Literatura científica selecionada sobre o tema "Évaluation de la fibrose"
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Artigos de revistas sobre o assunto "Évaluation de la fibrose"
Guéchot, Jérôme. "Évaluation de la fibrose hépatique". Revue Française des Laboratoires 2003, n.º 358 (dezembro de 2003): 39–43. http://dx.doi.org/10.1016/s0338-9898(03)90045-x.
Texto completo da fonteTaibi, Ludmia, e Jérôme Guéchot. "Évaluation non invasive de la fibrose hépatique". Revue Francophone des Laboratoires 2017, n.º 491 (abril de 2017): 38–44. http://dx.doi.org/10.1016/s1773-035x(17)30117-x.
Texto completo da fonteKalla, Nabila, Souhila Aouidane, Faiza Megaache e Soraya Tebbal. "Evaluation of the performance and concordance of Fibroscan and the APRI score in patients with chronic hepatitis C". Batna Journal of Medical Sciences (BJMS) 7, n.º 1 (2 de maio de 2020): 19–23. http://dx.doi.org/10.48087/bjmsoa.2020.7105.
Texto completo da fonteTantaoui, H., K. Nassar e S. Janani. "Évaluation non invasive de la fibrose hépatique induite par méthotrexate". Revue du Rhumatisme 88 (dezembro de 2021): A298. http://dx.doi.org/10.1016/j.rhum.2021.10.509.
Texto completo da fonteCalès, P., F. Oberti, I. Hubert, S. Michalak, I. Valo, Y. Gallois, Y. Tourmen, G. Soulard, F. Moal e M. C. Rousselet. "CA1 - Évaluation non invasive des caractéristiques de la fibrose hépatique". Gastroentérologie Clinique et Biologique 28, n.º 8-9 (agosto de 2004): 778. http://dx.doi.org/10.1016/s0399-8320(04)95095-6.
Texto completo da fontede Lédinghen, V., T. Poynard, C. Wartelle e E. Rosenthal. "Évaluation non-invasive de la fibrose hépatique au cours de l’hépatite C". Gastroentérologie Clinique et Biologique 32, n.º 3 (março de 2008): S90—S95. http://dx.doi.org/10.1016/s0399-8320(08)73271-8.
Texto completo da fonteGharbi, O., M. Medhioub, M. Yakoubi, M. L. Hamzaoui, E. Chelbi, A. Khsiba, M. Mahmoudi e M. M. Azzouz. "Évaluation clinicobiologique non invasive de la fibrose au cours de la NASH". La Revue de Médecine Interne 39 (dezembro de 2018): A210. http://dx.doi.org/10.1016/j.revmed.2018.10.207.
Texto completo da fonteAlfidja, A. T., M. Badiane, A. Mbaye, Y. Dial, J. Richter e S. Ba Diop. "Fibrose périportale chez les enfants en zone d’endémie à Schistosoma mansoni : évaluation échographique". Journal de Radiologie 85, n.º 6 (junho de 2004): 763–67. http://dx.doi.org/10.1016/s0221-0363(04)97679-2.
Texto completo da fonteLe Bail, B., V. De Lédinghen, P. Bioulac-Sage e T. Lamireau. "Évaluation de la fibrose hépatique chez l’enfant : la biopsie sera t-elle supplantée ?" Annales de Pathologie 26 (novembro de 2006): 125. http://dx.doi.org/10.1016/s0242-6498(06)78425-5.
Texto completo da fonteFalque, L., M. Husson, M. Jaillet, A. Cazes, B. Crestani e A. Mailleux. "Fibrose Pulmonaire Idiopathique et cancer : évaluation ex vivo du rôle oncogénique du micro environnement". Revue des Maladies Respiratoires 38, n.º 6 (junho de 2021): 591. http://dx.doi.org/10.1016/j.rmr.2021.02.047.
Texto completo da fonteTeses / dissertações sobre o assunto "Évaluation de la fibrose"
Mezni, Imen. "Évaluation d'un marqueur précoce de la dysfonction chronique du greffon rénal : la PCR urinaire de l'ARNm de la Vimentine". Thesis, Sorbonne université, 2018. http://www.theses.fr/2018SORUS088.
