コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 injection) and dexamethasone (20 mg oral or intravenous infusion).
2 hcare professional or self-administered) via intravenous infusion.
3 an acceptable safety profile after a single intravenous infusion.
4 re capable of homing back to the marrow post-intravenous infusion.
5 ry application of adenosine against standard intravenous infusion.
6 dose of AMPH (0.1 mg/kg) was administered by intravenous infusion.
7 nd gave a stable aqueous system suitable for intravenous infusion.
8 tion by either intramuscular autoinjector or intravenous infusion.
9 mens including 750-1350mg orally, or a 600mg intravenous infusion.
10 administered in 28-day cycles by continuous intravenous infusion.
11 etermined with the use of a [1-(13)C]leucine intravenous infusion.
12 ns including 750-1350 mg orally, or a 600-mg intravenous infusion.
13 o system-level resilience when administering intravenous infusions.
14 ong preference or if difficulties occur with intravenous infusions.
15 essure (MAP) and heart rate 24 h/day and for intravenous infusions.
16 thy incompletely attenuated by synthetic GAA intravenous infusions.
17 practices and their effects on the safety of intravenous infusions.
18 g/m(2) per day on days 2-6), and idarubicin (intravenous infusion 10 mg/m(2) per day on days 2-4 in u
19 ) yields identical FFR results compared with intravenous infusion (140 mug/kg per minute), while requ
20 30 mg/m(2) per day on days 2-6), cytarabine (intravenous infusion 2000 mg/m(2) per day on days 2-6),
21 ay subcutaneously on days 1-5), fludarabine (intravenous infusion 30 mg/m(2) per day on days 2-6), cy
22 or 1000 mg (n = 7) dosing arms of rituximab intravenous infusions (500 or 1000 mg), given at study d
23 Rats anesthetized with isoflurane were given intravenous infusions (9 mL/kg over 1 min) of either 20%
24 osertib 1800 mg per 24 h via 72-h continuous intravenous infusion administered every other week or be
25 ods study of errors and policy deviations in intravenous infusion administration across 16 English ho
26 d anti-ZEBOV siRNAs (2 mg/kg per dose, bolus intravenous infusion) after 30 min, and on days 1, 3, an
27 posal in rats, pigs and dogs during constant intravenous infusion and euglycemic clamp conditions.
28 raised plasma fibrinogen levels in mice via intravenous infusion and induced thrombosis by ferric ch
29 tes and nitrates [NOx]) after (15)N-arginine intravenous infusion and on asymmetric dimethylarginine
30 midazolam were independently administered by intravenous infusion and plasma and brain concentrations
31 s are trapped in the lungs immediately after intravenous infusion and their survival time in the host
32 treatment and 11.1% that of daily continuous intravenous infusions and oral valganciclovir compared w
33 mit physiological insight, e.g. the need for intravenous infusions and restriction to short-term stud
34 es have been initiated, including continuous intravenous infusions and subcutaneous IL-15 administrat
35 2 of cycle 1; 56 mg/m(2) thereafter; 30 min intravenous infusion) and dexamethasone (20 mg oral or i
36 ), whereas direct intramyocardial injection, intravenous infusion, and intracoronary infusion indicat
37 ost-partum haemorrhage, needs refrigeration, intravenous infusion, and skilled providers for optimum
41 cycles of gemcitabine (1000 mg/m(2), 30 min intravenous infusion, at days 1, 8, and 15) and capecita
42 5% confidence interval, 2.7 to 11.3), as did intravenous infusion, but again intracoronary infusion d
43 practice are common in the administration of intravenous infusions, but not all result in negative co
44 y by transgenic overexpression or acutely by intravenous infusion caused hypophosphatemia, phosphatur
47 blocking agent be administered by continuous intravenous infusion early in the course of acute respir
49 .6, 0.9, or 1.2 mg/kg brentuximab vedotin by intravenous infusion every 2 weeks with either ABVD (25
51 cetaxel was given at a dose of 75 mg/m(2) by intravenous infusion every 3 weeks for up to six cycles.
