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1 hibition with picrotoxin or enhanced it with clonazepam.
2 r sertraline plus placebo or sertraline plus clonazepam.
3 d sertraline plus placebo or sertraline plus clonazepam.
4          One-half of these patients received clonazepam, 0.5 mg h.s. adjusted to two tablets by day 1
5  to groups receiving either 0.5 mg of active clonazepam 3 times daily or placebo clonazepam for the f
6 to 3.0 mg/day of clonazepam (sertraline plus clonazepam), a switch to up to 225 mg/day of venlafaxine
7 red network firing pattern was normalized by clonazepam, a positive modulator of the GABAA receptor.
8  27% of patients assigned to sertraline plus clonazepam achieved remission compared with patients ass
9 nt GABA neuronal response to benzodiazepine (clonazepam) administration.
10                           Midazolam, but not clonazepam, also augmented a form of spike inhibition af
11  compared midazolam, an anesthetic BDZ, with clonazepam, an anticonvulsant/anxiolytic BDZ that activa
12 A(A) receptor positive allosteric modulators clonazepam and allopregnanolone, and by the NMDA recepto
13 d group received a single oral dose of 0.5mg clonazepam, and the remaining patients received placebo.
14                                              Clonazepam augmentation correlated positively with the r
15 ach efficacy, the authors determined whether clonazepam augmentation of fluoxetine is superior to flu
16                                              Clonazepam augmentation of fluoxetine was superior to fl
17                The findings suggest that the clonazepam augmentation strategy provides relative benef
18  of mitochondrial Na(+)/Ca(2+) exchange with clonazepam blocked mitochondrial Ca(2+) efflux and resul
19              We confirm the effectiveness of clonazepam, but note that attention to the safety of the
20 2 microM) and the Na+/Ca2+ exchange blocker, clonazepam, (CLO, 20 microM) reversibly inhibited both t
21 oms can be safely achieved with a sertraline/clonazepam combination, supporting the clinical utility
22 r proportion of responders in the sertraline/clonazepam compared with the sertraline/placebo group at
23 he thalamic effects of the anti-absence drug clonazepam (CZP) are restricted to either relay or retic
24 CAP A3 and, partially, A2 subtypes), whereas clonazepam did the opposite, reducing non-rapid eye move
25                                          The clonazepam dose was then tapered during 3 weeks and disc
26 f variance confirmed a significant effect of clonazepam for average Hamilton depression scores.
27 f active clonazepam 3 times daily or placebo clonazepam for the first 4 weeks of the trial.
28  in the sertraline/placebo vs the sertraline/clonazepam group (38% vs 25%) (P =.5).
29 roportion of patients in the sertraline plus clonazepam group (56%) compared with the sertraline plus
30 week 3 with 14 (63%) of 22 of the sertraline/clonazepam group responding to treatment vs 8 (32%) of 2
31                                              Clonazepam had similar effects as CGP37157.
32                          The patients taking clonazepam improved significantly more during the first
33                           Midazolam, but not clonazepam, increased neurosteroid levels in CA1 pyramid
34 al period (occasionally prenatally) and that clonazepam is the treatment of choice (95% found it to b
35 7157 (CGP)], a benzothiazepine derivative of clonazepam, is commonly used as a blocker of the mitocho
36 o distinct cell populations that differed in clonazepam modulation and patterns of alpha-subunit expr
37 mmonly cited RBD treatments include low-dose clonazepam or high-dose melatonin taken orally at bedtim
38 f GABAergic transmission with tiagabine plus clonazepam partially rescues the effects of deletion of
39                                              Clonazepam/placebo was gradually discontinued during day
40 died, such as ketamine, midazolam, diazepam, clonazepam, propofol, pentobarbital, chloral hydrate, ha
41 levodopa, rotigotine, clozapine, duloxetine, clonazepam, ramelteon, gabapentin, zonisamide, and yokuk
42 e alone: the addition of up to 3.0 mg/day of clonazepam (sertraline plus clonazepam), a switch to up
43 10 were randomly assigned to sertraline plus clonazepam, switch to venlafaxine, or sertraline plus pl
44                                              Clonazepam treatment of RBD was completely or partially
45 tetrabenazine (one); and the introduction of clonazepam (two).
46 nerally similar, except for a notably higher clonazepam use in dementia convertors (OR = 2.6).
47                              Sertraline plus clonazepam was associated with a significantly greater d
48  selective TSPO agonist, or a combination of clonazepam with exogenous allopregnanolone.
49 ic effects were mimicked by a combination of clonazepam with FGIN (2-[2-(4-fluorophenyl)-1H-indol-3-y
50 st the efficacy of early coadministration of clonazepam with sertraline in the treatment of panic dis

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