BONOMI, MARCO
BONOMI, MARCO
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
2018 European Thyroid Association (ETA) Guidelines on the Diagnosis and Management of Central Hypothyroidism
2018 L. Persani, G. Brabant, M. Dattani, M. Bonomi, U. Feldt-Rasmussen, E. Fliers, A. Gruters, D. Maiter, N. Schoenmakers, A.S.P. van Trotsenburg
45,X/46,X,i(Yp) : Importance of Assessment and Support during Puberty and Adolescence
2019 R. Gaudino, E. Maines, F. Guizzardi, V. Vezzoli, C. Krausz, P. Cavarzere, G. Piacentini, F. Antoniazzi, M. Bonomi
A family with complete resistance to thyrotropin-releasing hormone
2009 M. Bonomi, M. Busnelli, P. Beck-Peccoz, D. Costanzo, F. Antonica, C. Dolci, A. Pilotta, F. Buzi, L. Persani
A Frequent Oligogenic Involvement in Congenital Hypothyroidism
2017 T. de Filippis, G. Gelmini, E. Paraboschi, M.C. Vigone, M. Di Frenna, F. Marelli, M. Bonomi, A. Cassio, D. Larizza, M. Moro, G. Radetti, M. Salerno, D. Ardissino, G. Weber, D. Gentilini, F. Guizzardi, S. Duga, L. Persani
A new variant in signal peptide of the human luteinizing hormone receptor (LHCGR) affects receptor biogenesis causing leydig cell hypoplasia
2015 V. Vezzoli, P. Duminuco, A. Vottero, G. Kleinau, R. Schülein, R. Minari, I. Bassi, S. Bernasconi, L. Persani, M. Bonomi
A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome
2018 E.F. Roche, A. Mcgowan, O. Koulouri, M. Turgeon, A.K. Nicholas, E. Heffernan, R. El-Khairi, N. Abid, G. Lyons, D. Halsall, M. Bonomi, L. Persani, M.T. Dattani, M. Gurnell, D.J. Bernard, N. Schoenmakers
A Rare SPRY4 Gene Mutation Is Associated With Anosmia and Adult-Onset Isolated Hypogonadotropic Hypogonadism
2019 R. Indirli, B. Cangiano, E. Profka, G. Mantovani, L. Persani, M. Arosio, M. Bonomi, E. Ferrante
Absence of primary hypothyroidism and goiter in Slc26a4(-/-) mice fed on a low iodine diet
2011 D. Calebiro, P. Porazzi, M. Bonomi, S. Lisi, A. Grindati, D. De Nittis, L. Fugazzola, M. Marinò, G. Bottà, L. Persani
Activator protein-1 and smad proteins synergistically regulate human follicle-stimulating hormone beta-promoter activity
2008 Y. Wang, J. Fortin, P. Lamba, M. Bonomi, L. Persani, MS. Roberson, DJ. Bernard
Addressing gaps in care of people with conditions affecting sex development and maturation
2019 O. Hiort, M. Cools, A. Springer, K. Mcelreavey, A. Greenfield, S.A. Wudy, A. Kulle, S.F. Ahmed, A. Dessens, A. Balsamo, M. Maghnie, M. Bonomi, M. Dattani, L. Persani, L. Audi
Approccio diagnostico alla paziente con insufficienza ovarica primaria
2022 S. Federici, L. Persani, M. Bonomi
Blood cell mitochondrial DNA content and premature ovarian aging
2012 M. Bonomi, E. Somigliana, C. Cacciatore, M. Busnelli, R. Rossetti, S. Bonetti, A. Paffoni, D. Mari, G. Ragni, L. Persani
Cardiovascular risk and testosterone – from subclinical atherosclerosis to lipoprotein function to heart failure
2021 B. Gencer, M. Bonomi, M.P. Adorni, C.R. Sirtori, F. Mach, M. Ruscica
Central hypogonadism in Klinefelter syndrome : report of two cases and review of the literature
2020 B. Cangiano, R. Indirli, E. Profka, E. Castellano, G. Goggi, V. Vezzoli, G. Mantovani, M. Arosio, L. Persani, G. Borretta, E. Ferrante, M. Bonomi
Central hypothyroidism
2015 L. Persani, M. Bonomi
Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH)
2018 M. Bonomi, V. Vezzoli, C. Krausz, F. Guizzardi, S. Vezzani, M. Simoni, I. Bassi, P. Duminuco, N. Di Iorgi, C. Giavoli, A. Pizzocaro, G. Russo, M. Moro, L. Fatti, A. Ferlin, L. Mazzanti, M.C. Zatelli, S. Cannavò, A. M Isidori, A.I. Pincelli, F. Prodam, A. Mancini, P. Limone, M.L. Tanda, R. Gaudino, M. Salerno, F. Pregnolato, M. Maghnie, M. Maggi, L. Persani
Clinical and genetic characterisation of a series of patients with triple A syndrome
2018 E. Kurnaz, P. Duminuco, Z. Aycan, Ş. Savaş-Erdeve, N.M. Sahin, Ş. Muratoğlu, M. Kestin, E. Bayramoğlu, M. Bonomi, S. Cetinkaya
Clinical benefits of sex steroids given as a priming prior to GH provocative test or as a growth-promoting therapy in peripubertal growth delays: Results of a retrospective study among ENDO-ERN centres
2020 E. Galazzi, N. Improda, M. Cerbone, D. Soranna, M. Moro, L.M. Fatti, A. Zambon, M. Bonomi, M. Salerno, M. Dattani, L. Persani
Congenital GnRH deficiency : a complex and genetically heterogeneous disease affecting human fertility and sexual development
2016 M. Bonomi, R. Quinton
Control of GnRH Secretion
2016 M. Bonomi, V. Vezzoli, A. Cariboni