Sfoglia per Autore  

Opzioni
Mostrati risultati da 1 a 20 di 30
Titolo Data di pubblicazione Autore(i) File
Sinus histiocytosis with massive lymphoadenopathy (Rosai-Dorfman disease). Clinico-pathological analysis of a paediatric case 1-gen-1992 Paulli, M; Locatelli, F; Kindl, S; Boveri, E; Facchetti, F; Porta, F; Rosso, R; Nespoli, L; Magrini, U
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.
PROTOCOLLO PER LA PREVENZIONE DELLE COMPLICANZE ODONTOSTOMATOLOGICHE DEL BAMBINO CANDIDATO AL TRAPIANTO DI MIDOLLO OSSEO 1-gen-1999 Majorana, Alessandra; M. M., Schubert; Savoldi, Enrico; Porta, Fulvio
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
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
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
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
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
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.
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
Single-center analysis of long-term outcome after hematopoietic cell transplantation in children with congenital severe T cell immunodeficiency 1-gen-2009 Mazzolari, E.; De Martiis, D.; Forino, C.; Lanfranchi, A.; Giliani, S.; Marzollo, R.; Airo, P.; Imberti, L.; Porta, F.; Notarangelo, L. 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
Oral Care in Paediatric Cancer Patients 1-gen-2010 Majorana, Alessandra; Porta, Fulvio
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
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
Risk factors for oral mucositis in children receiving hematopoietic cell transplantation for primary immunodeficiencies: a retrospective study. 1-gen-2013 Bardellini, Elena; Schumacher, F; Conti, G; Porta, Fulvio; Campus, G; Majorana, Alessandra
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutations 1-gen-2014 Notarangelo, Lucia Dora; Savoldi, Gianfranco; Cavagnini, Sara; Bennato, Veronica; Vasile, Sabrina; Pilotta, Alba; Plebani, Alessandro; Porta, Fulvio
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.
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.
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
Mostrati risultati da 1 a 20 di 30
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile