戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

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 + mood-stabilizer) or monotherapy (placebo + mood-stabilizer).
2  agonists, atomoxetine, antidepressants, and mood stabilizers).
3 thium fulfilled the a priori definition of a mood stabilizer.
4 oate (2-propylpentanoate) is a commonly used mood stabilizer.
5  which if any agents meet this definition of mood stabilizer.
6 four roles included in their definition of a mood stabilizer.
7 ssants was common, often in the absence of a mood stabilizer.
8 r disorder did not include prescription of a mood stabilizer.
9 [2.6] years) who initiated an anticonvulsant mood stabilizer.
10 with an antidepressant in conjunction with a mood stabilizer.
11 iving an antidepressant while treated with a mood stabilizer.
12 and those receiving an antidepressant plus a mood stabilizer.
13     Valproate (VPA) is a commonly prescribed mood stabilizer.
14 rupt/rapid versus gradual discontinuation of mood stabilizer.
15 ertraline, or venlafaxine as an adjunct to a mood stabilizer.
16 th therapeutic effects and were specific for mood stabilizers.
17 isorder is a useful tool in conjunction with mood stabilizers.
18 pathway may mediate the antimanic effects of mood stabilizers.
19 raging results when used in conjunction with mood stabilizers.
20 ents with mood disorders who were prescribed mood stabilizers.
21 red combinations of established and putative mood stabilizers.
22 rolled studies of the use of combinations of mood stabilizers.
23  inhibitors, memantine, antidepressants, and mood stabilizers.
24 56 (20.5%) SUD medications, and 1706 (12.2%) mood stabilizers.
25 s weight gain than commonly used alternative mood stabilizers.
26 ics in large measure supplanting traditional mood stabilizers.
27 sychoactive drugs such as antipsychotics and mood stabilizers.
28  benefits with antidepressants combined with mood stabilizers.
29 nt role in the actions of antispychotics and mood stabilizers.
30 ith ineffective regimens that do not include mood stabilizers.
31 tion of paliperidone and these two classical mood stabilizers.
32 wer antipsychotics with those of traditional mood stabilizers.
33  validated with several clinically effective mood stabilizers.
34 ated pathway and Bcl-2 are major targets for mood stabilizers.
35 and as a therapeutically relevant target for mood stabilizers.
36 ression but happened less in patients taking mood stabilizers (31.6% versus 84.2%).
37 antidepressant medications (14.4% to 48.6%), mood stabilizers (5.3% to 14.5%), stimulants (1.9% to 6.
38                           Despite the use of mood stabilizers, a significant proportion of patients w
39 vents provides a potential mechanism whereby mood stabilizers alleviate cerebral morphometric deficit
40  mood stabilizer was more efficacious than a mood stabilizer alone, and as efficacious as haloperidol
41  time to recovery relative to treatment with mood stabilizers alone, and treatment with antidepressan
42                     Lithium is a widely used mood stabilizer also proposed to act via synaptic scalin
43                       Valproic acid, another mood stabilizer, also increased the number of fluorescen
44 ave themselves been reported to be effective mood stabilizers, although the importance of increased c
45 ve recently reported that the anticonvulsant mood stabilizers (AMS), valproic acid, carbamazepine, an
46 Treatments and were currently treated with a mood stabilizer, an atypical antipsychotic, or their com
47                     Lithium (Li) is a potent mood stabilizer and displays neuroprotective and neuroge
48 21 is a key mediator of the effects of these mood stabilizers and a potential new therapeutic target
49 ably is involved in mechanisms of actions of mood stabilizers and antidepressants.
50 curring psychiatric conditions, or receiving mood stabilizers and antipsychotics were not included.
51  some pharmacological treatments - primarily mood stabilizers and atypical antipsychotics - augmented
52 sts that pharmacological interventions using mood stabilizers and atypical antipsychotics may be effe
53                                              Mood stabilizers and depressed episode reduced WM FA in
54 K-3beta) may mimic the therapeutic action of mood stabilizers and might therefore allow for the desig
55 sychotics, antidepressants, benzodiazepines, mood stabilizers and opioids.
56      Both the control and CT groups received mood stabilizers and regular psychiatric follow-up.
57 ent with antipsychotic, anxiolytic/hypnotic, mood stabilizer, and stimulant medications.
