Development and validation of a liquid chromatographic-tandem mass spectrometric method for the determination of galantamine in human heparinised plasma
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概要
- 論文の詳細を見る
- 2003-06-15
著者
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De Jong
Department Of Analytical Chemistry And Toxicology University Centre For Pharmacy
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Verhaeghe T.
Department Of Bioanalysis Johnson & Johnson Pharmaceutical Research And Development A Division O
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De Vries
Department Of Behavioral Biology Utrecht University
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DIELS L.
Department of Bioanalysis, Johnson & Johnson Pharmaceutical Research and Development, a Division of
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DE MEULDER
Department of Bioanalysis, Johnson & Johnson Pharmaceutical Research and Development, a Division of
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De Vries
Department Of Bioanalysis Johnson & Johnson Pharmaceutical Research And Development A Division O
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De Meulder
Department Of Bioanalysis Johnson & Johnson Pharmaceutical Research And Development A Division O
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De Jong
Department Of Analytical Biochemistry University Centre For Pharmacy
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De Jong
Department Of Bioanalysis Johnson & Johnson Pharmaceutical Research And Development A Division O
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Diels L.
Department Of Bioanalysis Johnson & Johnson Pharmaceutical Research And Development A Division Of Janssen Pharmaceutica N. V.
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