Littérature scientifique sur le sujet « Mouth diseases – drug therapy »
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Articles de revues sur le sujet "Mouth diseases – drug therapy"
Kolesova, V. V., A. M. Lunegov, I. V. Lunegova, V. A. Baryshev et V. M. Matveev. « Comparative pharmacorrection of diseases of the mouth in cats ». Legal regulation in veterinary medicine, no 4 (8 janvier 2023) : 112–14. http://dx.doi.org/10.52419/issn2782-6252.2022.4.112.
Texte intégralГригорьев, С., S. Grigoryev, А. Козьменко et A. Kozmenko. « A new drug for xerostomia combination therapy ». Actual problems in dentistry 12, no 2 (26 juillet 2016) : 2–10. http://dx.doi.org/10.18481/2077-7566-2016-12-2-2-10.
Texte intégralAbdollahi, Mohammad, Mania Radfar et Roja Rahimi. « Current Opinion on Drug-induced Oral Reactions : A Comprehensive Review ». Journal of Contemporary Dental Practice 9, no 3 (2008) : 1–15. http://dx.doi.org/10.5005/jcdp-9-3-1.
Texte intégralP R, Meenu, et Pradeep K. Kumar. « A REVIEW ON ASCHYOTANA THERAPY AND ITS YOGAS ». International Journal of Research in Ayurveda and Pharmacy 12, no 4 (28 août 2021) : 146–48. http://dx.doi.org/10.7897/2277-4343.1204124.
Texte intégralAditya, Vangara, et Kharidhi Laxman Vandana. « Evaluation of Different Local Drug Delivery Systems in Treatment of Periodontitis : An Institutional Study ». Journal of Multidisciplinary Dental Research 9, no 2 (24 décembre 2023) : 67–73. http://dx.doi.org/10.38138/jmdr/v9i2.23.19.
Texte intégralDemir, Mehmet Gökhan. « The Effect of Arthrocentesis Treatment for Maximum Mouth Opening and Pain in Temporomandibular Joint Diseases and the Effect of Splint, Drug, and Physical Therapy on This Treatment ». Medicina 59, no 10 (4 octobre 2023) : 1767. http://dx.doi.org/10.3390/medicina59101767.
Texte intégralVieri, Audrey Amber, Rosiliwati Wihardja et Tenny Setiani Dewi. « Clinical appearance of oral lesions in bronchial asthma patients using inhalation drug ». Padjadjaran Journal of Dentistry 32, no 3 (30 novembre 2020) : 207. http://dx.doi.org/10.24198/pjd.vol32no3.27472.
Texte intégralСериков, N. Serikov, Серикова, O. Serikova, Щербаченко et O. Shcherbachenko. « Use of Physiotherapy in the Treatment of Oral Muco-sa (brief message) ». Journal of New Medical Technologies 21, no 2 (13 août 2014) : 65–68. http://dx.doi.org/10.12737/5001.
Texte intégralJayachandran, Abirami Lakshmy, Radhika Katragadda, Ravinder Thyagarajan, Leela Vajravelu, Suganthi Manikesi, Shanmugam Kaliappan et Balaji Jayachandran. « Oral Candidiasis among Cancer Patients Attending a Tertiary Care Hospital in Chennai, South India : An Evaluation of Clinicomycological Association and Antifungal Susceptibility Pattern ». Canadian Journal of Infectious Diseases and Medical Microbiology 2016 (2016) : 1–6. http://dx.doi.org/10.1155/2016/8758461.
Texte intégralAouroud, Hala, Adil Ait Errami, Nayala Hanane Essaidi, FZ Lairani, O. Nacir, Sofia Oubaha, Zouhour Samlani et Khadija Krati. « Compliance to Drug Therapy in Inflammatory Bowel Diseases : A Monocentric Experience ». International Journal of Innovative Research in Medical Science 8, no 10 (13 octobre 2023) : 464–68. http://dx.doi.org/10.23958/ijirms/vol08-i10/1763.