58 cs, antidepressants, anxiolytics, hypnotics, mood stabilizers, and medications for attention-deficit/
59 otropic medications such as antidepressants, mood stabilizers, antianxiety drugs and opioid antagonis
60 ons can be induced by valproic acid (VPA), a mood-stabilizer, anticonvulsant and histone deacetylase
61  for attention-deficit/hyperactive disorder, mood stabilizers, antidepressants, benzodiazepines and r
62 and antidepressants, anxiolytics, hypnotics, mood stabilizers, antipsychotics and treatments for opio
63 0 to investigate which antipsychotics and/or mood stabilizers are better for patients with bipolar di
64                   Once the mechanisms of the mood stabilizers are identified, it is possible that a m
65 essive illness, and therapeutic mechanism of mood stabilizers are largely unknown.
66                                          New mood stabilizers are needed that possess efficacy for al
67 nd behavioral consequences to offspring when mood stabilizers are used during pregnancy.
68 ntipsychotic drugs (APD)s and anticonvulsant mood-stabilizers are now frequently used in combination
69 e whether zonisamide, another anticonvulsant mood stabilizer, as well as lithium, a mood stabilizer w
70  subjects with BD taking vs those not taking mood stabilizers, as well as in the left optic radiation
71   Despite important advances in the range of mood stabilizers available, the pharmacological treatmen
72 was partially (atypical APDs) or completely (mood-stabilizers) blocked by the serotonin (5-HT)1A rece
73 only the relative risks of fetal exposure to mood stabilizers but also the high risk of recurrence an
74             Valproate (VPA) is a widely used mood stabilizer, but its therapeutic mechanism of action
75 e found marginal efficacy for amantadine and mood stabilizers, but found no increased family history
76 tonin reuptake inhibitors, by 98% for use of mood stabilizers, by 171% for use of antipsychotics, and
77 tonin reuptake inhibitors, by 63% for use of mood stabilizers, by 60% for use of antipsychotics, and
78 te initiation in bipolar patients not taking mood stabilizers, careful assessment to rule out bipolar
79              The safest and most efficacious mood stabilizer combinations appear to be the mixtures o
80     There was no increase in prescription of mood stabilizer combinations.
81  up by querying the effect of treatment with mood stabilizers commonly prescribed in bipolar disorder
82                                 Lithium is a mood stabilizer, dampening both the manic and depressive
83                                       Use of mood stabilizers decreased from 62.3% of visits for bipo
84                               Treatment with mood stabilizers did not have a statistically significan
85                                              Mood stabilizers did not prevent cycle acceleration, rap
86 y and are known targets of the anti-suicidal mood stabilizer drug lithium, which increases their expr
87 in the mode of action of antidepressants and mood stabilizer drugs.
88 al prescription fills for antipsychotics and mood stabilizers during 4-week intervals.
89  disorder and the consequences of the use of mood stabilizers during pregnancy, and a consensus docum
90 who continued or discontinued treatment with mood stabilizers during pregnancy.
91                                              Mood stabilizers (e.g., valproic acid) and antipsychotic
92                                         Some mood stabilizers, e.g., sodium valproate and carbamazepi
93                               Anticonvulsant mood stabilizers, e.g., valproic acid and carbamazepine,
94             In contrast, only two studies of mood stabilizers evaluated SABV, with one noting a sex d
95 s, the authors examined trends in the use of mood stabilizers, first- and second-generation antipsych
96 mary psychiatric diagnosis, were receiving a mood stabilizer for 4 or more weeks, and had a Montgomer
97      Lithium (Li) remains the most effective mood stabilizer for BD, yet it benefits only a subset of
98   Lithium salts are commonly prescribed as a mood stabilizer for individuals with bipolar disorder.
99                Lithium is the most effective mood stabilizer for the treatment of bipolar disorder, b
100 d current substance dependence, treated with mood stabilizers for >or=2 weeks, were randomly assigned
101 m dose=1.7 mg/day, SD=1.3) added to existing mood stabilizers for 6 weeks.
