Zobrazeno 1 - 10
of 136
pro vyhledávání: '"E Vicens-Calvet"'
Publikováno v:
Endocrinología y Nutrición. 52:431-445
El pronostico del hipotiroidismo congenito ha cambiado radicalmente desde la instauracion en la mayoria de paises de las unidades de cribado precoz y seguimiento de esta endocrinopatia. Sin embargo, sus factores etiologicos aun son poco conocidos. En
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9dd85a74148faab0fe3fbac666a94ac9
https://doi.org/10.1016/s1575-0922(05)71041-x
https://doi.org/10.1016/s1575-0922(05)71041-x
Autor:
E. Vicens-Calvet, M. Bargadá
Publikováno v:
Endocrinología y Nutrición. 49:84-87
En los pacientes con hipotiroidismo congenito (HC), el inicio temprano del tratamiento previene del desarrollo de alteraciones mentales. Antes de la introduccion del cribado neonatal, los ninos con HC eran diagnosticados de forma tardia, cuando la si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2151f98f4fc1213abf70064585715a98
https://doi.org/10.1016/s1575-0922(02)74434-3
https://doi.org/10.1016/s1575-0922(02)74434-3
Autor:
E. Vilardell, G. Lloveras, E. Vicens-Calvet, J. Canela, F. Rodríguez-Hierro, Laura Audí, E. Sedano, A. Gilabert, C. Martí-Henneberg, Susan M. Webb
Publikováno v:
Hormone Research in Paediatrics. 57:113-119
Objectives: Epidemiologic and auxologic characteristics of patients treated with GH during childhood and adolescence and entered in a national registry in Catalonia were studied between 1988 and 1997. At the end of 1997, prevalence was 53.2 treatment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::beda592dc8ce2bb09fb057c3f5580e9c
https://doi.org/10.1159/000057961
https://doi.org/10.1159/000057961
Publikováno v:
Human Reproduction. 14:2735-2738
The meiotic or mitotic origin of most cases of Turner syndrome remains unknown, due to the difficulty in detecting hidden mosaicisms and to the lack of meiotic segregation studies. We have had the opportunity to study one pair of monozygotic twins co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce9fd8798f35ed4d8137f1c13235a5f2
https://doi.org/10.1093/humrep/14.11.2735
https://doi.org/10.1093/humrep/14.11.2735
Autor:
J. Egozcue, E. Vicens-Calvet, C. Templado, O. Martínez-Pasarell, Antonio Carrascosa, C. Nogués
Publikováno v:
Acta Paediatrica. 86:136-139
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1b9532dc7c9227df65cd66513825ea5
https://doi.org/10.1111/j.1651-2227.1997.tb18395.x
https://doi.org/10.1111/j.1651-2227.1997.tb18395.x
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 81:1237-1243
Previous studies have documented the association of insulin resistance and hyperandrogenism in adult women with functional ovarian hyperandrogenism (FOH) or polycystic ovary syndrome (a form of FOH). However, the possible impact of adrenal hyperandro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2168771b864a90a041a9558e930d960
https://doi.org/10.1210/jcem.81.3.8772605
https://doi.org/10.1210/jcem.81.3.8772605
Autor:
M. Gussinyé, P Saenger, A. Carrascosa, Neus Prat, N Potau, M Zampolli, Lourdes Ibáñez, E Vicens-Calvet
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 79:1778-1784
Functional ovarian hyperandrogenism (FOH) is characterized by an abnormal ovarian response to challenge with the GnRH analogs nafarelin and leuprolide acetate, similar to that observed in women with well defined polycystic ovary syndrome, regardless
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4a097e9eb43bc927bfb03722b72e02b
https://doi.org/10.1210/jcem.79.6.7989484
https://doi.org/10.1210/jcem.79.6.7989484
Autor:
Mónica Fernández-Cancio, J. Martínez-Mora, E. Vicens-Calvet, M. Carrera, M. Andrade, M. Gussinyé, Antonio Perez-Aytes, Emilio Suárez García, C. Piró, Teresa Vendrell, G. Lledó, M. Del Campo, Laura Audí, Pablo Lapunzina, L. Castaño, Diego Yeste, J. Sánchez del Pozo, José Luis Arroyo, Andrés Blanco Blanco, Maria Clemente, José I Labarta, A. Carrascosa, I. Hernández de la Calle, J. A. Bermúdez de la Vega, J. Forn, Joaquim Calaf, Pilar Andaluz, J. del Valle, E. Mayayo, Nuria Toran, E. Vilaró, Isabel Salinas, M. Beneyto, O. Angerri, Ángel Segura, María Caimari, Ricardo Gracia-Bouthelier, María Angeles Albisu, M. J. Martínez-Sopena, Elisabeth Gabau, V. Borrás, M. J. Martínez-Aedo, María Luisa Granada, Antonio M. Rodríguez
Publikováno v:
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Universitat Politècnica de Catalunya (UPC)
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Universitat Politècnica de Catalunya (UPC)
Background: Androgen receptor (AR) gene mutations are the most frequent cause of 46, XY disorders of sex development (DSD) and are associated with a variety of phenotypes, ranging from phenotypic women [complete androgen insensitivity syndrome (CAIS)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee95fe3c9ea372221848db8eb441771e
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=12781
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=12781
Autor:
A. Goday, C. Castell, R. Tresserras, J. Canela, J. L. Taberner, G. Lloveras, E. Aguadé, J. M. Albarran, X. Allué, M. Aliart, J. Anglada, J. Arroyo, M. Bergua, J. M. Calvet, J. F. Cano, R. Carrasco, A. Carrascosa, R. Clivillé, R. Corrales, B. Costa, M. Estruch, A. Famades, A. Felip, M. Fernandez-Castañer, D. Figuerola, X. Freixas, F. Gallo, A. Garcia-Rico, R. Gomis, A. Guarro, M. Gussinyé, A. Gutierrez, G. Hollenberg, L. Ibañez, F. Iniesta, A. de Leiva, T. Lezaun, J. Lopez Batllori, J. Marco, A. Martinez-Roig, I. Martinez, J. R. Masoliver, D. Mauricio, J. Mayos, M. T. Mengotti, J. Mesa, T. Micaló, M. Millan, E. Montaña, R. Nosas, A. Novials, A. Nubiola, M. Olesti, A. Palaudaries, C. Pavia, A. Perez, C. Perez, J. M. Pla, M. Porta, G. Prat, M. Prat, J. Querol, H. O. Rajmil, I. Recas, J. L. Reverter, W. Ricart, L. Riu, J. Rodriguez-Hierro, M. Roqueta, R. Rosell, M. D. Salcedo, A. Sanmarti, T. Sansa, J. M. Sans-Mallafré, P. Sardá, A. Sarto, J. Soler, M. Soler, E. Subiracs, R. Torras, P. Utges, J. Vendrell, E. Vicens-Calvet, J. Vidal-Bota, J. Viguera, L. Vila, M. Vila, E. Vilardell, C. Vilaseca, D. Yeste, V. Yetano
Publikováno v:
Diabetologia. 35:267-271
The incidence of Type 1 (insulin-dependent) diabetes mellitus was prospectively evaluated in Catalonia, Spain in patients up to 30 years of age during the period 1987–1990. The population at risk (0–29 years) consisted of 2,690,394 inhabitants (t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd42022d85f2736b5efd125ea96b9d29
https://doi.org/10.1007/bf00400928
https://doi.org/10.1007/bf00400928
Autor:
R Virdis, N Potau, L Ghizzoni, A. Carrascosa, S Bernasconi, M. A. Albisu, Lourdes Ibáñez, E Vicens-Calvet, M Zampolli
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 74:254-257
The natural history of girls with premature pubarche is reported to be normal, but the effects on puberty and on final height are not well documented. We assessed the outcome of a group of girls with premature pubarche from two Latin populations in w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c01d56e50eb41d8eaa3715d430bbcdda
https://doi.org/10.1210/jcem.74.2.1730803
https://doi.org/10.1210/jcem.74.2.1730803