Academic literature on the topic 'Ethanol Vaginosis, Bacterial Vaginosis, Bacterial'

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Journal articles on the topic "Ethanol Vaginosis, Bacterial Vaginosis, Bacterial"

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Wang, Jeff. "Bacterial vaginosis." Primary Care Update for OB/GYNS 7, no. 5 (September 2000): 181–85. http://dx.doi.org/10.1016/s1068-607x(00)00043-3.

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Hay, Phillip. "Bacterial vaginosis." Medicine 38, no. 6 (June 2010): 281–85. http://dx.doi.org/10.1016/j.mpmed.2010.03.008.

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Hay, Phillip. "Bacterial vaginosis." Medicine 42, no. 7 (July 2014): 359–63. http://dx.doi.org/10.1016/j.mpmed.2014.04.011.

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OSBORNE, NEWTON G. "Bacterial Vaginosis." Journal of Gynecologic Surgery 16, no. 2 (January 2000): 93–94. http://dx.doi.org/10.1089/gyn.2000.16.93.

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VEJTORP, MOGENS, ANNE CATHRINE BOLLERUP, LlSSlE VEJTORP, ERIK FANOE, EVA NATHAN, ANITA REITER, MARY E. ANDERSEN, BODIL STROMSHOLT, and STEEN STEENBEK SCHRODER. "Bacterial Vaginosis." Obstetrical & Gynecological Survey 44, no. 6 (June 1989): 471–72. http://dx.doi.org/10.1097/00006254-198906000-00020.

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Neri, A., D. Rabinerson, and B. Kaplan. "Bacterial Vaginosis." Obstetrical & Gynecological Survey 49, no. 12 (December 1994): 809–13. http://dx.doi.org/10.1097/00006254-199412000-00003.

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Young, H. "Bacterial vaginosis." Sexually Transmitted Infections 61, no. 3 (June 1, 1985): 213–14. http://dx.doi.org/10.1136/sti.61.3.213.

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Pattman, R. S. "Bacterial vaginosis." Sexually Transmitted Infections 64, no. 3 (June 1, 1988): 208. http://dx.doi.org/10.1136/sti.64.3.208.

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OʼBrien, Rebecca Flynn. "Bacterial Vaginosis." Postgraduate Obstetrics & Gynecology 25, no. 23 (November 2005): 1–7. http://dx.doi.org/10.1097/00256406-200511300-00001.

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&NA;. "Bacterial Vaginosis." Postgraduate Obstetrics & Gynecology 25, no. 23 (November 2005): 8. http://dx.doi.org/10.1097/00256406-200511300-00002.

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Dissertations / Theses on the topic "Ethanol Vaginosis, Bacterial Vaginosis, Bacterial"

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Bukusi, Elizabeth Anne. "Bacterial vaginosis : a randomized controlled trial to prevent recurrence /." Thesis, Connect to this title online; UW restricted, 2006. http://hdl.handle.net/1773/10880.

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Al-Mushrif, Shawqi A. "Pathogenicity of bacterial vaginosis." Thesis, University of Sheffield, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.310757.

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Eriksson, Katarina. "Bacterial Vaginosis : Diagnosis, Prevalence, and Treatment." Doctoral thesis, Linköpings universitet, Obstetrik och gynekologi, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-68812.