Texto completo da fonteChronic graft dysfunction is the major cause for end-stage renal failure after renal transplantation, both through immune and non-immune mechanisms. When the renal tubular epithelium undergoes epithelial phenotypic changes (EPC), reminiscent of epithelial mesenchymal transition (EMT), and associated with interstitial fibrosis and tubular atrophy, the prognosis is poor with a diminution of renal function and graft loss. In this prospective study. We studied the renal epithelial phenotype by immunohistochemistry and measured mRNA in urine of vimentin, CD45, GAPDH and uroplakin 1a by RT-PCR. We compared grafts from living donors and those from deceased donors. We evaluated the diagnostic performance of RT-PCR on urine for the diagnosis of epithelial phenotypic changes in transplant patients, with renal biopsy surveillance at 3 months and a biopsy on particular indication. We have shown that the EMT score on renal biopsy surveillance and the evolution of graft renal function were better in the patients from living donors than in those from cadaveric donors. The value of the mRNA of vimentin and CD45 relative to the uroplakin is correlated with the score in vimentin immunostaining in routine biopsies. These biomarkers could be used as a noninvasive tool to monitor the renal graft fibrogenesis. This test could be used for early detection of fibrotic diseases of the kidney transplant. In an independant study, the transcriptome in urine was analyzed, and it was found that normalization of mRNA with uroplakin mRNA was useful, and that EPC were associated with immune and inflammatory profiles
Cassinotto, Christophe. "Diagnostic et évaluation de la gravité des maladies chroniques du foie : impact de l’elastographie par ondes de cisaillement « supersonic shear imaging »". Thesis, Bordeaux, 2016. http://www.theses.fr/2016BORD0231/document.
Texto completo da fonteAbstract :The management and the prognosis for chronic liver diseases are widely based on the presence and the development of a liver fibrosis. The progressive worsening of liver fibrosis leads in a certain number of patients to the development of cirrhosis and its complications. Thus, the development of non-invasive diagnostic tools for the diagnosis and the monitoring of the liver fibrosis is of crucial interest. Liver elastography is one of the most promising techniques that have recently emerged in the field of chronic liver diseases. In this study, we aim to assess the diagnostic accuracy of a new elastography technique, named “Supersonic Shear Imaging” (SSI), and toanalyse its added value in the non invasive diagnosis of chronic liver diseases.In a first study, we prospectively analysed and compared the diagnostic performances of SSI elastography versus FibroScan and ARFI for the staging of liver fibrosis in a cohort of 349 patients with chronic liver diseases that consecutively underwent a liver biopsy. In a second study, we prospectively analysed the impact of liver and spleen SSI elastography in a cohortof 401 cirrhotic patients for the non invasive diagnosis of cirrhosis severity and oesophageal varices.In a third study, we assessed the clinical use of liver stiffness measurement evaluated by SSI, FibroScan,and ARFI in a cohort of nonalcoholic fatty liver disease patients who underwent liver biopsy. A total of 291 NAFLD patients were prospectively enrolled at 2 French university hospitals (Angers and Bordeaux)
Boulanger, Simon. "Évaluation du potentiel d'action de l'utilisation combinée de la tomatidine (ou son analogue : FC04-100) et d'aminoglycosides contre Staphylococcus aureus et Pseudomomas aeruginosa". Mémoire, Université de Sherbrooke, 2015. http://hdl.handle.net/11143/7533.
Texto completo da fonteLunven, Laurent. "Synthèse et évaluation d'aurones sur des modèles de fibres de tau". Thesis, Université Grenoble Alpes (ComUE), 2016. http://www.theses.fr/2016GREAV007/document.
Texto completo da fonteThe fibrillation of the tau protein occurs in many neurodegenerative diseases, including Alzheimer’s disease, and leads to the formation of amyloid fibres called neurofibrillary tangles. Using organic molecules able to mark these fibres or inhibit their formation provides an interest both in diagnosis and therapy in Alzheimer’s disease. A series of aurones was synthesized and their ability to interfere with the fibrillation process was evaluated in vitro on models of tau fibres developed in this project. This work shows that polyhydroxylated aurones are able to act both as probes and as inhibitors of the fibrillation process. The ligation of these aurones with biomolecules or their radiolabelling has also been investigated
Pham, Thi Minh Tam. "Évaluation de la combinaison échographie, élastométrie par onde de cisaillement, et biomarqueurs sériques pour le diagnostic ultra-précoce du carcinome hépatocellulaire". Thesis, Sorbonne université, 2019. http://www.theses.fr/2019SORUS309.
Texto completo da fonteBackground: Hepatocellular carcinoma (HCC) is the most common primary liver cancer. It occurs in 75% to 80% of cases on cirrhosis. The annual incidence in France is 10,624 cases and is responsible for 10,063 deaths per year. There is a relationship between tumor size and prognosis. It is therefore necessary to improve the screening and monitoring of patients with chronic liver disease and high risk of HCC. Objective: The objective of the thesis was to prospectively evaluate the effectiveness of day hospital screening of HCC by FibroTest, associated with shear wave elastometry / Shear-Wave-Elastography (SWE), morphological ultrasound in B mode associated with the alphafetoprotein (AFP) assay (FT-SWE surveillance). Methods: Patients of the Hepatocellular Carcinoma Multi-Technological Consortium (HECAM) were prospectively included between 2015 and 2018 in the Pitié-Salpêtrière Hospital Group for surveillance by SWE. They were matched to historical controls monitored by simple ultrasound, using a propensity score. The efficacy of FibroTest was compared to that of Fibroscan / Transient Elastography (TE) to identify subjects with severe fibrosis. Results: All comparisons, whether in terms of HCC-free survival or 10-year overall survival, showed superior survival in HECAM patients under FT-SWE surveillance compared to control patients under standard surveillance. FibroScan alone or associated with FibroTest is less effective than FibroTest alone. Conclusion: FT-SWE surveillance compared to control patients under standard surveillance
Bertho, Annaïg. "Lésions pulmonaires après irradiation stéréotaxique : modélisation préclinique et aspects radiopathologiques". Thesis, Sorbonne université, 2019. http://www.theses.fr/2019SORUS504.
Texto completo da fontePulmonary stereotactic radiation therapy uses high doses per fraction (6 to 20 Gy). Despite the decrease in irradiated volumes, patients still develop side effects as lung fibrosis. The lack of radiobiological data for high doses per fraction exposure remains an issue. The purpose is therefore to acquire, in vivo, original data in pulmonary radiopathology thanks to the SARRP. Effect of the irradiation volume is characterized by 4 different beam collimations at a dose of 90 Gy. The 3x3 mm² collimator allows observing radiation induced pulmonary fibrosis requiring depletion of club cells and reactive proliferation of type II pneumocytes. Dose effect study was conducted using a single dose range (from 20 to 120 Gy, 3x3mm²). A dose of 60 Gy is required to generate fibrosis. Study of fractionation effect show that a minimum BED3Gy (Biological Effective Dose) of 200 Gy was required to observe pulmonary fibrosis in mice. In vitro, different pulmonary cell lines were irradiated at variable doses per fraction but constant BED. Analysis of 44 genes suggests an epithelial to mesenchymal transition process. At constant BED, there is no significant effect of dose per fraction in our model
Malleville, Marie-Alicia. "Évaluation du potentiel des fibres apériodiques à très large aire modale pour la réalisation de sources laser impulsionnelles". Thesis, Limoges, 2020. http://www.theses.fr/2020LIMO0009.
Texto completo da fonteThese Ph.D work is conducted in the context of a long-term collaboration between Xlim laboratory and the company EOLITE Systems in order to develop new large mode area fibers typically capable of providing up to 200 W of average output power and a peak power of 1 MW while maintaining a transverse single-mode emission at 1030 nm. For that purpose, optical fibers with an aperiodic microstructuration (FA-LPF) were developed in order to improve the performances of commercial fibers, mainly by pushing further the transverse mode instabilities power threshold. An unprecedented experimental study has been conducted to investigate the influence of the fiber structure, the laser source architecture and the mode field diameter. Furthermore, by replacing the commercial fiber by a FA-LPF in an industrial laser prototype, as a proof-of-concept, the FA-LPF permits to obtain a laser source with at least similar properties as those of the laser sources of the company regarding the laser efficiency or the lifetime test. The feasibility of a microstructured fiber shorter and still efficient (50 cm-long), has also been studied, by increasing the ytterbium ions concentration in the FA-LPF core or by improving the core to clad ratio. Finally, a new concept of fiber with a depressed-index core led to core diameters higher than 110 μm while maintaining a transverse single-mode emission
Courtiol-Legourd, Stéphanie. "Conception, synthèse et évaluation d’inhibiteurs phosphoanalogues d’aldose-cétose isomérases". Thesis, Paris 11, 2013. http://www.theses.fr/2013PA112050.
