MARGAGLIONE, MAURIZIO
MARGAGLIONE, MAURIZIO
Dipartimento di Medicina Clinica e Sperimentale
"Genetic modulation of oral anticoagulantion with warfarin "
2000-01-01 Margaglione, Maurizio; Colaizzo, D; D'Andrea, Giovanna; Brancaccio, V; Ciampa, A; Grandone, E; Diminno, G.
. Impact of prothrombotic mutations and family history on the occurrence of intra-uterine fetal deaths. Haematologica 2002; 87(10):1118-9
2002-01-01 Grandone, E; Colaizzo, D; Brancaccio, V; Ciampa, A; Di Minno, G; Margaglione, M
. An unreported mutation within protein Z gene is associated with very low protein levels in women with fetal loss.Fertil Steril.
2008-01-01 Grandone, E; Colaizzo, D; Cappucci, F; D'Ambrosio, Rl; Vecchione, G; Margaglione, M
. PAI-1 4G/5G and ACE I/D gene polymorphisms and the occurrence of myocardial infarction in patients on intermittent dialysis. Nephrol Dial Transplant 2003; 18(6):1142-6
2003-01-01 Aucella, F; Margaglione, M; Vigilante, M; Gatta, G; Grandone, E; Forcella, M; Ktena, M; De Min, A; Salatino, G; Procaccini, Da; Stallone, C
.Adverse outcome in women with thrombophilia and bilateral uterine artery notches. Fertil Steril. 86(3):726-7; 2006
2006-01-01 Grandone, E; Colaizzo, D; Martinelli, P; Paladini, D; di Minno, G; Margaglione, M
.Homocysteine metabolism in families from southern Italy with neural tube defects: role of genetic and nutritional determinants. Prenat Diagn. 2006; 26(1):1-5
2006-01-01 Grandone, E; Corrao, Am; Colaizzo, D; Vecchione, G; Di Girgenti, C; Paladini, D; Sardella, L; Pellegrino, M; Zelante, L; Martinelli, P; Margaglione, M
.Risk factors and clinical presentation of portal vein thrombosis in patients with liver cirrhosis. J Hepatol. 2004; 40(5):736-41.
2004-01-01 Amitrano, L; Guardascione, Ma; Brancaccio, V; Margaglione, M; Manguso, F; Iannaccone, L; Grandone, E; Balzano, A
2014 Sep 8. A novel congenital dysprothrombinemia leading to defective prothrombin maturation
2014-01-01 Bafunno, V; Bury, L; Tiscia, Gl; Fierro, T; Favuzzi, G; Caliandro, R; Sessa, F; Grandone, E; Margaglione, M; Gresele, P
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions.
2008-01-01 D'Andrea, Giovanna; Bafunno, V.; DEL VECCHIO, L.; Amoriello, A.; Morabito, P.; Vecchione, G.; Grandone, E.; Margaglione, Maurizio
A comprehensive on-line digestion-liquid chromatography/mass spectrometry/collision-induced dissociation mass spectrometry approach for the characterization of human fibrinogen.
2001-01-01 Vecchione, G; Casetta, B; Santacroce, Rosa; Margaglione, Maurizio
A description of a new case of combined Factor V and Factor VIII deficiency: the LMAN1 M1T is a frequent cause in Italian patients.
2007-01-01 Dambrosio, R; Santacroce, Rosa; DI PERNA, P; Sarno, M; Romondia, A; Margaglione, Maurizio
A fast and accurate method for genotyping the angiotensin-converting enzyme I/D polymorphism.
1998-01-01 Mancini, Fp; Margaglione, Maurizio; Tufano, A; Celentano, A; Ferrara, La; Colantuoni, V; Di Minno, G.
A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo
2001-01-01 Margaglione, Maurizio; . VECCHIONE G, .; Santacroce, Rosa; Dangelo, F.; Casetta, B.; Papa, M. L.; Grandone, E.; DI MINNO, G.
