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Results:
1-7
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Results: 7
Authors:
Rogoff, D
Bergada, I
Venara, M
Chemes, H
Heinrich, JJ
Barontini, M
Citation: D. Rogoff et al., Intermittent hyperaldosteronism in a child due to an adrenal adenoma, EUR J PED, 160(2), 2001, pp. 114-116
Authors:
Bergada, I
Bergada, C
Campo, S
Citation: I. Bergada et al., Role of inhibins in childhood and puberty, J PED END M, 14(4), 2001, pp. 343-353
Authors:
Venara, M
Rey, R
Bergada, I
Mendilaharzu, H
Campo, S
Chemes, H
Citation: M. Venara et al., Sertoli cell proliferations of the infantile testis - An intratubular formof Sertoli cell tumor?, AM J SURG P, 25(10), 2001, pp. 1237-1244
Authors:
Dardis, A
Marino, R
Bergada, I
Escobar, ME
Gryngarten, M
Rivarola, MA
Belgorosky, A
Citation: A. Dardis et al., Molecular analysis of the most frequent mutations associated with congenital adrenal hyperplasia secondary to steroid 21-hydroxylase enzyme deficiency, MEDICINA, 61(1), 2001, pp. 28-34
Authors:
Bergada, I
Del Toro, K
Katz, O
Chemes, H
Campo, S
Citation: I. Bergada et al., Serum inhibin B concentration in a prepubertal boy with gynecomastia and Peutz-Jeghers syndrome, J PED END M, 13(1), 2000, pp. 101-103
Authors:
Bergada, I
Rojas, G
Ropelato, G
Ayuso, S
Bergada, C
Campo, S
Citation: I. Bergada et al., Sexual dimorphism in circulating monomeric and dimeric inhibins in normal boys and girls from birth to puberty, CLIN ENDOCR, 51(4), 1999, pp. 455-460
Authors:
Rogoff, D
Smolenicka, Z
Bergada, I
Vallejo, G
Barontini, M
Heinrich, JJ
Ferrari, P
Citation: D. Rogoff et al., The codon 213 of the 11 beta-hydroxysteroid dehydrogenase type 2 gene is ahot spot for mutations in apparent mineralocorticoid excess, J CLIN END, 83(12), 1998, pp. 4391-4393
Risultati:
1-7
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