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Статті в журналах з теми "Drug interactions Prevention"
Liekweg, A., and A. Hinnerkort. "311 Identification and prevention of drug-drug interactions." European Journal of Cancer Supplements 7, no. 2 (September 2009): 76. http://dx.doi.org/10.1016/s1359-6349(09)70264-2.
Повний текст джерелаWittkowsky, Ann K. "Workshop: Warfarin drug interactions: Detection, prediction, prevention." Journal of Thrombosis and Thrombolysis 2, no. 4 (March 1996): 295–99. http://dx.doi.org/10.1007/bf01061915.
Повний текст джерелаCavuto, N. J. "Pharmacies and prevention of potentially fatal drug interactions." JAMA: The Journal of the American Medical Association 275, no. 14 (April 10, 1996): 1086–87. http://dx.doi.org/10.1001/jama.275.14.1086.
Повний текст джерелаCavuto, Nicholas John. "Pharmacies and Prevention of Potentially Fatal Drug Interactions." JAMA: The Journal of the American Medical Association 275, no. 14 (April 10, 1996): 1086. http://dx.doi.org/10.1001/jama.1996.03530380028022.
Повний текст джерелаAliot, Etienne, and Josep Brugada. "Drug–Device Interactions." European Cardiology Review 6, no. 2 Supplement (2010): 8. http://dx.doi.org/10.15420/ecr.2010.6.2suppl.8.
Повний текст джерелаRIAZ, MUHAMMAD KASHIF. "POTENTIAL DRUG-DRUG INTERACTIONS AND STRATEGIES FOR THEIR DETECTION AND PREVENTION." FARMACIA 67, no. 4 (July 10, 2019): 572–79. http://dx.doi.org/10.31925/farmacia.2019.4.3.
Повний текст джерелаJyotsna, M., and Y. Hemalatha. "Drug–Drug, Drug–Disease and Disease–Disease Interactions in COVID-19 with Cardiovascular Diseases (CVDs)." Indian Journal of Cardiovascular Disease in Women WINCARS 5, no. 03 (September 2020): 216–22. http://dx.doi.org/10.1055/s-0040-1716786.
Повний текст джерелаNesar, Shagufta, Muhammad Harris Shoaib, Kiran Rafiq, Muhammad Azhar Mughal, Tayyaba Mumtaz, Ishrat Younus, and Arfa Akram. "Medication errors with influencing factors of polypharmacy among elderly patients using Calcium Chanel Blockers." International Journal of Endorsing Health Science Research (IJEHSR) 10, no. 2 (June 1, 2022): 144–49. http://dx.doi.org/10.29052/ijehsr.v10.i2.2022.144-149.
Повний текст джерелаGulick, Roy M., and Charles Flexner. "Long-Acting HIV Drugs for Treatment and Prevention." Annual Review of Medicine 70, no. 1 (January 27, 2019): 137–50. http://dx.doi.org/10.1146/annurev-med-041217-013717.
Повний текст джерелаBaumann, P. "Drug interactions in the treatment of Bipolar disorder." European Psychiatry 26, S2 (March 2011): 2028. http://dx.doi.org/10.1016/s0924-9338(11)73731-2.
Повний текст джерелаДисертації з теми "Drug interactions Prevention"
Åstrand, Bengt. "ePrescribing : Studies in Pharmacoinformatics." Doctoral thesis, Högskolan i Kalmar, Naturvetenskapliga institutionen, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:hik:diva-32.
