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Page 1
Novel (60%) and recurrent (40%) androgen receptor gene mutations in a series of 59 patients with a 46,XY disorder of sex development.
Audi L, Fernández-Cancio M, Carrascosa A, Andaluz P, Torán N, Piró C, Vilaró E, Vicens-Calvet E, Gussinyé M, Albisu MA, Yeste D, Clemente M, Hernández de la Calle I, Del Campo M, Vendrell T, Blanco A, Martínez-Mora J, Granada ML, Salinas I, Forn J, Calaf J, Angerri O, Martínez-Sopena MJ, Del Valle J, García E, Gracia-Bouthelier R, Lapunzina P, Mayayo E, Labarta JI, Lledó G, Sánchez Del Pozo J, Arroyo J, Pérez-Aytes A, Beneyto M, Segura A, Borrás V, Gabau E, Caimarí M, Rodríguez A, Martínez-Aedo MJ, Carrera M, Castaño L, Andrade M, Bermúdez de la Vega JA; Grupo de Apoyo al Síndrome de Insensibilidad a los Andrógenos (GrApSIA). Audi L, et al. Among authors: vicens calvet e. J Clin Endocrinol Metab. 2010 Apr;95(4):1876-88. doi: 10.1210/jc.2009-2146. Epub 2010 Feb 11. J Clin Endocrinol Metab. 2010. PMID: 20150575 Free article.
Source localization of androgen excess in adolescent girls.
Ibáñez L, Potau N, Zampolli M, Prat N, Gussinyé M, Saenger P, Vicens-Calvet E, Carrascosa A. Ibáñez L, et al. J Clin Endocrinol Metab. 1994 Dec;79(6):1778-84. doi: 10.1210/jcem.79.6.7989484. J Clin Endocrinol Metab. 1994. PMID: 7989484
Fetal growth regulation and intrauterine growth retardation.
Carrascosa A, Yeste D, Copil A, Audí L, Gusinyé M, Vicens-Calvet E, Clemente M. Carrascosa A, et al. Among authors: vicens calvet e. J Pediatr Endocrinol Metab. 2004 Mar;17 Suppl 3:435-43. J Pediatr Endocrinol Metab. 2004. PMID: 15134304 Review.
Natural history of premature pubarche: an auxological study.
Ibañez L, Virdis R, Potau N, Zampolli M, Ghizzoni L, Albisu MA, Carrascosa A, Bernasconi S, Vicens-Calvet E. Ibañez L, et al. J Clin Endocrinol Metab. 1992 Feb;74(2):254-7. doi: 10.1210/jcem.74.2.1730803. J Clin Endocrinol Metab. 1992. PMID: 1730803
36 results