Добірка наукової літератури з теми "Mucosa Orale"
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Статті в журналах з теми "Mucosa Orale"
Attuati, Sara, Valeria Martini, Riccardo Mauro Bonacina, and Umberto Mariani. "Neoformazione ulcerata della mucosa orale." Dental Cadmos 87, no. 04 (April 2019): 197. http://dx.doi.org/10.19256/d.cadmos.04.2019.03.
Повний текст джерелаDi Iorio, E. "Lesione esofitica della mucosa orale." Dental Cadmos 85, no. 06 (June 2017): 327. http://dx.doi.org/10.19256/d.cadmos.06.2017.04.
Повний текст джерелаBeauvillain de Montreuil, C., M. H. Tessier, and J. Billet. "Patologia benigna della mucosa orale." EMC - Otorinolaringoiatria 11, no. 3 (September 2012): 1–20. http://dx.doi.org/10.1016/s1639-870x(12)62051-0.
Повний текст джерелаBeauvillain de Montreuil, C., M. H. Tessier, and J. Billet. "Patologia benigna della mucosa orale." EMC - Otorinolaringoiatria 18, no. 2 (June 2019): 1–23. http://dx.doi.org/10.1016/s1639-870x(19)42040-0.
Повний текст джерелаDi lorio, E. "Pigmentazioni multiple della mucosa orale." Dental Cadmos 83, no. 7 (September 2015): 443–44. http://dx.doi.org/10.1016/s0011-8524(15)30062-3.
Повний текст джерелаBaart, J. A. "Oral medicine 6. Ulceraties van de orale mucosa." Nederlands Tijdschrift voor Tandheelkunde 120, no. 05 (May 10, 2013): 246–49. http://dx.doi.org/10.5177/ntvt.2013.05.12242.
Повний текст джерелаGrande, Francesco, and Claudio Marchetti. "Bolle ematiche ricorrenti sulla mucosa orale." Dental Cadmos 87, no. 01 (September 2019): 541. http://dx.doi.org/10.19256/d.cadmos.09.2019.03.
Повний текст джерелаMORO, A., C. DE WAURE, F. DI NARDO, F. SPADARI, M. D. MIGNOGNA, M. GIULIANI, L. CALIFANO, et al. "Il dispositivo medico GOCCLES® è in grado di individuare displasie e cancro orale se impiegato nel setting odontoiatrico. Risultati da uno studio multicentrico." Acta Otorhinolaryngologica Italica 35, no. 6 (December 2015): 449–54. http://dx.doi.org/10.14639/0392-100x-922.
Повний текст джерелаRooijers, W. "Medicaments and oral healthcare. Adverse effects of medications on the oral mucosa." Nederlands Tijdschrift voor Tandheelkunde 127, no. 07/08 (July 3, 2020): 434–40. http://dx.doi.org/10.5177/ntvt.2020.07/08.20007.
Повний текст джерелаMeleti, M., B. Bianchi, E. Merigo, M. Manfredi, R. Guidotti, C. Fornaini, A. Sarraj, G. Mergoni, L. Corcione, and P. Vescovi. "Pigmentazioni maculari acquisite delle labbra e della mucosa orale." Dental Cadmos 79, no. 2 (February 2011): 59–60. http://dx.doi.org/10.1016/j.cadmos.2010.11.001.
Повний текст джерелаДисертації з теми "Mucosa Orale"
Kinikoglu, Fatma Beste. "Tissue engineering of full-thickness human oral mucosa." Thesis, Lyon 1, 2010. http://www.theses.fr/2010LYO10310.
