Zobrazeno 1 - 10
of 97
pro vyhledávání: '"C Stuckens"'
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
Akademický článek
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Autor:
A Linglart, S Cabrol, P Berlier, C Stuckens, K Wagner, M de Kerdanet, C Limoni, J-C Carel, J-L Chaussain
Publikováno v:
European Journal of Endocrinology. 164:891-897
ObjectiveAdult height deficit seen in Turner syndrome (TS) originates, in part, from growth retardation in utero and throughout the first 3 years of life. Earlier diagnosis enables earlier therapeutic intervention, such as with recombinant human GH (
Publikováno v:
European Journal of Immunogenetics. 29:251-257
Summary Several studies have demonstrated an association of cytotoxic T lymphocyte-associated molecule 4 (CTLA-4) (IDDM 12) alanine 17 with type 1 diabetes, but we wished to study the parental effect of CTLA-4 49 A/G dimorphism in diabetic families.
Publikováno v:
Archives de Pédiatrie. 6:1077-1080
Resume La forme Ib du pseudo-hypoaldosteronisme est une affection hereditaire transmise sur le mode autosomique recessif et se traduisant par une perte de sel multiviscerale de decouverte neonatale. L'evolution est favorable vers l'âge de 18 mois a
Publikováno v:
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics. 29(3)
Several studies have demonstrated an association of cytotoxic T lymphocyte-associated molecule 4 (CTLA-4) (IDDM 12) alanine 17 with type 1 diabetes, but we wished to study the parental effect of CTLA-4 49 A/G dimorphism in diabetic families. The CTLA
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 6(10)
Type Ib pseudohypoaldosteronism is a congenital disorder characterized in the newborn by salt loss caused by multiple end-organ resistance to aldosterone. An autosomal recessive mode of inheritance has been reported. Its particularity is the spontane
Autor:
S Gondé, S. Vanderbecken, Jean-Pierre Farriaux, C. Stuckens, C. Ponte, M. Cartigny-Maciejewski, N Guilley, J Weill, E Paux
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 6(2)
Resume Le bilan du depistage neonatal de l'hyperplasie congenitale des surrenales par deficit en 21-hydroxylase dans la region Nord-Pasde-Calais de 1980 a 1996 par dosage sur papier buvard de la 17-hydroxyprogesterone chez 408 138 nouveau-nes est rap
Publikováno v:
1999 IEEE Transmission and Distribution Conference (Cat. No. 99CH36333).
The determination of ferroresonant oscillations in circuits with voltage transformers is a highly nonlinear problem due to the possible core saturation. It is achieved with an algorithm based upon the harmonic balance method in the frequency domain.