Zobrazeno 1 - 6
of 6
pro vyhledávání: '"María Cecilia García Rudaz"'
Publikováno v:
American Journal of Hypertension. 17:1107-1111
We report a novel germ-line point mutation in the von Hippel-Lindau (vhl) gene in a family with childhood occurrence of isolated pheochromocytoma. Two members of this family (the father and his son) were affected. The son had bilateral adrenal pheoch
Autor:
Johannes D. Veldhuis, Valentina Alexandrovna Peterkova, Paul Saenger, Marta Barontini, Ilknur Arslanoglu, Martijn H. Breuning, María Cecilia García Rudaz, W. Oostdijk, Delphine Mitanchez, Tomasz Romer, Pierre Chatelain, Marwa E. Fahmi, Hyi-Jeong Ji, Peter J Simm, Robert L. Rosenfield, María Gabriela Ropelato, Pinchas Cohen, Conrad Savoy, Guy Van Vliet, María Gabriela Ballerini, M.H. de Ru, Mirta Gryngarten, Jürgen Kratzsch, G Bona, Mohamed El Kholy, Eileen Fowler, Samia Selim, Margaret Zacharin, Wolfgang G. Sippell, Melanie Shim, J.M. Wit, Heba Elsedfy, Elena Bolshova-Zubkovskaya, William L. Oppenheim, A. Ferrandez-Longas, Ayman E. Nassar, A. Carrascosa, Claude J. Migeon, M E Escobar, F K Grote, H.M. Zonderland, Dragan Zdravkovic, Omar Ali, S.G. Kant
Publikováno v:
Hormone Research in Paediatrics. 68:327-329
Autor:
Johannes D. Veldhuis, María Gabriela Ropelato, María Cecilia García Rudaz, Marta Barontini, Sonia Bengolea, M E Escobar, María de Luján Calcagno
Publikováno v:
The Journal of clinical endocrinology and metabolism. 94(9)
Little is known about the neuroendocrine effects of androgens on the GnRH-LH unit in females.Our objective was to evaluate androgen negative feedback on the GnRH-LH axis in eumenorrheic and polycystic ovary syndrome (PCOS) adolescents.We conducted a
Autor:
María Gabriela Ropelato, M E Escobar, María Cecilia García Rudaz, Johannes D. Veldhuis, Mirta Gryngarten, Marta Barontini, María Gabriela Ballerini
Publikováno v:
Hormone research. 68(6)
Some adolescents with a history of idiopathic central precocious puberty (ICPP) develop hyperandrogenism. Hypothesis: Luteinizing hormone (LH) hypersecretion could be a common mechanism underlying ICPP and polycystic ovary syndrome. Aim: To explore t
Autor:
Gabriela Sanso, María Cecilia García Rudaz, Ana K. de Mondino, Marta Barontini, Alejandro Ring, Sonia Iorcansky, Eduardo Pusiol, Boris Elsner, Maria Roque, M M A Horacio Domene, Héctor Perinetti
Publikováno v:
Cancer. 94(2)
BACKGROUND Multiple endocrine neoplasia type 2 (MEN 2) is an inherited disease caused by germline mutations in the RET proto-oncogene, and is responsible for the development of endocrine neoplasia. Its prognosis is dependent on the appearance and spr
Autor:
Ayman E. Nassar, Samia Selim, Melanie Shim, A. Carrascosa, Valentina Alexandrovna Peterkova, A. Ferrandez-Longas, Dragan Zdravkovic, Pinchas Cohen, Marwa E. Fahmi, Eileen Fowler, María Gabriela Ropelato, F K Grote, H.M. Zonderland, G Bona, Heba Elsedfy, Conrad Savoy, M E Escobar, Omar Ali, Wolfgang G. Sippell, María Gabriela Ballerini, M.H. de Ru, Marta Barontini, Mirta Gryngarten, Delphine Mitanchez, J.M. Wit, Peter J Simm, Mohamed El Kholy, S.G. Kant, Tomasz Romer, Ilknur Arslanoglu, Jürgen Kratzsch, Robert L. Rosenfield, Claude J. Migeon, Guy Van Vliet, W. Oostdijk, Johannes D. Veldhuis, Martijn H. Breuning, Hyi-Jeong Ji, Paul Saenger, William L. Oppenheim, Margaret Zacharin, Elena Bolshova-Zubkovskaya, María Cecilia García Rudaz, Pierre Chatelain
Publikováno v:
Hormone Research in Paediatrics. 68:321-322