Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Hugo Scaglia"'
Autor:
Carlos Mastandrea, Beatriz Ludueña, Cecilia Franconi, Hugo Scaglia, Carlos Chichizola, Alfredo Ghione Pelayo
Publikováno v:
Bioquímica y Patología Clínica, Vol 73, Iss 3, Pp 9-23 (2009)
Muchos estudios vienen demostrando que el desarrollo humano puede ser feminizado por una exposición a químicos ambientales o estrogénicos. Como sabemos el estrógeno es la hormona clave en la iniciación de la pubertad y en el fi nal de la vida re
Externí odkaz:
https://doaj.org/article/411ab87ecd244945b038bad41eedbb34
Autor:
Rubén Lisker, Hugo Scaglia, Jorge Espinosa, Freddy Febres, Tomás Morato, Mario Shkurovich, Gregorio Pérez-Palacios
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 41:833-840
Gonadal function was studied in three post-pubertal siblings (two male and one female) and one unrelated male patient with myotonic dystrophy. The diagnosis was confirmed in all cases by electromyography and muscle biopsy. Basal levels of plasma immu
Autor:
R. Lisker, M. Maillard, Martha Medina, A. Pasapera, Gregorio Pérez-Palacios, Hugo Scaglia, M. Uribe
Publikováno v:
Acta Endocrinologica. 84:191-199
Pituitary and gonadal functions were evaluated in two pre-pubertal male siblings and in one unrelated adult male with the complete form of the Laurence-Moon-Biedl syndrome. The adult patient (19 years old) presented lack of secondary sex characterist
Autor:
Sylvia Ortiz, Tomas Morato, Rubén Lisker, Freddy Febres, Ezequiel Lopez-Amor, Hugo Scaglia, Gregorio Pérez-Palacios
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 41:946-952
A 16-yr-old 46 XY individual with a familial incomplete male pseudohermaphroditism closely resembling the syndrome described by Gilbert-Dreyfus et al. was studied. The patient's habitus was masculine despite the presence of a small phallus, pseudo-va
Publikováno v:
Fertility and Sterility. 27:243-249
Hypothalamic and pituitary gonadotropin function and responsiveness in four patients with well-documented Stein-Leventhal syndrome were studied. All patients were of reproductive age and had had menstrual disorders since menarche. Estrogen production
Autor:
Oscar Larraza, Hugo Scaglia, Gregorio Pérez-Palacios, Sergio Ochoa, O Dolores Saavedra, Susana Kofman-Alfaro, Ana E. Pérez
Publikováno v:
Acta endocrinologica. 98(1)
An inherited form of incomplete male pseudohermaphroditism was studied in two post-pubertal and one pre-pubertal sibling. All patients presented a 46XY karyotype, infantile female external genitalia, lack of breast development and sexual hair. Persis
Publikováno v:
The Journal of clinical endocrinology and metabolism. 43(5)
The circulating levels of of radioimmunoassayable LH and FSH in three postmenopausal women were measured in samples drawn at one minute intervals for a period of 150 or 300 min in order to ascertain the existance of short term oscillation on the plas
Autor:
Ada L. Pinto-Ferreira, Carlos Gual, Martha Medina, Guadalupe Vazques, Gregorio Pérez-Palacios, Hugo Scaglia
Publikováno v:
Acta endocrinologica. 81(4)
The plasma concentrations and episodic fluctuations of immunoreactive FSH and LH as well as the pituitary sensitivity to LH-RH stimulation were evaluated in post-menopausal women. The subjects were divided into 4 groups according to age. Group 1: 60
Autor:
Enrique Ferrusca, Gregorio Pérez-Palacios, Fernando Larrea, Georgina Benavides, Hugo Scaglia, Susana Kofman-Alfaro, Martha Medina
Publikováno v:
The Journal of clinical endocrinology and metabolism. 46(6)
Four postpubertal 46 XY male patients with an inherited form of bilateral gynecomastia were studied to delineate the nature of the disease. Normal serum FSH and moderately elevated serum LH with concomitantly increased circulating levels of testoster