52 mg/kg or 3.4 mg/kg belantamab mafodotin via intravenous infusion every 3 weeks on day 1 of each cycl
53 igned to receive either volasertib 300 mg by intravenous infusion every 3 weeks or an investigator's
54 mg/m(2) lurbinectedin administered as a 1-h intravenous infusion every 3 weeks until disease progres
55 LE trial and received patisiran 0.3 mg/kg by intravenous infusion every 3 weeks with plans to continu
56 domly assigned (2:1) to siltuximab (11 mg/kg intravenous infusion every 3 weeks) or placebo; all pati
57 etirinotecan pegol (145 mg/m(2) as a 90-min intravenous infusion every 3 weeks) or single-drug treat
60 300 mg twice daily and durvalumab 1.5 g via intravenous infusion every 4 weeks until disease progres
61 n every 8 h) or 1000 mg meropenem (by 30-min intravenous infusion every 8 h) for 7-14 days; regimens
62 mg ceftazidime and 500 mg avibactam (by 2 h intravenous infusion every 8 h) or 1000 mg meropenem (by
63 lus 500 mg avibactam, administered via a 2-h intravenous infusion every 8 h) or best available therap
64 in appearance to bimagrumab, administered as intravenous infusions every 4 weeks for at least 48 week
65 expression received avelumab (10 mg/kg, 1 h intravenous infusion) every 2 weeks until confirmed dise
66 isotopic labeling with 1-(13) C(1) -acetate intravenous infusion, followed by measurement of labeled
67 se of 20 mug/kg/d administered by continuous intravenous infusion for 10 days resulted in a massive (
68 monotherapy was administered via continuous intravenous infusion for 28 days then tapered to daily i
69 ion administered over 5-20 min or continuous intravenous infusion for 6-96 h on day 1 of every 21-day
70 limumab 10 mg/kg or 3 mg/kg, administered by intravenous infusion for 90 min every 3 weeks for four d
71 f approximately 18 hours, requiring frequent intravenous infusions for prophylaxis and treatment in p
72 s: 1) glucose gavage and 2) hyperinsulinemic intravenous infusion, for studies in either beta-cell sp
73 (1:1) to receive either infliximab (5 mg/kg intravenous infusion given over 2 h at baseline, and aga
74 , 252 patients were randomly assigned to the intravenous infusion group and 248 to the fixed-dose com
75 ent was reported in 25 (10%) patients in the intravenous infusion group and 26 (10%) patients in the
76 se event that led to death (urosepsis in the intravenous infusion group and acute myocardial infarcti
77 neutropenia (34 [13%] of 252 patients in the intravenous infusion group vs 35 [14%] of 248 patients i
79 mg/kg/day) was delivered through continuous intravenous infusion, hepatic SAMe levels reached 0.7 mM
83 The TERLI group received terlipressin by intravenous infusion, initially 3 mg/24 hours, progressi
84 vation that IL-15 administered by continuous intravenous infusion is able to induce markedly greater
89 y candidates, tumor size > 2 cm) received an intravenous infusion of (18)F-fluoropaclitaxel and then
91 is the first human study to demonstrate that intravenous infusion of 0.9% saline results in reduction
94 compared the safety and efficacy of a single intravenous infusion of 1500 mg of dalbavancin to the 2-
95 ation, rats were pretreated with either NAc (intravenous infusion of 50 mg/kg/h) or MK-801 (0.16 mg/k
96 nd 6, stratified by study site) to either an intravenous infusion of 500 mL of crystalloid solution o
97 re randomly assigned (2:1) to receive either intravenous infusion of 600 mg of ocrelizumab (two 300 m
99 es after drug injection, animals received an intravenous infusion of [1,6-(13)C2]glucose for 8 min to
102 e conducted two separate protocols utilizing intravenous infusion of a nitric oxide synthase inhibito
103 althy participants (Cohort A, n = 25) during intravenous infusion of a subanesthetic dose of ketamine
106 c), and 2 FFR measurements during continuous intravenous infusion of adenosine (140 mug/kg per minute
107 Intracoronary saline given on top of an intravenous infusion of adenosine did not further increa
108 escalation of treatment in such cases using intravenous infusion of adrenaline which has been adopte
110 optimal medical treatment were randomized to intravenous infusion of allogenic UC-MSCs (Cellistem, Ce
111 erate disease in 6 adult males who underwent intravenous infusion of an adeno-associated viral (AAV)
112 lysis to compare prolonged versus short-term intravenous infusion of antipseudomonal beta-lactams in
115 ited by 44% in LS; however, the simultaneous intravenous infusion of ascorbic acid or apocynin acutel
117 ulfan and fludarabine, patients received one intravenous infusion of autologous CD34+ cells genetical
118 m(2)] daily for 5 days, followed by a single intravenous infusion of autologous TILs and high-dose in
121 exercise, acute normobaric hypoxia, and the intravenous infusion of catecholamines, or absent/decrea
124 tion with [(11)C]CUMI-101 after receiving an intravenous infusion of citalopram 10 mg or placebo in a
126 uglycemic clamps with a physiologic low-dose intravenous infusion of cortisol to reproduce levels fou
127 C-verapamil (30-72 MBq/kg) before and during intravenous infusion of CsA (12 or 24 mg/kg/h, n = 2 eac
128 ned dose of oral decitabine on day -3, a 1-h intravenous infusion of decitabine 20 mg/m(2) on day 1,
130 ls of lithium or valproate received a single intravenous infusion of either ketamine hydrochloride (.