Повний текст джерелаTissue engineered human oral mucosa has the potential to fill tissue deficits caused by facial trauma or malignant lesion surgery. It can also help elucidate the biology of oral mucosa and serve as an alternative to in vivo testing of oral care products. The aim of this thesis was to construct a tissue engineered full-thickness human oral mucosa closely mimicking the native tissue. To this end, the feasibility of the concept was tested by co-culturing fibroblasts and epithelial cells isolated from normal human oral mucosa biopsies in a collagen-glycosaminoglycan-chitosan scaffold, developed in our laboratory to construct a skin equivalent. An oral mucosal equivalent closely mimicking the native one was obtained and characterized by histology, immunohistochemistry and transmission electron microscopy. Using the same model, the influence of mesenchymal cells on oral epithelial development was investigated by culturing epithelial cells on lamina propria, corneal stroma and dermal equivalents. They were found to significantly influence the thickness and the ultrastructure of the epithelium. Finally, in order to improve the adhesiveness of conventional scaffolds, an elastin-like recombinamer (ELR) containing the cell adhesion tripeptide, RGD, was used in the production of novel bilayer scaffolds employing lyophilization and electrospinning. These scaffolds were characterized by mercury porosimetry, scanning electron microscopy and mechanical testing. In vitro tests revealed positive contribution of ELR on the proliferation of both fibroblasts and epithelial cells. It was thus possible to construct a viable oral mucosa equivalent using the principles of tissue engineering
Gualerzi, A. "ANALISI MORFOLOGICA DELLA MUCOSA ORALE CHERATINIZZATA UMANA NORMALE DOPO ESPOSIZIONE A STIMOLI ESOGENI." Doctoral thesis, Università degli Studi di Milano, 2013. http://hdl.handle.net/2434/215122.
Повний текст джерелаPloyon, Sarah. "Interactions entre muqueuse orale, salive et molécules de la flaveur." Thesis, Dijon, 2016. http://www.theses.fr/2016DIJOS037/document.
Повний текст джерелаThe role of saliva in food sensory perception is increasingly recognized, especially through physicochemical interactions occurring between salivary proteins and food components. This work focuses on the mucosal pellicle, a layer of salivary proteins anchored onto epithelial cells, and aims at characterizing interactions that may occur between the proteins of the mucosal pellicle and flavour compounds. For that purpose, an in vitro model of oral mucosa was developed. A stable cell line (TR146/MUC1) was obtaining by transfecting the TR146 cell line in order to express the membrane bound mucin MUC1. In order to form a salivary pellicle, confluent cells were incubated with human saliva. A higher retention of salivary MUC5B by TR146/MUC1 cells was observed compared to TR146 cells, emphasising the involvement of MUC1 in MUC5B anchoring to epithelial cells. The model was applied to the investigation of interactions between the oral mucosa and aroma molecules and tannins. Measurements of partition coefficients by GC-FID revealed 1- the role of hydration of the mucosa on the release of the most hydrophilic compounds, 2- the ability of cells to metabolize some aroma compounds, 3- the absence of effect of the mucosal pellicle itself on aroma release at the thermodynamic equilibrium. Oppositely, analyses by PTR-MS evidenced an effect of the mucosa and of the pellicle on aroma release kinetic. Interactions between proteins of the mucosal pellicle and tannins modified structural characteristics of the pellicle, especially the coating of cells by salivary MUC5B. Sensory relevance for the phenomena of aroma persistence and astringency, respectively, are discussed
GIOVANNACCI, ILARIA. "Quantificazione spettrofotometrica dell'autofluorescenza come potenziale strumento diagnostico per lesioni maligne della cute e della mucosa orale." Doctoral thesis, Università degli studi di Modena e Reggio Emilia, 2020. http://hdl.handle.net/11380/1211519.
