Browsing Centre for Endocrinology by Author "Paganoni, A"
Now showing items 1-6 of 6
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Autism-linked NLGN3 is a key regulator of gonadotropin-releasing hormone deficiency
Oleari, R; Lettieri, A; Manzini, S; Paganoni, A; Andre, V; Grazioli, P; Busnelli, M; Duminuco, P; Vitobello, A; Philippe, C (2023) -
Combined omic analysis revealed autism-linked <i>NLGN3</i> as new candidate gene associated to GnRH neuron development and disease
Oleari, R; Lettieri, A; Paganoni, A; Howard, SR; Cariboni, A (2021) -
Rare variants in the MECP2 gene in girls with central precocious puberty: a translational cohort study
Canton, APM; Tinano, FR; Guasti, L; Montenegro, LR; Ryan, F; Shears, D; Melo, MED; Gomes, LG; Piana, MP; Brauner, R (2023) -
RF14 | PSAT120 X-Linked Central Precocious Puberty Associated with MECP2 Defects
Canton, A; Tinano, F; Guasti, L; Montenegro, L; Argente, J; Ryan, F; Shears, D; Melo, ME; Gomes, L; Piana, M (The Endocrine Society, 2022-11-01) -
Variants in Methyl-CpG-binding protein 2 (MECP2) are associated with X-Linked Central Precocious Puberty
E, RJ; Pinheiro-Machado, CA; Tinano, F; Guasti, L; Ribeiro, ML; Ryan, F; Shears, D; Paganoni, A; Korbonits, M; Jorge, A -
X-Linked Central Precocious Puberty Associated with MECP2 defects
Canton, A; Tinano, F; Guasti, L; Montenegro, L; Ryan, F; Shears, D; Melo, ME; Gomes, L; Piana, M; Brauner, R (2022)