Yannis L. Loukas

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代表论文

1. 1
   Validation of a novel LC‐MS/MS method for the quantitation of colistin A and B in human plasma

   57 次引用 · 2010
2. 2
   Quantitative determination of donepezil in human plasma by liquid chromatography/tandem mass spectrometry employing an automated liquid–liquid extraction based on 96-well format plates

   46 次引用 · 2006
3. 3
   Development of a high-throughput method for the determination of itraconazole and its hydroxy metabolite in human plasma, employing automated liquid–liquid extraction based on 96-well format plates and LC/MS/MS

   44 次引用 · 2005
4. 4
   An improved and fully validated LC–MS/MS method for the simultaneous quantification of simvastatin and simvastatin acid in human plasma

   42 次引用 · 2007
5. 5
   Turbulent flow and ternary column-switching on-line clean-up system for high-throughput quantification of risperidone and its main metabolite in plasma by LC–MS/MSApplication to a bioequivalence study

   32 次引用 · 2006
6. 6
   Application of a semi-automated 96-well format solid-phase extraction, column-switching, fluorescence detection protocol for the determination of alendronate in human urine samples obtained from a bioequivalence study

   24 次引用 · 2006
7. 7
   An improved high‐throughput liquid chromatographic/tandem mass spectrometric method for terbinafine quantification in human plasma, using automated liquid–liquid extraction based on 96‐well format plates

   21 次引用 · 2007
8. 8
   Development and validation of an improved high-throughput method for the determination of anastrozole in human plasma by LC–MS/MS and atmospheric pressure chemical ionization

   21 次引用 · 2008
9. 9
   Study of the effect of CYP2C19 polymorphisms on omeprazole pharmacokinetics by utilizing validated LC–MS/MS and Real Time-PCR methods

   17 次引用 · 2016
10. 10
    Validation of a fully automated high throughput liquid chromatographic/tandem mass spectrometric method for roxithromycin quantification in human plasma. Application to a bioequivalence study

    14 次引用 · 2007

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