Повний текст джерелаAutofluorescence (AF) is defined as the fluorescence emission observed when certain cell molecules are excited by UV or visible light of suitable wavelenghts. When a biologic molecule is illuminated at an excitation wavelength within the absorption spectrum of that molecule, it will absorb this energy and be activated from its ground state to an excited state. The molecule (fluorophore) can then relax back from the excited to the ground state by generating energy in the form of fluorescence, at emission wavelengths, which are longer than that of the excitation wavelength. The most important endogenous fluorophores are molecules widely distributed in cells and tissues, like proteins containing aromatic aminoacids, flavins and lipopigments. The main fluorophores of healthy skin are located in the epithelium (eg. keratin, nicotinamide adenine dinucleotide or NADH and flavin adenine dinucleotide or FAD) and the submucosa (e.g. collagen and elastin). These molecules when irradiated between the wavelengths from 375 and 440 nm, show fluorescence in the green spectral range. Nonmelanoma skin cancer (NMSC) is the most common malignancy worldwide. The developement of NMSC is accompanied by histopathological changes in epidermis such as loss of cellular maturation, alteration in keratin production, overall thickening of the epithelial layer and biochemical alterations (NADH decrease). NMSC is also accompanied by histopathological changes in the underlying stroma and submucosa, including neovascularization and destruction of the collagen cross-link by proteases. These alterations lead to a general decrease in AF due the alteration in distribution of the fluorochromes and in particular to NADH and collagen. In the last two decades, studies concerning cell and tissue AF has had a dramatic increase. AF studies have been performed both in vitro and in vivo, for the study of normal tissue and for the discrimination between normal tissues and neoplastic lesions of oral mucosa, skin, esophagus, colon, lung, bronchi, brain and bladder. The methods used are both direct visual fluorescence examination (DVFE) and spectrophotometry. In particular, DVFE has been widely used for clinical studies on oral mucosa. Regarding AF of the skin, this has been studied more frequently by using spectrophotometry. The principle is scanning and analyzing reflected light from the skin after exposure to an activating light source. AF spectroscopy is a very sensitive technique for quantitative measurements of tissue constituents. However, to date no methods have emerged that can be translated into clinical practice. The primary objective of this study is to investigate the correlation between spectral mesurement of cutaneous AF and the histopathological characteristics of malignant and pre-malignant skin in NMSC. Following surgical removal of the cancer, an ex vivo evaluation of the AF will be performed. The specimen will be irradiated with a probe that emits a light in the blue spectrum (wavelength 400-440 nm) and the fluorescence emitted by the tissue will be measured using a spectrophotometer in a standardized spot modality. Any changes detected will be reported on the surgical specimen with the application of a surgical mark. Histopathological examination of the lesion will be performed and any changes in the fluorescence pattern will be correlated with possible alterations in the histopathological pattern, referring to surgical marks. Alterations in AF spectral measurement correlate with histopathological alterations in NMSC. the spectral measurement can be a new support for the early diagnosis of NMSCs, a guide for the targeted incisional biopsies, a tool for the definition of the intraoperative surgical margins, and for the follow-up of treated patients.
Ruberti, Maristela 1975. "Caracterização fenotípica e funcional das células imunocompetentes da mucosa intestinal envolvidas na tolerância oral a ovalbumina." [s.n.], 2012. http://repositorio.unicamp.br/jspui/handle/REPOSIP/317404.
Повний текст джерелаTese (doutorado) - Universidade Estadual de Campinas, Instituto de Biologia
Made available in DSpace on 2018-08-20T10:43:40Z (GMT). No. of bitstreams: 1 Ruberti_Maristela_D.pdf: 10774061 bytes, checksum: 7afe7ee8aa8c7f97c1f80e66f0cd8bfa (MD5) Previous issue date: 2012
Resumo: Trabalhos anteriores de nosso laboratório mostraram que camundongos transgênicos DO11.10, cuja maioria dos linfócitos T expressam TCR específico para ovalbumina (OVA) no contexto de...Observação: O resumo, na íntegra, poderá ser visualizado no texto completo da tese digital
Abstract: Previous work from our laboratory showed that DO11.10 transgenic mice, in which the most of T lymphocytes express TCR specific for ovalbumin (OVA) in the context of...Note: The complete abstract is available with the full electronic document
Doutorado
Imunologia
Doutor em Genetica e Biologia Molecular
WACHSMANN, LEVY DOMINIQUE. "Immunite des muqueuses : etude de la reponse immune locale apres stimulation orale par des antigenes proteiques et polysaccharidiques de streptococcus mutans." Strasbourg 1, 1986. http://www.theses.fr/1986STR13125.