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Bacterial Vaginosis (BV) is a disorder of unknown etiology, characterized by a foul smelling vaginal discharge, loss or reduction of the normal vaginal Lactobacilli, and overgrowth of other anaerobic bacteria. Thus, it presents a formidable problem for clinicians as well as microbiologists researching its etiology, clinical course, treatment, and epidemiology. The present work focuses on the unresolved issues of the epidemiology and treatment of BV in order to provide valid methods for treatment studies of this condition and to describe the prevalence of BV in defined populations. The first study validates the use of PAP-stained smears in the diagnosis of BV. The study assesses the methods of Amsel’s clinical criteria and Nugent criteria on Gram-stain smears, against Pap-stained smears and also validates different observers. The result shows that the PAP-staining of vaginal smears is a good method in BV diagnosis; the kappa value is 0.86 (interobserver weighted kappa index) compared to 0.81 for Gram-stained smears, and 0.70 for rehydrated air-dried smears using the mean Nugent score as the criterion standard. This enables population based studies on archived PAP-stained smears from the screening of cervical cancer. In the second study, we use the knowledge gained from study one to investigate the prevalence of BV in a cohort from the population of Åland. The prevalences of BV on the Åland Islands were: 15.6 %, 11.9 %, 8.7 %, and 8.6% in 1993, 1998, 2003, and 2008, respectively. This means that the prevalence of BV decreased between1993-2008 from 15.6% to 8.6%. The confidence intervals are not overlapping, thus indicating a significant decrease in prevalence from 1993 to 2008. The third study is a prospective, double-blind placebo controlled treatment study of BV. After conventional treatment with clindamycin, the patients were treated with adjuvant treatment of Lactobacilli-loaded tampons or placebo. The study showed no differences between the treatment and the placebo group, indicating that the tampon does not work at all. There are a variety of possible explanations for the result, which are analyzed in this thesis. The fourth study aimed to evaluate whether clindamycin is retained for a long time in the vaginal mucosa, thus disturbing the Lactobacilli in an attempt to reimplant Lactobacilli in the probiotic treatment studies. In conventional treatment, it is also useful to know whether clindamycin is retained, especially when considering the pressure from antibiotics on the antimicrobial sensitivity pattern. In the study, we found that the clindamycin disappears rapidly. Conclusion: BV research requires effort from many different scientific disciplines and the riddle of this condition and its treatment can only be resolved by concerted actions in research and treatment. The vision for the future includes, among other factors, better molecular biology based diagnostic tools, and knowledge of population based bacterial floras.
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Brumley, Jessica. "Testing a Model of Bacterial Vaginosis among Black Women." Scholar Commons, 2012. http://scholarcommons.usf.edu/etd/3995.

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Bacterial Vaginosis is an inbalance of vaginal flora which has been associated with increased risk of numerous gynecological and obstetric morbidities including increased risk of acquisition of HIV from an infected partner and increased risk of preterm delivery. Black race has been consistently identified as a risk factor for BV. Black women also suffer from significant disparities in most of the morbidities also associated with BV when compared to women of other ethnicities and races. Traditional predictors of BV such as douching practices and sexual behaviors do not fully account for the racial disparities in BV prevalence. Researchers have begun to explore the potential relationship between stress and BV. Also, perceived racism has been identified as a potential stressor contributing to the health outcomes of Black women. The purpose of this study was to test a predictive model of bacterial vaginosis among Black women. The Allostatic Load Model was the theoretical framework. Participants (N=94) completed a self administered questionnaire and interview including measures of perceived stress, preceived racism, behavioral responses to stress and specific behavioral responses to racism along with traditional predictors of BV. Measurement scales included the Cohen Perceived Stress Scale, the John Henryism Scale of Active Coping, the Everyday Perceived Racial Discrimination Index, the Experiences of Discrimination Scale and the Vines Telephone Administered Perceived Racism Scale (TPRS) which included a behavioral responses to racism subscale. Bacterial vaginosis was diagnosed utilizing a self-collected vaginal swab which was analyzed utilizing the BVBlue point of care testing kit. Twenty percent (N=19) of participants screened positive for bacterial vaginosis. Douching and sexual activity in the last three months and education were significantly associated with bacterial vaginosis. Age, income, hormonal contraceptive use and condom use were not associated with BV. Neither perceived stress nor perceived racism were associated with bacterial vaginosis. After logistic regression analysis, only education continued to be a significant predictor of BV. The lack of an association between BV and the main study variables may have been related to young age of the sample or the low rates of high perceived stress and high perceived racism. Perceived stress was positively associated with perceived racism and behavioral responses to stress. This association is likely a reflection of the stressful nature of perceived racism. Further research is needed to better understand how the stressful nature of racism and behavioral responses to stressors may influence health outcomes and if interventions can be utilized to promote adaptive behavioral responses.
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McLean, Nigel W. "The role of lactobacilli in the prevention of bacterial vaginosis." Thesis, Glasgow Caledonian University, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.308801.

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Keane, Frances Emer. "Studies of the aetiologies of non-gonococcal urethritis and bacterial vaginosis." Thesis, Queen's University Belfast, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.287207.

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Ugwumadu, Austin Hayes Nnamdi. "The influence of bacterial vaginosis and intermediate flora on human pregnancy." Thesis, St George's, University of London, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.433661.

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Montoya, Vincent Keith. "Metagenomic analyses of two female genital tract diseases : bacterial vaginosis and ovarian cancer." Thesis, University of British Columbia, 2013. http://hdl.handle.net/2429/44333.

