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Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency. 1-gen-2002 Fiorini, Maurilia; Vermi, William; Facchetti, Fabio; Moratto, Daniele; Alessandri, Giulio; Notarangelo, L.; Caruso, Arnaldo; Grigolato, Pier Giovanni; Ugazio, Alberto Giovanni; Notarangelo, Luigi Daniele; Badolato, Raffaele
Functional defects of dendritic cells in patients with CD40 deficiency. 1-gen-2003 Fontana, S; Moratto, Daniele; Mangal, S; DE FRANCESCO, Maria Antonia; Vermi, William; Ferrari, S; Facchetti, Fabio; Kutukculer, N; Fiorini, C; Duse, M; Das, Pk; Notarangelo, Ld; Plebani, Alessandro; Badolato, Raffaele
Stem cell transplantation for the Wiskott-Aldrich syndrome: a single-center experience confirms efficacy of matched unrelated donor transplantation 1-gen-2006 Pai, S. Y.; Demartiis, D; Forino, Concetta; Cavagnini, Sara; Lanfranchi, Arnalda; Giliani, Silvia Clara; Moratto, Daniele; Mazza, C; Porta, Fulvio; Imberti, L; Notarangelo, Luigi Daniele; Mazzolari, Evelina
The Wiskott-Aldrich syndrome: From genotype-phenotype correlation to treatment 1-gen-2007 Moratto, Daniele; Giliani, Silvia Clara; Notarangelo, Ld; Mazza, C; Mazzolari, E; Notarangelo, Ld
Multi-lineage analysis of X-inactivation in female carriers of genetic alterations in the Wiskott-Aldrich syndrome protein (WASP) gene locus 1-gen-2008 Moratto, Daniele; Forino, C; Notarangelo, Luigi Daniele; Vielmi, V; Mazza, Cinzia; Soresina, A; Masi, M; Jankovic, M; Loffredo, P; Ruggeri, M; Zecca, M; Cancrini, C; Porta, Fulvio; Notarangelo, Ld; Giliani, Silvia Clara
Application of common recommendations for diagnosis and treatment of Wiskott-Aldrich syndrome and X-recessive piastrinopenia: clinical and immunological characteristics of 65 patients with WAS/XLT 1-gen-2008 Soresina, Sa; Mazzolari, E; Notarangelo, Ld; Ventura, A; Locatelli, F; Dufour, C; Galanello, R; Zanesco, L; Izzi, G; De Mattia, D; Azzari, C; Cornelli, Pe; Rossi, P; Mazza, Cinzia; Moratto, Daniele; Giliani, Silvia Clara; Rondelli, R; Pession, A; Ugazio, Ag; Plebani, Alessandro
Long-term outcome and lineage-specific chimerism in 194 Wiskott-Aldrich Syndrome patients treated by hematopoietic celltransplantation between 1980-2009: an international collaborative study. 1-gen-2011 Moratto, Daniele; Giliani, Silvia Clara; Bonfim, C; Mazzolari, Evelina; Fischer, A; Ochs, Hd; Cant, Aj; Thrasher, Aj; Cowan, Mj; Albert, Mh; Small, T; Pai, Sy; Haddad, E; Lisa, A; Hambleton, S; Slatter, M; Cavazzana Calvo, M; Mahlaoui, N; Picard, C; Torgerson, Tr; Burroughs, L; Koliski, A; Zanis Neto, J; Porta, Fulvio; Qasim, W; Veys, P; Kavanau, K; Hönig, M; Schulz, A; Friedrich, W; Notarangelo, Luigi Daniele
WASP-WIP DEFICIENCIES: NEW INSIGHTS IN WASP-WIP INTERACTION 1-gen-2012 Lanzi, Gaetana; Moratto, Daniele; Vairo, Donatella; Masneri, Stefania; Mazza, Cinzia; Tovo, P; Martino, S; Notarangelo, Luigi Daniele; Plebani, Alessandro; Geha, R; Notarangelo, Luigi Daniele; Giliani, Silvia Clara
CASE REPORT: IDENTIFICATION OF A PATIENT WITH FAMILIAR MUTATIONS AFFECTING BOTH WASP AND FOXP3 GENES 1-gen-2012 Mazza, Cinzia; Moratto, Daniele; Masneri, Stefania; Vairo, Donatella; Plebani, Alessandro; Rovelli, A; Balduzzi, A; Corti, P; Giliani, Silvia Clara
PROSPECTIVE STUDY OF 84 PATIENTS WITH WISKOTT-ALDRICH SYNDROME AND X-RECESSIVE PIASTRINOPENIA: RESULTS OF THE APPLICATION OF COMMON PROTOCOL FOR DIAGNOSIS AND TREATMENT OF WAS/XLT 1-gen-2012 Soresina, A; Notarangelo, Ld; Ventura, A; Locatelli, F; Dufour, C; Galanello, R; Zanesco, L; Biondi, A; De Mattia, D; Aiuti, A; Arico, M; Azzari, C; Cornelli, Pe; Rossi, P; Martino, S; Specchia, F; Pignata, C; Izzi, G; Mazza, Cinzia; Moratto, Daniele; Giliani, Silvia Clara; Rondelli, R; Pession, A; Ugazio, Alberto Giovanni; Plebani, Alessandro; Pietrogrande, Mc; Porta, Fulvio
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 1-gen-2012 Lougaris, Vassilios; Baronio, M; Vitali, M; Masneri, Stefania; Cattivelli, K; Folsi, V; Tampella, G; Moratto, Daniele; Soresina, A; Badolato, Raffaele; Giliani, Silvia Clara; Plebani, Alessandro
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in 3 brothers with diarrhea, eczema, and infections 1-gen-2013 Dinwiddie, D. L.; Kingsmore, S. F.; Caracciolo, S.; Rossi, G.; Moratto, D.; Mazza, C.; Sabelli, C.; Bacchetta, R.; Passerini, L.; Magri, C.; Bell, C. J.; Miller, N. A.; Hateley, S. L.; Saunders, C. J.; Zhang, L.; Schroth, G. P.; Barlati, S.; Badolato, R.
