Literatura académica sobre el tema "Oral Candidiasis"
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Artículos de revistas sobre el tema "Oral Candidiasis"
Marroquín-Remón, Rosmin y Patricia Chang. "Candidiasis oral". Revista médica (Colegio de Médicos y Cirujanos de Guatemala) 160, n.º 3 (8 de diciembre de 2021): 333–36. http://dx.doi.org/10.36109/rmg.v160i3.370.
Texto completoDellinger, Tracy M. y H. Mark Livingston. "Oral Candidiasis". Annals of Pharmacotherapy 37, n.º 10 (octubre de 2003): 1529. http://dx.doi.org/10.1345/aph.1d125.
Texto completoRay, Thomas L. "Oral Candidiasis". Dermatologic Clinics 5, n.º 4 (octubre de 1987): 651–62. http://dx.doi.org/10.1016/s0733-8635(18)30708-3.
Texto completoPeterson, Douglas E. "Oral Candidiasis". Clinics in Geriatric Medicine 8, n.º 3 (agosto de 1992): 513–28. http://dx.doi.org/10.1016/s0749-0690(18)30461-0.
Texto completoMillsop, Jillian W. y Nasim Fazel. "Oral candidiasis". Clinics in Dermatology 34, n.º 4 (julio de 2016): 487–94. http://dx.doi.org/10.1016/j.clindermatol.2016.02.022.
Texto completoAkpan, A. "Oral candidiasis". Postgraduate Medical Journal 78, n.º 922 (1 de agosto de 2002): 455–59. http://dx.doi.org/10.1136/pmj.78.922.455.
Texto completoLynch, Denis P. "Oral candidiasis". Oral Surgery, Oral Medicine, Oral Pathology 78, n.º 2 (agosto de 1994): 189–93. http://dx.doi.org/10.1016/0030-4220(94)90146-5.
Texto completoRavić-Nikolić, Ana. "Oral candidiasis". Galenika Medical Journal 1, n.º 4 (2022): 48–52. http://dx.doi.org/10.5937/galmed2204050r.
Texto completoLimbhore, Mayur Vilas, Shandilya Ramanojam, Pallavi Rathi, Vikrant Sane y Adil Mevawala. "ORAL CANDIDIASIS: AN OVERVIEW AND CASE REPORT". Era's Journal of Medical Research 6, n.º 2 (diciembre de 2019): 160–66. http://dx.doi.org/10.24041/ejmr2019.147.
Texto completoKim, Chorok y Jihyun Song. "Association between Candidiasis and Early Childhood Caries : Analysis Using Healthcare Big Data". JOURNAL OF THE KOREAN ACADEMY OF PEDTATRIC DENTISTRY 47, n.º 4 (30 de noviembre de 2020): 359–67. http://dx.doi.org/10.5933/jkapd.2020.47.4.359.
Texto completoTesis sobre el tema "Oral Candidiasis"
Samaranayake, Yuthika Hemamala. "Pathogenic attributes of candida krusei with particular reference to the oral cavity". Thesis, Hong Kong : University of Hong Kong, 1995. http://sunzi.lib.hku.hk/hkuto/record.jsp?B14024494.
Texto completoNaglik, Julian Richard. "Candida albicans secreted aspartyl proteinases and human mucosal candidiasis". Thesis, King's College London (University of London), 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.271292.
Texto completoQueiroz, Vanessa Cristina Pin Piazentin. "Avaliação do potencial antifúngico de própolis de Apis mellifera contra leveduras do gênero Candida". [s.n.], 2010. http://repositorio.unicamp.br/jspui/handle/REPOSIP/288528.
Texto completoDissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba
Made available in DSpace on 2018-08-16T16:26:49Z (GMT). No. of bitstreams: 1 Queiroz_VanessaCristinaPinPiazentin_M.pdf: 4355114 bytes, checksum: 2e7009da410cba032963dee4cd9aa7ac (MD5) Previous issue date: 2010
Resumo: A candidíase oral é uma infecção fúngica que tem sido relatada como problema de saúde pública e em decorrência de um crescente índice de cepas resistentes de Candida spp., tem-se aumentado o interesse em produtos naturais como fonte de novos compostos bioativos. Neste sentido, a própolis brasileira apresenta importantes propriedades farmacológicas como antimicrobiana e poderia ser estudada quanto à sua atividade antifúngica. Assim, o objetivo deste trabalho foi avaliar a atividade anti-Candida de três tipos de própolis brasileiras contra formas planctônicas e em biofilme de Candida spp. de maiores incidências em patologias da cavidade oral. Foram utilizados três tipos de própolis selecionadas por suas propriedades antimicrobianas em estudos prévios, os quais estão classificadas na literatura como: tipo 3 (interior do estado do Paraná), tipo 6 (região de mata atlântica do estado da Bahia) e tipo 13 (região de mangue da cidade de Maceió, estado de Alagoas). Para cada tipo de própolis foram obtidos o extrato etanólico (EEP) e suas respectivas frações com diferentes gradientes de polaridade (hexano, diclorometano e acetato de etila). Aos EEP e respectivas frações foram aplicadas as seguintes metodologias para avaliação da atividade antifúngica contra Candida spp. de forma a conduzir um estudo bioguiado: 1- Determinação da Concentração Inibitória Mínima (CIM) e Concentração Fungicida Mínima (CFM) dos EEP dos tipos 3, 6 e 13 e frações hexânica (fr-hex), diclorometânica (fr-dicloro) e acetato de etila (fr-acet) contra as formas planctônicas das leveduras, obtidas de um banco internacional de cepas Centraalbureau voor Schimmelcultures (CBS): Candida albicans (CBS 562), Candida dubliniensis (CBS 7987), Candida glabrata (CBS 07), Candida krusei (CBS 573), Candida parapsilosis (CBS 604), Candida tropicalis (CBS 94), pelo método da microdiluição. 2- Determinação da CIM das própolis 3 e 13 (EEP e respectivas frações diclorometânicas) sobre biofilmes em pré-adesão. 3- Verificação de possíveis alterações ou danos na estrutura celular das leveduras quando submetidas às própolis 3 e 13 (EEP e respectivas frações diclorometânicas) pela Microscopia Eletrônica de Varredura (MEV) em biofilmes em pré-adesão e formados. De maneira geral, as própolis dos tipos 3 e 13 demonstraram forte atividade anti-Candida contra as leveduras analisadas (valores mínimos e máximos de CIM 4,0 e 31,3 µg/mL para EEP da própolis 3 e 1,0 e 7,8 µg/mL para EEP da própolis 13) em relação a do tipo 6 que demonstrou baixa atividade. O EEP tipo 13 e respectiva fr-dicloro se destacaram, por apresentarem efeito fungicida contra todas as cepas analisadas com valores mínimos e máximos de CFM 125 e 500 µg/mL para a fr-dicloro tipo 13. As própolis 3 e 13 (EEP e respectivas fr-dicloro) apresentaram atividade anti-biofilme em pré-adesão com valores máximos de 250 µg/mL para EEP tipo 3 (C. parapsilosis) e 250 µg/mL para fr-dicloro tipo 3 (C. parapsilosis) e CIM 125 µg/mL para EEP tipo 13 (C. tropicalis) e 31,3 µg/mL para fr-dicloro tipo 13 (C. parapsilosis). As imagens de MEV mostram a interferência dos EEP tipos 3 e 13 e respectivas fr-dicloro sobre biofilmes em pré-adesão, entretanto as própolis não foram capazes de desagregar completamente os biofilmes formados de Candida spp se comparadas ao grupo controle (Nistatina). Conclui-se que os três tipos de própolis estudadas apresentaram atividade anti-Candida tanto em organização planctônica quanto em biofilme, entretanto, a fração diclorometânica da própolis do tipo 13 é a fração ativa, que contém importantes compostos efetivos contra Candida spp. e pode ser fonte de novos princípios bioativos para prevenção ou tratamento da candidíase oral, a qual deve ser objeto de estudos futuros
Abstract: Oral candidiasis is a fungal infection that has been reported as a public health problem and due to increased rate of resistant strains of Candida spp. has increased the interest in natural products as sources for new bioactive compounds. Brazilian propolis have important biological properties such as antimicrobial and anticariogenic activity, thus antifungal activity could also be evaluated. The aim of this study was to evaluate the anti-Candida activity of three Brazilian propolis against planktonic and biofilm forms of Candida spp. of higher incidences in oral cavity diseases.Three types of propolis were selected for antimicrobial properties in previous studies, which are classified in the literature as type 3 (within the state of Parana state), type 6 (Atlantic Rainforest of Bahia state) and type 13 (mangrove region, Maceió city, Alagoas state). For each type of propolis were obtained the ethanolic extract (EEP) and respective fractions with different gradient polarity (hexane, dichloromethane and ethyl acetate). The following methodologies were applied on EEP and correspondent fractions to evaluate antifungal activity against Candida spp. by a bioguided study: 1 - Determination of Minimum Inhibitory Concentration (MIC) and Minimum Fungicidal Concentrations (MFC) of EEP types 3, 6 and 13 and hexane (hex-fr), dichloromethane (dichlo-fr) and ethyl acetate (ethyl-fr) against planktonic forms of yeasts from an international bank Centraalbureau voor Schimmelcultures (CBS): Candida albicans (CBS 562), Candida dubliniensis (CBS 7987), Candida glabrata (CBS 07), Candida krusei (CBS 573), Candida parapsilosis (CBS 604), Candida tropicalis (CBS 94) using the microdilution method. 2 - Determination of MIC of propolis 3 and 13 (EEP and dichloromethane fractions) on preformed biofilm. 3 - Verification of possible changes or damages of the yeast cell structure when subjected to 3 and 13 propolis (EEP and dichloromethane fractions) by Scanning Electron Microscopy (SEM) in preformed and mature biofilms. In most cases, propolis types 3 and 13 demonstrated strong anti-Candida activity against the yeasts tested (minimum and maximum MIC values 4.0 and 31.3 µg/mL for EEP type 3 and 1.0 and 7.8 µg/mL for EEP type 13 compared to the low effect of propolis type 6. EEP type 13 and respective dichlo-fr had the best fungicidal effect against all strains (minimum and maximum MFC values 125 and 500 µg/mL). EEP type 3 and 13 and their dichlo-fr presented anti-biofilm activity 250 µg/mL for EEP type 3 (C. parapsilosis), 250 µg/mL for dichlo-fr type 3 (C. parapsilosis) and (maximum MIC 125 µg/mL for EEP type 13 (C. tropicalis), 31.3 µg/mL for dichlo-fr type 13 (C. parapsilosis). SEM images show the influence of propolis samples on preformed biofilms, however these samples were not capable of completely disrupting the mature biofilms, if compared to control (Nistatin). Thus, we concluded that the three types of propolis studied presented anti-Candida activity both in organization and in planktonic biofilm, however, the dichloromethane fraction of propolis type 13 is the active fraction, which contains important compounds effective against Candida spp. and could be a source of new bioactive principles for prevention or alternative treatment of oral candidiasis, which should be the object of future studies
Mestrado
Farmacologia, Anestesiologia e Terapeutica
Mestre em Odontologia
Jurevic, Richard Joseph. "Genetic variations in human beta defensin genes and their relationship to oral health and disease /". Thesis, Connect to this title online; UW restricted, 2004. http://hdl.handle.net/1773/6386.
Texto completoAlbougy, Hany Ahed. "A systematic review of the management of oral candidiasis associated with HIV/AIDS". Thesis, Stellenbosch : Stellenbosch University, 2002. http://hdl.handle.net/10019.1/52713.
Texto completoThesis (MSc)--Stellenbosch University, 2002.
