Zobrazeno 1 - 10
of 45
pro vyhledávání: '"G Ropelato"'
Autor:
M. G. Ropelato
Publikováno v:
Journal of Clinical Endocrinology & Metabolism. 84:4629-4636
Publikováno v:
Clinical Endocrinology. 51:455-460
BACKGROUND AND OBJECTIVE Inhibins are peptides, mainly of gonadal origin, that suppress FSH production. Dimeric forms of inhibin (A and B) have been proposed as peripheral markers of Sertoli and granulosa cell function. The aim of this study was to e
Autor:
Horacio M, Domené, Paula A, Scaglia, Alicia S, Martínez, Ana C, Keselman, Liliana M, Karabatas, Viviana R, Pipman, Sonia V, Bengolea, María C, Guida, María G, Ropelato, María G, Ballerini, Eva M, Lescano, Miguel A, Blanco, Juan J, Heinrich, Rodolfo A, Rey, Héctor G, Jasper
Publikováno v:
Hormone research in paediatrics. 80(6)
In acid-labile subunit (ALS)-deficient families, heterozygous carriers of IGFALS gene mutations are frequently shorter than their wild-type relatives, suggesting that IGFALS haploinsufficiency could result in short stature. We have characterized IGFA
Autor:
Miguel L. Podesta, Cesar Bergada, Ricardo Medel, Emilio Quesada, G. Ropelato, Silvia Gottlieb
Publikováno v:
Journal of Urology. 152:794-797
Preoperative and postoperative testicular volume, serum testosterone, follicle-stimulating hormone and luteinizing hormone were determined in 25 patients 8 to 19 years old (mean age 13.2 +/- 1.63) with grades 2 and 3 unilateral varicocele. Testicular
Autor:
Romina P, Grinspon, María G, Ropelato, Patricia, Bedecarrás, Nazareth, Loreti, María G, Ballerini, Silvia, Gottlieb, Stella M, Campo, Rodolfo A, Rey
Publikováno v:
Clinical endocrinology. 76(5)
The biphasic ontogeny of serum gonadotrophins observed in normal children also exists in girls with gonadal dysgenesis, although with higher levels. However, limited data exist in prepubertal boys with anorchia.To investigate whether the existence of
Autor:
R P, Grinspon, P, Bedecarrás, M G, Ballerini, G, Iñiguez, A, Rocha, E A, Mantovani Rodrigues Resende, V N, Brito, C, Milani, V, Figueroa Gacitúa, A, Chiesa, A, Keselman, S, Gottlieb, M F, Borges, M G, Ropelato, J-Y, Picard, E, Codner, R A, Rey
Publikováno v:
International journal of andrology. 34(5 Pt 2)
Male patients with an extra sex chromosome or autosome are expected to present primary hypogonadism at puberty owing to meiotic germ-cell failure. Scarce information is available on trisomy 21, a frequent autosomal aneuploidy. Our objective was to as
Publikováno v:
The Journal of clinical endocrinology and metabolism. 86(1)
The present study explores the postulate that the polycystic ovarian syndrome (PCOS) is marked by failure of physiological feedforward and feedback signaling between pituitary LH and ovarian androgens. To this end, we appraised the 3-fold simultaneou
Autor:
A S, Martínez, H M, Domené, M G, Ropelato, H G, Jasper, P A, Pennisi, M E, Escobar, J J, Heinrich
Publikováno v:
The Journal of clinical endocrinology and metabolism. 85(11)
We have studied the effect of estradiol (E2) on the GH-insulin-like growth factor (GH-IGF) axis in 15 prepubertal GH deficiency (GHD) children and 44 prepubertal or early pubertal children with idiopathic short stature (SS). All of them received a da
Publikováno v:
Clinical endocrinology. 51(4)
Inhibins are peptides, mainly of gonadal origin, that suppress FSH production. Dimeric forms of inhibin (A and B) have been proposed as peripheral markers of Sertoli and granulosa cell function. The aim of this study was to establish the relationship
Autor:
M C, García Rudaz, M G, Ropelato
Publikováno v:
Medicina. 59(1)