Sfoglia per Autore
Clinical and molecular evaluation of Italian patients affected by Pelizaeus-Merzbacher disease
1996-01-01 Terregino, C; Cardona, F; Barbetti, F; Antonozzi, I; Carducci, C
Increased OB gene expression leads to elevated plasma leptin concetrations in patients with chronic primary hyperinsulinemia
1998-01-01 D'Adamo, M; Buongiorno, A; Maroccia, E; Leonetti, F; Barbetti, F; Giaccari, A; Zorretta, D; Tamburrano, G; Sbraccia, P
Three novel missense mutations in the glucokinase gene (G80S; E221K; G227C) in Italian subjects with maturity-onset diabetes of the young (MODY). Mutations in brief no. 162. Online
1998-01-01 Guazzini, B; Gaffi, D; Mainieri, D; Multari, G; Cordera, R; Bertolini, S; Pozza, G; Meschi, F; Barbetti, F
Mutational analysis of the coding regions of the genes encoding protein kinase B-α and -β, phosphoinositide-dependent protein kinase-1, phosphatase targeting to glycogen, protein phosphatase inhibitor-1, and glycogenin: Lessons from a search for genetic variability of the insulin-stimulated glycogen synthesis pathway of skeletal muscle in NIDDM patients
1999-01-01 Hansen, L; Fjordvang, H; Rasmussen, Sk; Vestergaard, H; Echwald, Sm; Hansen, T; Alessi, D; Shenolikar, S; Saltiel, Ar; Barbetti, F; Pedersen, O
Role of proline 193 in the insulin receptor post-translational processing
1999-01-01 Maggi, D; Barbetti, F; Cordera, R
Missense mutations in the human insulin promoter factor-1 gene and their relation to maturity-onset diabetes of the young and late-onset type 2 diabetes mellitus in caucasians
2000-01-01 Hansen, L; Urioste, S; Petersen, Hv; Jensen, Jn; Eiberg, H; Barbetti, F; Serup, P; Hansen, T; Pedersen, O
MODY 2 presenting as neonatal hyperglycaemia: A need to reshape the definition of 'neonatal diabetes'? [2]
2000-01-01 Prisco, F; Iafusco, D; Franzese, A; Sulli, N; Barbetti, F
Neonatal diabetes mellitus due to complete glucokinase deficiency
2001-01-01 Njolstad, Pr; Sovik, O; Cuesta-Munoz, A; Bjorkhaug, L; Massa, O; Barbetti, F; Undlien, De; Shiota, C; Magnuson, Ma; Molven, A; Matschinsky, Fm; Bell, Gi
High prevalence of glucokinase mutations in Italian children with MODY. Influence on glucose tolerance, first-phase insulin response, insulin sensitivity and BMI
2001-01-01 Massa, O; Meschi, F; Cuesta-Munoz, A; Caumo, A; Cerutti, F; Toni, S; Cherubini, V; Guazzarotti, L; Sulli, N; Matschinsky, F; Lorini, R; Iafusco, D; Barbetti, F
The second activating glucokinase mutation (A456V): Implications for glucose homeostasis and diabetes therapy
2002-01-01 Christesen, Hbt; Jacobsen, Bb; Odili, S; Buettger, C; Cuesta-Munoz, A; Hansen, T; Brusgaard, K; Massa, O; Magnuson, Ma; Shiota, C; Matschinsky, Fm; Barbetti, F
Role of transglutaminase 2 in glucose tolerance: knockout mice studies and a putative mutation in a MODY patient
2002-01-01 Bernassola, F; Federici, M; Corazzari, M; Terrinoni, A; Hribal, Ml; De Laurenzi, V; Ranalli, M; Massa, O; Sesti, G; Irwin Mclean, W; Citro, G; Barbetti, F; Melino, G
The genetic abnormality in the beta cell determines the response to an oral glucose load
2002-01-01 Stride, A; Vaxillaire, M; Tuomi, T; Barbetti, F; Njolstad, Pr; Hansen, T; Costa, A; Conget, I; Pedersen, O; Sovik, O; Lorini, R; Groop, L; Froguel, P; Hattersley, At
Permanent diabetes mellitus in the first year of life
2002-01-01 Iafusco, D; Stazi, M; Cotichini, R; Cotellessa, M; Martinucci, M; Mazzella, M; Cherubini, V; Barbetti, F; Martinetti, M; Cerutti, F; Prisco, F
Renal cysts and diabetes syndrome linked to mutations of the hepatocyte nuclear factor-1β gene: Description of a new family with associated liver involvement
2002-01-01 Montoli, A; Colussi, G; Massa, O; Caccia, R; Rizzoni, G; Civati, G; Barbetti, F
Lack of the architectural factor HMGA1 causes insulin resistance and diabetes in humans and mice