Texto completo da fonteAldose-ketose isomerases are enzymes which catalyze the interconversion of an aldose and a ketose. We have studied three of them: phosphoribose isomerase (RPI), phosphomannose isomerase (PMI) and phosphoglucose isomerase (PGI). These enzymes play a major role in various metabolic pathways as glycolysis, neoglucogenesis, the pentoses phosphates pathways or the mannose metabolism. It has been shown to have a crucial role for the survival and development of several microorganisms responsible for diseases as the leishmaniose, the cystic fibrosis, the tuberculosis, the malaria or the insomnia. These enzymes are thus potential therapeutic targets. Consequently, strong inhibitors of these enzymes could provide efficient therapeutic tools against these deseases. The reactions catalyzed by these enzymes involve intermediaries of high energy (IHE) of 1,2-cis-enediol(ate) type. The synthesis of analogues of these intermediaries allowed to obtain in the laboratory, the best inhibitors known for these enzymes, the acid 5-phospho-D-arabononohydroxamique (5PAH, the best inhibitor of the PMI and PGI) and the 5-phospho-D-ribonate (5PRA, the best inhibitor of the RPI). However, these inhibitors possess a phosphate group which is easily hydrolysable in physiological environment, what makes them inactive in vivo. During this work of thesis, phosphoanalogues of the 5PAH, the 5-phospho-D-ribose (R5P, the substrate of the RPI) and of the 5PRA possessing a malonate, phosphonate, phosphorothiate, sulphate and sulfonate were obtained by multi-steps synthesis bringing in D-arabinose or D-ribose as starting product. The inhibitive properties of these compounds were then determined and their stability in physiological environment evaluated. The phosphoanalogue of the 5PAH of malonate type, the acid 5-desoxy-5-dicarboxyméthyl-D-arabinonohydroxamique (5DCAH) is a modest and stable inhibitor of the PMI of Escherichia Coli. Among the phosphoanalogues of the R5P, the compounds of sulphate and sulfonate types, respectively, the 5-sulfate-D-ribose (5SR) and 5-desoxy-sulfonomethyl-D-ribose (5SMR), are good inhibitors of three RPI (the RPI of spinach, the RPI of Escherichia Coli and the RPI of Micobacterium tuberculosis). Only the compound of sulfonate type is stable in physiological environment. The phosphoanalogue of malonate type, the 5-desoxy-5-dicarboxymethyl-D-ribose (5DCR) is a modest inhibitor of this three RPI. On the other hand, the phosphoanalogues of phosphorothioate and phosphonate types, respectively, the 5-desoxy-5-phosphorothioate-D-ribose (5PTR) and the 5-desoxy-5-phosphonomethyl-D-ribose (5PMR), are bad inhibitors. The phosphoanalogue of phosphonate type of the 5PRA, the 5-desoxy-5-phosphonomethyl-D-ribonate (5PMRA), is a good inhibitor of the RPI of Micobacterium tuberculosis. Furthermore, this compound is stable in physiological environment. It is on the other hand a bad inhibitor of the RPI of spinach and Escherichia Coli. These results are particularly promising because the 5PMRA is this day the best stable and specific inhibitor of the RPI of Micobacterium tuberculosis
Alexaline, Maïa. "Elaboration d’un épiderme de culture et évaluation non clinique sur un modèle de brûlure cutanée". Thesis, Paris 11, 2015. http://www.theses.fr/2015PA114816.
