Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Paule, Bayle"'
Autor:
Maryse Lapeyre-Mestre, Aude Lagarrigue, Emilie Jouanjus, Norbert Telmon, Dider Fabre, Marion Mongiatti, Paule Bayle
Publikováno v:
Thérapie
Thérapie, EDP Sciences, 2020, 75, pp.579-589. ⟨10.1016/j.therap.2020.06.017⟩
Thérapie, 2020, 75, pp.579-589. ⟨10.1016/j.therap.2020.06.017⟩
Thérapie, EDP Sciences, 2020, 75, pp.579-589. ⟨10.1016/j.therap.2020.06.017⟩
Thérapie, 2020, 75, pp.579-589. ⟨10.1016/j.therap.2020.06.017⟩
Summary Objective It is essential that health professionals who practice medicine in prison rely on accurate knowledge about their patients to provide them with adapted care. The use of cannabis can influence the health status of prisoners, but data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6e23e89fcff3857e810f9e8cd6fe448
https://pubmed.ncbi.nlm.nih.gov/32718583
https://pubmed.ncbi.nlm.nih.gov/32718583
Publikováno v:
Médecine Palliative : Soins de Support - Accompagnement - Éthique. 13:200-206
Summary More than 10 years after the establishment of the law of 4 March 2002 on patients’ rights and quality of health system, the application of one of its measures, suspension of sentence for medical reasons, remains poor. This arrangement shoul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f83904437fa628fb674b82aecb9e2b3
https://doi.org/10.1016/j.medpal.2014.03.002
https://doi.org/10.1016/j.medpal.2014.03.002
Autor:
Paule Bayle, Jacques Bazex
Publikováno v:
Bulletin de l'Académie Nationale de Médecine. 189:917-933
RESUME Le terme maladies neutrophiliques est retenu pour identifier un groupe d’affections, dont la plupart sont des dermatoses, definies par une accumulation tissulaire de polynucleaires neutrophiles en l’absence de germes microbiens. Les maladi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04928a47d89ef32218d63fbf827727e5
https://doi.org/10.1016/s0001-4079(19)33518-6
https://doi.org/10.1016/s0001-4079(19)33518-6
Publikováno v:
Bulletin de l'Académie Nationale de Médecine. 186:1479-1487
RESUME Le deficit en alpha1antitrypsine (AAT), transmis sur le mode autosomique codominant est caracterise par une production serique d’AAT insuffisante ou non fonctionnelle. Les deux manifestations cliniques les plus frequentes sont les emphysemes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::149b55057bd5f25e7c563a3a2f0b290c
https://doi.org/10.1016/s0001-4079(19)34146-9
https://doi.org/10.1016/s0001-4079(19)34146-9
Publikováno v:
Presse medicale (Paris, France : 1983). 38(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f8461201b97b34de636f8db523543ccc
https://pubmed.ncbi.nlm.nih.gov/19734004
https://pubmed.ncbi.nlm.nih.gov/19734004
Autor:
Jacques, Bazex, Paule, Bayle
Publikováno v:
Bulletin de l'Academie nationale de medecine. 189(5)
Neutrophilic diseases are a group of disorders--mainly dermatoses--in which polymorphonuclear neutrophils accumulate in the absence of an identified pathogen. Such neutrophil infiltration can lead to a variety of clinical manifestations, including in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d9fdd44d80d63d9b2b591300648716e
https://pubmed.ncbi.nlm.nih.gov/16433463
https://pubmed.ncbi.nlm.nih.gov/16433463
Autor:
Cécile, Marty, Antoine, Bennet, Paule, Bayle, Marie, Danjoux, Thibaud, Lalande, Marie-Claude, Marguery, Jacques, Bazex
Publikováno v:
Annales de medecine interne. 154(8)
We report a case of glucagonoma syndrome, revealed by a necrolytic migratory erythema that had developed for four Years, associated with anorexia, severe weight loss, anemia, hypoprotidemia, and hypoaminoacidemia. The fasting blood glucose level tend
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::981d2a612f9812ca7437a790682309d1
https://pubmed.ncbi.nlm.nih.gov/15037834
https://pubmed.ncbi.nlm.nih.gov/15037834
Publikováno v:
Contact dermatitis. 49(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14ef914fa380a77047b60c9e877a1bb8
https://pubmed.ncbi.nlm.nih.gov/14678215
https://pubmed.ncbi.nlm.nih.gov/14678215
Publikováno v:
Bulletin de l'Academie nationale de medecine. 186(8)
Alpha1 antitrypsin (AAT) deficiency is an autosomic codominant inherited disorder characterized by inefficient or non-functional serum AAT. The principal clinical manifestations are panlobular emphysema and cirrhoses. Among cutaneous aspects, about 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d17a8d4e2018fb90495cf32d48a9e8cd
https://pubmed.ncbi.nlm.nih.gov/12669363
https://pubmed.ncbi.nlm.nih.gov/12669363
Publikováno v:
La Presse Médicale. 38:1863-1864
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c1cad1865e555d095a29c2b38c6aad4
https://doi.org/10.1016/j.lpm.2009.07.005
https://doi.org/10.1016/j.lpm.2009.07.005