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1 pinal cord injury victims, and patients with prostatitis.
2 res the links between sexual dysfunction and prostatitis.
3 The d3tx male mice also developed autoimmune prostatitis.
4 the pathologically defined focus of chronic prostatitis.
5 imaging abnormality in the region of chronic prostatitis.
6 mal peripheral zone from prostate cancer and prostatitis.
7 hat PAP-specific CTLs can induce destructive prostatitis.
8 pathogenic E. coli virulence factor in acute prostatitis.
9 tes to E. coli virulence in a model of acute prostatitis.
10 er than Abs, mediates destructive autoimmune prostatitis.
11 e most likely secondary to radiation-induced prostatitis.
12 uced rapid and severe destructive autoimmune prostatitis.
13 oes not generate CTL or result in autoimmune prostatitis.
14 tant microorganisms in patients with chronic prostatitis.
15 weeks for people with febrile UTI and acute prostatitis.
16 for the prophylaxis or treatment of MDR-GNB prostatitis.
17 sy and possibly for the treatment of MDR-GNB prostatitis.
18 er and grade were positively correlated with prostatitis.
19 and compared with mice without induction of prostatitis.
20 l culture and in a murine model of bacterial prostatitis.
21 ical disease including urinary retention and prostatitis.
22 at immunity to SVS2 was sufficient to induce prostatitis.
23 s and central tolerance, develop spontaneous prostatitis.
24 pathologic examination to represent chronic prostatitis.
25 published epidemiologic research on chronic prostatitis.
26 may provide clues to the etiology of chronic prostatitis.
27 eliable tests to diagnose chronic abacterial prostatitis?
29 ic mice with this regimen resulted in marked prostatitis accompanied by destruction of epithelium, in
30 fidence interval: 1.43, 2.15) or young-onset prostatitis (adjusted OR = 1.55, 95% confidence interval
32 mong women and is frequently misdiagnosed as prostatitis and benign prostatic hyperplasia among men.
35 eviously healthy 38-year-old male with acute prostatitis and concurrent Pseudomonas aeruginosa urosep
37 oss leads to histological changes suggesting prostatitis and increases the number of intermediate cel
38 ive technique that shows differences between prostatitis and PCa in both the peripheral zone and cent
44 ary tract infection and a rat model of acute prostatitis and that a striking feature of the histopath
46 s (68%) in prostatodynia (chronic idiopathic prostatitis); and (iii) culture of difficult-to-grow cor
47 Gleason score >= 7), and benign lesions (eg, prostatitis); and justify classifications using PI-RADS
48 ents with benign prostate hyperplasia (BPH), prostatitis, and adenocarcinoma; and paraffin-embedded s
49 ks of fluoroquinolones for chronic bacterial prostatitis, and alpha-blockers for CP/CPPS with urinary
50 associated with strains from pyelonephritis, prostatitis, and bacteremia of urinary tract origin.
51 ute bacterial prostatitis, chronic bacterial prostatitis, and CP/CPPS, each of which is diagnosed and
52 sexually transmitted infections, young-onset prostatitis, and frequency of ejaculation, were investig
53 benign prostatic hyperplasia (BPH) nodules, prostatitis, and healthy tissue were delineated on T2-we
55 ndard diagnostic test for chronic abacterial prostatitis, and the methodologic quality of available s
63 nts data suggesting that possible causes for prostatitis (bacterial or otherwise) may be explained un
64 ents were significantly higher than those in prostatitis, benign prostate hyperplasia, and normal pro
65 ival probabilities for prostate disorder and prostatitis, but not for BPH, were observed among cohort
66 ct abnormalities of bacteriuria or bacterial prostatitis by traditional clinical tests, or of urethri
67 of (a) cancer versus NPZ, (b) cancer versus prostatitis, (c) prostatitis versus NPZ, and (d) high- o
68 er pathology) and few treatments for chronic prostatitis can be recommended on the basis of scientifi
70 category III), which accounts for 90%-95% of prostatitis cases, is of unknown etiology and is marked
72 ostatitis (category I) and chronic bacterial prostatitis (category II) are characterized by uropathog
85 of muscle) to better categorize male chronic prostatitis/chronic pelvic pain syndrome and interstitia
86 diagnosis, categorization, and treatment of prostatitis/chronic pelvic pain syndrome based on the Na
89 l cystitis/bladder pain syndrome and chronic prostatitis/chronic pelvic pain syndrome, collectively r
90 Urologic pain conditions such as chronic prostatitis/chronic pelvic pain syndrome, interstitial c
91 l cystitis/bladder pain syndrome and chronic prostatitis/chronic pelvic pain syndrome, is characteriz
95 mal DNA in the prostates of men with chronic prostatitis compared with controls are compatible with t
96 tions have been detected in men with chronic prostatitis compared with normal individuals, suggesting
97 tate tissues (adenocarcinoma and benign with prostatitis) compared those with normal prostate conditi
101 in conditions can be associated with chronic prostatitis/CPPS, including irritable bowel syndrome, fi
103 r findings support that chronic or recurrent prostatitis develops despite strong innate immune respon
107 istories of sexually transmitted infections, prostatitis, ejaculation frequency, surgery for an enlar
110 tic nephropathy, urinary bladder infections, prostatitis, gastric paresis, and impaired spermatogenes
111 ies show that microorganisms associated with prostatitis generally occur as complex microbial communi
113 ity of CAL > or = 2.7 mm and moderate/severe prostatitis have higher PSA levels than those with eithe
114 a major target Ag of experimental autoimmune prostatitis in a rat model and may serve as a target Ag
116 generates a CTL response and tissue-specific prostatitis in the absence of detectable PAP-specific Ab
117 e developed significant nonbacterial chronic prostatitis in the prostate gland with notable infiltrat
121 mal prostate, benign prostate hyperplasia or prostatitis indicating that Runx2 S319 phosphorylation i
122 mTmG model in concert with a murine model of prostatitis induced by infection from the uropathogenic
124 First-line therapy for chronic bacterial prostatitis is a minimum 4-week course of levofloxacin o
125 ide direct evidence that spontaneous chronic prostatitis is an autoimmune disease and is regulated by
133 d alpha-blockers to treat chronic abacterial prostatitis is not supported by the existing evidence.
