Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Christèle Derrien"'
Autor:
Jean‐Louis Pépin, Sébastien Bailly, Joelle B. Texereau, Emmanuel Sonnet, Sylvie Picard, Bruno Vergès, Christine Coffin Boutreux, Gwenaelle Arnault Ouary, Laurence Kessler, Bruno Guerci, Brigitte Anton Kuchly, Salha Fendri Gaied, Alain Cuperlier, Christel Voinot, Christèle Derrien, Séverine Dubois, Florent Lavergne, Anne Laure Borel, Renaud Tamisier, Pierre‐Yves Benhamou
Publikováno v:
D30. INTEGRATING OSA AND COMORBIDITIES FOR EFFECTIVE THERAPIES.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f12602f39478ad80a3b61101b3b6e76d
https://doi.org/10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a6508
https://doi.org/10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a6508
Autor:
Maurine Allard, Mathilde Barrallier, Hugo Pisaroni, Mathilde Fichet, Margot De La Vergne De Cerval, Robin Pflaum, Audrey Poisson, Christèle Derrien, Fabrice Bonnet, Patricia Vaduva
Publikováno v:
Annales d'Endocrinologie.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::906b0018850541a15b1cb60a13876499
https://doi.org/10.1016/j.ando.2023.01.007
https://doi.org/10.1016/j.ando.2023.01.007
Autor:
Mathilde Fichet, Ondine Delache, Margot De La Vergne de Cerval, Nina Kissel, Patricia Vaduva, Rémi Nguyen Van, Raphaël Guillin, Fabrice Bonnet, Christèle Derrien
Publikováno v:
Médecine des Maladies Métaboliques. 15:206-214
Resume Introduction la biopsie osseuse (BO) percutanee est le « gold standard » pour le diagnostic de l’osteite du pied diabetique (OPD), mais il existe des freins a sa realisation. La place de la BO percutanee et son impact diagnostique dans la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb8d93b1de0320d9321647ccf558492b
https://doi.org/10.1016/j.mmm.2021.01.003
https://doi.org/10.1016/j.mmm.2021.01.003
Autor:
Christèle Derrien, Michel Polak, Véronique David, Paul Czernichow, Nadine Lucidarme, Gabor Szinnai, Shinji Kosugi
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 91:1199-1204
Iodide transport defect (ITD) is an autosomal recessive disorder resulting in varying degrees of congenital hypothyroidism (CH) with goiter and low or absent radioiodide uptake (RIUT), as determined by thyroid scintigraphy, and low iodide saliva to p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6211dfa27cf0e80e00aa379d36b2a7e
https://doi.org/10.1210/jc.2005-1832
https://doi.org/10.1210/jc.2005-1832
Autor:
J.-F. Blickle, Edgar Kaloustian, A. Grimaldi, Sophie Caillat-Zucman, Pierre-Jean Guillausseau, Christèle Derrien, Henri Gin, Arnaud Murat, Béatrice Bouhanick, Frédérique Olivier, Bruno Guerci, Eric Bertin, Pierre-Henri Ducluzeau, Pascale Massin, P. Chedin, Véronique Paquis-Flucklinger, Julien Samuel-Lajeunesse, Guillaume Charpentier, Marie Virally, Juliette Cahen, Michel Paques, Danièle Dubois-Laforgue, Bernard Vialettes, José Timsit, Béatrice Porokhov
Publikováno v:
Scopus-Elsevier
Maternally inherited diabetes and deafness (MIDD), which is seen in 0.5% to 2.8% of patients with type 2 diabetes mellitus, is related to a point mutation at position 3243 of mitochondrial (mt) DNA. Its clinical description is incomplete.To study the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02622960cf140b7ab87a813e25996ccb
http://www.scopus.com/inward/record.url?eid=2-s2.0-0035341093&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0035341093&partnerID=MN8TOARS
