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1 ed patients with acute mania associated with bipolar I disorder.
2 ophrenia and to some extent among those with bipolar I disorder.
3 in recently manic or hypomanic patients with bipolar I disorder.
4 campal region in male patients with familial bipolar I disorder.
5 oliferation in this brain region in familial bipolar I disorder.
6 uronal dysfunction, or neuropil reduction in bipolar I disorder.
7 ing symptoms of acute mania in patients with bipolar I disorder.
8 suicidal behavior in high-risk patients with bipolar I disorder.
9 lated with a poorer outcome in patients with bipolar I disorder.
10 ) than normal comparison subjects (none) had bipolar I disorder.
11 psychotic and 18 nonpsychotic probands with bipolar I disorder.
12 malities were confirmed in the subgroup with bipolar I disorder.
13 t of 124 consecutively treated patients with bipolar I disorder.
14 te of poor outcome in the acute treatment of bipolar I disorder.
15 he acute treatment response of patients with bipolar I disorder.
16 n affectively ill relatives of probands with bipolar I disorder.
17 he psychosocial functioning of patients with bipolar I disorder.
18 th major depressive episodes associated with bipolar I disorder.
19 ecurrence of any mood episode in adults with bipolar I disorder.
20 Only 3% met DSM-IV criteria for bipolar I disorder.
21 alysis to family genetic studies of ADHD and bipolar I disorder.
22 reviewing family genetic studies of ADHD and bipolar I disorder.
23 either drug alone for relapse prevention in bipolar I disorder.
24 for 12.2% to bipolar II disorder and 7.5% to bipolar I disorder.
25 rent mood events in patients with stabilized bipolar I disorder.
26 showed individual genotypic association with bipolar I disorder.
27 pine as monotherapy in relapse prevention in bipolar I disorder.
28 th pharmacotherapy alone in the treatment of bipolar I disorder.
29 enia, schizoaffective disorder, or psychotic bipolar I disorder, 1,055 of their first-degree relative
31 as higher in the 169 trials in patients with bipolar I disorder (30.8%) than the 59 trials in patient
32 zoaffective disorder, and 115 with psychotic bipolar I disorder), 369 of their first-degree relatives
33 f 1,162 women with clinically treated DSM-IV bipolar I disorder (479 pregnancies/283 women), bipolar
34 es were 58 currently depressed patients with bipolar I disorder, 58 age- and sex-matched unipolar dep
35 6%), obsessive-compulsive disorder (9%), and bipolar I disorder (6%) were more common among patients
36 mpared with 4.0% of the asenapine group) and bipolar I disorder (6.3% compared with 1.6%) in the doub
39 nds and a significantly higher prevalence of bipolar I disorder among relatives of ADHD probands.
41 d in 15 euthymic male patients with familial bipolar I disorder and 20 healthy male comparison subjec
42 average density of 1 SNP per 11.9 kb in 323 bipolar I disorder and 274 schizophrenia or schizoaffect
43 rty-four lithium-free euthymic patients with bipolar I disorder and 31 healthy comparison subjects un
44 Patients with a primary DSM-IV diagnosis of bipolar I disorder and a current manic or mixed episode
46 ood disorder episodes, 12 were patients with bipolar I disorder and a positive history of psychotic s
48 line reduces cocaine use in outpatients with bipolar I disorder and current cocaine dependence and ac
49 postpartum mood disorder are more common in bipolar I disorder and manic and psychotic presentations
51 a trait-related abnormality in patients with bipolar I disorder and that male and female patients sho
52 ing recurrence of mood events in adults with bipolar I disorder and was generally well-tolerated.
53 order, and 129 of individuals with psychotic bipolar I disorder), and 200 healthy comparison subjects
54 e posed: Does stress precipitate episodes of bipolar I disorder, and does sensitivity to stress diffe
56 ubstance use disorders, major depressive and bipolar I disorders, and antisocial and borderline perso
60 mately 2 years apart for 35 adolescents with bipolar I disorder (BDI) and 37 healthy adolescents.
62 predicted lower lifetime prevalence rates of bipolar I disorder, bipolar II disorder, and bipolar spe
63 ing of perinatal mood episodes in women with bipolar I disorder, bipolar II disorder, and recurrent m
64 me prevalence rates in various countries for bipolar I disorder, bipolar II disorder, bipolar spectru
65 as affected if they had been diagnosed with bipolar I disorder; bipolar II disorder; or schizoaffect
66 ty in bipolar disorder is based primarily on bipolar I disorder (BP-I) and does not relate disability
67 f weekly symptomatic status of patients with bipolar I disorder (BP-I) during long-term follow-up.