Повний текст джерелаSaid, Zulfahmi. "Analysis of corticosteroid drug delivery using tissue engineered oral mucosa for the treatment of inflammatory mucosal diseases." Thesis, University of Sheffield, 2018. http://etheses.whiterose.ac.uk/22529/.
Повний текст джерелаSukotjo, Cortino. "Wit 3.0, a novel gene derived from edentulous oral mucosa, encodes cytoplasmic molecules facilitating oral mucosa wound contraction." Restricted to subscribing institutions, 2002. http://proquest.umi.com/pqdweb?did=1568361991&sid=1&Fmt=2&clientId=1564&RQT=309&VName=PQD.
Повний текст джерелаFonollosa, Pla José María. "Influencia del monómero residual, el diseño y la falta de ajuste de las prótesis dentales con soporte mucoso, en las lesiones de la mucosa oral." Doctoral thesis, Universitat Autònoma de Barcelona, 2021. http://hdl.handle.net/10803/671700.
Повний текст джерелаIntroducción. La patología de la mucosa oral incluye lesiones y alteraciones relacionadas con el uso de prótesis dentales de soporte mucoso elaboradas con materiales acrílicos, tanto recientes como antiguas. Su etiología puede deberse al traumatismo de un mal ajuste o diseño que no consigue transmitir de forma homogénea las fuerzas oclusales y/o genera roces, contactos y sobrepresiones, sobre la mucosa oral y los tejidos blandos adyacentes. En otras ocasiones serán los elementos químicos de los materiales los responsables de determinadas reacciones mucosas, tanto por restos de monómero libre como de otros compuestos de las resinas acrílicas. Las hipótesis de trabajo, por un lado, apuntan hacia los diseños incorrectos y a la falta de ajuste como posibles causas de determinadas lesiones en la mucosa oral y, por otro, a las técnicas aplicables a los sistemas de procesado del material acrílico autopolimerizable para reducir la presencia de monómero residual y, en consecuencia, evitar reacciones que pueden generar una estomatitis alérgica de contacto en el paciente. Objetivo. Determinar la relación entre las lesiones de los tejidos bucales de etiología protésica, en pacientes portadores de prótesis dentales completas, con aspectos de su diseño, de su falta de ajuste y con los procedimientos de polimerización de los materiales acrílicos con los que se fabrican. Método. Se ha realizado un estudio observacional, descritivo, transversal, de serie de casos, prevalentes, por lo tanto retrospectivo, en pacientes portadores de prótesis dentales completas, completas unimaxilares y parciales removible clase I y II de Kennedy Resultados. Sobre 144 pacientes se han analizado 288 prótesis superiores e inferiores que han originado lesiones agudas y crónicas en un 18,40% por diseño incorrecto y en un 12,15 % por falta de ajuste. Las resinas autopolimerizables con tratamiento durante y después de la polimerización no han generado estomatitis alérgica de contacto en 25 pacientes con prótesis completas - 50 prótesis-, 59 pacientes con prótesis completa unimaxilar y 154 prótesis parciales clase I y II de Kennedy. Conclusión. El diseño incorrecto y la falta de ajuste de las prótesis completase están relacionados con algunas lesiones de la mucosa oral. El tratamiento térmico e hídrico en las resinas autopolimerizables durante y después de su polimerización ha resultado eficaz para evitar la presencia de estomatitis alérgica de contacto.
