molecular Vision
|
May 21, 2004
Inward rectifying currents stabilize the membrane potential in dendrites of mouse amacrine cells: patch-clamp recordings and single-cell RT-PCR
Amane Koizumi, Tatjana C Jakobs, Richard H Masland
Lancet (London, England)
|
November 4, 1989
Vigabatrin therapy in patient with succinic semialdehyde dehydrogenase deficiency
K M Gibson, D C DeVivo, C Jakobs
Journal of Inherited Metabolic Disease
|
January 1, 1992
D-glyceric aciduria: new development
C Largillière, M Fontaine, C Jakobs, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Prenatal detection of Canavan disease (aspartoacylase deficiency) by DNA analysis
O N Elpeleg, A Shaag, Y Anikster, et al.
European Journal of Biochemistry
|
July 1, 1997
The promoter of the human type I 5'-deiodinase gene--mapping of the transcription start site and identification of a DR+4 thyroid-hormone-responsive element
T C Jakobs, C Schmutzler, J Meissner, et al.
Journal of Inherited Metabolic Disease
|
November 7, 2008
The biochemistry, metabolism and inherited defects of the pentose phosphate pathway: a review
M M C Wamelink, E A Struys, C Jakobs
Prenatal Diagnosis
|
February 1, 1993
Prenatal detection of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria)
C Jakobs, H Ogier, D Rabier, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
Stable isotope dilution analysis of 3-hydroxyisovaleric acid in amniotic fluid: contribution to the prenatal diagnosis of inherited disorders of leucine catabolism
C Jakobs, L Sweetman, W L Nyhan, et al.
Journal of Lipid Research
|
October 9, 2001
A rapid screening procedure for cholesterol and dehydrocholesterol by electrospray ionization tandem mass spectrometry
D W Johnson, H J ten Brink, C Jakobs
Page
of 42
Search research articles
Search
Showing results (51-60 of 417) with videos related to
Sort By:
Page
of 42
European Journal of Pediatrics
|
January 1, 1993
Long-term outcome in 134 patients with galactosaemia
S Schweitzer, Y Shin, C Jakobs, et al.
Molecular Vision
|
May 21, 2004
Inward rectifying currents stabilize the membrane potential in dendrites of mouse amacrine cells: patch-clamp recordings and single-cell RT-PCR
Amane Koizumi, Tatjana C Jakobs, Richard H Masland
Lancet (London, England)
|
November 4, 1989
Vigabatrin therapy in patient with succinic semialdehyde dehydrogenase deficiency
K M Gibson, D C DeVivo, C Jakobs
Journal of Inherited Metabolic Disease
|
January 1, 1992
D-glyceric aciduria: new development
C Largillière, M Fontaine, C Jakobs, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Prenatal detection of Canavan disease (aspartoacylase deficiency) by DNA analysis
O N Elpeleg, A Shaag, Y Anikster, et al.
European Journal of Biochemistry
|
July 1, 1997
The promoter of the human type I 5'-deiodinase gene--mapping of the transcription start site and identification of a DR+4 thyroid-hormone-responsive element
T C Jakobs, C Schmutzler, J Meissner, et al.
Journal of Inherited Metabolic Disease
|
November 7, 2008
The biochemistry, metabolism and inherited defects of the pentose phosphate pathway: a review
M M C Wamelink, E A Struys, C Jakobs
Prenatal Diagnosis
|
February 1, 1993
Prenatal detection of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria)
C Jakobs, H Ogier, D Rabier, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
Stable isotope dilution analysis of 3-hydroxyisovaleric acid in amniotic fluid: contribution to the prenatal diagnosis of inherited disorders of leucine catabolism
C Jakobs, L Sweetman, W L Nyhan, et al.
Journal of Lipid Research
|
October 9, 2001
A rapid screening procedure for cholesterol and dehydrocholesterol by electrospray ionization tandem mass spectrometry
D W Johnson, H J ten Brink, C Jakobs
Page
of 42