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BARBETTI, FABRIZIO

BARBETTI, FABRIZIO  

Dipartimento di Medicina Sperimentale  

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Risultati 1 - 20 di 113 (tempo di esecuzione: 0.045 secondi).
Data di pubblicazione Titolo Autore(i) Tipo File
16-gen-2014 A possible role of transglutaminase 2 in the nucleus of INS-1E and cells of human pancreatic islets. Sileno, S; D’Oria, V; Stucchi, R; Alessio, M; Petrini, S; Bonetto, V; Maechler, P; Bertuzzi, F; Grasso, V; Paolella, K; Barbetti, F; Massa, O Articolo su rivista
1-gen-2024 A rare cause of transient neonatal diabetes mellitus: Spontaneous HNF1B splice variant Pezzino, G; Ruta, R; Rapini, N; Chiodo, Dc; Mucciolo, M; Tomaselli, L; Cianfarani, S; Barbetti, F Articolo su rivista
1-gen-1985 Amniotic membrane chambers for pancreatic islet transplantation: The diffusion patterns of glucose and insulin Maldonato, A; Cama, A; Marani, F; Lucisano, A; Maniccia, E; Luciani, G; Cascella, V; Barbetti, F; Falucca, F; Andreani, D Articolo su rivista
1-gen-2007 An ATP-binding mutation (G334D) in KCNJ11 is associated with a sulfonylurea-insensitive form of DEND (Developmental Delay, Epilepsy, and Neonatal Diabetes) Masia, R; Koster, J; Tumini, S; Chiarelli, F; Colombo, C; Nichols, C; Barbetti, F Articolo su rivista
6-nov-2018 b Cell Replacement after Gene Editing of a Neonatal Diabetes-Causing Mutation at the Insulin Locus Ma, S; Viola, R; Sui, L; Cherubini, V; Barbetti, F; Egli, D Articolo su rivista
1-set-2018 Can HbA1c combined with fasting plasma glucose help to assess priority for GCK-MODY vs HNF1A-MODY genetic testing? Delvecchio, M; Salzano, G; Bonura, C; Cauvin, V; Cherubini, V; D’Annunzio, G; Franzese, A; Giglio, S; Grasso, V; Graziani, V; Iafusco, D; Iughetti, L; Lera, R; Maffeis, C; Maltoni, G; Mantovani, V; Menzaghi, C; Oater, P; Rabbone, I; Reinstadler, P; Scelfo, S; Tinto, N; Toni, S; Tumini, S; Lombardo, F; Nicolucci, A; Barbetti, F Articolo su rivista
1-gen-2021 Case report: coeliac disease as a cause of secondary failure of glyburide therapy in a patient with permanent neonatal diabetes due to KCNJ11/R201C mutation Iafusco, D; Zanfardino, A; Piscopo, A; Casaburo, F; De Nigris, A; Alfiero, S; Russo, G; Arenella, M; Russo, M; Barbetti, F Articolo su rivista
1-gen-1996 Clinical and molecular evaluation of Italian patients affected by Pelizaeus-Merzbacher disease Terregino, C; Cardona, F; Barbetti, F; Antonozzi, I; Carducci, C Articolo su rivista
1-gen-2011 Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation. KATP channel inactivation mechanism and clinical management. Loechner, K; Akrouh, A; Kurata, H; Dionisi Vici, C; Maiorana, A; Pizzoferro, M; Rufini, V; DE VILLE DE GOYET, J; Colombo, C; Barbetti, F; Koster, J; Nichols, Cg Articolo su rivista
1-gen-2016 Consulenza genetica e diabete Barbetti, F; Buzzetti, R; Cerutti, F; Copetti, M; Dauriz, M; Penno, G; Trischitta, V Contributo in libro
1-gen-2022 Contribution of ONECUT1 variants to different forms of non-autoimmune diabetes mellitus in Italian patients Prudente, S; Andreozzi, F; Mercuri, L; Alberico, F; Digiamberardino, A; Mannino, G; Ludovico, O; Piscitelli, P; Di Paola, R; Morano, S; Penno, G; Carella, M; De Cosmo, S; Trischitta, V; Barbetti, F Articolo su rivista
1-gen-1994 Deletion of exon 3 of the insulin receptor gene in a kindred with a familial form of insulin resistance Wertheimer, E; Litvin, Y; Ebstein, Rp; Bennett, Er; Barbetti, F; Accili, D; Taylor, Si Articolo su rivista
1-gen-1992 Detection of mutations in insulin receptor gene by denaturing gradient gel electrophoresis Barbetti, F; Gejman, Pv; Taylor, Si; Raben, N; Cama, A; Bonora, E; Pizzo, P; Moghetti, P; Muggeo, M; Roth, J Articolo su rivista
1-gen-2015 Diabete tipo 1, tipo 2 e tipo X. Ipeglicemia in età pediatrica: quale diabete ? Iafusco, D; Barbetti, F; Massimi, A; Grasso, V; Rabbone, I; Casaburo, F; Cocca, A; Confetto, S; Galderisi, A; Paccone, A; Picariello, S; Piscopo, A; Russo, L; Villano, P; Zanfardino, A; Prisco, F; Tinto, N; Mazzaccara, C; Pirozzi, D; De Sanctis, P; Pinelli, M; Acquaviva, F; Sacchetti, L Articolo su rivista
1-gen-2016 Diabetes associated with dominant insulin gene mutations: outcome of 24-month, sensor-augmented insulin pump treatment Ortolani, F; Piccinno, E; Grasso, V; Papadia, F; Panzeca, R; Cortese, C; Tummolo, A; Vendemiale, M; Barbetti, F Articolo su rivista
1-gen-2007 Diagnosis of neonatal and infancy-onset diabetes Barbetti, F Contributo in libro
1-gen-2021 Differences between transient neonatal diabetes mellitus subtypes can guide diagnosis and therapy Bonfanti, R; Iafusco, D; Rabbone, I; Diedenhofen, G; Bizzarri, C; Patera, P; Reinstadler, P; Costantino, F; Calcaterra, V; Iughetti, L; Savastio, S; Favia, A; Cardella, F; Lopresti, D; Girtler, Y; Rabbiosi, S; D’Annunzio, G; Zanfardino, A; Piscopo, A; Casaburo, F; Pintomalli, L; Russo, L; Grasso, V; Minuto, N; Mucciolo, M; Novelli, A; Marucci, A; Piccini, B; Toni, S; Silvestri, F; Carrera, P; Rigamonti, A; Frontino, G; Trada, M; Tinti, D; Delvecchio, M; Rapini, N; Schiaffini, R; Mammì, C; Barbetti, F Articolo su rivista
1-gen-1987 Dose-response effect of somatostatin-14 on human basal pancreatic hormones Annibale, B; Delle Fave, G; Barbetti, F; De Magistris, L; Puoti, M; Giordano, E; Leonetti, F; Tamburrano, G Articolo su rivista
4-giu-2018 Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study. Bowman, P; Sulen, A; Barbetti, F; Beltrand, J; Svalastoga, P; Codner, E; Tessmann Ellen, H; Juliusson Petur, B; Skrivarhaug, T; Pearson Ewan, R; Flanagan Sarah, E; Babiker, T; Thomas Nicholas, J; Shepherd Maggie, H; Ellard, S; Klimes, I; Szopa, M; Polak, M; Iafusco, D; Hattersley Andrew, T; Njølstad Pål, R Articolo su rivista
1-ott-1982 Effects of somatostatin on established induced ketosis Fallucca, F; Barbetti, F; Maldonato, A; Spallone, V; Giangrande, L; Gambardella, S Articolo su rivista