ENGLISH ABSTRACT: The purpose of this review was to investigate the management of oral candidiasis in HIV/AIDS patients and to evaluate the different guidelines that are available for its management. To achieve this aim, three objectives were identified: (i) to identify and report on the different interventions used to manage oral candidiasis, in patients with HIV/AIDS, (ii) to determine the efficacy of these interventions, and (iii) to provide guidelines for management. A thorough systematic search of the literature was carried out and all relevant papers were graded into three levels of evidence (A, B, and C) and scored for quality according to set criteria. A number of topical and systemic antifungal medications are used to treat oral candidiasis in HIV-positive patients. These include the poleyne antibiotics, nystatin and amphotericin B. Milder episodes of oral candidiasis respond to topical therapy with nystatin, clotrimazole troches or oral ketoconazole. Fluconazole has been extensively evaluated as a treatment for candidiasis. With HIV-infection, a cure rate of 82% has been achieved with a daily oral dose of 50 mg. Fluconazole was found to be a better choice of treatment for relapsing oropharyngeal candidiasis, resulting in either better cure rates or better prevention of relapse. Intravenous amphotericin B has been found to be effective therapy in azole refractory candidiasis where it was shown to be safe and well tolerated. Topical therapies were found to be effective treatment for uncomplicated oropharyngeal candidiasis, however patients relapsed more quickly than those treated with oral systemic antifungal therapy. Overall, nystatin appears less effective than clotrimazole and the azoles in the treatment of oropharyngeal candidiasis. With regard to the resolution of clinical symptoms, clotrimazole was found to be just as effective as the azoles, except when patient compliance was poor. Fluconazole-treated patients were more likely to remain disease-free during the fluconazole follow-up period than with those treated with other interventions. Relatively few studies were qualified to address the provision of guidelines for the management of oral candidiasis in primary health care settings. Most of the studies found were of moderate and low quality level of evidence. These studies included the assessment of different guidelines for identification, treatment and dental needs. They stressed that patients with HN need dentists who will act as primary health care providers, together with other providers to ensure adequate overall care. Given the level of interest and importance of candidiasis associated with treatment of HN -positive patients, it is surprising to find that little high quality research has been undertaken. As such, it is hoped that this review would provide researchers, oral health care workers and other health care providers with an overview of the management of oral candidiasis associated with HN/AIDS.
AFRIKAANSE OPSOMMING: Die doelstelling van die oorsig was om ondersoek in te stel na die hantering van orale kandidiase in HIV/AIDS pasiënte asook om die verskillende beskikbare riglyne vir die behandeling daarvan te evalueer. Ter verwesenliking van hierdie doelstelling is drie doelwitte geïdentifiseer: (i) om die intervensies wat gebruik word in die hantering van orale kandidiase behandeling te identifiseer, (ii) om die effektiwiteit van hierdie intervensies te identifiseer en (iii) om op grond hiervan riglyne vir die hantering voor te stel. 'n Sistematiese literatuursoektog is uitgevoer en alle relevante artikels is in drie groepe geklassifiseer (A, B en C) op grond van die data kwaliteit. 'n Verskeidenheid topikale en sistemiese antifungale middels word gebruik om orale kandidiase in HIV-positiewe pasiënte te behandel. 'n Sukseskoers van 82% is met die gebruik van 'n daaglikse dosis van 50 mg medikament gerapporteer. Fluconazole was die beter keuse van middel vir die behandeling van terugkerende orofaringeale kandidiase. Topikale behandeling was effektief in die behandeling van ongekompliseerde orofaringeale kandidiase, hoewel die kans op terugkeer van die toestand groter was as met die sistemiese middels. Pasiënte wat met flukonasool behandel is, het 'n groter kans gehad om siektevry te bly vergeleke met pasiënte op die ander intervensies. Meeste van die studies was van middelmatige tot lae kwaliteit en gevolglik was dit moeilik om behandelingsriglyne te stel. Wat egter wel duidelik is, is dat HIV pasiënte primêre mondsorg benodig wat saam met ander versorging omvattende sorg sal verseker.
Schmidt-Westhausen, Andrea Maria. "Experimentelle Untersuchungen zur Pathogenese und Therapie der oralen Candidiasis bei Immundefizienz". Doctoral thesis, Humboldt-Universität zu Berlin, Medizinische Fakultät - Universitätsklinikum Charité, 2001. http://dx.doi.org/10.18452/13748.
