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1 h medical and public discourse about 'Female Sexual Dysfunction'.
2 urvivors (BCSs) with a DSM-IV diagnosis of a sexual dysfunction.
3 ter cope with their posttreatment urinary or sexual dysfunction.
4 uch as bladder stones, increased the rate of sexual dysfunction.
5 lationships and masculinity, which accompany sexual dysfunction.
6 including hot flashes, vaginal dryness, and sexual dysfunction.
7 suggested a causal relation between BPH and sexual dysfunction.
8 nd only small increased risks of fatigue and sexual dysfunction.
9 on with symptoms of depression, fatigue, and sexual dysfunction.
10 ntial roles as therapeutic agents for female sexual dysfunction.
11 evelop appropriate management strategies for sexual dysfunction.
12 mining the pharmacological aspects of female sexual dysfunction.
13 bo in ameliorating antidepressant-associated sexual dysfunction.
14 gs in the evaluation and treatment of female sexual dysfunction.
15 ial groups demonstrate different patterns of sexual dysfunction.
16 the adjuvant setting experienced symptoms of sexual dysfunction.
17 ated complications, including, unexpectedly, sexual dysfunction.
18 al sexual differentiation and any associated sexual dysfunction.
19 ty-of-life impairment, including itching and sexual dysfunction.
20 ention that was implemented to alleviate the sexual dysfunction.
21 en do not receive adequate support to manage sexual dysfunction.
22 e link between metabolic syndrome (MetS) and sexual dysfunction.
23 emerged pointing to a relationship with male sexual dysfunction.
24 n and urinary tract erosion, thigh pain, and sexual dysfunction.
25 tions in testosterone truly account for male sexual dysfunction.
26 ypogonadism and its correlation with QoL and sexual dysfunction.
27 to be associated with increased urinary and sexual dysfunction.
28 e baseline function had similar increases in sexual dysfunction.
29 l in the evaluation and treatment outcome of sexual dysfunction.
30 itted by SRIs but who were also experiencing sexual dysfunction.
31 brief sexual counseling can often alleviate sexual dysfunction.
32 obesity, cancer, cardiovascular disease and sexual dysfunction.
33 g with treatment-related urinary, bowel, and sexual dysfunction.
34 symptom in men with CP/CPPS as it relates to sexual dysfunction.
35 fects older men and is often associated with sexual dysfunction.
36 used to identify factors associated with the sexual dysfunction.
37 nderlying the link between LUTS/BPH and male sexual dysfunction.
38 mage, and menopausal symptoms in BCSs with a sexual dysfunction.
39 ed for the association between LUTS and male sexual dysfunction.
40 rofiles, and signs of prolactin elevation or sexual dysfunction.
41 f attempted suicide, child abuse, and recent sexual dysfunction.
42 d mean baseline scores were 41.8 to 46.4 for sexual dysfunction, 20.8 to 22.8 for urinary obstruction
43 nificant annual increase in risk of reported sexual dysfunction (5 per 1000 patients; 95% CI, 2-8), e
44 problems (7.7 [7.8] vs 7.9 [9.1]; P = .70), sexual dysfunction (68.2 [34.6] vs 65.9 [34.7]; P = .65)
47 determined potential confounding factors of sexual dysfunction: age; disease duration; physical disa
48 tures, myocardial infarction, and markers of sexual dysfunction, although there are few studies for e
50 opriate screening, information, and support, sexual dysfunction and accompanying distress can be sign
54 Previously reported associations between sexual dysfunction and hypertension, diabetes, and depre
55 henotypes in this syndrome, such as obesity, sexual dysfunction and possibly sleep abnormalities.
