MARTINO, Silvana
MARTINO, Silvana
SCIENZE DELLA SANITA' PUBBLICA E PEDIATRICHE
A diagnostic score for molecular analysis of hereditary autoinflammatory syndromes with periodic fever in children
2008-01-01 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)
2012-01-01 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
2012-01-01 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 PAW? YES, THANK YOU AN ANIMAL ASSISTED INTERVENTION (AAI) PILOT PROJECT FOR CHILDREN WITH JUVENILE IDIOPATHIC ARTHRITIS (JIA)
2020-01-01 U. Viora, P. Ponzio, M. T. Mascarino, B. Picco, P. Guiso, E. Battista, S. Martino, D. Montin, M. Dellepiane, G. Rosso .
A prospective study on children with initial diagnosis of transient hypogammaglobulinemia of infancy: results from the Italian Primary Immunodeficiency Network
2008-01-01 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.
2012-01-01 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.
2004-01-01 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
2008-01-01 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.
1993-01-01 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
2016-01-01 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
2014-01-01 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
2008-01-01 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.
2011-01-01 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
2007-01-01 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.
2002-01-01 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.
2013-01-01 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.
2011-01-01 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.
2016-01-01 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?
1985-01-01 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
2006-01-01 TRIFARI S; SITIA G; AIUTI A; SCARAMUZZA S; MARANGONI F; GUIDOTTI LG; MARTINO S; SARACCO P; NOTARANGELO LD; RONCAROLO MG; DUPRE L
| 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 PAW? YES, THANK YOU AN ANIMAL ASSISTED INTERVENTION (AAI) PILOT PROJECT FOR CHILDREN WITH JUVENILE IDIOPATHIC ARTHRITIS (JIA) | 2020 | U. Viora, P. Ponzio, M. T. Mascarino, B. Picco, P. Guiso, E. Battista, S. Martino, D. Montin, M. Dellepiane, G. Rosso . | |
| 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 |