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Metagenomics is a rapidly evolving field that has facilitated the expansion of microbiology into new areas of human and environmental health. Metagenomic studies have expanded the phylogenetic tree of life by increasing taxonomic resolution in individual phyla as well as adding entirely new branches of life. This revolution in microbiology has been made possible by the introduction of second-generation high-throughput sequencing, the associated methods for preparing DNA sequencing libraries, as well as new bioinformatic algorithms for analyzing these new types of data. Because of the novelty of these methods, very few have been systematically tested for their sensitivities and specificities outside of the initial development process. As the interpretation of metagenomic studies utilizing these tools depends greatly upon their efficiencies in both detection and classification, it is essential to best determine the performance of each tool. In this study, a variety of novel techniques were utilized and tested in their abilities to characterize the microbial populations in two regions of the female genital tract: ovarian cancer tissue and the vaginal microbiome. Although a diverse microbial population was initially observed in the transcriptome sequence data for ovarian cancer using next generation sequencing, we were unable to recover these microbial sequences through PCR and Sanger sequencing approaches. Optimized methods were applied to healthy vaginal microbiome samples and tested for their ability to differentiate them from a polymicrobial disease of the vagina, bacterial vaginosis. In addition to a high correlation between a microbial scoring system for bacterial vaginosis, this novel metagenomic pipeline also revealed microorganisms not yet associated with the vaginal microbiome such as specific Bifidobacteria spp., various bacteriophage, and Debaryomyces. Collectively, both of these studies provide unique insights into each disease as well as illustrate both the limitations and potential of the rapidly growing field of metagenomics.
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Eiderbrant, Kristina. "Development of quantitative PCR methods for diagnosis of bacterial vaginosis and vaginal yeast infection." Thesis, Linköpings universitet, Institutionen för klinisk och experimentell medicin, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-68269.

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Vaginitis is a vaginal infection which affects many women all over the world. The disorder is characterized by an infection of the vaginal area which can cause problems like abnormal vaginal discharge, itching and redness. The two most common causes of vaginitis are bacterial vaginosis and Candida vaginitis. The prevalence of bacterial vaginosis in Sweden is around 10-20 % and approximately 75 % of all women will once in their lifetime suffer from vaginal yeast infection. The clinical symptoms of vaginal infections are not specific and the diagnosis methods of bacterial vaginosis and Candida vaginitis are subjective and depended on the acuity of the clinician. Due to the lack of standardized and objective diagnostic tools, misdiagnosis and consequently incorrect treatment may occur. As vaginal infections and symptoms impact greatly of women´s quality of life and vaginitis have been associated with serious public health consequences, it is essential to diagnose and treat the conditions correctly. Hence, there is a great need of better methods of diagnosing these conditions. The aim of this master thesis was to develop quantitative species-specific real-time PCR assays to use in diagnosing the two most common causes of vaginitis i.e. bacterial vaginosis and Candida vaginitis. Potential markers for bacterial vaginosis (Atopobium vaginae, BVAB2, Gardnerella vaginalis, Lactobacillus crispatus, Lactobacillus gasseri, Lactobacillus jensenii, Lactobacillus iners, Megasphaera type 1, Megasphaera type 2, Mobiluncus curtisii, Mobiluncus mulieris and Leptotrichia/Sneathia species) and Candida vaginitis (Candida albicans, Candida glabrata, Candida parapsilosis and Candida tropicalis) were chosen. Primers and probes were designed and tested on reference strains and vaginal samples. Single- and multiplex PCR reactions were successfully optimized with the designed oligonucleotides. Furthermore, standard curves with excellent linearity were created and covered more than five orders of magnitude. These developed quantitative species-specific real-time PCR assays will, in a prospective medical validation, quantify 300 vaginal samples from women visiting the RFSU Clinic in Stockholm.
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Gottschick, Cornelia Verfasser], and Irene [Akademischer Betreuer] [Wagner-Döbler. "The microbiome of bacterial vaginosis - clinical studies and model biofilms / Cornelia Gottschick ; Betreuer: Irene Wagner-Döbler." Braunschweig : Technische Universität Braunschweig, 2017. http://d-nb.info/1175969842/34.

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Books on the topic "Ethanol Vaginosis, Bacterial Vaginosis, Bacterial"

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Parker, James N., and Philip M. Parker. The official patient's sourcebook on bacterial vaginosis. Edited by Icon Group International Inc and NetLibrary Inc. San Diego, Calif: Icon Health Publications, 2002.

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Thomason, J. L. Bacterial vaginosis (Current concepts). The Upjohn Co, 1990.

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Meijden, W. I. Van Der. Bacterial Vaginosis: Clue Cell-Positive Discharge : Diagnostic, Ultra-Structural, and Therapeutic Aspects. Van Gorcum Ltd, 1987.