57 mpare higher doses of bupropion for treating sexual dysfunction and should include a greater number o
58 ata from individual studies showed that male sexual dysfunction and urinary dysfunction (three studie
61 bladder irritability, by increasingly severe sexual dysfunction and, in men aged more than 65 years,
63 ween primary treatment, urinary dysfunction, sexual dysfunction, and general health-related quality o
64 effective procedure, with low morbidity, no sexual dysfunction, and good short- and intermediate-ter
65 th adverse birth outcomes, hyperandrogenism, sexual dysfunction, and impaired implantation in humans,
67 studies of combination therapy for LUTS/BPH, sexual dysfunction, and other age-associated comorbiditi
69 ence, cognitive changes, somatic complaints, sexual dysfunction, and reduced quality of life may be s
72 erectile dysfunction, epidemiologic data on sexual dysfunction are relatively scant for both women a
74 as chronic diarrhea, dizziness, fatigue, and sexual dysfunction, are due to cholinergic autonomic dys
75 uate discrimination on 4 of the 5 domains of sexual dysfunction (area under the receiver operating ch
76 east 6 weeks, who were euthymic, and who had sexual dysfunction as determined by a total score greate
77 buspirone and amantadine in the treatment of sexual dysfunction associated with fluoxetine administra
78 other aspects of sexual function in men with sexual dysfunction associated with the use of SRI antide
82 yndromes that are reported after HCT include sexual dysfunction, cognitive problems, fatigue, insomni
86 ptors as possible treatments for obesity and sexual dysfunction due to the role of these receptors in
87 he route of administration, risk of fatigue, sexual dysfunction, dysphagia, shortness of breath and/o
92 ease associated pelvic pain; infertility and sexual dysfunction have a significant adverse clinical,
93 tion in women with antidepressant-associated sexual dysfunction have been reported, and there is unce
94 ng an integrative treatment model to address sexual dysfunction in a cancer survivorship treatment se
96 luate the hypothesis that fluoxetine-induced sexual dysfunction in female rats derived from disruptio
97 arizes current knowledge about the nature of sexual dysfunction in gynecological cancers, highlightin
98 nesis, testosterone deficiency, and physical sexual dysfunction in male pubertal, adolescent, and you
101 is study population, sildenafil treatment of sexual dysfunction in women taking SRIs was associated w
103 tions of female sexual problems, and 'Female Sexual Dysfunction' in particular, throughout the 20th c
105 depending upon their age, have complaints of sexual dysfunction, including decreased libido, vaginal
108 cts of the SSRI fluoxetine, and reversed the sexual dysfunction induced by chronic fluoxetine treatme
109 sustained-release bupropion with placebo for sexual dysfunction induced by selective serotonin reupta
110 idimensional Fatigue Inventory), bladder and sexual dysfunction (International Prostate Symptom Score
123 l risks of depressive symptoms, fatigue, and sexual dysfunction is not supported by data from clinica
125 n treatment of BPH (or watchful waiting) and sexual dysfunction is usually coincidental, unless sympt
128 l sexual maturation, idiopathic infertility, sexual dysfunction, low serum testosterone concentration
129 e frequently interrupts sexual function, and sexual dysfunction may signal serious endocrine disease.
130 , 30-day mortality, bladder dysfunction, and sexual dysfunction, none showed a statistically signific
135 s, digoxin and thiazide diuretics may worsen sexual dysfunction owing to medication side effects.
136 Owing to the link between LUTS/BPH and male sexual dysfunction, patients presenting with one of thes
137 rols, each therapy group reported bothersome sexual dysfunction; radical prostatectomy was associated
138 ndomized studies exist to guide treatment of sexual dysfunction related to MetS; rather, most studies
141 Compared with active surveillance, mean sexual dysfunction scores worsened by 3 months for patie
145 ded about key risk factors and predictors of sexual dysfunction that can be used to guide appropriate
146 adverse effects such as urinary symptoms and sexual dysfunction that can negatively affect quality of
148 thematical model for quantifying the risk of sexual dysfunction through time for this group of patien
151 tion after 12 months, but the time course of sexual dysfunction varied by treatment and, for bowel fu
158 primary treatment, urinary dysfunction, and sexual dysfunction were independently associated with ge
159 OFS results in more menopausal symptoms and sexual dysfunction, which contributes to inferior self-r
160 dence of an association between LUTS/BPH and sexual dysfunction will be reviewed, as well as the effe
161 logists are benign prostatic hyperplasia and sexual dysfunction, with an increasing number of patient
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