SALINA, ALESSANDRO

SALINA, ALESSANDRO  

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Titolo Data di pubblicazione Autore(i) File
"Pesto" Mutation: Phenotypic and Genotypic Characteristics of Eight GCK/MODY Ligurian Patients 1-gen-2023 Salina, Alessandro; Bassi, Marta; Aloi, Concetta; Strati, Marina Francesca; Bocciardi, Renata; D'Annunzio, Giuseppe; Maghnie, Mohamad; Minuto, Nicola
A novel hepatocyte nuclear factor-1β (MODY 5) gene mutation in a Romanian boy with pancreatic calcifications, renal and hepatic dysfunction. 1-gen-2011 Banin, P; Giovannini, M; Raimondi, F; D'Annunzio, G; Sala, S; Salina, Alessandro; Aloi, C; De Sanctis, V.
An Atypical Case of Late-Onset Wolfram Syndrome 1 without Diabetes Insipidus 1-gen-2022 Rigoli, L.; Caruso, V.; Aloi, C.; Salina, A.; Maghnie, M.; D'Annunzio, G.; Lamacchia, O.; Salzano, G.; Lombardo, F.; Picca, G.
Comment on: Clinical application of best practice guidelines for genetic diagnosis of MODY2. 1-gen-2012 Salina, Alessandro; Aloi, C; Pasquali, L; Mascagni, A; Cassanello, M; Tallone, R; Lugani, F; Lorini, RENATA GIUSEPPINA; D'Annunzio, G.
Diabetes Mellitus Diagnosed in Childhood and Adolescence With Negative Autoimmunity: Results of Genetic Investigation 1-gen-2022 Lezzi, Marilea; Aloi, Concetta; Salina, Alessandro; Fragola, Martina; Bassi, Marta; Strati, Marina Francesca; D'Annunzio, Giuseppe; Minuto, Nicola; Maghnie, Mohamad
Hyperglycaemia and beta-cell antibodies: is it always pre-type 1 diabetes? 1-gen-2013 D'Annunzio, G; Marchi, M; Aloi, C; Salina, Alessandro; Lugani, F; Lorini, RENATA GIUSEPPINA
Mother and daughter carrying the same KCNJ11 mutation but with a different response to switching from insulin to sulfonylurea. 1-gen-2011 Russo, C; Salina, Alessandro; Aloi, C; Iafusco, D; Lorini, RENATA GIUSEPPINA; D'Annunzio, G.
Next Generation Sequencing (NGS) Target Approach for Undiagnosed Dysglycaemia 1-gen-2023 Aloi, Concetta; Salina, Alessandro; Caroli, Francesco; Bocciardi, Renata; Tappino, Barbara; Bassi, Marta; Minuto, Nicola; D’Annunzio, Giuseppe; Maghnie, Mohamad
The coexistence of type 1 diabetes, MODY2 and metabolic syndrome in a young girl. 1-gen-2012 Calcaterra, V; Martinetti, M; Salina, Alessandro; Aloi, C; Larizza, D.
Wolfram syndrome: new mutations, different phenotype 1-gen-2012 Aloi, C; Salina, Alessandro; Pasquali, L; Lugani, F; Perri, K; Russo, C; Tallone, R; Ghiggeri, Gm; Lorini, RENATA GIUSEPPINA; D'Annunzio, G.