Sfoglia per Autore
Protein Z gene polymorphisms are associated with protein Z plasma levels
2004-01-01 Santacroce, Rosa; Cappucci, F; DI PERNA, P; Sessa, F; Margaglione, Maurizio
A novel mutation in HERG gene, a490p, found in a large family with autosomal dominant long QT syndrome
2006-01-01 Pellegrino, P. L.; Bafunno, V.; Ieva, R.; Brunetti, NATALE DANIELE; Mavilio, G.; Sessa, F.; De Gennaro, L.; Casavecchia, G.; Margaglione, Maurizio; DI BIASE, Matteo
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia
2006-01-01 Santacroce, Rosa; Vecchione, G; Tomaiuolo, M; Sessa, F; Sarno, M; Colaizzo, D; Grandone, E; Margaglione, Maurizio
Low protein Z levels and risk of occurrence of deep vein thrombosis
2006-01-01 Santacroce, Rosa; Sarno, M.; Cappucci, F.; Sessa, F.; Colaizzo, D.; Brancaccio, V.; Grandone, E.; Margaglione, Maurizio
A Novel Mutation In HERG Gene, A490P, Found In A Large Family With Autosomal Dominant Long QT Syndrome
2007-01-01 Pellegrino, Pl; Bafunno, V; Ieva, R; Brunetti, NATALE DANIELE; Mavilio, G; Sessa, F; Grimaldi, M; Margaglione, Maurizio; DI BIASE, Matteo
Screening of mutations of hemophilia A in 40 Italian patients: a novel G-to-A mutation in intron 10 of the F8 gene as a putative cause of mild hemophilia A in southern Italy
2008-01-01 Santacroce, Rosa; Santoro, R.; Sessa, F.; Iannaccaro, P.; Sarno, M.; Longo, V.; Gallone, A.; Vecchione, G.; Muleo, G.; Margaglione, Maurizio
Coexistence of beta-thalassemia and hereditary hemochromatosis in homozygosity: a possible synergic effect?
2009-01-01 Bukvic, N; Sportelli, F; Sessa, F; Longo, V; Roberti, Mg; Santacroce, Rosa; Margaglione, Maurizio
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A.
2009-01-01 Bafunno, V; Santacroce, Rosa; Chetta, M; D'Andrea, Giovanna; Pisanelli, D; Sessa, F; Trotta, Teresa; Tagariello, G; Peyvandi, F; Margaglione, Maurizio
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification
2009-01-01 Santacroce, Rosa; Longo, V.; Bafunno, V.; Sessa, F.; Chetta, M.; Sarno, M.; Bukvic, N.; D'Andrea, Giovanna; Tomaiuolo, M.; Margaglione, Maurizio
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A
2010-01-01 Bafunno, V.; Santacroce, R.; Chetta, M.; D'Andrea, G.; Pisanelli, D.; Sessa, F.; Trotta, T.; Tagariello, G.; Peyvandi, F.; Margaglione, M.
Familial X;Y translocation with distinct phenotypic consequences: Characterization using FISH and array CGH.
2010-01-01 Bukvic, N.; Carri, V. D.; DI COSOLA, M. L.; Pustorino, G.; Cesarano, C.; Chetta, M.; Santacroce, Rosa; Sarno, M.; Sessa, F.; Longo, V.; Novelli, A.; Gentile, M.; Margaglione, Maurizio
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A
2010-01-01 Bafunno, V.; Santacroce, Rosa; Chetta, M.; D'Andrea, Giovanna; Pisanelli, D.; Sessa, F.; Trotta, Teresa; Tagariello, G.; Peyvandi, F.; Margaglione, Maurizio
Lo sport come mediatore tra mente e corpo
2011-01-01 Petito, Annamaria; Iuso, S.; Sessa, F.; Margaglione, Maurizio; Bellomo, Antonello
Gene polymorphisms and sport attitude in italian athletes.