102  cardiovascular disorders, arthritis, and as mood stabilizers for bipolar disorder; however, the mech
103 nd that lithium and valproate, commonly used mood stabilizers for the treatment of manic-depressive i
104 ne, and as efficacious as haloperidol plus a mood stabilizer, for the rapid control of manic symptoms
105                        Lithium, a well-known mood stabilizer, has both neuroprotective, pro-neurogeni
106                                              Mood stabilizers have an effect on mitochondrial functio
107 sychotics (HR, 0.45 [95% CI, 0.23-0.88]) and mood stabilizers (HR, 0.64 [95% CI, 0.46-0.90]) were ass
108 definition by which an agent is considered a mood stabilizer if it has efficacy in treating acute man
109 ark pharmacotherapy, functioning as a potent mood stabilizer in most, but not all patients.
110 ipolar course had received prescriptions for mood stabilizers in any follow-up year.
111            A lower level of effectiveness of mood stabilizers in children cannot be ruled out.
112 icle is to review the safety and efficacy of mood stabilizers in combinations.
113 ent and pattern of blood serum monitoring of mood stabilizers in Medicaid patients with bipolar disor
114 ety of risperidone as an adjunctive agent to mood stabilizers in the treatment of acute mania.
115 nical synergism of an APD and anticonvulsant mood-stabilizer in improving the cognitive deficits pres
116  mood disorders, whereas antidepressants and mood stabilizers increase Bcl-2 levels.
117  Prescription of an antidepressant without a mood stabilizer increased substantially, from 17.9% in t
118 es despite the prescription of commonly used mood stabilizers, into a CT group or control group.
119                                    The term "mood stabilizer" is widely used in the context of treati
120 ith infants exposed to another commonly used mood stabilizer, lamotrigine.
121 kin to the antipsychotic haloperidol and the mood stabilizer lithium carbonate.
122  3beta (GSK3beta) inhibitors, especially the mood stabilizer lithium chloride, are also used as neuro
123 to account for the behavioral actions of the mood stabilizer lithium in various animal models of mood
124                Chronic administration of the mood stabilizer lithium returns many of these behavioral
125 ere attenuated by chronic treatment with the mood stabilizer lithium.
126 ctions of the structurally highly dissimilar mood stabilizers lithium and valproate: BAG-1 [BCL-2 (B-
127 citotoxicity, and that co-treatment with the mood stabilizers lithium and valproic acid (VPA) induces
128 urrent manic or mixed episode who received a mood stabilizer (lithium or divalproex) and placebo, ris
129 a typical antipsychotic (perphenazine) and a mood stabilizer (lithium, carbamazepine, or valproate),
130 lar disorder, or psychosis or treatment with mood stabilizer (lithium, valproate, or carbamazepine),
131  relationship of adherence to treatment with mood stabilizers (lithium, carbamazepine, and sodium val
132    Current treatments include the so-called "mood stabilizers," lithium and valproic acid.
133 tidepressant treatment in combination with a mood stabilizer may be warranted in some patients with b
134 bits glucocorticoid activation suggests that mood stabilizers may counteract the deleterious effects
135 2%]; 20.3% decrease), with antipsychotic and mood stabilizer medication prescription fills (216 468 [
136 re-CVD, and antipsychotic and anticonvulsant/mood stabilizer medication prescriptions.
137 o have used antianxiety, antidepressant, and mood stabilizer medications, and those with borderline o
138 did not yield higher recovery rates than did mood stabilizer monotherapy.
139 of and the response to antidepressants (AD), mood stabilizers (MS), and antipsychotics (AP) in the tr
140   Treatment with antidepressants (AD) in MD, mood-stabilizers (MS) in BD, and antipsychotics (AP) in
141 ng older patients with bipolar disorder with mood stabilizers need evidence from age-specific randomi
142     Among patients treated with a concurrent mood stabilizer, no acute change in risk of mania was ob
143 epressants, antipsychotics, benzodiazepines, mood stabilizers, opioids, and stimulants.
144 f these patients were receiving a concurrent mood stabilizer or an atypical antipsychotic.
145 ributable to treatment with antidepressants, mood stabilizers or electroconvulsive therapy (ECT).
146 andomized to receive cotherapy (olanzapine + mood-stabilizer) or monotherapy (placebo + mood-stabiliz
147      Because antipsychotic drugs are used as mood stabilizers our studies focused on a newly-marketed
148                           Discontinuation of mood stabilizer, particularly abruptly, during pregnancy
149 d 51 of the 187 subjects (27.3%) receiving a mood stabilizer plus a matching placebo (P=0.40).