Texte intégralThèses sur le sujet "Mouth diseases – drug therapy"
Tavari, Mohsen. « Hybrid molecules as inhibitors of the monoamine oxidases and caspase 3 for neurodegenerative disorders ». University of the Western Cape, 2016. http://hdl.handle.net/11394/5069.
Texte intégralNeurodegenerative diseases are multifactorial in nature, and taking the complex nature of these disorders into consideration, multi-target directed ligands may present as better options to treat these disorders than the classic ‘one molecule, one target’ approach. Neurotransmitter amines are catabolized by monoamine oxidase A and B (MAO-A and MAO-B), therefore they have been targeted for the treatment of neuropsychiatric and neurodegenerative diseases. Besides offering a potential antidepressant action in PD, MAO-A inhibitors may also provide a symptomatic benefit by reducing MAO-A-catalysed oxidation of dopamine. The oxidative deamination reaction catalyzed by MAO-B is one of the major catabolic pathways of dopamine in the brain. Inhibition of this enzyme leads to enhanced dopaminergic neurotransmission and are currently used in the symptomatic treatment of PD. Furthermore, MAO-B inhibitors may also exert neuroprotective effects by reducing the concentration of potentially hazardous by-products produced by MAO-B-catalysed dopamine oxidation. Apoptosis or programmed cell death occurs in a number of neurodegenerative disorders and it has been proven that inhibition of the executing enzyme, caspases-3, slows down or even stops apoptosis. Having this in mind we focused on the propargylamine function of selegiline and the fluorophenyl function of safinamide, because of their inherent monoamine oxidase inhibitory activities; and isatin as a non-peptide inhibitor of caspase-3. Therefore we attempted to design and synthesize multifunctional hybrid molecules acting simultaneously to halt the apoptotic neuronal breakdown process and eliminate the signs and symptoms of diseases such as PD. Seven novel compounds were successfully synthesized utilizing multistep processes. The synthesis of 5 chlorosulfonyl isatin was accomplished starting from the commercially available isatin in two steps, which were, sulfonation using tetramethylene sulfone and chlorination with POCl₃. Next 5-chlorosulfonyl isatin was conjugated to the fluorophenylamine derivative with the fluoro-function at either the ortho, meta or para position through a nucleophilic substitution reaction on the chlorosulfonyl position. The resultant compounds were coupled on the N position of the isatin function with propargyl bromide, using a microwave synthesis procedure, in a nucleophilic substitution reaction. The structures and purity were confirmed by nuclear magnetic resonance (NMR) and mass spectrometry (MS). In the biological evaluations recombinant human MAO-A, MAO-B and caspase 3 enzymatic assays were performed to determine the activity of the novel compounds at an enzymatic level. The inhibition percentages for these compounds were calculated and plotted against the logarithm 8 of the inhibitor concentrations to obtain a sigmoidal dose-response curve and consequently the IC50 value. The synthesized compounds showed inhibition of the MAO-A, MAO-B and caspase-3 enzymes at low to high micro molar concentrations. The role of the fluorophenylamine moiety in the synthesized compounds was significant for their multifunctional activity as shown by compounds 3 and 4 having good inhibitory activity towards MAO-A, MAO-B and also excellent inhibitory activity against caspase 3, making those ideal candidates for further lead compound development and multifunctional drug design. The introduction of the propargylamine moiety only increased the MAO-A inhibitory activity; this was shown by compounds 7, 8 and 9 which exhibit good MAO-A selectivity with low MAO-B and caspase-3 inhibitory activities.
Zent, Clive Steven, et Clive Steven Zent. « The use of aminoglycoside antibiotic therapy in neutropaenic patients with haematological disease ». Master's thesis, University of Cape Town, 1991. http://hdl.handle.net/11427/24969.