Introduction. The pathology of the oral mucosa includes injuries and alterations related to the use of mucosal-bearing dental prostheses made with acrylic materials, both recent and old. Its etiology may be due to the trauma of a poor fit or design that fails to transmit the occlusal forces in a homogeneous way and / or generates friction, contacts and overpressures on the oral mucosa and adjacent soft tissues. On other occasions, the chemical elements of the materials will be responsible for certain mucosal reactions, both due to free monomer residues and other compounds of acrylic resins. The working hypotheses, on the one hand, point to incorrect designs and a lack of fit as possible causes of certain lesions in the oral mucosa and, on the other, to the techniques applicable to the processing systems of self-curing acrylic material to reduce the presence of residual monomer and, consequently, avoid reactions that can generate allergic contact stomatitis in the patient. Objective. To determine the relationship between oral tissue injuries of prosthetic etiology, in patients with complete dental prostheses, with aspects of their design, their lack of fit and with the polymerization procedures of the acrylic materials with which they are manufactured. Method. An observational, descriptive, cross-sectional, case series study, prevalent, therefore retrospective, has been carried out in patients with complete, complete unimaxillary and partial removable Kennedy class I and II dental prostheses. Results. Out of 144 patients, 288 upper and lower prostheses have been analyzed that have caused acute and chronic injuries in 18.40% due to incorrect design and in 12.15 % due to lack of adjustment. Self-curing resins with treatment during and after polymerization have not generated allergic contact stomatitis in 25 patients with complete dentures - 50 dentures -, 59 patients with unimaxillary full dentures, and 154 Kennedy class I and II partial dentures. Conclusion. Incorrect design and poor fit of complete dentures are related to some lesions of the oral mucosa. Heat and water treatment of self-curing resins during and after polymerization has been effective in preventing the presence of allergic contact stomatitis.
Gibson, Rachel J. "Chemotherapy-induced mucositis : mechanisms of damage, time course of events and possible preventative strategies /." Title page, table of contents and abstract only, 2004. http://web4.library.adelaide.edu.au/theses/09PH/09phg4481.pdf.
Повний текст джерелаКниги з теми "Mucosa Orale"
Squier, Christopher, and Kim A. Brogden, eds. Human Oral Mucosa. West Sussex, UK: John Wiley & Sons, Ltd., 2011. http://dx.doi.org/10.1002/9781118710470.
Повний текст джерелаMorteau, Olivier. Oral tolerance: The response of the intestinal mucosa to dietary antigens. Georgetown, Tex: Landes Bioscience/Eurekah.com, 2004.
Знайти повний текст джерелаMorteau, Olivier. Oral tolerance: The response of the intestinal mucosa to dietary antigens. Georgetown, Tex: Landes Bioscience/Eurekah.com, 2004.
Знайти повний текст джерелаMorteau, Olivier. Oral tolerance: The response of the intestinal mucosa to dietary antigens. Georgetown, TX: Landes Bioscience, 2001.
Знайти повний текст джерелаSquier, Christopher A. Human oral mucosa: Development, structure, and function. Chichester, West Sussex, UK: Wiley-Blackwell, 2011.
Знайти повний текст джерелаSchmidt, Enno, ed. Diseases of the Oral Mucosa. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-82804-2.
Повний текст джерела1921-, Pindborg J. J., and Wahi P. N, eds. Histological typing of cancer and precancer of the oral mucosa. 2nd ed. Berlin: Springer, 1997.
Знайти повний текст джерелаBergmeier, Lesley Ann, ed. Oral Mucosa in Health and Disease. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-56065-6.
Повний текст джерелаVedtofte, Poul. Cellemembranbundne kulhydrater i humant oralt epitel: Blodtypeantigener og lektinreceptorer som differentieringsmarkører i epitel fra mundslimhinde, tandanlæg, odontogene cyster og ameloblastomer. København: Institutterne for tand-, mund- og kæbekirurgi samt patologi og medicin, Københavns tandlægehøjskole og Afdelingen for tand-, mund- og kæbesygdomme, Rigshospitalet, 1986.
Знайти повний текст джерелаGünther, Veltman, Loevy Hannelore Taschini, and Taschini Pierangelo, eds. Differential diagnosis of diseases of the oral mucosa. Chicago: Quintessence Pub. Co., 1989.
Знайти повний текст джерелаЧастини книг з теми "Mucosa Orale"
Allam, Jean-Pierre, and Natalija Novak. "Mucosal Homeostasis of the Oral Mucosa." In Oral Mucosa in Health and Disease, 69–76. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-56065-6_5.
Повний текст джерелаSquier, Christopher, and Kim A. Brogden. "Oral Epithelium." In Human Oral Mucosa, 19–52. West Sussex, UK: John Wiley & Sons, Ltd., 2013. http://dx.doi.org/10.1002/9781118710470.ch3.