Texto completo da fonteThe deep and large injuries caused by massive burns prevent the use of split-thickness skin autografts. Today, autologous epidermal substitutes constitute an alternative treatment for skin regeneration. In fact tissue engineering allows the production of Cultured Epithelial Autografts (CEA) by in vitro keratinocyte amplification from a small healthy skin biopsy. The clinical use of CEA since the 1980’s has allowed an increase in the survival rate of burnt patients. However, CEAs present numerous drawbacks, among them the high fragility of keratinocyte sheets, and the immaturity of the dermal-epidermal junction leading to heavy cosmetic and functional sequelae.This thesis focuses on the bioengineering of epidermal substitute for clinical burn treatment to enhance wound healing and skin regeneration, from a translational research point of view. This work also includes the development of an animal model of third degree burn for the evaluation of epidermal substitute.We first developed a new epidermal substitute cultured on a fibrin matrix from human plasma (hPBES: human Plasma-Based Epidermal Substitute). Then we characterized this new substitute with phenotypical and functional analyses, using as a reference the epidermal substitute Epicel® (Genzyme, US). We observed properties more favorable with hPBES than with Epicel® in terms of clonogenicity, stemness, differentiation level, proliferation, migration potential and basement membrane protein conservation.The influence of the plasma-based fibrin matrix on keratinocytes was studied in comparison with a culture on a fibrin from purified fibrinogen, and with a culture with no matrix. For this study we focused our analysis on the role of the released factors from fibrin matrices during epidermal substitute culture. Both fibrin matrices improved epidermal substitute properties: reduction of terminal differentiation, enhancement of migration potential, secretion of wound healing enhancing factors. Besides, plasma-based fibrin specifically promote epidermal morphogenesis, keratinocyte proliferation and clonogenicity.The culture process was adapted to European regulation requirements without diminishing its regenerative potential: substitution of murine feeder cells by human dermal fibroblasts, adaptation of culture medium and plasma viral inactivation using amotosalen treatment.A burn model including all the surgical steps used in clinics for CEA grating was developed on nude rats. However the evaluation of hPBES on this model could not be achieved due to graft rejection. Therefore we evaluated epidermal regeneration after hPBES graft on acute wounds on NOD-SCID mice. We showed a good graft rate, with the regeneration of a human epidermis close to healthy epidermis with a well-organized dermal-epidermal junction two weeks after hPBES grafting
Mottais, Angélique. "Thérapie génique non-virale de la mucoviscidose : évaluation des voies d'administration et adaptation des formulations". Thesis, Brest, 2017. http://www.theses.fr/2017BRES0146/document.
Texto completo da fonteCystic fibrosis is a genetic disease with lung damages as the current main causes of death. Due to the absence or dysfunction of the CFTR chloride channel, CF patients have hyper-viscous mucus, particularly in the respiratory tract. This mucus is an environment favorable to infection development by opportunistic bacteria such as Staphylococcus aureus or Pseudomonas aeruginosa. The chronicity of infections coupled with significant inflammation leads to the progressive degradation of respiratory functions. Currently, apart from the heart-lung transplantation, no cure is still available for all patients.The approach by gene therapy appears to be a good strategy to cure all patients regardless of the type of mutations they have. It is a matter of bringing a healthy copy of the CFTR gene into the cells so that they express a functional protein. To do this, many barriers must be overcome. Among them, the presence of bacteria in the cellular environment is a brake against the transfer of genes in particular by vectors. It seems pertinent to develop a multifunctional formulation that on the one hand eliminates surface bacteria and on the other hand transfect the target cells. This formulation must remain effective after it has been aerosolized. During this work, several formulations, incorporating cationic lipids and silver compounds, have been developed
Livros sobre o assunto "Évaluation de la fibrose"
Reinhardt, Dietrich, Manfred Götz, Richard Kraemer e Martin H. Schöni, eds. Cystische Fibrose. Berlin, Heidelberg: Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/978-3-642-56796-4.
Texto completo da fonteKraemer, Richard, e Martin Kistler. Cystische Fibrose/Mukoviszidose. Basel: Birkhäuser Basel, 1992. http://dx.doi.org/10.1007/978-3-0348-5655-3.
Texto completo da fonteSchmitt, Gustel Matthias. Cystische Fibrose: Leben mit einer chronischen Krankheit. Göttingen: Hogrefe, 1991.
Encontre o texto completo da fonteTélé-université, Université du Québec, ed. Évaluation environnementale. Sainte-Foy: Télé Université, 1998.
Encontre o texto completo da fonteDéry, Lucie. L' évaluation. Toronto: Ministère de la formation professionnelle de l'Ontario, 1989.
Encontre o texto completo da fonteBraun, Claude M. J. Évaluation neuropsychologique. Montréal, Qué: Décarie, 1997.
Encontre o texto completo da fonteTagliante, Christine. L' évaluation. [Paris]: Clé International, 1991.
Encontre o texto completo da fonteE, Hodson Margaret, Geddes Duncan M e Bush, Andrew, 1954 Apr. 24-, eds. Cystic fibrosis. 3a ed. London: Hodder Arnold, 2007.
Encontre o texto completo da fontePena, Felipe. No jornalismo não há fibrose: E outros ensaios críticos sobre a imprensa. Rio de Janeiro: Cassará, 2012.
Encontre o texto completo da fonteDennis, Shale, ed. Cystic fibrosis. London: BMJ Publishing Group, 1996.