Texte intégralThomson, William Murray. « Medications, dry mouth and dental caries among older people : a longitudinal study / ». Title page, contents and abstract only, 1999. http://web4.library.adelaide.edu.au/theses/09PH/09pht4858.pdf.
Texte intégralYu, Zhen. « Altered drug responses in diabetic and hypertensive-diabetic cardiomyopathy ». Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/29406.
Texte intégralPharmaceutical Sciences, Faculty of
Graduate
Flood, Lars. « Glucocorticosteroid therapy and steroid resistance in inflammatory bowel disease / ». Stockholm, 2004. http://diss.kib.ki.se/2004/91-7140-020-6/.
Texte intégralKucukturhan, Aysu. « Bioactive Agent Carrying Plga Nanoparticles In Thetreatment Of Skin Diseases ». Master's thesis, METU, 2012. http://etd.lib.metu.edu.tr/upload/12614551/index.pdf.
Texte intégral1.5%. L929 fibroblast and Saos 2 human osteosarcoma cells were used to study the uptake of NPs by the cells. Particles accumulate near the nucleus. The characterization and cell viability tests, and drug release behavior indicate the suitability of these NPs for further testing to develop a patient specific skin diseases treatment approach.
Törneke, Karolina. « Pharmacological aspects of adrenoceptor drugs in the horse / ». Uppsala : Swedish Univ. of Agricultural Sciences (Sveriges lantbruksuniv.), 1999. http://epsilon.slu.se/avh/1999/91-576-5431-X.pdf.
Texte intégralCameli, Paolo. « The impact of antifibrotic therapy in the management of idiopathic pulmonary fibrosis and progressive fibrosing interstitial lung diseases : a real-world comparative study of efficacy between pirfenidone and nintedanib ». Doctoral thesis, Università di Siena, 2021. http://hdl.handle.net/11365/1159047.
Texte intégralWang, Jianghai. « Human deoxyribonucleoside kinases : their substrate recognition and implications for chemotherapy / ». Uppsala : Swedish Univ. of Agricultural Sciences (Sveriges lantbruksuniv.), 1999. http://epsilon.slu.se/avh/1999/91-576-5427-1.pdf.
Texte intégralHorn, Je'nine. « The analysis of 6- and 24-hour iodine-131 thyroid uptake in patients with Graves' disease at Universitas Hospital ». Thesis, [Bloemfontein?] : Central University of Technology, Free State, 2007. http://hdl.handle.net/11462/102.
Texte intégralIn the South African Health Services (SAHS) it is each health worker’s responsibility to find ways to reduce health care cost and improve health service to the public. The measurement of radioactive iodine uptake (RAIU) by the thyroid gland for diagnostic purposes has been used as early as the 1940s. The 24-hour (hr) iodine-131 (131I) uptake measurement is traditionally used for the calculation of the 131I administered activity for therapy dosage. This entails that the patient’s hospitalisation is prolonged, which increases the costs. The literature also indicates that the 24-hr 131I uptake value can be discarded and only the 6-hr 131I uptake measurement is needed to calculate administered activity for therapeutic dosages for Graves’ patients. Therefore, if it can be confirmed that the 6-hr 131I uptake measurement alone is needed, the SAHS could decrease hospitalisation costs. The overall goal of the investigation was to analyse the 6-hr and 24-hr 131I uptake measurements of patients with Graves’ disease at the Universitas Hospital. The aim was to determine the relationship between the 6-hr and 24- hr RAIU values to establish the therapeutic dosage for Graves’ disease. To achieve the aim, three objectives were set. First, to serve as a background to the investigation, a literature survey relating to the RAIU measurements of patients with Graves’ disease was made. Second, a retrospective analysis was performed by collecting the 6-hr and 24-hr 131I uptake measurements of patients with proven Graves’ disease at the Universitas Nuclear Medicine Department (UNMD). Finally, the data obtained from the retrospective analysis was analysed, summarised and compared to answer