Зміст
Добірка наукової літератури з теми "Foie – Maladies – Chimiothérapie"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "Foie – Maladies – Chimiothérapie".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Статті в журналах з теми "Foie – Maladies – Chimiothérapie"
Abdalla, S., and A. Brouquet. "Place de la chimiothérapie préopératoire dans le traitement des cancers du rectum localement avancés." Côlon & Rectum 13, no. 3 (August 2019): 137–46. http://dx.doi.org/10.3166/cer-2019-0092.
Повний текст джерелаde Nonneville, A., and A. Gonçalves. "Cancers du sein triple-négatifs : données actuelles et perspectives d’avenir." Oncologie 21, no. 1-4 (January 2019): 33–39. http://dx.doi.org/10.3166/onco-2019-0039.
Повний текст джерелаMercier, Marie, Emmanuelle Bocquet, Michel Danguy, and Monique-Marie Rousset. "Planification des soins bucco-dentaires et des traitements ODF chez les enfants atteints d’une hémopathie maligne." L'Orthodontie Française 82, no. 3 (September 2011): 299–306. http://dx.doi.org/10.1051/orthodfr/2011133.
Повний текст джерелаBaldé, S. "C95: Place de l’Evérolimus dans le cancer du sein avancé M+ RH+/Her2- : Stratégies thérapeutiques." African Journal of Oncology 2, no. 1 Supplement (March 1, 2022): S40—S41. http://dx.doi.org/10.54266/ajo.2.1s.c95.hcih5777.
Повний текст джерелаLèye, PA, TB Ly, PI Ndiaye, I. Gaye, EHB Ba, MD Bah, and E. Diouf. "C61: Gestion périopératoire de la transfusion sanguine en chirurgie carcinologique." African Journal of Oncology 2, no. 1 Supplement (March 1, 2022): S26—S27. http://dx.doi.org/10.54266/ajo.2.1s.c61.wpvk8511.
Повний текст джерелаWidlöcher, D. "Depression. Indices biologiques et indices cliniques." Psychiatry and Psychobiology 1, no. 1 (1986): 12–18. http://dx.doi.org/10.1017/s0767399x00000316.
Повний текст джерелаThéron, Alexandre, Anne-Charlotte Teyssier, Aziz Abgaou, and Anne Sirvent. "Les complications de la greffe de cellules souches hématopoïétiques chez l'enfant." Médecine Intensive Réanimation, November 22, 2023. http://dx.doi.org/10.37051/mir-00188.
Повний текст джерелаGelli, M., and I. Sourrouille. "Métastases péritonéales de cancer colorectal Cas particuliers : découverte peropératoire, métastases péritonéales et autres sites métastatiques, récidive après chirurgie de cytoréduction." Côlon & Rectum, 2020. http://dx.doi.org/10.3166/cer-2020-0159.
Повний текст джерелаAdmin - JAIM. "Résumés des conférences JRANF 2021." Journal Africain d'Imagerie Médicale (J Afr Imag Méd). Journal Officiel de la Société de Radiologie d’Afrique Noire Francophone (SRANF). 13, no. 3 (November 17, 2021). http://dx.doi.org/10.55715/jaim.v13i3.240.
Повний текст джерелаДисертації з теми "Foie – Maladies – Chimiothérapie"
Marimoutou, Catherine. "Evolution de la prise en charge de l'infection par le VIH à l'ère des multithérapies : expériences des Cohortes Aquitaine et MANIF 2000 : et du département de recherche clinique du CISIH-Sud de Marseille." Bordeaux 2, 2003. http://www.theses.fr/2003BOR21085.
Повний текст джерелаThis work presents the results observed through three different cohorts of HIV infected patients and focused on changes in morbidity and mortality of HIV infected patients since HAART era. First, we observed the decraese in deaths and AIDS cases following the large diffusion of HAART in 1996 and persisting nowadays. Non AIDS deaths were mainly due to liver or heart failures and neoplasia. In patients infected through injecting drug use, deaths due to liver failure were as frequent as AIDS deaths. These results underlined the necessity to manage the hepatitis C virus (HCV) coinfection. The main barrier to this management seemed to be the complete realization of the HCV screening, particularly the performance of liver biopsy. However, 1/2 HIV-VHC coinfected patients had a biopsy performed and 1/5 were treated for HCV. Among treated patients, the pejorative role of HAART with PI on HCV therapeutic response underlined the problem of therapeutic interaction in such coinfected patients
Delaporte, Flavien. "Évaluation de la toxicité des nanocapsules lipidiques sur des cellules hépatiques et immunitaires : influence de paramètres physico-chimiques." Electronic Thesis or Diss., Angers, 2024. https://dune.univ-angers.fr/documents/dune19058.
Повний текст джерелаThis PhD thesis evaluates the biodistribution and cellular toxicity of nanovectors: the lipid nanocapsules (LNCs). Physico-chemical parameters (size, charge and surface coating) can influence cellular interaction. The strong hepatic tropism of LNCs guided the first study on the evaluation of interactions between LNCs, with a diameter of 50 and 100 nm, and hepatocytes, represented by HepG2 and HepaRG cells. A relatively weak toxicity, concentration, size and time dependent was demonstrated. The 50 nm LNCs, although slower to be internalized than 100 nm ones, exhibited a higher toxicity, notably on cancer cells (HepG2 cell line). Exposure to LNCs generated lipid peroxidation which led to cells death via ferroptosis. A higher toxicity has been observed after 2 (vs. 24 h) and 4 weeks of exposure (vs. 2 weeks) for 50 nm LNCs. The 100 nm LNC seemed to be less toxic because their cytotoxicity did not increase between 2 and 4 weeks of exposure. A 2nd study allowed us to better characterized the influence of size and pegylation,parameters modified to improve blood and hepatic stealthness. LNCs of 50 and 100 nm, pegylated or not, have been exposed to human blood (ex vivo) in order to analyze the blood distribution. Circulating phagocytes (monocytes and neutrophiles) quickly internalized LNCs, without influence of size nor pegylation. An in vitro assessment was performed in order to complete the biodistribution study in hepatic cells (endotelial cell line, human macrophages and hepatocytes). It has been confirmed that LNCs preferentially distributed in liver cancer cells (vs. differentiated ones), as well as in primary human macophages and endotelial cells. Except for human macrophages, an increase in size improved internalization whereas pegylation decreased it. Finally, LNCs dit not seem to be immunomodulators. In conclusion, the passive distribution into liver cancer cells, associated with a high cytotoxicity, and the good tolerance observed with the other cells studied (hepatic in vitro and in blood ex vivo), suggest that LNCs could be considered as vectors for hepatocarcinoma treatment
Edeline, Julien. "Radiothérapie interne sélective et traitements systémiques dans les tumeurs hépatiques primitives : associations et comparaison des résultats." Thesis, Rennes 1, 2015. http://www.theses.fr/2015REN1B031/document.
Повний текст джерелаSelective Internal Radiation Therapy (SIRT) with microspheres loaded with Yttrium-90 is an emerging locoregional treatment of liver malignancies. In this work, we studied potential relationships between systemic treatment and SIRT in an in vitro model and two retrospective clinical studies. The results obtained may generate new hypotheses for clinical development. Regarding cholangiocarcinoma, concomitant use of chemotherapy may be associated with better outcomes, as suggested by both the in vitro and clinical retrospective data. Regarding hepatocellular carcinoma, our results confirmed previous interest in SIRT in case of portal vein thrombosis; our results might also suggest potential improvement by increasing the dose delivered, and the need to select patients with good targeting of the thrombosis as better candidate for SIRT. These results should be confirmed in prospective studies, currently ongoing