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Publications, ICON Health. Bacterial Vaginosis - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References. ICON Health Publications, 2003.

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Swidsinski, Alexander, Mario Vaneechoutte, and Nuno Cerca, eds. Bacterial Vaginosis, a Model of True Polymicrobial Infections: Genetics, Evolution, Clinical and Socio-Clinical Implications. Frontiers Media SA, 2020. http://dx.doi.org/10.3389/978-2-88966-222-7.

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Publications, ICON Health. The Official Patient's Sourcebook on Bacterial Vaginosis: A Revised and Updated Directory for the Internet Age. Icon Health Publications, 2002.

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F, Easmon C. S., ed. The diagnosis and management of bacterial vaginosis: Proceedings of a Round Table meeting held at Robinson College, Cambridge, on 4 July 1993. London: Royal Society of Medicine Services, 1993.

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Török, M. Estée, Fiona J. Cooke, and Ed Moran. Sexually transmitted infections. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199671328.003.0018.

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This chapter covers the diagnosis and management of sexually transmitted infections, including bacterial vaginosis, with causes including vaginal discharge, vulvovaginal candidiasis, and trichomoniasis. The chapter also covers vulvovaginal candidiasis, genital warts or anogenital warts caused by human papillomavirus, tropical genital ulceration (which is commoner in patients presenting with sexually transmitted infections in the developing world and is an important factor in the spread of HIV), genital herpes, pelvic inflammatory disease, toxic shock syndrome, gonorrhoea, chlamydia, trichomoniasis, and syphilis.
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Holst, John. Pelvic Inflammatory Disease and Tubo-Ovarian Abscess. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199976805.003.0040.

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Pelvic inflammatory disease (PID) consists of inflammation in various parts of the upper genital tract and includes endometritis, salpingitis, tubo-ovarian abscess (TOA), and/or pelvic peritonitis. Overt acute PID patients typically present as ill-appearing with pain, fever, chills, purulent vaginal discharge, nausea, vomiting, and elevated white blood cells. “Silent” PID presents with dyspareunia, irregular bleeding, and urinary and gastrointestinal complaints. Bacterial vaginosis (BV) and associated microorganisms are present in acute PID patients. PID coverage is focused on a polymicrobial infection. HIV patients typically have more severe symptoms and are more likely to have a TOA than an immunocompetent patient, but HIV alone does not mandate hospital admission nor does parenteral therapy improve outcomes compared to non-HIV patients. Gonorrhea and chlamydia cases must be reported to the local health department; it is not mandatory for PID patients to remove an intrauterine device at the time of diagnosis.
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Book chapters on the topic "Ethanol Vaginosis, Bacterial Vaginosis, Bacterial"

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Sonnex, Christopher. "Bacterial Vaginosis." In In Clinical Practice, 17–23. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-21638-6_4.

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Eschenbach, David A. "Bacterial Vaginosis." In Sexually Transmitted Diseases and Adverse Outcomes of Pregnancy, 101–23. Washington, DC, USA: ASM Press, 2014. http://dx.doi.org/10.1128/9781555818210.ch7.

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Rubins, A. "Bacterial Vaginosis." In Sexually Transmitted Infections and Sexually Transmitted Diseases, 203–6. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14663-3_19.

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Rosca, Aliona, and Nuno Cerca. "Bacterial Vaginosis." In Diagnostics to Pathogenomics of Sexually Transmitted Infections, 257–75. Chichester, UK: John Wiley & Sons, Ltd, 2018. http://dx.doi.org/10.1002/9781119380924.ch13.

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Sobel, Jack D. "Bacterial Vaginosis." In Sexually Transmitted Infections in HIV-Infected Adults and Special Populations, 165–74. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-56694-8_9.

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Piot, Peter. "Bacterial Vaginosis." In Laboratory Diagnosis of Infectious Diseases, 94–99. New York, NY: Springer New York, 1988. http://dx.doi.org/10.1007/978-1-4612-3898-0_9.

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Fujisaki, Midori. "Bacterial Vaginosis." In Preterm Labor and Delivery, 175–80. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-9875-9_18.

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Marrazzo, Jeanne M. "Bacterial Vaginosis." In Sexually Transmitted Diseases, 54–63. Oxford, UK: Wiley-Blackwell, 2012. http://dx.doi.org/10.1002/9781118314937.ch7.

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Tao, Lin, Sylvia I. Pavlova, and Ali O. Kiliç. "Phages and Bacterial Vaginosis." In Phages, 256–79. Washington, DC, USA: ASM Press, 2014. http://dx.doi.org/10.1128/9781555816506.ch13.

