Human infertility: meiotic genes as potential candidates 1Cliniciens participant au projet : J. Belaisch (Hoˆpital de Se`vres, France), B. Beartov (Bar-Ilan University, Israe¨l), T. Bienvenu (Hoˆpital Cochin, Paris), P. Bouchard (Hop. St-Antoine, Paris), S. Christin (Hop. St-Antoine, Paris), J. Don (Bar-Ilan University, Israe¨l), P. Jouannet (Hop. Cochin, Paris), F. Kutten (Hop. Necker, Paris), C. Lecointre (CHU, Rouen, France), H. Lejeune (Hop. de l'Antiquaille, Lyon), F. Morel (Fac. de Me´decine, Brest, France), G. Schaison (Hop. de Biceˆtre, Paris), S. Shalev (Hop. Haemek, Israe¨l), JP Siffroi (Hop. Tenon, Paris), P. Touraine (Hop. Necker, Paris).

Autor: Mandon-Pépin, B.¹ pepin@jouy.inra.fr, Derbois, C.², Matsuda, F.², Cotinot, C.¹, Wolgemuth, D.J.³, Smith, K.⁴, McElreavey, K.⁵, Nicolas, A.⁴, Fellous, M.⁵

Publikováno v: Gynecologie Obstetrique & Fertilite. Oct2002, Vol. 30 Issue 10, p817. 5p.

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

Hypothyroïdie congénitale: devenir adulte

Autor: C. Lecointre, J.-M. Kuhn, M.-H. Ragault, P. Leclerc, G. Travert, S. Marret, L. Berani

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

A central role for the syntenin exosomal pathway on the SRC metastatic function in colorectal cancer

Autor: P. Zimmermann, C. Lecointre, V. Simon, N.S. Imjeti, F. Lembo, S. Roche

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

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