136 Epidemiological studies have confirmed that "prostatitis" is common, with a prevalence of 10-15%.
137 sometimes called prostatodynia or abacterial prostatitis, is a commonly diagnosed and poorly treated
138 specimens that contained regions of chronic prostatitis larger than 6 mm in the peripheral zone.
144 ic imaging, pathologically confirmed chronic prostatitis may demonstrate metabolic abnormality that l
145 that antibiotic therapy in chronic bacterial prostatitis may not be due to altered antibiotic pharmac
146 munities distinct from those associated with prostatitis may occur at low levels in normal prostatic
147 e prostate, and previous bouts of CD8-driven prostatitis may promote invasion in the Pten(+/-) model
149 pathologically identified regions of chronic prostatitis, MR spectroscopic imaging data in nine of 12
151 olates showed that pyelonephritis (n=23) and prostatitis (n=17) isolates exhibited more virulence fac
152 treatment of patients diagnosed with chronic prostatitis (NIH classification types II, IIIa/IIIb and
153 tal rectal examination, dysplastic glands or prostatitis on biopsy, ultrasound gland volume, urinary
154 ntigenic targets for experimental autoimmune prostatitis on the assumption that such proteins might a
156 distinguish tumors from benign tissue (BPH, prostatitis, or healthy tissue) and high-grade tumors fr
159 cess (P < 0.001), osteomyelitis (P < 0.001), prostatitis (P < 0.001), diabetic retinopathy (P < 0.001
160 NA sequence study after we found that 77% of prostatitis patients were PCR positive for prokaryotic r
163 y our observation that patients with chronic prostatitis possessed specific autoantibodies against th
164 ibacterium acnes, causative agent of chronic prostatitis possibly culminating in prostate cancer, is
165 smitted infection can experience urethritis, prostatitis, reduced fertility, and amplified human immu
166 ods were used to select 135 men with chronic prostatitis refractory to multiple previous courses of a
167 with inflammation, the contribution of CA to prostatitis-related symptoms of unknown etiology or to p
169 rea of histopathologically confirmed chronic prostatitis, seven of 12 patients had focal low SI that
172 oad-spectrum antibiotics for acute bacterial prostatitis (such as piperacillin-tazobactam, ceftriaxon
174 The National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI) measures symptom se
175 with a National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI) score of at least 1
177 This review describes the current status of prostatitis syndromes and explores the future prospects
180 mplex series of syndromes (NIH category I-IV prostatitis) that vary widely in clinical presentation a
181 he most common grade 3-4 adverse events were prostatitis (three [2%] in the vascular-targeted photody
182 rsus NPZ, (b) cancer versus prostatitis, (c) prostatitis versus NPZ, and (d) high- or intermediate-gr
184 eadache was 4% (2-9); chronic pelvic pain or prostatitis was 11% (8-17); and fibromyalgia was 4% (3-7
185 he most common MR imaging finding in chronic prostatitis was focal low SI that was not specific for c
186 flammation on Nxk3.1 accumulation, bacterial prostatitis was induced by intraurethral inoculation of
189 mice developed spontaneous inflammation, and prostatitis was similar among groups of mice at 8 and 12
190 link, the POET3 mouse, an inducible model of prostatitis, was crossed with a Pten-loss model of prost
193 ugh the median ADCs of biopsy specimens with prostatitis were significantly higher compared with low-
194 s been a recent surge of interest in chronic prostatitis, which hopefully will translate into advance