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De Seta, Francesco, Manola Comar, Secondo Guaschino, and Bryan Larsen. "Bacterial Vaginitis and Vaginosis." In Sexually Transmitted Infections, 277–94. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-02200-6_14.

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Conference papers on the topic "Ethanol Vaginosis, Bacterial Vaginosis, Bacterial"

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Baker, Yolanda S., Rajeev Agrawal, James A. Foster, Daniel Beck, and Gerry Dozier. "Detecting bacterial vaginosis using machine learning." In the 2014 ACM Southeast Regional Conference. New York, New York, USA: ACM Press, 2014. http://dx.doi.org/10.1145/2638404.2638521.

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Lokken, E. "S01.2 Bacterial vaginosis, vaginal microbiota, and fecundability." In Abstracts for the STI & HIV World Congress, July 14–17 2021. BMJ Publishing Group Ltd, 2021. http://dx.doi.org/10.1136/sextrans-2021-sti.20.

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Baker, Yolanda S., Rajeev Agrawal, James A. Foster, Daniel Beck, and Gerry Dozier. "Applying machine learning techniques in detecting Bacterial Vaginosis." In 2014 International Conference on Machine Learning and Cybernetics (ICMLC). IEEE, 2014. http://dx.doi.org/10.1109/icmlc.2014.7009123.

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Eleuterio, Renata Mirian Nunes, José Eleutério Junior, Paulo Giraldo, Ana Katherine Gonçalves, Beatriz Gordiano Valente, and Fernanda Queiroz. "P5.28 Diagnosis of bacterial vaginosis with affirm vpiii." In STI and HIV World Congress Abstracts, July 9–12 2017, Rio de Janeiro, Brazil. BMJ Publishing Group Ltd, 2017. http://dx.doi.org/10.1136/sextrans-2017-053264.644.

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Lithgow, K., V. Buchholz, S. Konschuh, and L. Sycuro. "O02.5 Secreted Proteolytic Activity of Bacterial Vaginosis-Associated Bacteria." In Abstracts for the STI & HIV World Congress, July 14–17 2021. BMJ Publishing Group Ltd, 2021. http://dx.doi.org/10.1136/sextrans-2021-sti.60.

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Muzny, Christina, Kristal Aaron, Angela Pontius, Cheri Aycock, and Jane Schwebke. "P375 Risk factors for incident bacterial vaginosis among heterosexual women." In Abstracts for the STI & HIV World Congress (Joint Meeting of the 23rd ISSTDR and 20th IUSTI), July 14–17, 2019, Vancouver, Canada. BMJ Publishing Group Ltd, 2019. http://dx.doi.org/10.1136/sextrans-2019-sti.477.

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Mitchell, Caroline. "S17.2 Treatment of bacterial vaginosis: how, when and how much?" In Abstracts for the STI & HIV World Congress (Joint Meeting of the 23rd ISSTDR and 20th IUSTI), July 14–17, 2019, Vancouver, Canada. BMJ Publishing Group Ltd, 2019. http://dx.doi.org/10.1136/sextrans-2019-sti.78.

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Carter, Joi, Daniel Beck, Henry Williams, Gerry Dozier, and James A. Foster. "GA-based selection of vaginal microbiome features associated with bacterial vaginosis." In GECCO '14: Genetic and Evolutionary Computation Conference. New York, NY, USA: ACM, 2014. http://dx.doi.org/10.1145/2576768.2598378.

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Beamer, May, Leslie Meyn, Melinda Petrina, Lisa Cosentino, Hilary Avolia, Michele Austin, Allison Demarco, Victoria Gould, and Sharon Hillier. "P365 Microbial risk factors for acquisition of symptomatic Bacterial Vaginosis (BV)." In Abstracts for the STI & HIV World Congress (Joint Meeting of the 23rd ISSTDR and 20th IUSTI), July 14–17, 2019, Vancouver, Canada. BMJ Publishing Group Ltd, 2019. http://dx.doi.org/10.1136/sextrans-2019-sti.467.

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Mbugua, Njeri, Elizabeth Ann Bukusi, and Waiyaki Peter. "P3.172 Bacterial vaginosis: risk factors among kenyan women and their male partners." In STI and HIV World Congress Abstracts, July 9–12 2017, Rio de Janeiro, Brazil. BMJ Publishing Group Ltd, 2017. http://dx.doi.org/10.1136/sextrans-2017-053264.407.

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