Texto completoThis study applied an animal model to address the following questions: 1. Does a dose/effect relationship exist between C. albicans load and the emergence of an oral C. albicans infection, 2. which cellular immune response takes place following inoculation with defined pathogen loads, 3. is it possible to inhibit C. albicans adhesion to murine epithelium cells through the local application of mucine metabolites (glycopeptides). Material and methods: Immunocompetent inbred mice (Balb/c) (n=27) and mice with combined B- and T-cell defects (SCID) (n=30) were orally inoculated with pathogen loads between 10^4 and 10^8 C. albicans cells/10 microl (strain DSM 3454). Moreover, Balb/c mice (n=8) were inoculated with 10^8 C. albicans cells in combination with glycopeptides; SCID mice (n=8) were inoculated with 10^5 cells, also in combination with glycopeptides. One half of the tongue tissue was histochemically examined with the Periodic Acid Schiff (PAS) Method for displaying the invasion of hyphae. The other half of the tissue was examined by immune peroxidase technique for analysing the distribution of immunocompetent cells (CD4, CD13, ICAM-1, E-Selectin, CD74, CD80, CD86, CD103) in the epithelial layers and subepithelial connective tissue. Results: One week following the inoculation, neither group's tissue showed clinical signs of oral candidiasis. Following histochemical preparation (PAS-Reaction) the tongue mucosa showed signs of infection (hyphae) with the inoculation dose of 10^8 C. albicans cells in the case of Balb/c mice and a load of 10^5 pathogens in the case of SCID mice. The extent of the immunologic reaction depended both on the inoculation dose given to the animals and on their immune status. The results of an inoculation of 10^8 C. albicans cells in combination with glycopeptides showed hyphae invasion of the tongue epithelium in 2/8 Balb/c mice. Following an inoculation of 10^5 pathogens in combination with glycopeptides hyphae invasion could be demonstrated in 0/8 SCID mice. The results of immunohistochemical studies showed that the host's reaction to combined glycopeptide-pathogen-inoculation correspond to the reaction without inoculation. Conclusion: Despite the lack of clinical signs of oral candidiasis in neither group's tissue, non-apparent infections of the tongue epithelium were evident leading to immunologic reactions of the tongue mucosa. Inoculation of C. albicans cells in combination with glycopeptides resulted in decreased infection rate compared to a corresponding inoculation dose without glycopeptides. As no side effects have been documented for the oral application of these antiadhesive agents, their use as complimentary therapy for patients at an increased risk for oral candidiasis should be considered.
Paporn, Kaveewatcharanont. "The effect of fixed orthodontic appliances on the oral carriage of Candida species and coliforms in adolescents". Thesis, Hong Kong : University of Hong Kong, 1993. http://sunzi.lib.hku.hk/hkuto/record.jsp?B13436004.
Texto completoTorrealba, Durán Claudia Cecilia. "Susceptibilidad in vitro de levaduras del género cándida aisladas de un grupo de pacientes con candidiasis oral frente a azoles y polienos". Tesis, Universidad de Chile, 2007. http://repositorio.uchile.cl/handle/2250/139076.
