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Life Sciences|January 1, 1996
Prenatal exposure to carbon monoxide and vascular responsiveness of rat resistance vesselsM Montagnani, M Serio, M A Potenza, et al.Journal of Andrology|July 1, 1988
Simultaneous determination of testosterone, dihydrotestosterone and 5 alpha-androstan-3 alpha,-17 beta-diol by isotopic dilution mass spectrometry in plasma and prostatic tissue of patients affected by benign prostatic hyperplasia. Effects of 3-month treatment with a GnRH analogR Salerno, G Moneti, G Forti, et al.Journal of Endocrinological Investigation|May 1, 1995
Genetic screening to identify the gene carrier in Italian and German kindreds affected by multiple endocrine neoplasia type 1 (MEN 1) syndromeA Morelli, A Falchetti, R Castello, et al.The Journal of Clinical Endocrinology and Metabolism|July 21, 2000
Effect of a vitamin D3 analogue on keratinocyte growth factor-induced cell proliferation in benign prostate hyperplasiaC Crescioli, M Maggie, G B Vannelli, et al.Journal of Endocrinological Investigation|November 1, 1990
Pulsatile secretion of luteinizing hormone in agonadal men before and during testosterone replacement therapyA D Genazzani, G Forti, M Maggi, et al.Hypertension (Dallas, Tex. : 1979)|September 18, 1999
In vivo evidence that endogenous dopamine modulates sympathetic activity in manM Mannelli, L Ianni, C Lazzeri, et al.Bioorganic & Medicinal Chemistry|June 16, 2001
Effect of C-ring modifications in benzo[c]quinolizin-3-ones, new selective inhibitors of human 5 alpha-reductase 1A Guarna, E G Occhiato, F Machetti, et al.Journal of Reproduction and Fertility|July 1, 1994
Antagonists for the human oxytocin receptor: an in vitro studyM Maggi, G Fantoni, E Baldi, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|May 30, 2013
SPIDIA-DNA: an External Quality Assessment for the pre-analytical phase of blood samples used for DNA-based analysesF Malentacchi, M Pazzagli, L Simi, et al.Journal of Medical Genetics|August 3, 2005
Phenotype variability of neural crest derived tumours in six Italian families segregating the same founder SDHD mutation Q109XL Simi, R Sestini, P Ferruzzi, et al.Pageof 37