PORTA, Fulvio

PORTA, Fulvio  

Dipartimento di Scienze Cliniche e Sperimentali  

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Titolo Data di pubblicazione Autore(i) File
A INNOVATIVE TOPICAL THERAPY IN SEVERE ORAL GRAFT VERSUS HOST DISEASE GvHD IN CHILDREN UNDERGOING HEMATOPOIETIC CELL TRANSPLANTATION 1-gen-2000 Majorana, Alessandra; Porta, Fulvio; S., Pasini; Bardellini, Elena; E., Mazzolari; V., Mondini; Sapelli, Pierluigi
Analysis of X-chromosome inactivation in bone marrow precursors from carriers of Wiskott-Aldrich syndrome and X-linked severe combined immunodeficiency: Evidence that the Wiskott-Aldrich gene is expressed prior to granulocyte-macrophage colony-forming-unit 1-gen-1993 Mantuano 1, E; Candotti, F; Giliani, S; Parolini, O; Lusardi, M; Zucchi, M; Lanfranchi, A; Porta, F; Airò, P; Albertini, A; Et, Al.
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.
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients. 1-gen-2009 Tassone, Laura; Notaralgelo, Ld; Bonomi, V; Savoldi, G; Sensi, A; Soresina, A; Smith, Ci; Porta, Fulvio; Plebani, Alessandro; Notarangelo, Ld; Badolato, Raffaele
Clinical and Prognostic Role of 18F-FDG PET/CT in Pediatric Ewing Sarcoma 1-gen-2020 Albano, Domenico; Dondi, Francesco; Schumacher, Richard Fabian; D'Ippolito, Carmelita; Porta, Fulvio; Giubbini, Raffaele; Bertagna, Francesco
Clinical and transcriptomic characteristics of a novel SMARCD2 mutation that disrupts neutrophil maturation and function 1-gen-2023 Dotta, L.; Baresi, G.; Tamassia, N.; Calzetti, F.; Bianchetto-Aguilera, F.; Gasperini, S.; Gardiman, E.; Chiarini, M.; Moratto, D.; Martellosio, G.; Serana, F.; Micheletti, M.; Tregambe, D.; Pintabona, V.; Soncini, E.; Meini, A.; Girelli, M. F.; Beghin, A.; Lanfranchi, A.; Bugatti, M.; Brugnoni, D.; Soresina, A.; Plebani, A.; Cassatella, M.; Vermi, W.; Porta, F.; Badolato, R.
F-BAR domain only protein 1 (FCHO1) deficiency is a novel cause of combined immune deficiency in human subjects 1-gen-2019 Calzoni, Enrica; Platt, Craig D.; Keles, Sevgi; Kuehn, Hye Sun; Beaussant-Cohen, Sarah; Zhang, Yu; Pazmandi, Julia; Lanzi, Gaetana; Pala, Francesca; Tahiat, Azzeddine; Artac, Hasibe; Heredia, Raul Jimenez; Dmytrus, Jasmin; Reisli, Ismail; Uygun, Vedat; Uygun, Dilara; Bingol, Aysen; Basaran, Erdem; Djenouhat, Kamel; Benhalla, Nafissa; Bendahmane, Chafa; Emiroglu, Melike; Kirchhausen, Tomas; Pasham, Mithun; Jones, Jennifer; Wallace, Jacqueline G.; Zheng, Lixin; Boisson, Bertrand; Porta, Fulvio; Rosenzweig, Sergio D.; Su, Helen; Giliani, Silvia; Lenardo, Michael; Geha, Raif S.; Boztug, Kaan; Chou, Janet; Notarangelo, Luigi D.
G-CSF treatment of Severe Congenital Neutropenia reverses neutropenia but does not correct the underlying functional deficiency of the neutrophil in defending against microorganisms. 1-gen-2007 Donini, M; Fontana, Stefania; Savoldi, Gianfranco; Vermi, William; Tassone, Laura; Gentili, Francesca; Zenaro, E; Ferrari, Daniela; Notarangelo, Luigi Daniele; Porta, Fulvio; Facchetti, Fabio; Dusi, S; Badolato, Raffaele
Hematopoietic stem cell transplantation in Omenn syndrome: a single-center experience 1-gen-2005 Mazzolari, Evelina; Moshous, D; Forino, Concetta; DE MARTIIS, Donatella; Offer, C; Lanfranchi, Arnalda; Giliani, Silvia Clara; Imberti, L; Pasic, S; Ugazio, Alberto Giovanni; Porta, Fulvio; Notarangelo, Luigi Daniele
How to remove a tunneled and cuffed central venous catheter quickly and safely? A little trick useful in children 1-gen-2023 Benvenuti, Stefano; Finetti, Federico; Porteri, Elena; Ceresoli, Rosanna; Pintossi, Cristian; Annovazzi, Caterina; Zanatta, Francesca; Bartolini, Gabriele; Facchini, Federica; Porta, Fulvio; Alberti, Daniele
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 1-gen-2016 Prandini, Alberto; Salvi, Valentina; Colombo, Francesca; Moratto, Daniele; Lorenzi, Luisa; Vermi, William; DE FRANCESCO, Maria Antonia; Notarangelo, Lucia Dora; Porta, Fulvio; Plebani, Alessandro; Facchetti, Fabio; Sozzani, Silvano; Badolato, Raffaele
Long-term analysis of immune reconstitution and clinical status after hematopoietic cell transplantation for severe T-cell immunodeficiencies 1-gen-2008 Notarangelo, Ld; Porta, Fulvio; de Martiis, D; Forino, C; Marzollo, R; Giliani, Silvia Clara; Airo, P; Imberti, L; Lanfranchi, A; Mazzolari, E.
Long-term immune reconstitution and clinical outcome after stem cell transplantation for severe T-cell immunodeficiency 1-gen-2007 Mazzolari, Evelina; Forino, Concetta; Guerci, Sara; Imberti, L; Lanfranchi, Arnalda; Porta, Fulvio; Notarangelo, Luigi Daniele
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
Long-Term Outcome of WHIM Syndrome in 18 Patients: High Risk of Lung Disease and HPV-Related Malignancies 1-gen-2019 Dotta, L.; Notarangelo, L. D.; Moratto, D.; Kumar, R.; Porta, F.; Soresina, A.; Lougaris, V.; Plebani, A.; Smith, C. I. E.; Norlin, A. -C.; Gomez Raccio, A. C.; Bubanska, E.; Bertolini, P.; Amendola, G.; Visentini, M.; Fiorilli, M.; Venuti, A.; Badolato, R.
Long-Term Survival After Hematopoietic Stem Cell Transplantation for Complete STAT1 Deficiency 1-gen-2017 Naviglio, Samuele; Soncini, Elena; Vairo, Donatella; Lanfranchi, Arnalda; Badolato, Raffaele; Porta, Fulvio
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
Omenn Syndrome due to RAG1 Mutation Presenting With Nonimmune Hydrops Fetalis in Two Siblings 1-gen-2022 Valeri, L; Lugli, L; Iughetti, L; Soresina, A; Giliani, S; Porta, F; Berardi, A.
Optimization of the procedure for obtaining DPSCs by means of fragile fracture in clean room conditions 1-gen-2014 Paganelli, Corrado; Lanfranchi, Arnalda; Porta, Fulvio; Valdivia Gandur, I; Arroyo Bote, S; Martínez Arroyo, J; Martínez Osorio, J; Carvalho Lobato, P; Tallón Walton, V; Manzanares Céspedes, M.
Oral Care in Paediatric Cancer Patients 1-gen-2010 Majorana, Alessandra; Porta, Fulvio