131 c levels of lithium or valproate received an intravenous infusion of either ketamine hydrochloride (0
133 acute heart failure to receive a continuous intravenous infusion of either ularitide at a dose of 15
134 stable lipid-lowering therapy to receive an intravenous infusion of evinacumab (at a dose of 15 mg p
137 on imaging through the imaging window during intravenous infusion of fluorescently labeled low and hi
138 s, and 141 patients to receive 1000 mg/m2 of intravenous infusion of gemcitabine once a week for 3 of
141 under baseline conditions (n = 4) and during intravenous infusion of high-dose erlotinib (10 mg/kg/h,
145 tomy for esophageal adenocarcinoma) received intravenous infusion of IdU (200 mg/m(2) body surface ar
146 ral nervous uptake of the IN 210 IU dose via intravenous infusion of ins-asp at a dose of 0.12 IU/kg/
148 is hypothesis, a GABA deficit was induced by intravenous infusion of iomazenil (IOM; 3.7 mug/kg), an
149 ts were randomized 1:1:1 to receive a single intravenous infusion of KB001, 3 mg/kg (n=13) or 10 mg/k
150 ive Battery (MCCB) before and after a single intravenous infusion of ketamine (0.5 mg/kg) or midazola
151 ere randomly assigned to receive a 40-minute intravenous infusion of ketamine (0.5 mg/kg) or midazola
154 east an initial partial response to a single intravenous infusion of ketamine 0.5 mg/kg were randomiz
155 order patients received a single, open-label intravenous infusion of ketamine hydrochloride (.5 mg/kg
157 double-blind conditions to receive a single intravenous infusion of ketamine or midazolam in a 2:1 r
158 ore symptoms within 2 h of a single low-dose intravenous infusion of ketamine with effects lasting up
159 ptoms within two hours of a single, low-dose intravenous infusion of ketamine, with effects lasting u
160 ealthy young male volunteers underwent a 7-h intravenous infusion of l-[ring-(2)H5]phenylalanine on t
163 ed Sprague-Dawley rats received a continuous intravenous infusion of LPS (15 microg kg(-1) h(-1)), De
167 mia were not observed in rhesus monkeys when intravenous infusion of MK-3682 was completed after AMIO
168 C]raclopride displacement) in response to an intravenous infusion of morphine, and its relationship w
169 placebo-controlled trial using a continuous intravenous infusion of NAC (150 mg/kg/day in 5% dextros
170 ly assigned 452 patients to receive a single intravenous infusion of neutralizing antibody LY-CoV555
172 continuous feeding on two occasions: during intravenous infusion of niacin (2.8 mg/min) and saline.