Повний текст джерелаSquier, Christopher, and Kim A. Brogden. "Homologies in Structure and Function Among Mucosae: Oral, Esophageal, and Vaginal Mucosa." In Human Oral Mucosa, 145–57. West Sussex, UK: John Wiley & Sons, Ltd., 2013. http://dx.doi.org/10.1002/9781118710470.ch9.
Повний текст джерелаLucas, R. B., and J. W. Eveson. "The Oral Mucosa." In Atlas of Oral Pathology, 47–65. Dordrecht: Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-009-5580-6_5.
Повний текст джерелаSquier, Christopher, and Kim A. Brogden. "The Functions of Oral Mucosa." In Human Oral Mucosa, 1–7. West Sussex, UK: John Wiley & Sons, Ltd., 2013. http://dx.doi.org/10.1002/9781118710470.ch1.
Повний текст джерелаSquier, Christopher, and Kim A. Brogden. "The Organization of Oral Mucosa." In Human Oral Mucosa, 9–17. West Sussex, UK: John Wiley & Sons, Ltd., 2013. http://dx.doi.org/10.1002/9781118710470.ch2.
Повний текст джерелаSquier, Christopher, and Kim A. Brogden. "The Interface Between Epithelium and Connective Tissue." In Human Oral Mucosa, 53–58. West Sussex, UK: John Wiley & Sons, Ltd., 2013. http://dx.doi.org/10.1002/9781118710470.ch4.
Повний текст джерелаSquier, Christopher, and Kim A. Brogden. "Connective Tissue." In Human Oral Mucosa, 59–75. West Sussex, UK: John Wiley & Sons, Ltd., 2013. http://dx.doi.org/10.1002/9781118710470.ch5.
Повний текст джерелаSquier, Christopher, and Kim A. Brogden. "Regional Differences in the Oral Mucosa." In Human Oral Mucosa, 77–98. West Sussex, UK: John Wiley & Sons, Ltd., 2013. http://dx.doi.org/10.1002/9781118710470.ch6.
Повний текст джерелаSquier, Christopher, and Kim A. Brogden. "Development and Aging of the Oral Mucosa." In Human Oral Mucosa, 99–111. West Sussex, UK: John Wiley & Sons, Ltd., 2013. http://dx.doi.org/10.1002/9781118710470.ch7.
Повний текст джерелаТези доповідей конференцій з теми "Mucosa Orale"
Majumdar, S. K., A. Uppal, and P. K. Gupta. "Autofluorescence spectroscopy of oral mucosa." In BiOS '98 International Biomedical Optics Symposium, edited by Alexander V. Priezzhev, Toshimitsu Asakura, and J. D. Briers. SPIE, 1998. http://dx.doi.org/10.1117/12.311884.
Повний текст джерелаTIMOSHIN, Anton, Aleksei DOROFEEV, Kirill ERSHOV, Inna PUSTOKHINA, and Elena EMELINA. "EVALUATION OF THE EFFECTIVENESS OF TREATMENT OF THE ORAL MUCOSA WITH PHYTO-OINTMENT BASED ON PHYTOECDYSTEROIDS." In SOUTHERN BRAZILIAN JOURNAL OF CHEMISTRY 2021 INTERNATIONAL VIRTUAL CONFERENCE. DR. D. SCIENTIFIC CONSULTING, 2022. http://dx.doi.org/10.48141/sbjchem.21scon.09_abstract_timoshin.pdf.
Повний текст джерелаRoy, Krishnendu, Ian Bottrill, Duncan R. Ingrams, Michail M. Pankratov, Elie E. Rebeiz, Peak Woo, Sadru Kabani, et al. "Diagnostic fluorescence spectroscopy of oral mucosa." In Photonics West '95, edited by R. Rox Anderson, Graham M. Watson, Rudolf W. Steiner, Douglas E. Johnson, Stanley M. Shapshay, Michail M. Pankratov, George S. Abela, et al. SPIE, 1995. http://dx.doi.org/10.1117/12.209094.