the investigation questions. The investigation group included patients with confirmed Graves’ disease who had undergone both the 6- and 24-hr 131I RAIU at the Universitas Hospital from the beginning of 2004 to the end of 2005. Graves’ disease is confirmed by the following factors at the UNMD, namely: Suppressed TSH, elevated T4 and T3 values, an increased uptake on the 99mTc-pertechnetate scan and increased 6- and 24-hr 131I RAIU values. The UNMD statistics show that 178 patients were diagnosed with Graves’ disease during this period. The patients of the investigation group included both male and female patients from different races, ranging from 15-75 years. In order to increase the validity of the investigation, all factors that could influence the accuracy of the 131I thyroid uptake test were excluded. After the exclusion and inclusion criteria had been applied, the final investigation group was made up of 124 Graves’ disease patients. The data obtained from the patient files was noted on the different data sheets (see Appendix A) for further analysis. The information from these data sheets was then used to obtain the investigation results. The Department of Biostatistics of the University of the Free State (UFS) was consulted for recommendations regarding the management of data and the processing of results. All values were summarised by means and Standard Deviations (SD) or percentiles. Mean or median differences were calculated with a 95% Confidence Interval (CI). A regression analysis was made between the 6-hr and 24-hr 131I RAIU values. The highest RAIU value is the best to calculate the therapeutic dosage, as this gives a true reflection of the thyroid function of a Graves’ disease patient. In the investigation group the median of the 24-hr 131I RAIU values was higher than the 6-hr 131I RAIU values. The findings showed that the 24-hr 131I RAIU in most of the investigation group was the highest value and most effective to calculate the 131I therapeutic dosage. At a time when research-based practice is taking on an increasingly important role, it is essential for nuclear medicine departments to make evidence-based recommendations. This investigation found that the correlation between the 6-hr and 24-hr RAIU clearly justified the cost spent on Graves’ disease patients who must stay overnight for the 24-hr 131I RAIU procedure.
Livres sur le sujet "Mouth diseases – drug therapy"
Robert, Newland J., dir. Oral soft tissue diseases : A reference manual for diagnosis & management. Hudson, Ohio : Lexi-Comp, 2001.
Trouver le texte intégralNewland, J. Robert. Oral hard tissue diseases : A reference manual for radiographic diagnosis. 3e éd. Hudson, Ohio : Lexi-Comp, 2012.
Trouver le texte intégralZambito, Raymond F. Immunology and infectious diseases of the mouth, head, and neck. St. Louis : Mosby Year Book, 1991.
Trouver le texte intégralSeymour, R. A. Adverse drug reactions in dentistry. 2e éd. Oxford : Oxford University Press, 1996.
Trouver le texte intégralSeymour, R. A. Adverse drug reactions in dentistry. Oxford : Oxford University Press, 1988.
Trouver le texte intégralH, Messerli Franz, dir. Cardiovascular drug therapy. 2e éd. Philadelphia : Saunders, 1996.
Trouver le texte intégralKhan, M. Gabriel. Cardiac drug therapy. 3e éd. London : W.B. Sanders, 1992.
Trouver le texte intégralJ, Eadie Mervyn, dir. Drug therapy in neurology. Edinburgh : Churchill Livingstone, 1992.
Trouver le texte intégralCorporation, Springhouse, dir. Cardiovascular drug therapy. Springhouse, Pa : Springhouse Corp., 1995.
Trouver le texte intégralKhan, M. I. Gabriel. Manual of cardiac drug therapy. 2e éd. London : Bailliere Tindall, 1988.
Trouver le texte intégralChapitres de livres sur le sujet "Mouth diseases – drug therapy"
Merk, Hans F., et Daniela Höller Obrigkeit. « Drug Reactions ». Dans Therapy of Skin Diseases, 297–319. Berlin, Heidelberg : Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-78814-0_29.
