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Human Reproduction (Oxford, England)|September 7, 2013
Y-chromosome microdeletions are not associated with SHOX haploinsufficiencyC Chianese, D Lo Giacco, F Tüttelmann, et al.
European Journal of Pain (London, England)|June 26, 2012
Investigating the role of pain-modulating pathway genes in musculoskeletal painK L Holliday, J McBeth, G Macfarlane, et al.
Molecular and Cellular Endocrinology|August 6, 2002
Identification, localization and functional activity of oxytocin receptors in epididymisS Filippi, G B Vannelli, S Granchi, et al.
Clinical Chemistry and Laboratory Medicine|July 4, 2001
Real-Time quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) for the measurement of prostate-specific antigen mRNA in the peripheral blood of patients with prostate carcinoma using the taqman detection systemS Gelmini, C Tricarico, G Vona, et al.
International Journal of Impotence Research|August 12, 2011
Childhood maltreatment in subjects with male-to-female gender identity disorderE Bandini, A D Fisher, V Ricca, et al.
Journal of Endocrinological Investigation|June 5, 2009
Persistence of expression of the TMPRSS2:ERG fusion gene after pre-surgery androgen ablation may be associated with early prostate specific antigen relapse of prostate cancer: preliminary resultsL Bonaccorsi, G Nesi, F Nuti, et al.
Journal of Endocrinological Investigation|December 4, 2009
Epidemiology, diagnosis, and treatment of male hypogonadotropic hypogonadismA Lenzi, G Balercia, A Bellastella, et al.
Alimentary Pharmacology & Therapeutics|August 21, 2013
Randomised clinical trial: mesalazine and/or probiotics in maintaining remission of symptomatic uncomplicated diverticular disease--a double-blind, randomised, placebo-controlled studyA Tursi, G Brandimarte, W Elisei, et al.
European Journal of Endocrinology|October 19, 2014
Associations of obesity with socioeconomic and lifestyle factors in middle-aged and elderly men: European Male Aging Study (EMAS)T S Han, D M Lee, M E J Lean, et al.
Journal of Medical Genetics|September 11, 2008
Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal backgroundC Krausz, C Giachini, Y Xue, et al.
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