MARTINO, Silvana

MARTINO, Silvana  

SCIENZE DELLA SANITA' PUBBLICA E PEDIATRICHE  

Risultati 1 - 20 di 64 (tempo di esecuzione: 0.026 secondi).
Titolo Data di pubblicazione Autore(i) File
A diagnostic score for molecular analysis of hereditary autoinflammatory syndromes with periodic fever in children 2008 M. Gattorno; M. P. Sormani; A. D'Osualdo; M. A. Pelagatti; F. Caroli; S. Federici; M. Cecconi; N. Solari; A. Meini; F. Zulian; L. Obici; L. Breda; S. Martino; A. Tommasini; G. Bossi; A. Govers; I. Touitou; P. Woo; J. Frenkel; I. Koné-Paut; M. Baldi; I. Ceccherini; A. Martini
A long-term follow-up study of methotrexate in juvenile localized scleroderma (morphea) 2012 Zulian F; Vallongo C; Patrizi A; Belloni-Fortina A; Cutrone M; Alessio M; Martino S; Gerloni V; Vittadello F; Martini G.
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP 2012 Lanzi G; Moratto D; Vairo D; Masneri S; Delmonte O; Paganini T; Parolini S; Tabellini G; Mazza C; Savoldi G; Montin D; Martino S; Tovo P; Pessach IM; Massaad MJ; Ramesh N; Porta F; Plebani A; Notarangelo LD; Geha RS; Giliani S.
A prospective study on children with initial diagnosis of transient hypogammaglobulinemia of infancy: results from the Italian Primary Immunodeficiency Network 2008 V. Moschese; S. Graziani; M. A. Avanzini; R. Carsetti; M. Marconi; M. La Rocca; L. Chini; C. Pignata; A. R. Soresina; R. Consolini; G. Bossi; A. Trizzino; S. Martino; F. Cardinale; P. Bertolini; G. L. Marseglia; M. Zecca; S. Di Cesare; I. Quinti; R. Rondelli; M. C. Pietrogrande; P. Rossi; A. Plebani
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia. 2012 Zannolli, Raffaella; Buoni, Sabrina; Betti, Gianni; Salvucci, Sara; Plebani, Alessandro; Soresina, Annarosa; Pietrogrande, Maria C; Martino, Silvana; Leuzzi, Vincenzo; Finocchi, Andrea; Micheli, Roberto; Rossi, Livia Nicoletta; Brusco, Alfredo; Misiani, Filippo; Fois, Alberto; Hayek, Joseph; Kelly, Colleen; Chessa, Luciana
Anemia di Diamond Blackfan (DBA) : Studio dell’espressione genica. 2004 QUARELLO P; CAMPAGNOLI MF; GARELLI E; CARANDO A; CRESCENZIO N; DORIA A; MARTINO S; RENGA D; U. RAMENGHI; DIANZANI I
Angiogenesis, tumor necrosis factor-alpha and procoagulant factors in coronaryartery giant aneurysm of a fatal infantile Kawasaki disease 2008 Pucci A; Martino S; Celeste A; Linari A; Tibaldi M; Camosso E; Muscio M; Barattia G; Riva C; Bartoloni G.
Chimerism and tolerance to host and donor in severe combined immunodeficiencies transplanted with fetal liver stem cells. 1993 Bacchetta R; Vandekerckhove BA; Touraine JL; Bigler M; Martino S; Gebuhrer L; de Vries JE; Spits H; Roncarolo MG.
Chronic nonbacterial osteomyelitis may be associated with renal disease and bisphosphonates are a good option for the majority of patients 2016 Pastore, Serena; Ferrara, Giovanna; Monasta, Lorenzo; Meini, Antonella; Cattalini, Marco; Martino, Silvana; Alessio, Maria; La Torre, Francesco; Teruzzi, Barbara; Gerloni, Valeria; Breda, Luciana; Taddio, Andrea; Lepore, Loredana
Clinical features and follow-up in patients with 22q11.2 deletion syndrome 2014 Cancrini C, Puliafito P, Digilio MC, Soresina A, Martino S, Rondelli R, Consolini R, Ruga EM, Cardinale F, Finocchi A, Romiti ML, Martire B, Bacchetta R, Albano V, Carotti A, Specchia F, Montin D, Cirillo E, Cocchi G, Trizzino A, Bossi G, Milanesi O, Azzari C, Corsello G, Pignata C, Aiuti A, Pietrogrande MC, Marino B, Ugazio AG, Plebani A, Rossi P; Italian Network for Primary Immunodeficiencies: Pierani P, Gabrielli A, Danieli MG, De Mattia D, Sisto C, Dammacco F, Ranieri G, Pession A, Ricci G, Minelli P, Lougaris V, Badolato R, Cattaneo R, Airò P, Mura RM, Cossu F, Del Giacco S, Manconi PE, Consarino C, Dello Russo AM, Miniero R, Anastasio E, Marino S, Russo G, Paganelli R, Sperlì D, Carpino L, Aricò