Texto completoAutor no autoriza el acceso a texto completo de su documento
Las infecciones fúngicas son comúnmente provocadas por hongos del género Candida.(6) C.albicans es la especie más frecuente(17)y en menor proporción otras como:glabrata, tropicalis y krusei. (8) Candida dubliniensis es una nueva especie identificada recientemente de cavidad oral en pacientes VIH.Estudios recientes muestran un notable incremento en el diagnóstico de Candidiasis orales(8),debido a diferentes factores facilitadores.(5,9) Así,el objetivo de este trabajo fue determinar la susceptibilidad “in vitro” de levaduras del género Candida, aisladas de pacientes chilenos con Candidiasis oral, a Nistatina, Fluconazol, Itraconazol y Voriconazol.Nuestra hipótesis plantea que la susceptibilidad de levaduras del género Candida, (Candida albicans y Candida no albicans,) aisladas de pacientes con Candidiasis oral dependen tanto de la especie de Candida como del antifúngico empleado (Azoles y Polienos). El estudio incluyó 74 cepas tales como; 41 Candida albicans,16 Candida dubliniensis,6 Candida glabrata,4 Candida famata,3 Candida krusei, 2 Candida lusitanie y 1 Candida.parapsilosis agrupadas en Candida albicans y Candida no albicans (n=33) que fueron evaluados por el método de microdilución en caldo según el documento M27-A (NCCLS)(13) Candida albicans (n=41)fueron sensibles a Fluconazol y 27 (n=33) Candida no albicans.Las especies no sensibles a Fluconazol fueron albicans, glabrata y krusei.38 Candida albicans (n=41) y 26 cepas de Candida no albicans (n=33) fueron sensibles a Itraconazol.Las especies no sensibles a Itraconazol fueron albicans, glabrata, lusitanie y dubliniensis . Las 74 especies, tanto Candida albicans como Candida no albicans, fueron sensibles a Voriconazol y Nistatina. Con el análisis estadísticos se concluyó que la susceptibilidad de levaduras del género Candida, agrupadas en Candida albicans y Candida no albicans, aisladas de pacientes chilenos con Candidiasis oral, depende tanto de la especie de Candida como del antifúngico empleado (Azoles y Polienos). (p=0,014).
Al-Dwairi, Ziad Nawaf. "Risk factors associated with oral candidiasis in elderly diabetic and non-diabetic patients wearing removable acrylic prostheses". Thesis, Queen's University Belfast, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.394634.
Texto completoFerreira, Elisangela Noborikawa. "Estudo comparativo de dois meios cromogênicos para identificação de espécies do gênero Candida, isoladas da mucosa oral de pacientes portadores de próteses totais completas ou uni maxilares superiores, com ou sem suspeita de candidíase oral". Universidade de São Paulo, 2011. http://www.teses.usp.br/teses/disponiveis/23/23139/tde-06032012-170254/.
Texto completoThe genus Candida includes several species of medical importance and although some will acquire increasing interest, Candida albicans remains the most important and responsible for more infections. Found in the microbiota of healthy humans, is responsible for the most common oral fungal infection in very close relation with denture stomatitis (EP). This is a frequent inflammation of the oral mucosa in complete or partial dentures wearers, where may also be present other microorganisms, interacting with several factors linked to the host and the microorganisms present themselves, in the inner surface of the biofilm of the prostheses. Most cases are asymptomatic and some patients report pain, itching or burning sensation. The diagnosis is clinical, supplemented by tests such as cytological and mycological. Treatment is often empiric, with no clear certainty whether the individual is only a carrier of yeast and if other species are involved. The chromogenic media enabled advances in the diagnosis of oral candidiasis. Its use facilitates the identification of these yeasts, resulting in less time than those of already standardized methods for other species of Candida. The CHROMagar Candida (CC) is the reference, providing results in 48 hours from the material collection. The medium called Chromogenic Candida Agar (CCA) was recently launched in our market and in view of its low cost seems to be one more tool for the diagnosis of candidiasis, although there is a lack of literature available on it. The objective of this study was to compare this new medium to CHROMagar Candida for sensitivity and specificity in the isolation of species of genus Candida from the oral mucosa of patients with upper dentures with or without symptoms of EP. Sixty one patients of both genders were recruited wearing complete dentures (45.9%) or uni upper jaw (54.1%) prostheses. Among the 61 samples, 45 (73.77%) were positive for yeasts in CC, and C. albicans (38 samples, 24 unique and 14 (36.84%) mixed. From these, 8 of C. albicans + C. tropicalis (21.05%), 3 of C. albicans + C. glabrata (7.89%), 3 of C. tropicalis + C. albicans + C. glabrata (7.89%). Other species were present, being 15 C. tropicalis (33.33%). Two unique isolates (13.33%), two mixed: C. tropicalis + C. glabrata (13.33%) and C. tropicalis + C. parapsilosis (6.66%). In CCA, from the 45 samples, 39 were positive (86.6%). C. albicans was the most frequent, with 33 isolates (84.6%), being unique in 25 (75.75%) and eight in mixed cultures (24.25%). Thus, C. albicans + C. tropicalis (5 - 12.82%); C. albicans + C. glabrata (2 - 5.13%), C. tropicalis + C. albicans + C. glabrata (1- 2.56%). Other species isolated were C. tropicalis (3 7.7%) and C. glabrata, C. krusei and C. parapsilosis (one of each - 2.56%). It was possible to conclude that CHROMagar Candida was more sensitive (100% vs. 65%) and more specific for C. albicans (84.4% vs. 73.3%), C. tropicalis (33.3% vs. 20.0%) and C. glabrata (17.7% vs. 8.8%). Both media showed the same specificity (2.2%), for C. krusei and C. parapsilosis.