Повний текст джерелаThe thesis aimed to study the developments, in the area of pharmacoinformatics, of the electronic prescribing and dispensing processes of drugs - in medical praxis, follow-up, and research. For hundreds of years, the written prescription has been the method of choice for physicians to communicate decisions on drug therapy and for pharmacists to dispense medication. Successively the prescription has also become a source of information for the patient about how to use the medication to maximize its benefit. Currently, the medical prescription is at a transitional stage between paper and web, and to adapt a traditional process to the new electronic era offers both opportunities and challenges The studies in the thesis have shown that the exposure of prescribed drugs in the general population has increased considerably over three decades. The risk of receiving potentially interacting drugs was also strongly correlated to the concomitant use of multiple drugs, polypharmacy. The pronounced increase in polypharmacy over time constitutes a growing reason for prescribers and pharmacists to be aware of drug interactions. Still, there were relatively few severe potential drug interactions. Recently established national prescription registers should be evaluated for drug interaction vigilance, both clinically and epidemiologically. The Swedish National Pharmacy Register provides prescription dispensing information for the majority of the population. The medication history in the register may be accessed online to improve drug utilization, by registered individuals, prescribers, and pharmacists in a safe and secure way. Lack of widespread secure digital signatures in healthcare may delay general availability. With a relatively high prevalence of dispensed drugs in the population, the National Pharmacy Register seems justified in evaluating individual medication history. With a majority of prescriptions transferred as ePrescriptions, the detected increased risk for prescription errors warrants quality improvement, if the full potential of ePrescriptions is to be fulfilled. The main conclusion of the studies was that ePrescribing with communication of prescribed drug information, storing and retrieving dispensed drug information, offers new opportunities for clinical and scientific
Gildenhuys, Johandie. "Interactions of quinoline antimalarial drugs with ferrihaem : structural and kinetic insights into the inhibition of malaria pigment formation." Thesis, Stellenbosch : Stellenbosch University, 2013. http://hdl.handle.net/10019.1/85621.
Повний текст джерелаENGLISH ABSTRACT: The work in this dissertation provides structural and kinetic insight into the mechanism of action of quinoline antimalarial drugs which may aid rational drug design. Quinoline antimalarial drug-ferrihaem (Fe(III)PPIX) complexes were investigated. Single crystal Xray diffraction (SCD) structures of the complexes formed between Fe(III)PPIX and the quinoline methanol antimalarials quinine, quinidine and mefloquine have been determined, and are the first observed structures of complexes formed between free Fe(III)PPIX and quinoline antimalarial compounds. Quinine, quinidine and mefloquine are shown to have a three-point binding mode to Fe(III)PPIX, which comprises direct coordination of the drug to the Fe(III) centre through its benzylic alcohol functionality, π-stacking between the drug and porphyrin aromatic systems, and intramolecular hydrogen bond formation between the porphyrin propionate group and the protonated quinuclidine nitrogen atom of the drug in the case of quinine and quinidine, and formation of an intramolecular hydrogen bonding network in the case of mefloquine. Extended X-ray absorption fine structure spectroscopy (EXAFS) was use to elucidate structural information of Fe(III)PPIX-drug complexes in solution, and indicates that coordination persists in solution. The protocol for lipid-mediated formation of β-haematin, where monopalmitic glycerol was used as a model lipid, was successfully modified to incorporate antimalarial drugs into the aqueous layer in order to investigate drug activity under biologically-relevant conditions. Four compounds were chosen, namely chloroquine and amodiaquine, both 4- aminoquinolines and quinine and quinidine. IC50 values for the inhibition of β-haematin formation show good correlation with biological activities determined against a chloroquine-sensitive Plasmodium falciparum strain. The lipid-water interface system was further used to investigate the effects of quinine, quinidine chloroquine and amodiaquine on the kinetics of β-haematin formation. The results led to the development of a kinetic model based on the Avrami equation and the Langmuir isotherm. The data strongly support a mechanism of antimalarial drug action by adsorption to the growing face of haemozoin, with precipitation of Fe(III)PPIX at high drug concentrations accounting for decreased yields. Adsorptions constants (log Kads) determined for each drug show a strong correlation with biological activity. Finally, the first SCD structure of the μ-propionato dimer of Fe(III)PPIX, the structural unit of haemozoin, has been determined as its DMSO solvate. EXAFS suggests that this species is only formed upon nucleation, with the π-π dimer species being favoured in solution.