2005-01-01 Foti, D; Chiefari, E; Fedele, M; Iuliano, R; Brunetti, L; Paonessa, F; Manfioletti, G; Barbetti, F; Brunetti, A; Croce, Cm; Fusco, A; Brunetti, A
Insights into the structure and regulation of glucokinase from a novel mutation (V62M), which causes maturity-onset diabetes of the young
2005-01-01 Gloyn, Al; Odili, S; Zelent, D; Buettger, C; Castleden, Haj; Steele, Am; Stride, A; Shiota, C; Magnuson, Ma; Lorini, R; D'Annunzio, G; Stanley, Ca; Kwagh, J; Van Schaftingen, E; Veiga-Da-Cunha, M; Barbetti, F; Dunten, P; Han, Y; Grimsby, J; Taub, R; Ellard, S; Hattersley, At; Matschinsky, Fm
KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes
2005-01-01 Massa, O; Iafusco, D; D'Amato, E; Gloyn, Al; Hattersley, At; Pasquino, B; Tonini, G; Dammacco, F; Zanette, G; Meschi, F; Porzio, O; Bottazzo, G; Crino, A; Lorini, R; Cerutti, F; Vanelli, M; Barbetti, F
Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation
2005-01-01 Colombo, C; Delvecchio, M; Zecchino, C; Faienza, Mf; Cavallo, L; Barbetti, F
Search for genetic variants in the p66 Shc longevity gene by PCR-single strand conformational polymorphism in patients with early-onset cardiovascular disease.
2006-01-01 Sentinelli, F; Romeo, S; Barbetti, F; Berni, A; Filippi, E; Fanelli, M; Fallarino, M; Baroni, M
Sulfonylurea treatment outweighs insulin therapy in short-term metabolic control of patients with permanent neonatal diabetes mellitus due to activating mutations of the KCNJ11 (KIR6.2) gene
2006-01-01 Tonini, G; Bizzarri, C; Bonfanti, R; Vanelli, M; Cerutti, F; Faleschini, E; Meschi, F; Prisco, F; Ciacco, E; Cappa, M; Torelli, C; Cauvin, V; Tumini, S; Iafusco, D; Barbetti, F
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 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-1998 | Increased OB gene expression leads to elevated plasma leptin concetrations in patients with chronic primary hyperinsulinemia | D'Adamo, M; Buongiorno, A; Maroccia, E; Leonetti, F; Barbetti, F; Giaccari, A; Zorretta, D; Tamburrano, G; Sbraccia, P | Articolo su rivista | |
| 1-gen-1998 | Three novel missense mutations in the glucokinase gene (G80S; E221K; G227C) in Italian subjects with maturity-onset diabetes of the young (MODY). Mutations in brief no. 162. Online | Guazzini, B; Gaffi, D; Mainieri, D; Multari, G; Cordera, R; Bertolini, S; Pozza, G; Meschi, F; Barbetti, F | Articolo su rivista | |
| 1-gen-1999 | Mutational analysis of the coding regions of the genes encoding protein kinase B-α and -β, phosphoinositide-dependent protein kinase-1, phosphatase targeting to glycogen, protein phosphatase inhibitor-1, and glycogenin: Lessons from a search for genetic variability of the insulin-stimulated glycogen synthesis pathway of skeletal muscle in NIDDM patients | Hansen, L; Fjordvang, H; Rasmussen, Sk; Vestergaard, H; Echwald, Sm; Hansen, T; Alessi, D; Shenolikar, S; Saltiel, Ar; Barbetti, F; Pedersen, O | Articolo su rivista | |
| 1-gen-1999 | Role of proline 193 in the insulin receptor post-translational processing | Maggi, D; Barbetti, F; Cordera, R | Articolo su rivista | |
| 1-gen-2000 | Missense mutations in the human insulin promoter factor-1 gene and their relation to maturity-onset diabetes of the young and late-onset type 2 diabetes mellitus in caucasians | Hansen, L; Urioste, S; Petersen, Hv; Jensen, Jn; Eiberg, H; Barbetti, F; Serup, P; Hansen, T; Pedersen, O | Articolo su rivista | |
| 1-gen-2000 | MODY 2 presenting as neonatal hyperglycaemia: A need to reshape the definition of 'neonatal diabetes'? [2] | Prisco, F; Iafusco, D; Franzese, A; Sulli, N; Barbetti, F | Articolo su rivista | |
| 1-gen-2001 | Neonatal diabetes mellitus due to complete glucokinase deficiency | Njolstad, Pr; Sovik, O; Cuesta-Munoz, A; Bjorkhaug, L; Massa, O; Barbetti, F; Undlien, De; Shiota, C; Magnuson, Ma; Molven, A; Matschinsky, Fm; Bell, Gi | Articolo su rivista | |