Libros sobre el tema "Oral Candidiasis"
R, Tyldesley William, ed. Oral candidosis. Middlesex [Eng]: E.R. Squibb, 1985.
Buscar texto completoRosa, Edvaldo Antonio Ribeiro. Oral Candidosis: Physiopathology, Decision Making, and Therapeutics. Springer, 2015.
Buscar texto completoRosa, Edvaldo Antonio Ribeiro. Oral Candidosis: Physiopathology, Decision Making, and Therapeutics. Springer, 2016.
Buscar texto completoLevine, Steven. Herbs for Oral Thrush: Complete Guide on How to Treat Oral Candidiasis Using Natural Remedies. Independently Published, 2021.
Buscar texto completoGerd, Mindel. Miconazole: Cure for Vaginal Candidiasis, Jock Itch, Skin Infection, Oral Thrush. Independently Published, 2018.
Buscar texto completoP, Samaranayake Lakshman y MacFarlane T. Wallace, eds. Oral candidosis: Edited by Lakshman P. Samaranayake, T. Wallace MacFarlane ; with a foreword by Jen J. Pindborg. London: Wright, 1990.
Buscar texto completoRose, Canida. Metronidazole: Cure for Most Bacterial and Fungi Infection Like Bacterial Vaginosis, Oral Candidiasis and Thrush. Independently Published, 2018.
Buscar texto completoCrack, Jader. Ketoconazole: Ultimate Treatment for Fungal Infection Like Oral Thrush, Candidiasis, Toe Nail Infection, Jock Itch. Independently Published, 2018.
Buscar texto completoJack, Jery. Metronidazole: Treatment of Bacteria and Fungi Infection Like Vaginosis, Candidiasis, Oral Thrush and Skin Rash. Independently Published, 2018.
Buscar texto completoKoto, Cori. Metronidazole: Medication for the Treatment of Parasitic, Bacteria, Fungi Infection Like Bacterial Vaginosis, Candidiasis, Oral Thrush. Independently Published, 2018.
Buscar texto completoCapítulos de libros sobre el tema "Oral Candidiasis"
De Rossi, Scott S. y Katharine Ciarrocca. "Oral Candidiasis". En Orofacial Disorders, 53–60. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-51508-3_6.
Texto completoGelwan, Jeffrey S., Burton M. Gold, Henry J. Shih y Crescens Pellecchia. "Oral candidiasis and AIDS". En Acquired Immunodeficiency Syndrome, 123–24. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4613-0807-2_35.
Texto completoRezaei, Nima. "Oral Ulcers and Candidiasis". En Pediatric Immunology, 259–63. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-21262-9_51.
Texto completoKragelund, Camilla, Jesper Reibel y Anne Marie Lynge Pedersen. "Management of Patients with Oral Candidiasis". En Oral Infections and General Health, 137–44. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-25091-5_13.
Texto completoDongari-Bagtzoglou, Anna. "Innate Defense Mechanisms in Oral Candidiasis". En Fungal Immunology, 13–35. Boston, MA: Springer US, 2005. http://dx.doi.org/10.1007/0-387-25445-5_2.
Texto completoÖner, Ümran, Fatih Öner, Cemal Cingi y Torello M. Lotti. "Oral Candidiasis in Infants and Children". En Pediatric ENT Infections, 489–501. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-80691-0_42.