Повний текст джерелаSEVBITOV, Andrey, Aleksey DOROFEEV, Sergey MIRONOV, Samer AL-KHOURY, and Anton TIMOSHIN. "PREVENTION OF CANDIDIASIS IN PATIENTS USING REMOVABLE DENTURES." In 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.
Повний текст джерелаRubins, Uldis, Zbignevs Marcinkevics, Robert Andrianirina Muckle, Ieva Henkuzena, Andris Roze, and Andris Grabovskis. "Remote photoplethysmography for assessment of oral mucosa." In Preclinical and Clinical Optical Diagnostics, edited by J. Quincy Brown and Ton G. van Leeuwen. SPIE, 2019. http://dx.doi.org/10.1117/12.2526979.
Повний текст джерелаBehl, Isha, Hitesh Mamgain, Atul Deshmukh, Lekha Kukreja, Arti R. Hole, and C. Murali Krishna. "Raman microspectroscopic study of oral buccal mucosa." In SPIE BiOS, edited by Robert R. Alfano and Stavros G. Demos. SPIE, 2014. http://dx.doi.org/10.1117/12.2033933.
Повний текст джерелаZHUO, SHUANGMU, JIANXIN CHEN, XINGSHAN JIANG, ZUFANG HUANG, and SHUSEN XIE. "NONLINEAR OPTICAL MICROSCOPY OF MOUSE ORAL MUCOSA." In Proceedings of the 6th International Conference on Photonics and Imaging in Biology and Medicine (PIBM 2007). WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812832344_0040.
Повний текст джерелаde Veld, D. C. G., M. J. H. Witjes, J. L. N. Roodenburg, W. M. Star, and H. J. C. M. Sterenborg. "Optical detection of (pre-)malignant lesions of the oral mucosa: autofluorescence characteristics of healthy mucosa." In European Conference on Biomedical Optics. Washington, D.C.: Optica Publishing Group, 2001. http://dx.doi.org/10.1364/ecbo.2001.4432_196.
Повний текст джерелаEdward, Kert, Tuya Shilagard, Suimin Qiu, and Gracie Vargas. "Two-photon autofluorescence spectroscopy of oral mucosa tissue." In SPIE BiOS, edited by Ammasi Periasamy, Karsten König, and Peter T. C. So. SPIE, 2011. http://dx.doi.org/10.1117/12.875049.
Повний текст джерелаde Veld, Diana C. G., Max Witjes, Jan L. Roodenburg, Willem M. Star, and Hericus J. C. M. Sterenborg. "Optical detection of (pre-)malignant lesions of the oral mucosa: autofluorescence characteristics of healthy mucosa." In European Conference on Biomedical Optics, edited by Theodore G. Papazoglou and Georges A. Wagnieres. SPIE, 2001. http://dx.doi.org/10.1117/12.447135.
Повний текст джерелаЗвіти організацій з теми "Mucosa Orale"
Feinberg, Stephen E. Phase 2 Clinical Trial of Intraoral Grafting of Human Tissue-Engineered Oral Mucosa. Fort Belvoir, VA: Defense Technical Information Center, October 2013. http://dx.doi.org/10.21236/ada591622.
Повний текст джерелаBimbas, E. S., and A. S. Shishmareva. Prevention of children’s dental anomalies with anomalies of the oral mucosa. Early orthodontic treatment. SIB-Expertise, December 2022. http://dx.doi.org/10.12731/er0640.15122022.
Повний текст джерелаClements, John D. Oral Adjuvant Therapy in the Development of Immunological Protection Against Mucosal Pathogens. Fort Belvoir, VA: Defense Technical Information Center, July 1995. http://dx.doi.org/10.21236/ada302243.
Повний текст джерелаZeng, Qingxiang, Junjiang Liu, Fanglong Wu, and Hongmei Zhou. The optimal oral biopsy site in the diagnosis of oral mucosal autoimmune bullous disorders: a systematic review and meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, August 2020. http://dx.doi.org/10.37766/inplasy2020.8.0024.
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