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1 stered at 8 mg/kg (IP) and Met at 140 mg/kg (per os).
2  reduced starting dose sorafenib (< 800 mg/d per os).
3 rge of the patient with amoxicillin (2 g tid per os).
4 ven ad libitum access to fentanyl (10 ug/ml, per os) across pregnancy and until weaning [postnatal da
5  which mice were exposed to aerosolized LPS, per os administration of 3T mannodendrimer was found to
6 uced through the administration of metformin per os and an intraperitoneal injection of lactic acid.
7 ctive, and liberates more than 120 equiv NH3 per Os center in a single batch experiment using Cp*2Co
8  procedure impacted infection outcomes after per os challenge with exogenous bacteria (Enterobacter s
9   Rats were treated with FK506 (1-1.5 mg/kg, per OS daily) for three days beginning 24 hours before e
10  atorvastatin and pravastatin administration per os for up to 7 mo, only long-term atorvastatin, but
11 pared famciclovir (Famvir, 500 mg 3x/day po [per os] for 5 days) and topical fluocinonide (0.05% Lide
12 t in vivo, having ED(50) = 0.6 +/- 0.3 mg/kg per os in mice for inhibition of brain N(tau)-methylhist
13 ebral cortex synaptosomes) and in vivo (ED50 per os in mice on brain tele-methylhistamine levels).
14          The dose of gabapentin was 1,800 mg per os, in a single administration.
15  the bite site of the triatomine vector, but per os infection is also a well-documented mode of trans
16                                              Per os infectivity factors PIF1 (Ac119) and PIF2 (Ac022)
17 od that was not significantly different from per os inoculation of the same dose of the HY TME agent.
18                          We isolated the nil per os (npo) mutation, which arrests morphogenesis and c
19  to standard of care plus pacritinib (400 mg per os on day 1 followed by 200 mg twice daily on days 2
20 kg body weight in corn oil or corn oil alone per os on days after inoculation (DAI) -1, +1, and +3 wi
21 gens 0.625 mg per os per day, ramipril 10 mg per os per day, and combination estrogens and ramipril.
22 nt with conjugated equine estrogens 0.625 mg per os per day, ramipril 10 mg per os per day, and combi
23 a was uniquely more active when administered per os (po) than subcutan (sc).
24 owth inhibition (TGI) = 75% at 25 mg/kg.day, per os (po)).
25 ided into six groups (enrofloxacin 10 mg/kg, per os (PO), every 24 h (q24), amoxicillin-clavulanic ac
26 e archaic practice of patients remaining nil per os postoperatively until return of bowel sounds.
27     Shikonin dose-dependently (0.5-50 mg/kg, per os) prevented DM/hypoxia-induced lesions.
28                     At 1.0 mg kg(-1) day(-1) per os, Pz-1 abrogated the formation of tumors induced b
29 in vivo FRZ treatment (40-110 mg/kg per day, per os) resulted in a dramatic loss of mIPSCs in CA1 neu
30  that intestinal LEPR-B could be a potential per os target for prevention against obesity.
31 m analgesic activities (ED50 < or = 4 mg/kg, per os) that are reversible with an adenosine receptor a
32     The virus was experimentally transmitted per os to several mosquito species.
33 standard starting dosage sorafenib (800 mg/d per os) versus that of patients who were prescribed redu
34 e detected in workers, fed individually once per os with 10 uL of 25 mM LiCl in sucrose solution (6.5
35 experiment 2, two piglets each were infected per os with A. butzleri ATCC 49616, A. cryaerophilus 1A
36 experiment 1, two piglets each were infected per os with either Arcobacter butzleri ATCC 49616, Arcob
37 y, groups of 10 C57BL/6 mice were inoculated per os with H. hepaticus, Helicobacter muridarum, or H.