2011-01-01 Sessa, Francesco; Chetta, M; Petito, Annamaria; Franzetti, M; Bafunno, V; Pisanelli, D; Sarno, M; Iuso, S; Margaglione, Maurizio
Polymorphic miRNA-mediated gene contribution to inhibitor development in haemophilia A
2012-01-01 Bafunno, V; Santacroce, Rosa; Chetta, M; Peyvandi, F; Sessa, Francesco; Chinni, E; Longo, V; Margaglione, Maurizio
De novo homozygous mutation of the C1 inhibitor gene in a patient with hereditary angioedema
2013-01-01 Bafunno, Valeria; Divella, Chiara; Sessa, Francesco; Tiscia, Giovanni Luca; Castellano, Giuseppe; Gesualdo, Loreto; Margaglione, Maurizio; Montinaro, Vincenzo
De novo homozygous mutation of the C1 inhibitor gene in a patient with hereditary angioedema
2013-01-01 Bafunno, Valeria; Divella, Chiara; Sessa, Francesco; Tiscia, Giovanni Luca; Castellano, Giuseppe; Gesualdo, Loreto; Margaglione, Maurizio; Montinaro, Vincenzo
Fatal outcome after minor trauma: Necrotizing fasciitis (Fournier’s gangrene) or complicated appendicitis?
2014-01-01 Neri, Margherita; Riezzo, Irene; Sessa, Francesco; Angelo, Montana; Bello, STEFANIA CONCETTA
Volatile Organic Compounds — From Science to Victim Recovery Canine Training: A Method to Aid in Determining the Location of Human Remains
2014-01-01 Rendine, M.; Fiore, C.; Bellifemina, A.; Sessa, F.; Neri, Margherita; Fortarezza, P.; Riezzo, Irene
A novel congenital dysprothrombinemia leading to defective prothrombin maturation
2014-01-01 Bafunno, Valeria; Bury, Loredana; Tiscia, Giovanni Luca; Fierro, Tiziana; Favuzzi, Giovanni; Caliandro, Rocco; Sessa, Francesco; Grandone, Elvira; Margaglione, Maurizio; Gresele, Paolo
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Protein Z gene polymorphisms are associated with protein Z plasma levels | 1-gen-2004 | Santacroce, Rosa; Cappucci, F; DI PERNA, P; Sessa, F; Margaglione, Maurizio | |
A novel mutation in HERG gene, a490p, found in a large family with autosomal dominant long QT syndrome | 1-gen-2006 | Pellegrino, P. L.; Bafunno, V.; Ieva, R.; Brunetti, NATALE DANIELE; Mavilio, G.; Sessa, F.; De Gennaro, L.; Casavecchia, G.; Margaglione, Maurizio; DI BIASE, Matteo | |
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia | 1-gen-2006 | Santacroce, Rosa; Vecchione, G; Tomaiuolo, M; Sessa, F; Sarno, M; Colaizzo, D; Grandone, E; Margaglione, Maurizio | |
Low protein Z levels and risk of occurrence of deep vein thrombosis | 1-gen-2006 | Santacroce, Rosa; Sarno, M.; Cappucci, F.; Sessa, F.; Colaizzo, D.; Brancaccio, V.; Grandone, E.; Margaglione, Maurizio | |
A Novel Mutation In HERG Gene, A490P, Found In A Large Family With Autosomal Dominant Long QT Syndrome | 1-gen-2007 | Pellegrino, Pl; Bafunno, V; Ieva, R; Brunetti, NATALE DANIELE; Mavilio, G; Sessa, F; Grimaldi, M; Margaglione, Maurizio; DI BIASE, Matteo | |
Screening of mutations of hemophilia A in 40 Italian patients: a novel G-to-A mutation in intron 10 of the F8 gene as a putative cause of mild hemophilia A in southern Italy | 1-gen-2008 | Santacroce, Rosa; Santoro, R.; Sessa, F.; Iannaccaro, P.; Sarno, M.; Longo, V.; Gallone, A.; Vecchione, G.; Muleo, G.; Margaglione, Maurizio | |
Coexistence of beta-thalassemia and hereditary hemochromatosis in homozygosity: a possible synergic effect? | 1-gen-2009 | Bukvic, N; Sportelli, F; Sessa, F; Longo, V; Roberti, Mg; Santacroce, Rosa; Margaglione, Maurizio | |
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. | 1-gen-2009 | Bafunno, V; Santacroce, Rosa; Chetta, M; D'Andrea, Giovanna; Pisanelli, D; Sessa, F; Trotta, Teresa; Tagariello, G; Peyvandi, F; Margaglione, Maurizio | |
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification | 1-gen-2009 | Santacroce, Rosa; Longo, V.; Bafunno, V.; Sessa, F.; Chetta, M.; Sarno, M.; Bukvic, N.; D'Andrea, Giovanna; Tomaiuolo, M.; Margaglione, Maurizio | |
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A | 1-gen-2010 | Bafunno, V.; Santacroce, R.; Chetta, M.; D'Andrea, G.; Pisanelli, D.; Sessa, F.; Trotta, T.; Tagariello, G.; Peyvandi, F.; Margaglione, M. | |
Familial X;Y translocation with distinct phenotypic consequences: Characterization using FISH and array CGH. | 1-gen-2010 | Bukvic, N.; Carri, V. D.; DI COSOLA, M. L.; Pustorino, G.; Cesarano, C.; Chetta, M.; Santacroce, Rosa; Sarno, M.; Sessa, F.; Longo, V.; Novelli, A.; Gentile, M.; Margaglione, Maurizio | |
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A | 1-gen-2010 | Bafunno, V.; Santacroce, Rosa; Chetta, M.; D'Andrea, Giovanna; Pisanelli, D.; Sessa, F.; Trotta, Teresa; Tagariello, G.; Peyvandi, F.; Margaglione, Maurizio | |
Lo sport come mediatore tra mente e corpo | 1-gen-2011 | Petito, Annamaria; Iuso, S.; Sessa, F.; Margaglione, Maurizio; Bellomo, Antonello | |
Gene polymorphisms and sport attitude in italian athletes. | 1-gen-2011 | Sessa, Francesco; Chetta, M; Petito, Annamaria; Franzetti, M; Bafunno, V; Pisanelli, D; Sarno, M; Iuso, S; Margaglione, Maurizio | |
Polymorphic miRNA-mediated gene contribution to inhibitor development in haemophilia A | 1-gen-2012 | Bafunno, V; Santacroce, Rosa; Chetta, M; Peyvandi, F; Sessa, Francesco; Chinni, E; Longo, V; Margaglione, Maurizio | |
De novo homozygous mutation of the C1 inhibitor gene in a patient with hereditary angioedema | 1-gen-2013 | Bafunno, Valeria; Divella, Chiara; Sessa, Francesco; Tiscia, Giovanni Luca; Castellano, Giuseppe; Gesualdo, Loreto; Margaglione, Maurizio; Montinaro, Vincenzo | |
De novo homozygous mutation of the C1 inhibitor gene in a patient with hereditary angioedema | 1-gen-2013 | Bafunno, Valeria; Divella, Chiara; Sessa, Francesco; Tiscia, Giovanni Luca; Castellano, Giuseppe; Gesualdo, Loreto; Margaglione, Maurizio; Montinaro, Vincenzo | |
Fatal outcome after minor trauma: Necrotizing fasciitis (Fournier’s gangrene) or complicated appendicitis? | 1-gen-2014 | Neri, Margherita; Riezzo, Irene; Sessa, Francesco; Angelo, Montana; Bello, STEFANIA CONCETTA | |
Volatile Organic Compounds — From Science to Victim Recovery Canine Training: A Method to Aid in Determining the Location of Human Remains | 1-gen-2014 | Rendine, M.; Fiore, C.; Bellifemina, A.; Sessa, F.; Neri, Margherita; Fortarezza, P.; Riezzo, Irene | |
A novel congenital dysprothrombinemia leading to defective prothrombin maturation | 1-gen-2014 | Bafunno, Valeria; Bury, Loredana; Tiscia, Giovanni Luca; Fierro, Tiziana; Favuzzi, Giovanni; Caliandro, Rocco; Sessa, Francesco; Grandone, Elvira; Margaglione, Maurizio; Gresele, Paolo |
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