AFRIKAANSE OPSOMMING: Die werk in die dissertasie verleen struktuur en kinetiese insig in the meganisme van aktiwiteit vir kinolien antimalariamiddels wat kan bydra tot die ontwikkeling van nuwe medisyne. Kinolien antimalariamiddel-ferriheem (Fe(III)PPIX) komplekse was ondersoek. Navorsing is gedoen op die enkelkristal X-straaldiffraksie strukture van die komplekse gevorm tussen Fe(III)PPIX en die kinolien metanol antimalaria middels kinien, kinidien en mefloquine. Die strukture is die eerste komplekse wat waargeneem is tussen vrye Fe(III)PPIX en kinolien antimalariamiddels. Kinien, kinidien en mefloquine het ʼn driepunt bindingsvorm, direkte koördinasie met die Fe(III) deur die bensielalkohol groep, ʼn π- stapel tussen die middel en die porfirien aromatiese sisteem, ʼn intramolekulêre waterstofbinding tussen the porfirienpropionaat funksie en die geprotoneerde kinuklidien stikstofatoom (kinien en kinidien) en ʼn netwerk van intramolekulêre waterstof bindings (mefloquine) insluit. Uitgebreide X-straal absorpsie fyn struktuur spektroskopie (EXAFS) is gebruik om inligting oor Fe(III)PPIX-middel komplekse in oplossing te verkry en het aangedui dat die koördinasie in oplossing voorkom. Deur gebruik te maak van monopalmitiengliserol as die lipid in the lipid-water interfase sisteem, waar antimalariamiddels suksesvol in die buffer geïnkorporeer was, was die middel se aktiwiteit onder biologiese kondisies geondersoek. Vier middels was gekies naamlik, chloroquine en amodiaquine, albei 4-aminokinoliene en kinien en kinidien om die IC50-waarde vir inhibisie van β-hematien vorming te bepaal. Die IC50 waardes het ʼn goeie korrelasie met biologiese aktiwiteite teen die chloroquine-sensitiewe Plasmodium falciparum stam gewys. Die lipid-water interfase-sisteem was ook gebruik om die effek van kinien, kinidien, chloroquine en amodiaquine op die kineties effek op die vorming van β-hematien te ondersoek. Die resultate het gelei to die ontwikkeling van die kinetiese model gebaseer op die Avrami vergelyking en die Langmuir isoterm. Die data ondersteun ʼn meganisme van middel aksie waar die middel teen die groeiende vlak van hemosoïen kristal adsorbeer. Die neerslag van Fe(III)PPIX wat vorm by hoë konsentrasies, het gelei tot laer opbrengste. Die adsorpsiekonstante (log Kads) bepaal vir elke middel, het goeie korrelasie met biologiese aktiwiteit getoon. Enkelkristal X-straaldiffraksie strukture van μ- propionatodimeer van Fe(III)PPIX, die struktuur eenheid van hemosoïen, was bepaal as ʼn DMSO solvaat. EXAFS het aangedui dat die spesie slegs by kernvorming ontstaan en dat die π-π dimeerspesie in oplossing voorkom.
Lindh, Ludwig, and Simon Marjanovic. "”Droger är ju olagligt så därför ska man hålla sig borta från det” : En kvalitativ studie om vad professionella uppfattar är viktigt vid det narkotikaförebyggande arbetet bland ungdomar." Thesis, Karlstads universitet, Institutionen för sociala och psykologiska studier (from 2013), 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kau:diva-76723.
Повний текст джерелаThe purpose of the study is to investigate what aspects professionals working with youth find important in order to prevent drug use among youth. To understand to what extent the youths’ environment can influence to their use of drugs the paper uses the Bronfenbrenner’s ecological systems theory. Five people, who in different ways work with drug prevention among youth, were interviewed. Qualitative content analysis was applied. The result shows that many of the interviewees had similar perceptions on how to prevent drug use amongst youth and stressed the importance of trying to collect information on the effects of using such substances. Moreover, the interviewees expressed the significant influence that the parents have on the individual and the importance of having a good environment at home and in school as well as the importance of including youth in the society.