Encontre o texto completo da fonteCapítulos de livros sobre o assunto "Évaluation de la fibrose"
Hebestreit, H., e A. Hebestreit. "Zystische Fibrose". In Pädiatrie, 499–505. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-34269-1_22.
Texto completo da fonteRohde, V. "Retroperitoneale Fibrose". In Facharztwissen Urologie, 243–47. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-01626-4_18.
Texto completo da fonteRaimbourg, Q., e E. Daugas. "Fibrose rétropéritonéale". In Maladies rares en médecine d’urgence, 317–29. Paris: Springer Paris, 2013. http://dx.doi.org/10.1007/978-2-8178-0350-0_19.
Texto completo da fonteBargon, J., e W. F. Caspary. "Zystische Fibrose". In Therapie von Leber- und Gallekrankheiten, 105–9. Berlin, Heidelberg: Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/978-3-642-56819-0_9.
Texto completo da fonteTeschendorf, C., e W. Schmiegel. "Zystische Fibrose". In Klinische Gastroenterologie und Stoffwechsel, 811–22. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57194-7_70.
Texto completo da fonteTiddens, H. A. W. M., J. M. Hulst e H. M. Janssens. "Cystische fibrose". In Compendium kindergeneeskunde, 343–53. Houten: Bohn Stafleu van Loghum, 2018. http://dx.doi.org/10.1007/978-90-368-1792-9_33.
Texto completo da fonteGötz, M., J. Henker e M. J. Lentze. "Zystische Fibrose". In Pädiatrie, 1061–73. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-09176-0_147.
Texto completo da fontevan den Berg, H., E. Erren, M. E. H. Reijers, M. Wittebrood e G. de Vries. "Cystic fibrose". In Verpleegkundig Vademecum, 189–94. Houten: Bohn Stafleu van Loghum, 2008. http://dx.doi.org/10.1007/978-90-313-7326-0_38.
Texto completo da fonteStern, Martin. "Zystische Fibrose". In Pädiatrische Gastroenterologie, Hepatologie und Ernährung, 575–83. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-24710-1_24.
Texto completo da fonteGallati, S., D. Hartl, N. Derichs, M. H. Schöni, B. Tümmler, D. Staab, S. Junge et al. "Zystische Fibrose". In Pädiatrische Pneumologie, 587–631. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-34827-3_28.
Texto completo da fonteTrabalhos de conferências sobre o assunto "Évaluation de la fibrose"
Jambon, Francis, Caroline Golanski e Pierre-Jacques Pommier. "Évaluation des dispositifs mobiles". In the 18th international conference. New York, New York, USA: ACM Press, 2006. http://dx.doi.org/10.1145/1132736.1132741.
Texto completo da fonteSaint-Aimé, Sébastien, Brigitte Le Pévédic e Dominique Duhaut. "Évaluation du modèle computationnel d'émotions iGrace". In the 21st International Conference. New York, New York, USA: ACM Press, 2009. http://dx.doi.org/10.1145/1629826.1629857.
Texto completo da fonteAmazonas de Albuquerque, Sandra Mara, e Judis Blacher. "Fibrose Cística: Atendimento Pedagógico e Multidisciplinaridade". In Forúm Nacional de Atendimento Escolar Hospitalar. São Paulo - SP, Brazil: Galoa, 2006. http://dx.doi.org/10.17648/afnaeh-2006-74091.
Texto completo da fonteSattler, B., A. Huber, L. Gantner, S. Kellnar, F. Edler von Koch e B. Schiessl. "Intrauteriner Volvolus bei Cystischer Fibrose (CF)". In 28. Deutscher Kongress für Perinatale Medizin. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1607895.
Texto completo da fonteBrun, Frédéric. "Sites nucléaires et évaluation des risques chimiques". In Chimie du nucléaire et prise en compte de l’environnement. Les Ulis, France: EDP Sciences, 2013. http://dx.doi.org/10.1051/jtsfen/2013chi04.
Texto completo da fonteHadjar, Omar R., e Ronald Beaubrun. "Implémentation et évaluation de la technologie HSDPA". In 2006 Canadian Conference on Electrical and Computer Engineering. IEEE, 2006. http://dx.doi.org/10.1109/ccece.2006.277645.