150  plus adjunctive antidepressant therapy or a mood stabilizer plus a matching placebo, under condition
151 -two of the 179 subjects (23.5%) receiving a mood stabilizer plus adjunctive antidepressant therapy h
152 o receive up to 26 weeks of treatment with a mood stabilizer plus adjunctive antidepressant therapy o
153 ficant trends favoring the group receiving a mood stabilizer plus placebo were observed across the se
154 combination of adequate doses of established mood stabilizers plus at least one antidepressant.
155 administration of lithium, a clinically used mood stabilizer, promoted the proliferation of neuronal
156  addition of an antidepressant to an ongoing mood stabilizer regimen were followed prospectively for
157 idepressants combined with antipsychotics or mood stabilizers, relatively few controlled studies have
158 Although the underlying mechanism(s) of this mood stabilizer remains controversial, recent evidence l
159              Consistent with these findings, mood stabilizers such as lithium ion and valproic acid,
160                  First-line therapy includes mood stabilizers, such as lithium, anticonvulsants, such
161              Long-term treatment consists of mood stabilizers, such as lithium, valproate, and lamotr
162 view will focus on four molecular targets of mood stabilizers that are known to play integral roles i
163             By contrast, for patients taking mood stabilizers, the risk of mania was lower after star
164 der (seven medication free and six receiving mood stabilizer therapy) who had been euthymic for more
165 iagnosis of mania/hypomania or initiation of mood stabilizer therapy.
166 (5-20 mg/d) vs placebo when added to ongoing mood-stabilizer therapy as measured by reductions in You
167 -blind treatment in which in addition to the mood stabilizer they received either continued perphenaz
168                      Lithium is an effective mood stabilizer treatment for BD, but only a minority of
169                            We postulate that mood stabilizer treatment has a profound effect on mitoc
170                               Anticonvulsant mood stabilizer treatment is associated with an increase
171 ts were euthymic at conception and continued mood stabilizer treatment or discontinued treatment prox
172 mong women who discontinued versus continued mood stabilizer treatment, recurrence risk was twofold g
173 ed 20-65 years) who initiated anticonvulsant mood stabilizer treatment.
174 te, olanzapine, or quetiapine as maintenance mood stabilizer treatment.
175 t the effects of antipsychotics when used as mood stabilizer treatment.
176 nd 1376 prescribed quetiapine as maintenance mood stabilizer treatment.
177 77), or quetiapine (n = 1376) as maintenance mood stabilizer treatment.
178 r increase in Cck expression in the VTA with mood stabilizer treatment.
179 , this risk is reduced markedly by continued mood stabilizer treatment.
180 rbidity associated with stopping maintenance mood stabilizer treatment.
181  In contrast, behaviorally effective chronic mood stabilizer treatments in mice inhibit GSK3beta and
182 comorbidities and concomitant antidepressant/mood stabilizer use.
183                              The widely used mood stabilizer valproate (VPA) causes perturbation of e
184          It was previously reported that the mood stabilizer valproate (VPA) increased phosphorylatio
185 ntial clinical utility of the anticonvulsant mood stabilizer, valproate, in bipolar disorder with co-
186 d risperidone, as well as the anticonvulsant mood-stabilizers, valproic acid (VPA), zonisamide, and c
187 ider the relative risks of fetal exposure to mood stabilizers versus the high recurrence risks after
188                           Risperidone plus a mood stabilizer was more efficacious than a mood stabili
189 0.62; 95% CI, 0.45-0.86), whereas the use of mood stabilizers was associated with increased odds of i
190  The treatment recommendation for adjunctive mood stabilizers was the only recommendation for which c
191 sant medication, as compared with the use of mood stabilizers, was not associated with increased effi
192                                          For mood stabilizers, whereas carbamazepine and topiramate c
193  Thus, pharmacological interventions such as mood stabilizers, which dampen limbic irritability, or s
194 ession that was inadequately responsive to a mood stabilizer with or without concomitant antidepressa
195 d in obstacles to discovering more effective mood stabilizers with fewer adverse side effects.
196 ia (OR, 6.75; 99% CI, 3.52-12.92); 2 or more mood stabilizers, with bipolar disorder (OR, 15.46; 99%
197  antipsychotics, anxiolytics, hypnotics, and mood-stabilizers, with statins as a negative control out
198 lsant mood stabilizer, as well as lithium, a mood stabilizer without anticonvulsant properties, also

 
Page Top