VITALI, Massimiliano
VITALI, Massimiliano
Dipartimento di Scienze Cliniche e Sperimentali
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity
2014-01-01 Giagulli, Cinzia; Caccuri, Francesca; Cignarella, Francesca; Lougaris, Vassilios; Martorelli, D; Bugatti, Antonella; Rusnati, Marco; Dolcetti, R; Vitali, Massimiliano; Plebani, Alessandro; Fiorentini, Simona; Caruso, Arnaldo
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family.
2012-01-01 Lougaris, Vassilios; Gallizzi, R; Vitali, Massimiliano; Baronio, Manuela; Salpietro, A; Bergbreiter, A; Salzer, U; Badolato, Raffaele; Plebani, Alessandro
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a.
2014-01-01 Khalili, A; Plebani, Alessandro; Vitali, Massimiliano; Abolhassani, H; Lougaris, Vassilios; Mirminachi, B; Rezaei, N; Aghamohammadi, A.
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation.
2014-01-01 Lougaris, Vassilios; Vitali, Massimiliano; Baronio, Manuela; Moratto, D; Tampella, Giacomo; Biasini, A; Badolato, Raffaele; Plebani, Alessandro
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency.
2012-01-01 Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Soresina, A; Badolato, Raffaele; Plebani, Alessandro
BAFF-R mutations in Good's syndrome.
2014-01-01 Lougaris, Vassilios; Vitali, Massimiliano; Baronio, Manuela; Tampella, Giacomo; Plebani, Alessandro
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation.
2014-01-01 Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Cattalini, Marco; Tassone, L; Soresina, A; Badolato, Raffaele; Plebani, Alessandro
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency
2015-01-01 Gualdi, G; Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Moratto, D; Tanghetti, P; Monari, P; CALZAVARA PINTON, Piergiacomo; Plebani, Alessandro
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects
2016-01-01 Abolhassani, Hassan; Vitali, Massimiliano; Lougaris, Vassilios; Giliani, Silvia Clara; Parvaneh, Nima; Parvaneh, Leila; Mirminachi, Babak; Cheraghi, Taher; Khazaei, Hosseinali; Mahdaviani, Seyed Alireza; Kiaei, Fatemeh; Tavakolinia, Naiimeh; Mohammadi, Javad; Negahdari, Babak; Rezaei, Nima; Hammarstrom, Lennart; Plebani, Alessandro; Aghamohammadi, Asghar
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease
2015-01-01 Lougaris, Vassilios; Tabellini, Giovanna; Vitali, Massimiliano; Baronio, Manuela; Patrizi, Ornella; Tampella, Giacomo; Biasini, Augusto; Moratto, Daniele; Parolini, Silvia; Plebani, Alessandro
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity.
2012-01-01 Lopez Herrera, G.; Tampella, Giacomo; Pan Hammarstrom, Q.; Herholz, P.; Trujillo Vargas, C. M.; Phadwalk, ; Simon, A. K.; Moutschen, M.; Etzioni, A.; Mory, A.; Srugo, I.; Melamed, D.; Hultenby, K.; Liu, C.; Baronio, Manuela; Vitali, Massimiliano; Philippet, P.; Dideberg, V.; Aghamohammadi, A.; Rezaei, N.; Enright, V.; Du, L.; Salzer, U.; Eibel, H.; Pfeifer, D.; Veelken, H.; Stauss, H.; Lougaris, Vassilios; Plebani, Alessandro; Gertz, E. M.; Schaffer, A. A.; Hammarstrom, L.; Grimbacher, B.
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency.