70 enazi pedigrees with a proband affected with bipolar I disorder (BPI) and at least one other member a
71 ion downregulation in euthymic subjects with bipolar I disorder (BPI) and healthy control subjects.
72 ainment of families, most linkage studies of Bipolar I disorder (BPI) have used relatively small samp
73 atives ascertained through a proband who had bipolar I disorder (BPI) were interviewed by a psychiatr
75 schizoaffective disorder, bipolar type, and bipolar I disorder, but the generalizability of these fi
76 to determine whether comorbidity of ADHD and bipolar I disorder constitutes a familial subtype distin
77 e to the comparison group, the patients with bipolar I disorder demonstrated significantly lower conc
80 rticipants with nondeficit schizophrenia and bipolar I disorder did not show significant differences
81 to cortical disconnectivity in patients with bipolar I disorder (diffusion-weighted magnetic resonanc
82 s, family history, and treatment patterns to bipolar I disorder document the validity of the bipolar
83 oup, fixed-dose study in adult patients with bipolar I disorder experiencing a current major depressi
86 330 patients aged 16 years and older with bipolar I disorder from 41 sites in the UK, France, USA,
87 on deficit hyperactivity disorder (ADHD) and bipolar I disorder has been documented in clinical and e
88 s provided 12 estimates of the prevalence of bipolar I disorder in 1,877 relatives of ADHD probands a
90 esponse to lithium maintenance treatment for bipolar I disorder in patients of Han Chinese descent.
91 Study participants included 15 patients with bipolar I disorder in the euthymic state and 25 normal c
96 rder phenotype was defined as current DSM-IV bipolar I disorder (manic or mixed phase) with at least
98 of 116 outpatients 7 to 18 years of age with bipolar I disorder, manic or mixed, were recruited at 20
99 ded individuals with schizophrenia (n = 36), bipolar I disorder (n = 29), and healthy controls (n = 3
100 from two academic centers and patients with bipolar I disorder (n = 39) and matched healthy controls
102 st-degree relatives (N=966) of probands with bipolar I disorder (N=192) and schizoaffective disorder,
104 t total of 413 youths (ages 7-17 years) with bipolar I disorder (N=244), bipolar II disorder (N=28),
106 studies that included both individuals with bipolar I disorder (n=4270) and those with bipolar II di
108 2B, IL2RB, and TUBA8) met this criterion for bipolar I disorder; only DAO has been previously associa
110 rence was examined among 1,177 patients with bipolar I disorder or bipolar II disorder, including 458
113 clinical armamentarium for the management of bipolar I disorder, particularly with respect to prophyl
114 ays relapse into subsequent mood episodes in bipolar I disorder patients who responded to open-label
115 s whether a prepubertal and early-adolescent bipolar I disorder phenotype (PEA-BP-I) is the same illn
119 ed magnetic resonance imaging on 25 euthymic bipolar I disorder subjects and 24 gender- and age-equiv
121 marker, was lower in subjects with familial bipolar I disorder than in healthy comparison subjects,
122 ng chart review of 184 adult inpatients with bipolar I disorder, the authors assessed patients' past
123 ve been implicated in the pathophysiology of bipolar I disorder, the neural mechanisms underlying bip
124 We compared this prevalence in people with bipolar I disorder versus those with bipolar II disorder
125 ing of psychosis was also apparent when only bipolar I disorder was considered the affected phenotype
126 follow-up, from adolescence into adulthood, bipolar I disorder was rare among bipolar offspring.
127 ates of suicide attempts among patients with bipolar I disorder were compared to rates during a 2-yea
132 Subjects with Research Diagnostic Criteria bipolar I disorder were prospectively followed up for as
135 Families ascertained through probands with bipolar I disorder were stratified into three groups bas
136 redicted mood-incongruence in relatives with bipolar I disorder when compared with all other subjects
138 recurrence of mood episodes in patients with bipolar I disorder who had recently experienced a manic
139 atients and outpatients age 60 or older with bipolar I disorder who presented with a manic, hypomanic
141 s were 65 patients in the depressed phase of bipolar I disorder who were enrolled in a larger ongoing
142 mples from one subgroup of 294 patients with bipolar I disorder who were receiving lithium treatment.
143 of 1761 patients of Han Chinese descent with bipolar I disorder who were recruited by the Taiwan Bipo
144 ment outcome in a group of 175 patients with bipolar I disorder who were treated for an acute affecti
145 schizophrenia, schizoaffective disorder, and bipolar I disorder with psychosis) is as important for d
146 schizoaffective disorder [SAD; N = 129] and bipolar I disorder with psychotic features [BPD+; N = 26
147 c remission from a manic or mixed episode of bipolar I disorder (Young Mania Rating Scale [YMRS] tota
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