173 nts were randomly assigned 2:1 to receive an intravenous infusion of nivolumab 1 mg/kg plus ipilimuma
174 response system) patients 2:1 to receive an intravenous infusion of nivolumab 3 mg/kg every 2 weeks
175 d ifosfamide were randomly assigned (1:1) to intravenous infusion of ombrabulin 25 mg/m(2) plus cispl
176 , 34 healthy men received a 6-h double-blind intravenous infusion of omecamtiv mecarbil or placebo on
177 use of interactive responsive technology to intravenous infusion of pamrevlumab 30 mg/kg or placebo
178 response system, to standard care plus 48-h intravenous infusion of placebo (n=62) or relaxin 10 mic
179 e randomized to receive a double-blind, 48-h intravenous infusion of placebo or OM in 3 sequential, e
180 ulin 25 mg/m(2) plus cisplatin 75 mg/m(2) or intravenous infusion of placebo plus cisplatin 75 mg/m(2
181 tivity, were randomly assigned to receive an intravenous infusion of PLD 30 mg/m(2) followed by a 3-h
183 rticipants with magnetoencephalography after intravenous infusion of psilocybin--prodrug of the nonse
184 one for 1 month (control) or to add a single intravenous infusion of rituximab (375 mg/m(2); interven
185 revious randomised controlled phase 2 trial, intravenous infusion of salbutamol for up to 7 days in p
186 rticipants were randomized to receive a 6-hr intravenous infusion of saline (control), an intermediat
187 g healthy males: (1) NVC was assessed during intravenous infusion of saline (placebo) and the non-sel
188 ter presentation to receive either a 48-hour intravenous infusion of serelaxin (30 mug per kilogram o
189 s in mean arterial pressure (MAP) induced by intravenous infusion of sodium nitroprusside (SNP) and p
190 th untreated or relapsed BPDCN to receive an intravenous infusion of tagraxofusp at a dose of 7 mug o
191 can and a second scan either with concurrent intravenous infusion of the ABCB1 inhibitor tariquidar (
192 oom temperature (22 degrees C) for 4 h or by intravenous infusion of the alpha-adrenergic receptor an
195 gether with duodenal nutrition perfusion and intravenous infusion of the glucagon-like peptide 1 (GLP
196 que monkey under control conditions or after intravenous infusion of the NET inhibitor desipramine (D
197 uted tomography (SPECT) images obtained with intravenous infusion of the radioactive tracer Technetiu
198 with type 2 diabetes, we also observed that intravenous infusion of the same n-apo AI (CSL111, 80 mg
199 to discrete pulses of activity revealed that intravenous infusion of the synthetic mixed glucocortico
200 CSF for 5 days followed by leukapheresis and intravenous infusion of three doses of CD133-positive ha
205 urs following no infusion (controls; n=6) or intravenous infusion of ultrasmall superparamagnetic par
206 diac arrest undergoing CPR to either a rapid intravenous infusion of up to 2 L of cold saline or stan
208 Patients were randomly assigned to receive intravenous infusion of vitamin C (50 mg/kg in dextrose
212 who were 50 to 85 years of age to receive an intravenous infusion of zoledronic acid (5 mg) or placeb
216 or greater were randomized to 3 once-monthly intravenous infusions of 10 mg/kg GSK679586 (n = 99) or
217 nteractive voice response system, to receive intravenous infusions of 10 mg/kg ipilimumab or placebo
218 to 400 m on 6 MWT, were randomized to weekly intravenous infusions of 30 or 50 mg/kg/wk eteplirsen or
219 cular lymphoma were assigned 1:1 to CVP plus intravenous infusions of 375 mg/m(2) CT-P10 or rituximab
220 onditions and during 4 postprandial hours by intravenous infusions of [3,3,3-(2)H3]-leucine and [ring
221 ate days in randomized, double-blinded order intravenous infusions of A) GIP(3-30)NH(2) (800 pmol/kg/
222 tients with AATD were treated with 12 weekly intravenous infusions of AAT augmentation therapy before
223 andomized equally to receive 15 double-blind intravenous infusions of adjunctive lanicemine 50 mg, la
224 th prodromal or mild AD, one year of monthly intravenous infusions of aducanumab reduces brain Abeta
225 t desmopressin (1 nmol.kg(-1)) or continuous intravenous infusions of arginine vasopressin (3 pmol.kg
227 atomegaly also occurs when animals are given intravenous infusions of bacterial lipopolysaccharide (L
228 ) patients with cancer who were treated with intravenous infusions of bisphosphonates between January
229 rrent hemophilia treatment involves frequent intravenous infusions of clotting factors, which is asso
231 of 179 (44-384) mL/min/1.73m2, who received intravenous infusions of colistimethate each 8 hours.
233 eal was used to measure energy intake during intravenous infusions of either PYY(3-36) or oxyntomodul
234 ntuximab, 50 mg (week 1), followed by weekly intravenous infusions of girentuximab, 20 mg (weeks 2-24
235 intravenous infusions of placebo plus MTX or intravenous infusions of golimumab at a dose of 2 mg/kg
236 in autonomic and respiratory responses after intravenous infusions of hypertonic sodium lactate.
