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Clinical Pharmacology and Therapeutics
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August 1, 1996
Disposition of fluvoxamine in humans is determined by the polymorphic CYP2D6 and also by the CYP1A2 activity
J A Carrillo, M L Dahl, J O Svensson, et al.
Acta Psychiatrica Scandinavica
|
March 1, 1984
CSF monoamine metabolites in melancholia
M Asberg, L Bertilsson, B Mårtensson, et al.
Analytical Chemistry
|
July 1, 1972
Quantitative determination of 5-hydroxyindole-3-acetic acid in cerebrospinal fluid by gas chromatography-mass spectrometry
L Bertilsson, A J Atkinson, J R Althaus, et al.
Clinical Pharmacology and Therapeutics
|
December 1, 1999
The roles of cytochrome P450 3A4 and 1A2 in the 3-hydroxylation of quinine in vivo
R A Mirghani, U Hellgren, P A Westerberg, et al.
Regulatory Peptides
|
February 24, 1994
Quantitation of N-terminally extended tachykinins in cerebrospinal fluid from healthy subjects
G Toresson, E Brodin, C de las Carreras, et al.
Pharmacogenetics
|
February 1, 1992
Polymorphic hydroxylation of S-mephenytoin and omeprazole metabolism in Caucasian and Chinese subjects
T Andersson, C G Regårdh, Y C Lou, et al.
Clinical Pharmacology and Therapeutics
|
August 10, 2007
Effect of terbinafine and voriconazole on the pharmacokinetics of the antidepressant venlafaxine
V-V Hynninen, K T Olkkola, L Bertilsson, et al.
Lakartidningen
|
May 6, 1992
[Genotyping for drug metabolism capacity can give valuable clinical information]
M Ingelman-Sundberg, I Johansson, M L Dahl, et al.
Clinical Pharmacology and Therapeutics
|
October 24, 2001
Inhibition of cytochrome P4502D6 activity with paroxetine normalizes the ultrarapid metabolizer phenotype as measured by nortriptyline pharmacokinetics and the debrisoquin test
K Laine, G Tybring, S Härtter, et al.
Clinical Pharmacology and Therapeutics
|
September 1, 1984
Nortriptyline and debrisoquine hydroxylations in Ghanaian and Swedish subjects
N M Woolhouse, K K Adjepon-Yamoah, B Mellström, et al.
Page
of 27
Search research articles
Search
Showing results (201-210 of 263) with videos related to
Sort By:
Page
of 27
Clinical Pharmacology and Therapeutics
|
August 1, 1996
Disposition of fluvoxamine in humans is determined by the polymorphic CYP2D6 and also by the CYP1A2 activity
J A Carrillo, M L Dahl, J O Svensson, et al.
Acta Psychiatrica Scandinavica
|
March 1, 1984
CSF monoamine metabolites in melancholia
M Asberg, L Bertilsson, B Mårtensson, et al.
Analytical Chemistry
|
July 1, 1972
Quantitative determination of 5-hydroxyindole-3-acetic acid in cerebrospinal fluid by gas chromatography-mass spectrometry
L Bertilsson, A J Atkinson, J R Althaus, et al.
Clinical Pharmacology and Therapeutics
|
December 1, 1999
The roles of cytochrome P450 3A4 and 1A2 in the 3-hydroxylation of quinine in vivo
R A Mirghani, U Hellgren, P A Westerberg, et al.
Regulatory Peptides
|
February 24, 1994
Quantitation of N-terminally extended tachykinins in cerebrospinal fluid from healthy subjects
G Toresson, E Brodin, C de las Carreras, et al.
Pharmacogenetics
|
February 1, 1992
Polymorphic hydroxylation of S-mephenytoin and omeprazole metabolism in Caucasian and Chinese subjects
T Andersson, C G Regårdh, Y C Lou, et al.
Clinical Pharmacology and Therapeutics
|
August 10, 2007
Effect of terbinafine and voriconazole on the pharmacokinetics of the antidepressant venlafaxine
V-V Hynninen, K T Olkkola, L Bertilsson, et al.
Lakartidningen
|
May 6, 1992
[Genotyping for drug metabolism capacity can give valuable clinical information]
M Ingelman-Sundberg, I Johansson, M L Dahl, et al.
Clinical Pharmacology and Therapeutics
|
October 24, 2001
Inhibition of cytochrome P4502D6 activity with paroxetine normalizes the ultrarapid metabolizer phenotype as measured by nortriptyline pharmacokinetics and the debrisoquin test
K Laine, G Tybring, S Härtter, et al.
Clinical Pharmacology and Therapeutics
|
September 1, 1984
Nortriptyline and debrisoquine hydroxylations in Ghanaian and Swedish subjects
N M Woolhouse, K K Adjepon-Yamoah, B Mellström, et al.
Page
of 27