Montagu, Angélique. "Composants aromatiques nano-encapsulés : une alternative face à la résistance aux antibiotiques : Démonstration des effets biologiques seuls ou nano-encapsulés de l’in vitro à l’in vivo Prevention of Bacterial Infections Using Encapsulated Phytophenolic Actives Aromatic and terpenic compounds loaded in lipidic nanocapsules: activity against multi-drug resisant Acinobacter baumannii assessed in vitro and in a murine model of sepsis Demonstration of the interactions between aromatic compound-loaded lipid nanocapsules and Acinetobacter baumannii bacterial membrane." Thesis, Angers, 2016. http://www.theses.fr/2016ANGE0072.
Повний текст джерелаFaced with the rise of multidrug-resistant bacteria, the discovery of new antibacterial strategies is imperative. An alternative is the use of antibacterial active substances from essential oils. These lipophilic compounds were encapsulated via lipidic nanocapsules(LNC) allowing a use by systemic way. The efficacy of actives loaded LNC has been showed in a murine model of sepsis against Acinetobacter baumannii with a survival rate of 45% to 55%. Our study showed the power of attraction and penetration of the encapsulated carvacrol (Car) via the hydroxyl functions. The biological effects of these compounds were characterized by a degradation of rRNA, an over expression of genes encoding heat shock proteins. A catalase overexpression was also observed which is related to an oxidative stress (role of detoxification). Our works showed that bacteria could use in this process, a defense strategy against Car using the endogenous reactive oxygen species in response to environmental stress. These biological effects are preserved after encapsulation by LNC. In an in vivo model of pneumonia, no animal survival has been observed, despite the use of pegylated LNC, which is supposed to increase their stealth in the blood. Pulmonary infection did not promote the LNC accumulation in the lungs. This phenomenon could be explained by the metabolization of Cin in cinnamic acid in the blood, the oxidized form ofthe compound which would drastically reduce the antibacterial activity of Car-Cin loaded LNC
Algarni, Amnah Abdullah A. 1983. "Interaction between tin/flouride-containing solutions and artificially created dental pellicles on erosion prevetion in vitro." Thesis, 2013. http://hdl.handle.net/1805/3717.
Повний текст джерелаBACKGROUND: Fluoride and stannous ions have been reported to be relevant for dental erosion prevention. However, their interaction with the acquired dental pellicle (ADP), a clinically relevant erosion protective factor, is not well known and needs to be investigated. OBJECTIVES: To investigate the anti-erosive properties of fluoride-containing solutions and stannous solutions on enamel and dentin surfaces with a previously formed ADP. To characterize the protein profile of the ADP treated with the test solutions. METHODS: Phase I tested four solutions: SnCl2/NaF, NaF, SnCl2 and deionized water (DIW) (as negative control). Forty bovine enamel and dentin specimens 104 (4x4x2 mm3) were prepared and randomly distributed into 4 groups (n = 10). The specimens were incubated in clarified human saliva (CHS) for 24 h for pellicle formation and then they were subjected to a cycling procedure that included a 5-min erosive challenge (0.3-percent citric acid, pH 2.6); a 2-min treatment with the solution (between 1st, 3rd and 6th cycles); a 2-h immersion in CHS, and overnight immersion in CHS. Cycles were repeated 6x/day for 5 days. The outcome measure was surface loss (SL) using profilometry. Phase II: Thirty-two (32) bovine enamel specimens (882 mm3) (n = 8) were similarly prepared and incubated in saliva for 24 h and then treated with the solutions for 2 min followed by CHS immersion for 2 h. This cycle was repeated 3x for one day. The pellicles formed and treated with the test rinse solutions were collected, digested, and analyzed for specific protein content using liquid chromatography electrospray ionization tandem mass spectrometry (LCESI-MS/MS). RESULTS: Phase I: for enamel, SnCl2/NaF, SnCl2, NaF solutions provided 89 percent, 67 percent, and 42 percent SL reduction respectively compared with the control, while in dentin they provided 60 percent, 23 percent, and 36 percent, respectively, all significant at p < 0.05. Phase II: Seventy-two (72) common proteins were identified in all groups, 30 exclusive to DIW, 20 to SnCl2/NaF, 19 to NaF, and 13 to SnCl2. SnCl2/NaF increased the abundance of pellicle proteins than each one alone. CONCLUSION: SnCl2/NaF showed the best anti-erosive effect on both enamel and dentin. The findings suggest that the composition of acquired pellicle changes with different solutions, which may be related to their anti-erosive effect.
