Letteratura scientifica selezionata sul tema "Sclérose latérale amyotrophique – Soins médicaux"
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Articoli di riviste sul tema "Sclérose latérale amyotrophique – Soins médicaux":
Gonzalez-Bermejo, Jésus, Amélie Hurbault, Christophe Coupé, Vincent Meininger e Thomas Similowski. "Soins palliatifs et ventilation mécanique dans la sclérose latérale amyotrophique (SLA)". Médecine Palliative : Soins de Support - Accompagnement - Éthique 9, n. 6 (dicembre 2010): 309–17. http://dx.doi.org/10.1016/j.medpal.2010.09.008.
Marcos, Isabelle, e Benoît Burucoa. "La psychomotricité en unité de soins palliatifs : au sujet d’une personne atteinte de sclérose latérale amyotrophique (SLA)". Médecine Palliative : Soins de Support - Accompagnement - Éthique 11, n. 3 (giugno 2012): 142–47. http://dx.doi.org/10.1016/j.medpal.2011.11.006.
Danel-Brunaud, V., L. Laurier, K. Parent, C. Moreau, L. Defebvre, D. Jacquemin e A. Destée. "Les enjeux de la loi Leonetti : participation des patients atteints de sclérose latérale amyotrophique à une discussion anticipée sur la réanimation respiratoire et les soins de fin de vie". Revue Neurologique 165, n. 2 (febbraio 2009): 170–77. http://dx.doi.org/10.1016/j.neurol.2008.08.008.
Tesi sul tema "Sclérose latérale amyotrophique – Soins médicaux":
Cardoso, Sonia Filomena. "Apports de la modélisation ontologique pour l’analyse des ruptures de parcours de soins dans la Sclérose Latérale Amyotrophique". Thesis, Sorbonne université, 2019. http://www.theses.fr/2019SORUS587.
Patients with ALS require multidisciplinary support during their course. Pathology causes many disabilities and disabilities. This complex management can lead to situations of course failure through absence, cessation or difficulties of management, however the causes of these breaks are not known. The city hospital coordination network SLA Île-de-France has a textual coordination base, on which the needs and demands of patients are described throughout their journey. To this end, we propose to analyze this basis in order to extract knowledge and describe the patient pathways. For this we use a semantic annotation tool that uses as a resource an ontology of the domain that we have created OntoParon. OntoParon is a modular ontology composed of a medical module, a socio-environmental module, a coordination module, a core module and a consolidation module. These ontological modules make it possible to take into account the dimensions involved in patients' journeys. Defined concepts, reporting on important themes such as the exhaustion of the caregiver or even the presence of social problems were created to detect the difficulties encountered. The annotation of 931 patient files has shown that not all patients have the same needs or the same demands, some themes are expressed differently depending on the age, the pathology or the lifestyle of the patients
Bramucci, Maryline. "Eléments de guidance pour le médecin praticien des malades atteints d'une sclérose latérale amyotrophique traités à domicile". Nancy 1, 1993. http://www.theses.fr/1993NAN11003.
Le, Forestier Nadine. "Les Passeurs de mots. Une éthique philosophique du soin : à propos d’une enquête nationale au sein des Centres SLA de France". Thesis, Paris 11, 2014. http://www.theses.fr/2014PA11T098/document.
The teaching of Doctor-Patient relationship, in particular in making announcement of the diagnosis, makes progress in the Faculties of Medicine. But in practice, communicating the thruth of a disease with fatal issue remains a distressing time because still badly told. Amyotrophic Lateral Sclerosis, a motor neuron disease, is the most pejorative diagnosis to make in Neurology. In the controversy surrounding the time of the announcement of the diagnosis, and, by examining the results of 203 ALS Patients’ and their Caregivers’ questionnaires, we compare with the results of 38 ALS Centre Neurologists’ interviews. Through bringing an epistemological, ethical and philosophical analysis into focus, we argue that, in the rational multidisciplinary of the care in a rapid and incurable disease, the evolution of the clearly medical information changes the Doctor-Patient relationship into a moral injunction of presence for the Caregivers and the families. Only through the training of Doctors and a certain conception of Patient information in palliative care can the harmful consequences of such a trend be limited
Capitoli di libri sul tema "Sclérose latérale amyotrophique – Soins médicaux":
Gonzalez-Bermejo, J. "Soins palliatifs dans l’insuffisance respiratoire de la sclérose latérale amyotrophique". In Enjeux éthiques en réanimation, 409–16. Paris: Springer Paris, 2010. http://dx.doi.org/10.1007/978-2-287-99072-4_44.