Texte intégralWehling, Martin. « Obstructive Lung Diseases ». Dans Drug Therapy for the Elderly, 135–42. Vienna : Springer Vienna, 2012. http://dx.doi.org/10.1007/978-3-7091-0912-0_11.
Texte intégralWu, Gencheng, Yanqing Wang et Xiaoding Cao. « Acupuncture-Drug Balanced Anesthesia ». Dans Acupuncture Therapy for Neurological Diseases, 143–61. Berlin, Heidelberg : Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-10857-0_6.
Texte intégralSepúlveda, Maria, Albert Saiz et Francesc Graus. « Targeting B Cells in Neurological Autoimmune Diseases ». Dans Milestones in Drug Therapy, 219–46. Basel : Springer Basel, 2013. http://dx.doi.org/10.1007/978-3-0348-0706-7_12.
Texte intégralBosch, Xavier, Pilar Brito-Zerón, Munther A. Khamashta et Manuel Ramos-Casals. « Targeting B Cells in Other Systemic Autoimmune Diseases ». Dans Milestones in Drug Therapy, 247–58. Basel : Springer Basel, 2013. http://dx.doi.org/10.1007/978-3-0348-0706-7_13.
Texte intégralLaird, Glen. « Introduction to Rare Disease Therapy Development ». Dans Drug Development for Rare Diseases, 1–6. Boca Raton : Chapman and Hall/CRC, 2023. http://dx.doi.org/10.1201/9781003080954-1.
Texte intégralFeng, Yi, et Boying Chen. « Effect of Acupuncture on Drug Addiction ». Dans Acupuncture Therapy for Neurological Diseases, 460–72. Berlin, Heidelberg : Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-10857-0_18.
Texte intégralChow, Shein-Chung. « Gene Therapy for Rare Diseases ». Dans Innovative Methods for Rare Disease Drug Development, 247–64. Boca Raton, FL : CRC Press, 2021. | : Chapman and Hall/CRC, 2020. http://dx.doi.org/10.1201/9781003049364-13.
Texte intégralWinchester, James F. « Acute Drug Intoxications ». Dans Therapy of Renal Diseases and Related Disorders, 639–48. Boston, MA : Springer US, 1991. http://dx.doi.org/10.1007/978-1-4613-0689-4_40.
Texte intégralRobinson, Peter. « Cell and Gene Therapy in Rare Diseases ». Dans Rare Disease Drug Development, 249–61. Cham : Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-78605-2_16.
Texte intégralActes de conférences sur le sujet "Mouth diseases – drug therapy"
Silveira, Rayanne Maria Brandão da, Marcela Marques de Oliveira Gregório, Elza Marcia Targar Yacubian et Laura Maria de Figueiredo Ferreira Guilhoto. « Cardiovascular risk in adults with drug-resistant epilepsy submitted to the modified atkins diet ». Dans XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.728.
Texte intégralThomas, E., et F. Blotman. « SP0064 Drug therapy in fibromyalgia. a review ». Dans Annual European Congress of Rheumatology, Annals of the rheumatic diseases ARD July 2001. BMJ Publishing Group Ltd and European League Against Rheumatism, 2001. http://dx.doi.org/10.1136/annrheumdis-2001.20.
Texte intégralХИЗРИЕВ, М. Д., И. Э. АТАШЕВА et З. О. ГАРУНОВ. « Drug therapy of patients with stable angina pectoris ». Dans II Международная научно-практическая конференция "Преобразование современного мира : проблемы и возможности". Crossref, 2024. http://dx.doi.org/10.26118/5186.2024.80.69.007.
Texte intégralBorges, Érico Induzzi, André Lopez Fernandez, Louis Fernando Marques de Almeida, Juline do Prado Paes, Jandey da Glória Bigonha, Antônio José da Rocha, Herval Soares Ribeiro Neto et Sônia Maria Cesar de Azevedo Silva. « Progressive Multifocal Leukoencephalopathy following Daratumumab therapy for refractory Multiple Myeloma – a case report ». Dans XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.441.