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in three brothers with diarrhea, eczema and infections. 1-gen-2013 Darrell L., Dinwiddie; Stephen F., Kingsmore; Sonia, Caracciolo; Giuseppe, Rossi; Moratto, Daniele; Cinzia, Mazza; Cristiano, Sabelli; Rosa, Bacchetta; Laura, Passerini; Magri, Chiara; Callum J., Bell; Neil A., Miller; Shannon L., Hateley; Carol J., Saunders; Lu, Zhang; Gary P., Schroth; Barlati, Sergio; Badolato, Raffaele
α- and β-Papillomavirus infection in a young patient with an unclassified primary T-cell immunodeficiency and multiple mucosal and cutaneous lesions 1-gen-2014 Landini, Manuela M.; Borgogna, Cinzia; Peretti, Alberto; Colombo, Enrico; Zavattaro, Elisa; Boldorini, Renzo; Miglio, Umberto; Doorbar, John; Ravanini, Paolo; Kumar, Rajesh; Moratto, Daniele; Badolato, Raffaele; De Andrea, Marco; Gariglio, Marisa
Aicardi Goutieres Syndrome: New Insights on a Novel Set of Inborn Errors of Immunity 1-gen-2014 Vairo, Donatella; Ferraro, R. M.; Moratto, Daniele; Pizzi, S.; Cattalini, Marco; Orcesi, S.; Tincani, Angela; Facchetti, Fabio; Galli, Jessica; Plebani, Alessandro; Crow, Y.; Notarangelo, L. D.; Plevani, P.; Fazzi, Elisa Maria; Giliani, Silvia Clara
Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia 1-gen-2015 Crestani, Elena; Volpi, Stefano; Candotti, Fabio; Giliani, Silvia Clara; Notarangelo, Lucia Dora; Chu, Julia; Aldave Becerra, Juan Carlos; Buchbinder, David; Chou, Janet; Geha, Raif S.; Kanariou, Maria; King, Alejandra; Mazza, Cinzia; Moratto, Daniele; Sokolic, Robert; Garabedian, Elizabeth; Porta, Fulvio; Putti, Maria Caterina; Wakim, Rima H.; Tsitsikov, Erdyni; Pai, Sung Yun; Notarangelo, Luigi D.
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
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 1-gen-2015 Lougaris, Vassilios; Faletra, Flavio; Lanzi, Gaetana; Vozzi, Diego; Marcuzzi, Annalisa; Valencic, Erica; Piscianz, Elisa; Bianco, Annamonica; Girardelli, Martina; Baronio, Manuela; Loganes, Claudia; Fasth, Anders; Salvini, Filippo; Trizzino, Antonino; Moratto, Daniele; Facchetti, Fabio; Giliani, Silvia Clara; Plebani, Alessandro; Tommasini, Alberto
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 1-gen-2015 Lougaris, Vassilios; Baronio, Manuela; Masneri, Stefania; Lorenzini, Tiziana; Cattivelli, Kim; Tampella, Giacomo; Soresina, Annarosa; Moratto, Daniele; Plebani, Alessandro
Evaluation of a novel human IgG1 anti-claudin3 antibody that specifically recognizes its aberrantly localized antigen in ovarian cancer cells and that is suitable for selective drug delivery 1-gen-2015 Romani, Chiara; Cocco, Emiliano; Bignotti, Eliana; Moratto, Daniele; Bugatti, Antonella; Todeschini, Paola; Bandiera, Elisabetta; Tassi, Renata Alessandra; Zanotti, Laura; Pecorelli, Sergio; Sartori, Enrico; Odicino, Franco; De Marco, Ario; Santin, Alessandro Davide; Ravaggi, Antonella; Mitola, Stefania Maria Filomena
Mostrati risultati da 1 a 20 di 62
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