Texto completoKragelund, Camilla, Jesper Reibel y Anne Marie Lynge Pedersen. "Oral Candidiasis and the Medically Compromised Patient". En Oral Infections and General Health, 65–77. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-25091-5_8.
Texto completoJunqueira, Juliana Campos. "Models Hosts for the Study of Oral Candidiasis". En Advances in Experimental Medicine and Biology, 95–105. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-5638-5_10.
Texto completoAshman, Robert B. y Camile S. Farah. "Oral Candidiasis: Clinical Manifestations and Cellular Adaptive Host Responses". En Fungal Immunology, 59–83. Boston, MA: Springer US, 2005. http://dx.doi.org/10.1007/0-387-25445-5_4.
Texto completoChallacombe, Stephen J., Durdana Rahman, Mukesh Mistry y Julian R. Naglik. "Humoral Factors in the Protection of the Oral Cavity against Candidiasis". En Fungal Immunology, 37–57. Boston, MA: Springer US, 2005. http://dx.doi.org/10.1007/0-387-25445-5_3.
Texto completoActas de conferencias sobre el tema "Oral Candidiasis"
SEVBITOV, Andrey, Aleksey DOROFEEV, Sergey MIRONOV, Samer AL-KHOURY y Anton TIMOSHIN. "PREVENTION OF CANDIDIASIS IN PATIENTS USING REMOVABLE DENTURES". En SOUTHERN BRAZILIAN JOURNAL OF CHEMISTRY 2021 INTERNATIONAL VIRTUAL CONFERENCE. DR. D. SCIENTIFIC CONSULTING, 2022. http://dx.doi.org/10.48141/sbjchem.21scon.04_abstract_sevbitov.pdf.
Texto completoFemilian, Afryla. "Salivary Calprotectin in Patient With Oral Candidiasis". En 4th International Conference on Sustainable Innovation 2020–Health Science and Nursing (ICoSIHSN 2020). Paris, France: Atlantis Press, 2021. http://dx.doi.org/10.2991/ahsr.k.210115.060.
Texto completoBaggott, R., S. Glavey, M. Power y A. O'Regan. "Prevalence of Oral Candidiasis at Bronchoscopy and Response to Treatment." En American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a2591.
Texto completoKhan, Sanober, B. H. Harshitha Gowda, R. Deveswaran, Sweekriti Mishra y Anoop Sharma. "Comparison of fluconazole and tea tree oil hydrogels designed for oral candidiasis: An invitro study". En PROCEEDINGS OF INTERNATIONAL CONFERENCE ON ADVANCES IN MATERIALS RESEARCH (ICAMR - 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0022601.
Texto completoPierce, Christine M., Stephanie Hogue, Shirlene Paul, Bo-Young Hong, Wildson Vieira da Silva, Maria F. Gomez, Anna R. Giuliano, Jimmy J. Caudell y George M. Weinstock. "Abstract 3326: Mucositis, candidiasis, and associations with the oral microbiome in treatment naive patients with oropharyngeal cancer". En Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-3326.
Texto completoPierce, Christine M., Stephanie Hogue, Shirlene Paul, Bo-Young Hong, Wildson Vieira da Silva, Maria F. Gomez, Anna R. Giuliano, Jimmy J. Caudell y George M. Weinstock. "Abstract 3326: Mucositis, candidiasis, and associations with the oral microbiome in treatment naive patients with oropharyngeal cancer". En Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-3326.
Texto completoTozzo, Ana Claudia, Iasmine Guardia Dos Santos, Fabiane Froes Mattiuzi y Alcione De Oliveira Dos Santos. "FATORES ASSOCIADOS A CANDIDÍASE VAGINAL RECORRENTE". En I Congresso Brasileiro de Doenças Infectocontagiosas On-line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/2173.
Texto completoInformes sobre el tema "Oral Candidiasis"
Hu, Qiaoyu y Na Liu. A meta-analysis of the efficacy of photodynamic therapy for oral candidiasis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, diciembre de 2022. http://dx.doi.org/10.37766/inplasy2022.12.0053.
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