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Pharmacogenetics
|
June 1, 1993
Debrisoquine oxidation polymorphism: phenotypic consequences of a 3-base-pair deletion in exon 5 of the CYP2D6 gene
F Broly, U A Meyer
Annales Pharmaceutiques Francaises
|
November 23, 2006
[Therapeutic failure: importance of genes?]
M Lhermitte, D Allorge, F Broly
Journal of Chromatography
|
October 14, 1988
High-performance liquid chromatographic assay for mexiletine hydroxylation in microsomes of human liver
F Broly, C Libersa, M Lhermitte
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
May 1, 1990
Mexiletine metabolism in vitro by human liver
F Broly, C Libersa, M Lhermitte
Clinical Neuropharmacology
|
October 1, 1994
Genetic polymorphism of cytochrome P450 2D6 in idiopathic Parkinson disease and diffuse Lewy body disease
R Bordet, F Broly, A Destee, et al.
British Journal of Clinical Pharmacology
|
October 1, 1991
The metabolism of mexiletine in relation to the debrisoquine/sparteine-type polymorphism of drug oxidation
F Broly, N Vandamme, C Libersa, et al.
Advances in Neurology
|
January 1, 1996
Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease
R Bordet, F Broly, A Destée, et al.
Revue Neurologique
|
April 13, 2011
[L-carnitine treatment and fish odor syndrome: an unwaited adverse effect]
F Rocher, C Caruba, F Broly, et al.
Biochemical Pharmacology
|
March 15, 1990
Inhibitory studies of mexiletine and dextromethorphan oxidation in human liver microsomes
F Broly, C Libersa, M Lhermitte, et al.
Pharmacopsychiatry
|
April 30, 1998
Ultrarapid metabolism of clomipramine in a therapy-resistant depressive patient, as confirmed by CYP2 D6 genotyping
P Baumann, F Broly, M Kosel, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 68) with videos related to
Sort By:
Page
of 7
Pharmacogenetics
|
June 1, 1993
Debrisoquine oxidation polymorphism: phenotypic consequences of a 3-base-pair deletion in exon 5 of the CYP2D6 gene
F Broly, U A Meyer
Annales Pharmaceutiques Francaises
|
November 23, 2006
[Therapeutic failure: importance of genes?]
M Lhermitte, D Allorge, F Broly
Journal of Chromatography
|
October 14, 1988
High-performance liquid chromatographic assay for mexiletine hydroxylation in microsomes of human liver
F Broly, C Libersa, M Lhermitte
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
May 1, 1990
Mexiletine metabolism in vitro by human liver
F Broly, C Libersa, M Lhermitte
Clinical Neuropharmacology
|
October 1, 1994
Genetic polymorphism of cytochrome P450 2D6 in idiopathic Parkinson disease and diffuse Lewy body disease
R Bordet, F Broly, A Destee, et al.
British Journal of Clinical Pharmacology
|
October 1, 1991
The metabolism of mexiletine in relation to the debrisoquine/sparteine-type polymorphism of drug oxidation
F Broly, N Vandamme, C Libersa, et al.
Advances in Neurology
|
January 1, 1996
Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease
R Bordet, F Broly, A Destée, et al.
Revue Neurologique
|
April 13, 2011
[L-carnitine treatment and fish odor syndrome: an unwaited adverse effect]
F Rocher, C Caruba, F Broly, et al.
Biochemical Pharmacology
|
March 15, 1990
Inhibitory studies of mexiletine and dextromethorphan oxidation in human liver microsomes
F Broly, C Libersa, M Lhermitte, et al.
Pharmacopsychiatry
|
April 30, 1998
Ultrarapid metabolism of clomipramine in a therapy-resistant depressive patient, as confirmed by CYP2 D6 genotyping
P Baumann, F Broly, M Kosel, et al.
Page
of 7