Zobrazeno 1 - 10 of 278 pro vyhledávání: '"V, Kerlan"'
1
Bed bug infestation in a French university hospital: control strategy, financial impact and perspectives
Autor: A, Gressier, N, Galakhoff, P, Thuillier, V, Kerlan, V, Cogulet, M, Cosse, L, Daniel, M, Canevet, S, Cabon, A, Le Grand, R, Baron, P, Saliou
Publikováno v: Journal of Hospital Infection. 126:81-86
With the increase in international travel and development of insecticide resistance, a re-emergence of the bed bug has been observed since the 2000s and it is becoming a worldwide public health problem. Hospitals and other medical settings have not b
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9745c1a7159efc2dcf96282ce26ef7c6
https://doi.org/10.1016/j.jhin.2022.05.014
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3
Endocrinology of bone mineralization: An update
Autor: A. Jannin, V. Kerlan, R. Desailloud
Publikováno v: Annales d'endocrinologie. 83(1)
Throughout the world, millions of people suffer from fragilizing osteopathies such as osteomalacia and osteoporosis. Osteomalacia is a rare disorder, corresponding to mineralization abnormalities in adult bone, as opposed to rickets in children. Rena
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::656bd93f24f20730aedfaa379af74144
https://pubmed.ncbi.nlm.nih.gov/34921812
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5
Akademický článek
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6
X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood
Autor: Elodie Fiot, Delphine Zénaty, Priscilla Boizeau, Jérémie Haignere, Sophie Dos Santos, Juliane Léger, J C Carel, S Cabrol, P Chanson, S Christin-Maitre, C Courtillot, B Donadille, J Dulon, M Houang, M Nedelcu, I Netchine, M Polak, S Salenave, D Samara-Boustani, D Simon, P Touraine, M Viaud, H Bony, K Braun, R Desailloud, A M Bertrand, B Mignot, F Schillo, P Barat, V Kerlan, C Metz, E Sonnet, Y Reznik, V Ribault, H Carla, I Tauveron, C Bensignor, F Huet, B Verges, O Chabre, C Dupuis, A Spiteri, M Cartigny, C Stuckens, J Weill, A Lienhardt, C Naud-Saudreau, F Borson-Chazot, A Brac de la Perriere, M Pugeat, T Brue, R Reynaud, G Simonin, F Paris, C Sultan, B Leheup, G Weryha, S Baron, B Charbonnel, S Dubourdieu, E Baechler, P Fenichel, K Wagner, F Compain, H Crosnier, C Personnier, B Delemer, A C Hecart, P F Souchon, M De Kerdanet, F Galland, S Nivot-Adamiak, M Castanet, C Lecointre, O Richard, N Jeandidier, S Soskin, P Lecomte, M Pepin-Donat, P Pierre
Publikováno v: European Journal of Endocrinology
European Journal of Endocrinology, 2019, 180 (6), pp.397-406. ⟨10.1530/EJE-18-0878⟩
European Journal of Endocrinology, BioScientifica, 2019, 180 (6), pp.397-406. ⟨10.1530/EJE-18-0878⟩
ObjectiveTurner Syndrome is associated with several phenotypic conditions associated with a higher risk of subsequent comorbidity. We aimed to evaluate the prevalence of congenital malformations and the occurrence of age-related comorbid conditions a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90141f9c76344ac051168fc9f8ff886a
https://doi.org/10.1530/eje-18-0878
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7
Akademický článek
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8
Évaluation d’un programme de suivi de patientes avec un diabète gestationnel par télémédecine : expérience brestoise
Autor: G. Crouzeix, P. Thuillier, S. Gaulier, V. Kerlan, E. Sonnet, Ahcène Bounceur
Publikováno v: Médecine des Maladies Métaboliques
Médecine des Maladies Métaboliques, Elsevier, 2017, 11 (6), pp.494-500. ⟨10.1016/S1957-2557(17)30117-7⟩
Resume L’augmentation de la prevalence du diabete gestationnel et l’interet de son traitement incitent les professionnels de sante a optimiser sa prise en charge. Notre service hospitalier a mis en place un projet de telemedecine appele « SUIDIA
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff227674e37938d113305e0a9b9b66f1
https://doi.org/10.1016/s1957-2557(17)30117-7
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9
La chirurgie d’épargne surrénalienne : du cortex à la médulla
Autor: V. Kerlan, A. Tabarin, A. Ferriere
Publikováno v: Annales d'Endocrinologie. 78:S11-S20
The 2017 Endocrine Society annual meeting included several communications and debates on the conservative adrenal surgery in bilateral hereditary pheochromocytomas (BHP), bilateral adrenal macronodular hyperplasia (BAMH) and primary hyperaldosteronis
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5fc471af4be1ff85b2c6dab9fb43b0e1
https://doi.org/10.1016/s0003-4266(17)30921-6
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10
Significant prevalence of NR3C1 mutations in incidentally discovered bilateral adrenal hyperplasia: results of the French MUTA-GR Study
Autor: Géraldine Vitellius, Séverine Trabado, Christine Hoeffel, Jérôme Bouligand, Antoine Bennet, Frederic Castinetti, Bénédicte Decoudier, Anne Guiochon-Mantel, Marc Lombes, Brigitte Delemer, F Amiot-Chapoutot, D Ancelle, F Bertoin, T Brue, P Caron, F Borson-Chazot, S Christin-Maitre, O Chabre, R Dessailloud, B Estour, H Grulet, F Illouz, N Jeandidier, V Kerlan, M Klein, A Penfornis, P Pierre, A Tabarin, P Touraine, M C Vantyghem, J Young
Publikováno v: European Journal of Endocrinology
European Journal of Endocrinology, BioScientifica, 2018, 178 (4), pp.411-423. ⟨10.1530/EJE-17-1071⟩
Background Recently discovered mutations of NR3C1 gene, encoding for the GR, in patients with glucocorticoid resistance and bilateral adrenal incidentalomas prompted us to investigate whether GR mutations might be associated with adrenal hyperplasia.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c70dcdb1bcc4e2418bac6738f99a40dc
https://hal.univ-reims.fr/hal-01822592
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