Texte intégralCheung, S., F. Kudaeva, P. Heidari et D. Truong. « AB1665-PARE DRUG PERSISTENCE WITH THERAPY OF ADALIMUMAB BIOSIMILAR, MSB11022, IN RHEUMATOLOGIC DISEASES ». Dans EULAR 2024 European Congress of Rheumatology, 12-15 June. Vienna, Austria. BMJ Publishing Group Ltd and European League Against Rheumatism, 2024. http://dx.doi.org/10.1136/annrheumdis-2024-eular.5499.
Texte intégralBarzizza, F., G. Belloni, E. Trespi, A. Venturini et I. Richichi. « HYPOGLYCEMIC EFFECT OF INDOBUFEN,AN ANTIAGGREGATING AGENT,IN ELDERLY DIABETIC PATIENTS ». Dans XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643100.
Texte intégralKim, Jinho, et Jim S. Chen. « Effect of Inhaling Patterns on Aerosol Drug Delivery : CFD Simulation ». Dans ASME 2008 International Mechanical Engineering Congress and Exposition. ASMEDC, 2008. http://dx.doi.org/10.1115/imece2008-66685.
Texte intégralOkun', Dmitriy. « FORMAL REPRESENTATION OF KNOWLEDGE ABOUT MEDICAMENTAL THERAPY FOR ISCHEMIC HEART DISEASES (detail) ». Dans XIV International Scientific Conference "System Analysis in Medicine". Far Eastern Scientific Center of Physiology and Pathology of Respiration, 2020. http://dx.doi.org/10.12737/conferencearticle_5fe01d9bce39f8.78028503.
Texte intégralCanzian, Kássia Braga, Marcella Canato Toloi, David Vargas Freitas Teixeira, Vanessa de Freitas Moreira, Amanda Freitas Alves, Eric Dupont, Fernanda Maria Gonçalves de Sousa Moura, Isabela de Almeida Stella, Thiago Ivan Vilchez Santillan et Herval Ribeiro Soares Neto. « Chronic paraneoplastic polyradiculoneuropathy during colorectal cancer : a case report ». Dans XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.633.
Texte intégralSheenkova, M. V. « ON THE PATHOGENESIS OF GASTRODUODENAL ZONE LESIONS IN VARIOUS VARIANTS OF DRUG THERAPY FOR OCCUPATIONAL RESPIRATORY DISEASES ». Dans The 16th «OCCUPATION and HEALTH» Russian National Congress with International Participation (OHRNC-2021). FSBSI “IRIOH”, 2021. http://dx.doi.org/10.31089/978-5-6042929-2-1-2021-1-575-578.
Texte intégralRapports d'organisations sur le sujet "Mouth diseases – drug therapy"
Grueso-Navarro, Elena, Leticia Rodríguez-Alcolado, Ángel Arias, Emilio J. Laserna-Mendieta et Alfredo J. Lucendo. Influence of HLA-DQA1*05 allele in the response to anti-TNFα drugs in inflammatory bowel diseases. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, février 2023. http://dx.doi.org/10.37766/inplasy2023.2.0076.
Texte intégralLI, jianhong, Zhuang LI, Yalin SHE et Guohua LIN. Assessment of acupuncture for treating herpes zoster:a protocol for an umbrella systematic review and meta analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, avril 2022. http://dx.doi.org/10.37766/inplasy2022.4.0010.
Texte intégralTang, Jiqin, Gong Zhang, Jinxiao Xing, Ying Yu et Tao Han. Network Meta-analysis of Heat-clearing and Detoxifying Oral Liquid of Chinese Medicines in Treatment of Children’s Hand-foot-mouth Disease:a protocol for systematic review. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, janvier 2022. http://dx.doi.org/10.37766/inplasy2022.1.0032.
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