2011-01-01 Tampella, Giacomo; Baronio, Manuela; Vitali, Massimiliano; Soresina, A; Badolato, Raffaele; Giliani, Silvia Clara; Plebani, Alessandro; Lougaris, Vassilios
Successful Anti-TNF-α Treatment in a Girl with LAD-1 Disease and Autoimmune Manifestations
2014-01-01 Marsili, Manuela; Lougaris, Vassilios; Lucantoni, Marta; Di Marzio, Daniele; Baronio, Manuela; Vitali, Massimiliano; Lombardi, Giuliano; Chiarelli, Francesco; Breda, Luciana
The nested graft acts by inducing the process of de-senescence of the fibroblasts in chronic venous ulcers
2016-01-01 Gualdi, Giulio; Crotti, Silvia; Monari, Paola; CALZAVARA PINTON, Piergiacomo; Vitali, Massimiliano; Baronio, Manuela; Lougaris, Vassilios
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity | 1-gen-2014 | Giagulli, Cinzia; Caccuri, Francesca; Cignarella, Francesca; Lougaris, Vassilios; Martorelli, D; Bugatti, Antonella; Rusnati, Marco; Dolcetti, R; Vitali, Massimiliano; Plebani, Alessandro; Fiorentini, Simona; Caruso, Arnaldo | |
| A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. | 1-gen-2012 | Lougaris, Vassilios; Gallizzi, R; Vitali, Massimiliano; Baronio, Manuela; Salpietro, A; Bergbreiter, A; Salzer, U; Badolato, Raffaele; Plebani, Alessandro | |
| Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. | 1-gen-2014 | Khalili, A; Plebani, Alessandro; Vitali, Massimiliano; Abolhassani, H; Lougaris, Vassilios; Mirminachi, B; Rezaei, N; Aghamohammadi, A. | |
| Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. | 1-gen-2014 | Lougaris, Vassilios; Vitali, Massimiliano; Baronio, Manuela; Moratto, D; Tampella, Giacomo; Biasini, A; Badolato, Raffaele; Plebani, Alessandro | |
| B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. | 1-gen-2012 | Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Soresina, A; Badolato, Raffaele; Plebani, Alessandro | |
| BAFF-R mutations in Good's syndrome. | 1-gen-2014 | Lougaris, Vassilios; Vitali, Massimiliano; Baronio, Manuela; Tampella, Giacomo; Plebani, Alessandro | |
| Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. | 1-gen-2014 | Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Cattalini, Marco; Tassone, L; Soresina, A; Badolato, Raffaele; Plebani, Alessandro | |
| Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency | 1-gen-2015 | Gualdi, G; Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Moratto, D; Tanghetti, P; Monari, P; CALZAVARA PINTON, Piergiacomo; Plebani, Alessandro | |
| Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects | 1-gen-2016 | Abolhassani, Hassan; Vitali, Massimiliano; Lougaris, Vassilios; Giliani, Silvia Clara; Parvaneh, Nima; Parvaneh, Leila; Mirminachi, Babak; Cheraghi, Taher; Khazaei, Hosseinali; Mahdaviani, Seyed Alireza; Kiaei, Fatemeh; Tavakolinia, Naiimeh; Mohammadi, Javad; Negahdari, Babak; Rezaei, Nima; Hammarstrom, Lennart; Plebani, Alessandro; Aghamohammadi, Asghar | |
| Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease | 1-gen-2015 | Lougaris, Vassilios; Tabellini, Giovanna; Vitali, Massimiliano; Baronio, Manuela; Patrizi, Ornella; Tampella, Giacomo; Biasini, Augusto; Moratto, Daniele; Parolini, Silvia; Plebani, Alessandro | |
| Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. | 1-gen-2012 | Lopez Herrera, G.; Tampella, Giacomo; Pan Hammarstrom, Q.; Herholz, P.; Trujillo Vargas, C. M.; Phadwalk, ; Simon, A. K.; Moutschen, M.; Etzioni, A.; Mory, A.; Srugo, I.; Melamed, D.; Hultenby, K.; Liu, C.; Baronio, Manuela; Vitali, Massimiliano; Philippet, P.; Dideberg, V.; Aghamohammadi, A.; Rezaei, N.; Enright, V.; Du, L.; Salzer, U.; Eibel, H.; Pfeifer, D.; Veelken, H.; Stauss, H.; Lougaris, Vassilios; Plebani, Alessandro; Gertz, E. M.; Schaffer, A. A.; Hammarstrom, L.; Grimbacher, B. | |
| Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency. | 1-gen-2011 | Tampella, Giacomo; Baronio, Manuela; Vitali, Massimiliano; Soresina, A; Badolato, Raffaele; Giliani, Silvia Clara; Plebani, Alessandro; Lougaris, Vassilios | |
| Successful Anti-TNF-α Treatment in a Girl with LAD-1 Disease and Autoimmune Manifestations | 1-gen-2014 | Marsili, Manuela; Lougaris, Vassilios; Lucantoni, Marta; Di Marzio, Daniele; Baronio, Manuela; Vitali, Massimiliano; Lombardi, Giuliano; Chiarelli, Francesco; Breda, Luciana | |
| The nested graft acts by inducing the process of de-senescence of the fibroblasts in chronic venous ulcers | 1-gen-2016 | Gualdi, Giulio; Crotti, Silvia; Monari, Paola; CALZAVARA PINTON, Piergiacomo; Vitali, Massimiliano; Baronio, Manuela; Lougaris, Vassilios |