Texto completo da fonteSilva, Amanda Lorraine Pereira, CINTIA GRAZIELY MIRANDA AZEVEDO e MARIA CAROLINA BEZERRA DI MEDEIROS LEAL. "ATRIBUIÇÃO DO CANAL CFTR NA FIBROSE CÍSTICA". In III Congresso Brasileiro de Biologia Molecular On-line. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/iii-conbramol/11708.
Texto completo da fonteVASCONCELOS, GUSTAVO BENTO, HÍGOR CHAGAS CARDOSO, RODRIGO ELIAS SOUZA PINTO, DÉBORA COSTA NOLETO e BRUNO YUJI HAMAOKA DE MELO. "O TRATAMENTO DA FIBROSE CÍSTICA EM CRIANÇAS". In III Congresso Brasileiro de Saúde On-line. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/iii-conbrasau/11725.
Texto completo da fontePEREIRA, CECÍLIA CANGERANA, VINICIUS ALVES DE ANDRADE, VICENTE CANGERANA PEREIRA e FERNANDA ALVES CANGERANA PEREIRA. "Fibrose Cística: Doença Pulmonar e Poluição Atmosférica". In II Brazilian Congress of Health. HEALTH2021, 2021. http://dx.doi.org/10.51162/health2021-0014.
Texto completo da fonteDavid, Christopher, Isabelle Care e José Veau. "Évaluation de débitmètres à effet vortex par l’EXERA". In 16th International Congress of Metrology, editado por J. R. Filtz, B. Larquier, P. Claudel e J. O. Favreau. Les Ulis, France: EDP Sciences, 2013. http://dx.doi.org/10.1051/metrology/201302002.
Texto completo da fonteRelatórios de organizações sobre o assunto "Évaluation de la fibrose"
Toutin, Th. Évaluation de la géométrie des images RADARSAT : premiers résultats. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1997. http://dx.doi.org/10.4095/219005.
Texto completo da fonteToutin, Th. Évaluation de la précision géométrique des images de RADARSAT. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1998. http://dx.doi.org/10.4095/219137.
Texto completo da fonteBerry, P., e R. Schnitter. Évaluation nationale du changement climatique et de la santé. Natural Resources Canada/CMSS/Information Management, 2022. http://dx.doi.org/10.4095/329609.
Texto completo da fonteMul, M., E. Obuobie, R. Appoh, K. Kankam-Yeboah, E. Bekoe-Obeng, B. Amisigo, F. Y. Logah, B. Ghansah e M. McCartney. Évaluation des ressources en eau du bassin de la Volta. International Water Management Institute (IWMI)., 2016. http://dx.doi.org/10.5337/2016.201.
Texto completo da fonteBird, T. D., J. E. Barclay, R. I. Campbell e P. J. Lee. Partie I: analyse géologique des zones gazéifères et évaluation des ressources. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1994. http://dx.doi.org/10.4095/194158.
Texto completo da fonteBird, T. D., J. E. Barclay, R. I. Campbell e P. J. Lee. Partie I: analyse géologique des zones gazéifères et évaluation des ressources. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1994. http://dx.doi.org/10.4095/194799.
Texto completo da fonteReinson, G. E., P. J. Lee, W. Warters, K. G. Osadetz, L L Bell, P. R. Price, F. Trollope, R. I. Campbell e J E Barclay. Partie I : analyse géologique des zones gazéifères et évaluation des ressources. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1993. http://dx.doi.org/10.4095/195158.
Texto completo da fonteBarclay, J. E., G. D. Holmstrom, P. J. Lee, R. I. Campbell e G E Reinson. Partie I : Analyse géologique des zones gazéifères et évaluation des ressources. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1997. http://dx.doi.org/10.4095/208997.
Texto completo da fonteAuer, Daniel, Denise Efionayi-Mäder, Fehlmann Joëlle, Mirjam Suri, Dina Bader, Giuliano Bonoli, Michael Morlok e Johanna Probst. Suivi et évaluation du programme pilote « Encouragement précoce de la langue ». Université de Neuchâtel – Swiss Forum for Migration and Population Studies (SFM), junho de 2023. http://dx.doi.org/10.35662/unine-sfmstudies-84f.
Texto completo da fonteHicks, Jacqueline, Alamoussa Dioma, Marina Apgar e Fatoumata Keita. Premiers résultats d'une évaluation de recherche-action systémique au Kangaba, Mali. Institute of Development Studies, abril de 2024. http://dx.doi.org/10.19088/ids.2024.019.
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