237 Patients were assigned randomly to receive intravenous infusions of infliximab 5 mg/kg at weeks 0,
238 lesions report panic anxiety in response to intravenous infusions of isoproterenol, a beta-adrenergi
239 ) patients were randomized to receive either intravenous infusions of LOLA (n = 98), 30 g daily, or p
241 twice daily on days 1-10 of 28-day cycles); intravenous infusions of mitoxantrone (8 mg/m(2) per day
242 , experimentally induced asthma received six intravenous infusions of MSCs (0.36-2.5 x 10E7 MSCs/infu
245 d by study centre to standard care plus 48-h intravenous infusions of placebo or serelaxin (30 mug/kg
246 or > or = 4 weeks were randomized to receive intravenous infusions of placebo plus MTX or intravenous
248 uropathic pain)-and a control group received intravenous infusions of saline in an initial session an
249 hyroid eye disease in a 1:1 ratio to receive intravenous infusions of the IGF-IR inhibitor teprotumum
250 inuation of ART, participants received eight intravenous infusions of UB-421, at a dose of either 10
251 lve healthy adult male subjects received 1-L intravenous infusions of Voluven or PVR over 30 minutes
252 e or the current standard of care plus three intravenous infusions of ZMapp (50 mg per kilogram of bo
253 However, catheter-based delivery, but not intravenous infusion, of LNA-92a significantly (P<0.05)
255 1 ratio), to receive docetaxel 75 mg/m(2) by intravenous infusion on day 1 plus either nintedanib 200
257 56 mg/m(2) thereafter) was given as a 30-min intravenous infusion on days 1, 2, 8, 9, 15, and 16 of 2
258 eceived romidepsin at 14 mg/m(2) as a 4-hour intravenous infusion on days 1, 8, and 15 every 28 days.
259 d induction chemotherapy (daunorubicin bolus intravenous infusion on days 1-3 [90 mg/m(2) for patient
261 aged >60 years], plus cytarabine continuous intravenous infusion on days 1-7 [100 mg/m(2)]), with el
262 les with loading doses of 10 mg/kg by 60 min intravenous infusions on days 1, 3, and 5 in the first w
263 days) (n = 551) or gemcitabine (1000 mg/m(2) intravenous infusion once a week for 3 of every 4 weeks)
265 o receive 0.3 mg/kg patisiran or placebo via intravenous infusion once every 3 weeks for 18 months.
268 near-constant obsessions received two 40-min intravenous infusions, one of saline and one of ketamine
270 ow oral availability and requires continuous intravenous infusion or multiple gram doses to ensure su
271 s infusion) and dexamethasone (20 mg oral or intravenous infusion) or bortezomib (1.3 mg/m(2); intrav
272 ntravenous bolus on day 1 or 72 h continuous intravenous infusion) or intensified doxorubicin (75 mg/
273 ays and 28 mug/day thereafter) by continuous intravenous infusion over 4 weeks every 6 weeks (up to f
274 m2 intravenous, and fluorouracil, 2400 mg/m2 intravenous infusion over 46-48 hours) on days 1 and 15
275 e plus 16 cycles of 7.5 mg/kg bevacizumab by intravenous infusion over 90 min on day 1 of each cycle.
277 receive ozanezumab (15 mg/kg) or placebo as intravenous infusions over 1 h every 2 weeks for 46 week
278 lve healthy adult male subjects received 2-L intravenous infusions over 1 hour of 0.9% saline or Plas
280 ts) at a dose of 7.4 GBq every 8 weeks (four intravenous infusions, plus best supportive care includi
281 d through systemic administration (typically intravenous infusion), precluding the feasible dosing of
282 n dose levels of IPH4102, administered as an intravenous infusion, ranging from 0.0001 mg/kg to 10 mg
283 s compare the efficacy of different forms of intravenous infusion sedation for critically ill patient
284 f mechanically ventilated patients receiving intravenous infusion sedation has increased over time.
286 Imetelstat was administered as a 2-hour intravenous infusion (starting dose, 9.4 mg per kilogram
288 ndomly assigned to receive either continuous intravenous infusion (TERLI-INF group) at the initial do
289 on of TKM-130803 at a dose of 0.3 mg/kg/d by intravenous infusion to adult patients with severe EVD w
290 time to FFR was 100 +/- 27 s for continuous intravenous infusion versus 23 +/- 14 s for intracoronar
291 administration of terlipressin as continuous intravenous infusion versus intravenous boluses in the t
293 eceived gemcitabine 1000 mg/m(2) as a 30-min intravenous infusion, weekly, for 7 weeks followed by a
296 as did direct intramyocardial injection and intravenous infusion, whereas intracoronary infusion dem
300 each diet, subjects cycled for 60 min after intravenous infusion with saline (CD and HFD) or dichlor