MAZZA, Cinzia

MAZZA, Cinzia  

Dipartimento di Scienze Cliniche e Sperimentali  

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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
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation 1-gen-2016 Tripodi, Serena Ilaria; Mazza, Cinzia; Moratto, Daniele; Ramenghi, Ugo; Caorsi, Roberta; Gattorno, Marco; Badolato, Raffaele
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.
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
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.
Lessons From the Clinic: ADPKD Genetic Test Unraveling Severe Phenotype, Intrafamilial Variability, and New, Rare Causing Genotype 1-gen-2022 Izzi, C.; Dordoni, C.; Delbarba, E.; Mazza, C.; Savoldi, G.; Econimo, L.; Cortinovis, R.; Zeni, L.; Martin, E.; Alberici, F.; Scolari, F.
Monocytes from Wiskott-Aldrich patients differentiate in functional mature dendritic cells with a defect in CD83 expression 1-gen-2001 Allavena, Paola; Badolato, Raffaele; Facchetti, Fabio; Vermi, William; Paganin, C; Luini, W; Giliani, Silvia Clara; Mazza, Cinzia; Bolzern, U; Chiesa, I; Notarangelo, Luigi Daniele; Mantovani, Alberto; Sozzani, Silvano
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
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
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