Postoperative inotropic treatment after combined beating heart coronary surgery and transmyocardial laser revascularization

por Guarracino, F, Triggiani, M, Benussi, S, Donatelli, F, De Stefani, R, Grossi, A
Publicado 1997

Bridging public health and primary care in an Italian Urban Area. Lessons learnt from pandemic

por Frisicale, E M, Barbara, A, Borghini, A, Carini, E, Grossi, A, Tanese, A, Goletti, M, Parente, P
Publicado 2023

Ukrainian refugee crisis: the experience of the Roman Local Health Authority “ASL Roma 1”: Andriy Melnyk

por Melnyk, A, Barone, LC, Messina, S, Grossi, A, Kohut, M, Cascini, F, Damiani, G, Parente, P, Goletti, M
Publicado 2022

The role of hybrid immunity after the administration of the first booster dose

por Pascucci, D, Nurchis, M C, Lontano, A, Marziali, E, Grossi, A, Capelli, G, Vetrugno, G, Damiani, G, Laurenti, P
Publicado 2023

Severe erytrodermic psoriasis and arthritis as clinical presentation of a CARD14-mediated psoriasis (CAMPS)

por Signa, S, Rusmini, M, Campione, E, Gueli, I, Grossi, A, Omenetti, A, Bianchi, L, Martini, A, Ceccherini, I, Gattorno, M
Publicado 2015

Prevalence of CECR1 mutations in pediatric patients with polyarteritis nodosa, livedo reticularis and/or stroke

por Caorsi, R, Grossi, A, Insalaco, A, Alessio, M, Martino, S, Cortis, E, Morreale, A, Caroli, F, Martini, A, Ceccherini, I, Gattorno, M
Publicado 2015

Whole genome sequencing in ROHHAD trios proved inconclusive: what’s beyond?

por Grossi, A., Rusmini, M., Cusano, R., Massidda, M., Santamaria, G., Napoli, F., Angelelli, A., Fava, D., Uva, P., Ceccherini, I., Maghnie, M.
Publicado 2023

P810: BONE MARROW FAILURE IN PATIENTS CARRYING VARIANTS ON CARD11 GENE.

por Beccaria, A., Grossi, A., Fioredda, F., Lanciotti, M., Palmisani, E., Terranova, P., Lupia, M., Dell’Orso, G., Ceccherini, I., Dufour, C., Miano, M.
Publicado 2022

Whole exome sequencing approach to childhood onset familial erythrodermic psoriasis unravels a novel mutation of CARD14 requiring unusual high doses of ustekinumab

por Signa, S., Campione, E., Rusmini, M., Chiesa, S., Grossi, A., Omenetti, A., Caorsi, R., Viglizzo, G. M., Galluzzo, M., Bianchi, L., Talamonti, M., Orlandi, A., Martini, A., Ceccherini, I., Gattorno, M.
Publicado 2019

A Next Generation Sequencing approach to the mutational screening of patients affected with systemic autoinflammatory disorders: diagnosis improvement and interpretation of complex...

por Rusmini, M, Federici, S, Caroli, F, Grossi, A, Baldi, M, Obici, L, Insalaco, A, Tommasini, A, Caorsi, R, Gallo, E, Olivieri, AN, Marzano, AV, Coviello, D, Ravazzolo, R, Martini, A, Gattorno, M, Ceccherini, I
Publicado 2015

B cells characterization in ADA2 Deficiency patients

por Schena, F, Volpi, S, Caorsi, R, Pastorino, C, Penco, F, Kalli, F, Omenetti, A, Chiesa, S, Bertoni, A, Picco, P, Filaci, G, Aksentijevich, I, Grossi, A, Ceccherini, I, Martini, A, Traggiai, E, Gattorno, M
Publicado 2015