Книги з теми "Drug interactions Prevention"
Drug interactions: Protecting yourself from dangerous drug, medication, and food combinations. New York: Rosen Pub. Group, 1999.
Знайти повний текст джерелаHarkness, Richard. The natural pharmacist: Drug-herb-vitamin interactions bible. Roseville, Calif: Prima, 2000.
Знайти повний текст джерелаStaines, Henry M. Treatment and Prevention of Malaria: Antimalarial Drug Chemistry, Action and Use. Basel: Springer Basel, 2012.
Знайти повний текст джерела1944-, Cooper James, ed. Geriatric drug therapy interventions. New York: Pharmaceutical Products Press, 1997.
Знайти повний текст джерелаJulian, Rosenthal C., and Rotman Marvin 1933-, eds. Infusion chemotherapy--irradiation interactions: Principles and applications to organ salvage and prevention of second primary neoplasms. New York: Elsevier, 1998.
Знайти повний текст джерелаAging, Illinois Alliance for. Driving, drinking, and medications: Developing a community response to older people at risk : a report on a series of roundtables. [Springfield, Ill.]: Illinois Dept. on Aging, 1995.
Знайти повний текст джерелаR, Hawes Gene, ed. Rx for recovery: The medical and health guide for alcoholics, addicts, and their families. New York: F. Watts, 1988.
Знайти повний текст джерелаMindell, Earl. The vitamin bible: How the right vitamins and nutrient supplements can revolutionise your life. London: BCA, 1986.
Знайти повний текст джерелаMindell, Earl. The vitamin bible: How the right vitamins and nutrient supplements can revolutionise your life. 2nd ed. London: Arlington Books, 1985.
Знайти повний текст джерелаMindell, Earl. Earl Mindell's vitamin bible: How the right vitamins and nutrient supplements can help turn your life around. New York: Warner, 1985.
Знайти повний текст джерелаЧастини книг з теми "Drug interactions Prevention"
Roe, Daphne A. "Prediction and Prevention of Drug-Nutrient Interactions Using Theoretical Models." In Diet and Drug Interactions, 161–76. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-011-6047-6_9.
Повний текст джерелаRoutledge, P. A. "Adverse Drug Reactions and Interactions: Mechanisms, Risk Factors, Detection, Management and Prevention." In Stephens' Detection of New Adverse Drug Reactions, 91–125. Chichester, UK: John Wiley & Sons, Ltd, 2005. http://dx.doi.org/10.1002/0470014199.ch2.
Повний текст джерелаAlakus, Talha Burak, and Ibrahim Turkoglu. "A Comparative Study of Amino Acid Encoding Methods for Predicting Drug-Target Interactions in COVID-19 Disease." In Modeling, Control and Drug Development for COVID-19 Outbreak Prevention, 619–43. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-72834-2_18.
Повний текст джерелаGoldstein, M. J. "The Interaction of Drug and Family Therapy in the Prevention of Relapse in Schizophrenia." In Guidelines for Neuroleptic Relapse Prevention in Schizophrenia, 55–66. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-86922-8_13.
Повний текст джерелаAasland, Aadne, and Anastasia Y. Meylakhs. "Adjusting the Scope of Interaction Between State and Civil Society: HIV Prevention Among Drug Users." In Governance in Russian Regions, 43–71. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-61702-2_3.
Повний текст джерелаThomas, David. "Drug–Nutrient Interactions." In Nutrition and Disease Prevention, 469–77. CRC Press, 2007. http://dx.doi.org/10.1201/9781420005493.ch29.
Повний текст джерелаA. Ochola, Lucy, and Eric M. Guantai. "Prevention of Hyperglycemia." In Metformin - Pharmacology and Drug Interactions. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.99342.
Повний текст джерелаNaveed, Safila, and Halima Sadia. "Interaction Studies of ACE Inhibitors with Antidiabetic Drugs." In Metformin - Pharmacology and Drug Interactions. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.99795.
