Browsing Centre for Endocrinology by Author "Quinton, R"
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Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures
Cassatella, D; Howard, SR; Acierno, JS; Xu, C; Papadakis, GE; Santoni, FA; Dwyer, AA; Santini, S; Sykiotis, GP; Chambion, C (2018-04) -
IGSF10 mutations dysregulate gonadotropin-releasing hormone neuronal migration resulting in delayed puberty
Howard, SR; Guasti, L; Ruiz-Babot, G; Mancini, A; David, A; Storr, H; Metherell, LA; Sternberg, MJE; Cabrera, CP; Warren, HR (2016-06) -
In-frame seven amino-acid duplication in AIP arose over the last 3000 years, disrupts protein interaction and stability and is associated with gigantism
Salvatori, R; Radian, S; Diekmann, Y; Iacovazzo, D; David, A; Gabrovska, P; Grassi, G; Bussell, A-M; Stals, K; Weber, A (2017-09) -
Outcomes and experiences of adults with congenital hypogonadism can inform improvements in the management of delayed puberty.
Howard, SR; Quinton, R (2024-01-29)Patients with congenital hypogonadism will encounter many health care professionals during their lives managing their health needs; from antenatal and infantile periods, through childhood and adolescence, into adult life ... -
An unusual phenocopy for postmenopausal ovarian hyperandrogenism: LH-driven testosterone secretion by adrenal adenoma expressing luteinising hormone-chorionic gonadotrophin receptor.
Ali, M; Rai, A; Howarth, S; Madathil, A; Rice, T; Boot, C; Quinton, R; Korbonits, M; Mamoojee, YH (2024-04)