A G-to A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing
2000-01-01 Margaglione, Maurizio; Santacroce, Rosa; Colaizzo, D.; Seripa, D.; Vecchione, G.; Lupone, M. R.; DE LUCIA, D.; Fortina, P.; Grandone, E.; Perricone, C.; DI MINNO, G.
A myoferlin gain-of-function variant associates with a new type of hereditary angioedema
2020-01-01 Ariano, A.; D'Apolito, M.; Bova, M.; Bellanti, F.; Loffredo, S.; D'Andrea, G.; Intrieri, M.; Petraroli, A.; Maffione, A. B.; Spadaro, G.; Santacroce, R.; Margaglione, M.
A new case of combined factor V and factor VIII deficiency further suggests that the LMAN1 M1T mutation is a frequent cause in Italian patients.
2007-01-01 D'Ambrosio, R; Santacroce, Rosa; Perna, Pd; Sarno, M; Romondia, A; Margaglione, Maurizio
A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis.
2007-01-01 Colaizzo, D; Amitrano, L; Tiscia, Gl; Grandone, E; Guardascione, Ma; Margaglione, Maurizio
A new method for determination of plasma homocystine by isotope dilution and electrospray tandem mass spectrometry. J
2006-01-01 Tomaiuolo, M; Vecchione, G; Grandone, E; Cocomazzi, N; Casetta, B; Di Minno, G; Margaglione, Maurizio
A New SERPINA-1 Missense Mutation Associated with Alpha-1 Antitrypsin Deficiency and Bronchiectasis
2017-01-01 Carpagnano, GIOVANNA ELISIANA; Santacroce, Rosa; Palmiotti, G. A; Leccese, A.; Giuffreda, E.; Margaglione, Maurizio; FOSCHINO BARBARO, MARIA PIA; Aliberti, S.; Lacedonia, Donato
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme
2007-01-01 D'Ambrosio, R. L.; D'Andrea, Giovanna; Cafolla, A.; Faillace, F.; Margaglione, Maurizio
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| "Genetic modulation of oral anticoagulantion with warfarin " | 1-gen-2000 | Margaglione, Maurizio; Colaizzo, D; D'Andrea, Giovanna; Brancaccio, V; Ciampa, A; Grandone, E; Diminno, G. | |
| . Impact of prothrombotic mutations and family history on the occurrence of intra-uterine fetal deaths. Haematologica 2002; 87(10):1118-9 | 1-gen-2002 | Grandone, E; Colaizzo, D; Brancaccio, V; Ciampa, A; Di Minno, G; Margaglione, M | |
| . An unreported mutation within protein Z gene is associated with very low protein levels in women with fetal loss.Fertil Steril. | 1-gen-2008 | Grandone, E; Colaizzo, D; Cappucci, F; D'Ambrosio, Rl; Vecchione, G; Margaglione, M | |
| . PAI-1 4G/5G and ACE I/D gene polymorphisms and the occurrence of myocardial infarction in patients on intermittent dialysis. Nephrol Dial Transplant 2003; 18(6):1142-6 | 1-gen-2003 | Aucella, F; Margaglione, M; Vigilante, M; Gatta, G; Grandone, E; Forcella, M; Ktena, M; De Min, A; Salatino, G; Procaccini, Da; Stallone, C | |
| .Adverse outcome in women with thrombophilia and bilateral uterine artery notches. Fertil Steril. 86(3):726-7; 2006 | 1-gen-2006 | Grandone, E; Colaizzo, D; Martinelli, P; Paladini, D; di Minno, G; Margaglione, M | |
| .Homocysteine metabolism in families from southern Italy with neural tube defects: role of genetic and nutritional determinants. Prenat Diagn. 2006; 26(1):1-5 | 1-gen-2006 | Grandone, E; Corrao, Am; Colaizzo, D; Vecchione, G; Di Girgenti, C; Paladini, D; Sardella, L; Pellegrino, M; Zelante, L; Martinelli, P; Margaglione, M | |