Повний текст джерела"Role of Nutritional Antioxidants in the Prevention and Treatment of Neurodegenerative Disorders." In Nutrient-Drug Interactions, 143–92. CRC Press, 2006. http://dx.doi.org/10.1201/9781420019131-9.
Повний текст джерелаEsposito, Ennio. "Role of Nutritional Antioxidants in the Prevention and Treatment of Neurodegenerative Disorders." In Nutrient-Drug Interactions, 129–78. CRC Press, 2006. http://dx.doi.org/10.1201/9781420019131.ch5.
Повний текст джерелаТези доповідей конференцій з теми "Drug interactions Prevention"
Kozloff, Kenneth M., Leo I. Volakis, Joan C. Marini, and Michelle S. Caird. "Near-Infrared Imaging Reveals Site- and Age-Specific Localization of Bisphosphonate Delivery and Retention in Model of Osteogenesis Imperfecta." In ASME 2009 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2009. http://dx.doi.org/10.1115/sbc2009-205344.
Повний текст джерелаZhukovets, T. A., M. А. Khancheuski, I. V. Koktysh, E. I. Kvasyuk, and A. G. Sysa. "ANTIOXIDANT EFFECTS OF EMOXYPINE AS ADJUVANT OF ANTI-CANCER DRUGS." In SAKHAROV READINGS 2021: ENVIRONMENTAL PROBLEMS OF THE XXI CENTURY. International Sakharov Environmental Institute of Belarusian State University, 2021. http://dx.doi.org/10.46646/sakh-2021-2-52-55.
Повний текст джерелаSantos, Nathalia Lima Schramm dos, William Wallace dos Santos Silva, Geovanna da Silva Campos Conceição, Gabriel Serra Almeida, Jacqueline Oliveira Freitas, Breno Silva Reis, and Lucas Santos Silva. "CGRP antagonists: Perspectives on migraine prophylaxis." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.193.
Повний текст джерелаOliveira, Ricardo F., Senhorinha F. Teixeira, Helena Maria Cabral Marques, and José Carlos Teixeira. "A Correlative CFD Study Between Recirculation Area and FPM in VHC Design." In ASME 2016 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/imece2016-67329.
Повний текст джерелаRabiei, Nastaran, and Carlos Hidrovo. "Effect of Wetted Microtexturing on Friction in Microchannel Flow." In ASME 2020 18th International Conference on Nanochannels, Microchannels, and Minichannels collocated with the ASME 2020 Heat Transfer Summer Conference and the ASME 2020 Fluids Engineering Division Summer Meeting. American Society of Mechanical Engineers, 2020. http://dx.doi.org/10.1115/icnmm2020-1083.
Повний текст джерелаApitz Castro, R., E. Ledezma, A. Jorquera, and M. K. Jain. "REVERSIBLE BLOCKADE OF PLATELET ACTIVATION DURING CARDIO-PUIMONAR BYPASS IN DOGS AFTER IV ADMINISTRATION OF AJOENE." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644820.
Повний текст джерелаLukinović, Mario, Larisa Jovanović, and Vladimir Šašo. "CHALLENGES IN MANAGING INTELLECTUAL PROPERTY RIGHTS DURING CORONAVIRUS PANDEMIC." In Fourth International Scientific Conference ITEMA Recent Advances in Information Technology, Tourism, Economics, Management and Agriculture. Association of Economists and Managers of the Balkans, Belgrade, Serbia, 2020. http://dx.doi.org/10.31410/itema.2020.239.
Повний текст джерелаKo, S. H., D. L. Rhode, and Z. Guo. "Computed Effects of Rim Seal Clearance and Cavity Width on Thermal Distributions." In ASME 1993 International Gas Turbine and Aeroengine Congress and Exposition. American Society of Mechanical Engineers, 1993. http://dx.doi.org/10.1115/93-gt-419.
Повний текст джерелаTsukimata, Márcio Yutaka, Bianca Lumi Inomata da Silva, and Jennison Alves Guimarães. "Açaí: potential anticonvulsant agent." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.064.
Повний текст джерела