Zobrazeno 1 - 10
of 187
pro vyhledávání: '"C, Lecointre"'
Akademický článek
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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⟩
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
https://doi.org/10.1530/eje-18-0878
Autor:
Alice Goldenberg, Didier Hannequin, D. Pouliquen, C. Lecointre, O. Martinaud, Valérie Cormier-Daire, J. Lechevallier
Publikováno v:
Journal of Clinical and Experimental Neuropsychology. 34:445-452
The Floating Harbor syndrome is a rare genetic disease characterized by a triad of clinical signs: specific dysmorphic facial features, short stature with delayed bone age, and language and speech disorders. These signs are, in most cases, associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75c2fe08054fa0bbd97d906b240bee7a
https://doi.org/10.1080/13803395.2011.646958
https://doi.org/10.1080/13803395.2011.646958
Publikováno v:
Archives de Pédiatrie. 14:1119-1122
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08408fed9587c4263f0de996a8a06a9c
https://doi.org/10.1016/j.arcped.2007.06.021
https://doi.org/10.1016/j.arcped.2007.06.021
Autor:
C. Pienkowski, Frédérique Dijoud, Marc Nicolino, Anne-Marie Bertrand, Juliane Léger, Claire Nihoul-Fékété, S. Soskin, M. Bost, C. Bouvatier, Y. Morel, Alaa El-Ghoneimi, Pierre Mouriquand, D. Zenaty, Sylvie Cabrol, G. Pinto, C. Lecointre
Publikováno v:
The Journal of Pediatrics. 149:687-691
Objective To analyze the clinical and histological findings in boys with bilateral anorchia and the response to testosterone treatment on penis length. Study design Patients were divided into two groups according to the absence (group A, n = 29) or t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e80a801c2321828d93a6bc9a7f3aaa4
https://doi.org/10.1016/j.jpeds.2006.07.044
https://doi.org/10.1016/j.jpeds.2006.07.044
Akademický článek
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A central role for the syntenin exosomal pathway on the SRC metastatic function in colorectal cancer
Publikováno v:
European Journal of Cancer. 61:S110
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0984d2c05fae9935a61b7ae624ae9a1b
https://doi.org/10.1016/s0959-8049(16)61389-8
https://doi.org/10.1016/s0959-8049(16)61389-8
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 14(9)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::515cb6fc0b0f03c6dac06de8856cac08
https://pubmed.ncbi.nlm.nih.gov/17669638
https://pubmed.ncbi.nlm.nih.gov/17669638
Publikováno v:
Appetite. 89:323
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::824796f0ae327fdbd0bb0bf84879f469
https://doi.org/10.1016/j.appet.2014.12.075
https://doi.org/10.1016/j.appet.2014.12.075
Autor:
E, Mallet, J, Gaudelus, P, Reinert, B, Le Luyer, C, Lecointre, J, Léger, C, Loirat, B, Quinet, J J, Bénichou, J, Furioli, G A, Loeuille, B, Roussel, M, Larchet, F, Freycon, M, Vidailhet, I, Varet
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 11(7)
Although systematic vitamin D supplementation in adolescents remains debated, rickets is nevertheless a well recognized pathology in this age group. Adolescence is an at-risk period because of rapid growth, insufficient calcium intake and/or vitamin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::14208af1ea1fe69b5a22c2677ad49400
https://pubmed.ncbi.nlm.nih.gov/15234392
https://pubmed.ncbi.nlm.nih.gov/15234392