M, Gambineri E, Lippi F, Canessa C, Maggi E, Romagnani S, Matucci A, Vultaggio A, Gattorno M, Castagnola E, Nigro G, Presta G, Civino A, Buzi F, Gambaretto G, Fasoli S, Salpietro C, Gallizzi R, Dellepiane RM, Panisi C, Fabio G, Carrabba M, Pietrogrande M, Roncarolo MG, Biondi A, Vallinoto C, Poggi V, Menna G, Di Nardo R, Sottile R, Marone G, Spadaro G, Carli M, Basso G, Putti C, Semenzato G, Agostini C, D'Angelo P, Izzi G, Bertolini P, Zecca M, Marseglia G, Maccario R, Felici L, Favre C, Vecchi V, Sacchini P, Rinaldi G, Livadiotti S, Simonetti A, Stabile A, Duse M, Iacobini M, Quinti I, Fiorilli M, Moschese V, Cecere F, D'Ambrosio A, De Zan G, Strafella S, Tamaro P, Rabusin M, Tommasini A, Tovo P, De Carli M, De Carli S, Nespoli L, Marinoni M, Porcellini A, Lunardi C, Patuzzo G, Boner A, Degani D
Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: an Italian multicenter study 2008 Martire B, Rondelli R, Soresina A, Pignata C, Broccoletti T, Finocchi A, Rossi P, Gattorno M, Rabusin M, Azzari C, Dellepiane RM, Pietrogrande MC, Trizzino A, Di Bartolomeo P, Martino S, Carpino L, Cossu F, Locatelli F, Maccario R, Pierani P, Putti MC, Stabile A, Notarangelo LD, Ugazio AG, Plebani A, De Mattia D; IPINET.
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 2011 Mazza C; Buzi F; Ortolani F; Vitali A; Notarangelo LD; Weber G; Bacchetta R; Soresina A; Lougaris V; Greggio NA; Taddio A; Pasic S; de Vroede M; Pac M; Kilic SS; Ozden S; Rusconi R; Martino S; Capalbo D; Salerno M; Pignata C; Radetti G; Maggiore G; Plebani A; Notarangelo LD; Badolato R.
Clinical manifestations in a cohort of 32 children with 22q11 deletion syndrome 2007 Delmonaco A.G; Ferrero G.B; Belligni E; Biamino E; Asnaghi V; Banaudi E; Martino S; Verdun Di Cantogno L; Forzano S; Cirillo Silengo M.
Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study. 2002 Plebani A, Soresina A, Rondelli R, Amato GM, Azzari C, Cardinale F, Cazzola G, Consolini R, De Mattia D, Dell'Erba G, Duse M, Fiorini M, Martino S, Martire B, Masi M, Monafo V, Moschese V, Notarangelo LD, Orlandi P, Panei P, Pession A, Pietrogrande MC, Pignata C, Quinti I, Ragno V, Rossi P, Sciotto A, Stabile A; Italian Pediatric Group for XLA-AIEOP.
Common variable immunodeficiency: Crossroads between infections, inflammation and autoimmunity. 2013 Baldovino S; Montin D; Martino S; Sciascia S; Menegatti E; Roccatello D.
Comparison of clinical features and drug therapies among European and Latin American patients with juvenile dermatomyositis. 2011 Guseinova D;Consolaro A;Trail L;Ferrari C;Pistorio A;Ruperto N;Buoncompagni A;Pilkington C;Maillard S;Oliveira SK;Sztajnbok F;Cuttica R;Corona F;Katsicas MM;Russo R;Ferriani V;Burgos-Vargas R;Solis-Vallejo E;Bandeira M;Baca V;Saad-Magalhaes C;Silva CA;Barcellona R;Breda L;Cimaz R;Gallizzi R;Garozzo R;Martino S;Meini A;Stabile A;Martini A;Ravelli A
Comparison of Two Available RNA Extraction Protocols for microRNA Amplification in Serum Samples. 2016 Bergallo, M; Gambarino, S; Martino, S; Montin, D; Montanari, P; Galliano, I; Tovo, Pa.
Defective interferon-alpha production in children with recurrent respiratory tract infections. A primary or secondary deficiency? 1985 Pugliese A; Salomone C; Martino S; Biglino A; Delpiano A; Tovo PA.
Defective Th1 cytokine gene transcription in CD4+ and CD8+ T cells from Wiskott-Aldrich syndrome patients 2006 TRIFARI S; SITIA G; AIUTI A; SCARAMUZZA S; MARANGONI F; GUIDOTTI LG; MARTINO S; SARACCO P; NOTARANGELO LD; RONCAROLO MG; DUPRE L
Development of a Low-Cost Stem-Loop Real-Time Quantification PCR Technique for EBV miRNA Expression Analysis 2016 Bergallo, Massimiliano; Merlino, Chiara; Montin, Davide; Galliano, Ilaria; Gambarino, Stefano; Mareschi, Katia; Fagioli, Franca; Montanari, Paola; Martino, Silvana; Tovo, Pier-Angelo