| .Risk factors and clinical presentation of portal vein thrombosis in patients with liver cirrhosis. J Hepatol. 2004; 40(5):736-41. | 1-gen-2004 | Amitrano, L; Guardascione, Ma; Brancaccio, V; Margaglione, M; Manguso, F; Iannaccone, L; Grandone, E; Balzano, A | |
| 2014 Sep 8. A novel congenital dysprothrombinemia leading to defective prothrombin maturation | 1-gen-2014 | Bafunno, V; Bury, L; Tiscia, Gl; Fierro, T; Favuzzi, G; Caliandro, R; Sessa, F; Grandone, E; Margaglione, M; Gresele, P | |
| A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. | 1-gen-2008 | D'Andrea, Giovanna; Bafunno, V.; DEL VECCHIO, L.; Amoriello, A.; Morabito, P.; Vecchione, G.; Grandone, E.; Margaglione, Maurizio | |
| A comprehensive on-line digestion-liquid chromatography/mass spectrometry/collision-induced dissociation mass spectrometry approach for the characterization of human fibrinogen. | 1-gen-2001 | Vecchione, G; Casetta, B; Santacroce, Rosa; Margaglione, Maurizio | |
| A description of a new case of combined Factor V and Factor VIII deficiency: the LMAN1 M1T is a frequent cause in Italian patients. | 1-gen-2007 | Dambrosio, R; Santacroce, Rosa; DI PERNA, P; Sarno, M; Romondia, A; Margaglione, Maurizio | |
| A fast and accurate method for genotyping the angiotensin-converting enzyme I/D polymorphism. | 1-gen-1998 | Mancini, Fp; Margaglione, Maurizio; Tufano, A; Celentano, A; Ferrara, La; Colantuoni, V; Di Minno, G. | |
| A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo | 1-gen-2001 | Margaglione, Maurizio; . VECCHIONE G, .; Santacroce, Rosa; Dangelo, F.; Casetta, B.; Papa, M. L.; Grandone, E.; DI MINNO, G. | |
| A G-to A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing | 1-gen-2000 | Margaglione, Maurizio; Santacroce, Rosa; Colaizzo, D.; Seripa, D.; Vecchione, G.; Lupone, M. R.; DE LUCIA, D.; Fortina, P.; Grandone, E.; Perricone, C.; DI MINNO, G. | |
| A myoferlin gain-of-function variant associates with a new type of hereditary angioedema | 1-gen-2020 | Ariano, A.; D'Apolito, M.; Bova, M.; Bellanti, F.; Loffredo, S.; D'Andrea, G.; Intrieri, M.; Petraroli, A.; Maffione, A. B.; Spadaro, G.; Santacroce, R.; Margaglione, M. | |
| A new case of combined factor V and factor VIII deficiency further suggests that the LMAN1 M1T mutation is a frequent cause in Italian patients. | 1-gen-2007 | D'Ambrosio, R; Santacroce, Rosa; Perna, Pd; Sarno, M; Romondia, A; Margaglione, Maurizio | |
| A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis. | 1-gen-2007 | Colaizzo, D; Amitrano, L; Tiscia, Gl; Grandone, E; Guardascione, Ma; Margaglione, Maurizio | |
| A new method for determination of plasma homocystine by isotope dilution and electrospray tandem mass spectrometry. J | 1-gen-2006 | Tomaiuolo, M; Vecchione, G; Grandone, E; Cocomazzi, N; Casetta, B; Di Minno, G; Margaglione, Maurizio | |
| A New SERPINA-1 Missense Mutation Associated with Alpha-1 Antitrypsin Deficiency and Bronchiectasis | 1-gen-2017 | Carpagnano, GIOVANNA ELISIANA; Santacroce, Rosa; Palmiotti, G. A; Leccese, A.; Giuffreda, E.; Margaglione, Maurizio; FOSCHINO BARBARO, MARIA PIA; Aliberti, S.; Lacedonia, Donato | |
| A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme | 1-gen-2007 | D'Ambrosio, R. L.; D'Andrea, Giovanna; Cafolla, A.; Faillace, F.; Margaglione, Maurizio |