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Fertility and Sterility|March 1, 1976
The Stein-Leventhal syndrome: a neuropituitary disorderH Scaglia, M Medina, C Gual, et al.Journal of Endocrinological Investigation|June 1, 1990
Analysis of the hypothalamic-pituitary-ovary axis in the neonatally-androgenized female ratE Spinedi, V Mariani, M Bulfon, et al.Journal of Medical Genetics|June 1, 1976
Pseudohermaphroditism due to XY gonadal absence syndromeS K Alfaro, D Saavedra, S Ochoa, et al.Calcified Tissue International|May 23, 1998
Bone mineral density and bone size in men with primary osteoporosis and vertebral fracturesE Vega, G Ghiringhelli, C Mautalen, et al.Reproduction, Nutrition, Development|July 20, 2002
Heterogeneity of circulating prolactin in the bitchC Gobello, M Colombani, H Scaglia, et al.The Journal of Clinical Endocrinology and Metabolism|November 1, 1975
Hypothalamic-pituitary-gonadal function in patients with myotonic dystrophyF Febres, H Scaglia, R Lisker, et al.Acta Endocrinologica|April 1, 1976
Pituitary LH and FSH secretion and responsiveness in women of old ageH Scaglia, M Medina, A L Pinto-Ferreira, et al.The Journal of Clinical Endocrinology and Metabolism|June 1, 1978
Gynecomastia as a familial incomplete male pseudohermaphroditism type 1: a limited androgen resistance syndromeF Larrea, G Benavides, H Scaglia, et al.The Journal of Clinical Endocrinology and Metabolism|November 1, 1975
Familial incomplete virilization due to partial end organ insensitivity to androgensG Perez-Palacios, S Ortiz, E López-Amor, et al.The Journal of Clinical Endocrinology and Metabolism|November 14, 1998
Recombinant human follicle-stimulating hormone administration increases testosterone production in men, possibly by a Sertoli cell-secreted nonsteroid factorO Levalle, C Zylbersztein, S Aszpis, et al.Pageof 2