| 1-gen-2001 | High prevalence of glucokinase mutations in Italian children with MODY. Influence on glucose tolerance, first-phase insulin response, insulin sensitivity and BMI | Massa, O; Meschi, F; Cuesta-Munoz, A; Caumo, A; Cerutti, F; Toni, S; Cherubini, V; Guazzarotti, L; Sulli, N; Matschinsky, F; Lorini, R; Iafusco, D; Barbetti, F | Articolo su rivista | |
| 1-gen-2002 | The second activating glucokinase mutation (A456V): Implications for glucose homeostasis and diabetes therapy | Christesen, Hbt; Jacobsen, Bb; Odili, S; Buettger, C; Cuesta-Munoz, A; Hansen, T; Brusgaard, K; Massa, O; Magnuson, Ma; Shiota, C; Matschinsky, Fm; Barbetti, F | Articolo su rivista | |
| 1-gen-2002 | Role of transglutaminase 2 in glucose tolerance: knockout mice studies and a putative mutation in a MODY patient | Bernassola, F; Federici, M; Corazzari, M; Terrinoni, A; Hribal, Ml; De Laurenzi, V; Ranalli, M; Massa, O; Sesti, G; Irwin Mclean, W; Citro, G; Barbetti, F; Melino, G | Articolo su rivista | |
| 1-gen-2002 | The genetic abnormality in the beta cell determines the response to an oral glucose load | Stride, A; Vaxillaire, M; Tuomi, T; Barbetti, F; Njolstad, Pr; Hansen, T; Costa, A; Conget, I; Pedersen, O; Sovik, O; Lorini, R; Groop, L; Froguel, P; Hattersley, At | Articolo su rivista | |
| 1-gen-2002 | Permanent diabetes mellitus in the first year of life | Iafusco, D; Stazi, M; Cotichini, R; Cotellessa, M; Martinucci, M; Mazzella, M; Cherubini, V; Barbetti, F; Martinetti, M; Cerutti, F; Prisco, F | Articolo su rivista | |
| 1-gen-2002 | Renal cysts and diabetes syndrome linked to mutations of the hepatocyte nuclear factor-1β gene: Description of a new family with associated liver involvement | Montoli, A; Colussi, G; Massa, O; Caccia, R; Rizzoni, G; Civati, G; Barbetti, F | Articolo su rivista | |
| 1-gen-2005 | Lack of the architectural factor HMGA1 causes insulin resistance and diabetes in humans and mice | Foti, D; Chiefari, E; Fedele, M; Iuliano, R; Brunetti, L; Paonessa, F; Manfioletti, G; Barbetti, F; Brunetti, A; Croce, Cm; Fusco, A; Brunetti, A | Articolo su rivista | |
| 1-gen-2005 | Insights into the structure and regulation of glucokinase from a novel mutation (V62M), which causes maturity-onset diabetes of the young | Gloyn, Al; Odili, S; Zelent, D; Buettger, C; Castleden, Haj; Steele, Am; Stride, A; Shiota, C; Magnuson, Ma; Lorini, R; D'Annunzio, G; Stanley, Ca; Kwagh, J; Van Schaftingen, E; Veiga-Da-Cunha, M; Barbetti, F; Dunten, P; Han, Y; Grimsby, J; Taub, R; Ellard, S; Hattersley, At; Matschinsky, Fm | Articolo su rivista | |
| 1-gen-2005 | KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes | Massa, O; Iafusco, D; D'Amato, E; Gloyn, Al; Hattersley, At; Pasquino, B; Tonini, G; Dammacco, F; Zanette, G; Meschi, F; Porzio, O; Bottazzo, G; Crino, A; Lorini, R; Cerutti, F; Vanelli, M; Barbetti, F | Articolo su rivista | |
| 1-gen-2005 | Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation | Colombo, C; Delvecchio, M; Zecchino, C; Faienza, Mf; Cavallo, L; Barbetti, F | Articolo su rivista | |
| 1-gen-2006 | Search for genetic variants in the p66 Shc longevity gene by PCR-single strand conformational polymorphism in patients with early-onset cardiovascular disease. | Sentinelli, F; Romeo, S; Barbetti, F; Berni, A; Filippi, E; Fanelli, M; Fallarino, M; Baroni, M | Articolo su rivista | |
| 1-gen-2006 | Sulfonylurea treatment outweighs insulin therapy in short-term metabolic control of patients with permanent neonatal diabetes mellitus due to activating mutations of the KCNJ11 (KIR6.2) gene | Tonini, G; Bizzarri, C; Bonfanti, R; Vanelli, M; Cerutti, F; Faleschini, E; Meschi, F; Prisco, F; Ciacco, E; Cappa, M; Torelli, C; Cauvin, V; Tumini, S; Iafusco, D; Barbetti, F | Articolo su rivista |
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