A novel in vitro pharmacokinetic/pharmacodynamic model based on two-compartment open model used to simulate serum drug concentration-time profiles.
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A novel in vitro pharmacokinetic/pharmacodynamic model based on two-compartment open model used to simulate serum drug concentration-time profiles.
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2007 nî lūn-bûn
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2007年の論文
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2007年学术文章
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2007年学术文章
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2007年学术文章
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2007年学术文章
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2007年學術文章
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name
A novel in vitro pharmacokinet ...... g concentration-time profiles.
@en
A novel in vitro pharmacokinet ...... g concentration-time profiles.
@nl
type
label
A novel in vitro pharmacokinet ...... g concentration-time profiles.
@en
A novel in vitro pharmacokinet ...... g concentration-time profiles.
@nl
prefLabel
A novel in vitro pharmacokinet ...... g concentration-time profiles.
@en
A novel in vitro pharmacokinet ...... g concentration-time profiles.
@nl
P2093
P2860
P1476
A novel in vitro pharmacokinet ...... g concentration-time profiles.
@en
P2093
Ayako Ozawa
Hitomi Moriyama
Ken Kikuchi
Tsutomu Tomita
Yoshifumi Takeda
Yuko Ohara-Nemoto
P2860
P304
P356
10.1111/J.1348-0421.2007.TB03934.X
P577
2007-01-01T00:00:00Z