Sfoglia per Autore
Assistential-diagnostic guidelines: Apparent life-threatening events (ALTE) [Linee guida diagnostico-assistenziale: ALTE (Apparent Life-Threatening Events)]
2009-01-01 Piumelli, R; Di Pietro, P; Longhi, L; Donzelli, G; Cutrera, R; Nespoli, L; Magnani, Cinzia; Nassi, N; Becherucci, P; Chiappini, E; Lapi, F; Vannacci, A; Mari, F; Nosetti, L; Rimini, A; Salvatore, S; Paglietti, Mg; Palmieri, A; Pomo, R; Vitale, A; Dalla Casa, P; DE ANGELIS, Gian Luigi; Macchiarini, A; NONNIS MARZANO, Francesco; Pisani, Francesco; Podestà, A.
Craniosynostosis, hydrocephalus, Chiari I malformation and radioulnar synostosis: Probably a new syndrome
2009-01-01 Valeria, Capra; Patrizia De, Marco; Elisa, Merello; Ave Maria, Baffico; Maurizia, Baldi; Maria Teresa, Divizia; Stefania, Gimelli; Delphine, Mallet; Alessandro, Raso; Samantha, Mascelli; Paolo, Toma`; Andrea, Rossi; Marco, Pavanello; Armando, Cama; Magnani, Cinzia
Evidence that polymorphic deletion of theGlutathione S-Transferase Gene, GSTM1,is associated with Esophageal Atresia.
2010-01-01 Filonzi, Laura; Magnani, Cinzia; DE ANGELIS, Gian Luigi; Dallaglio, S.; NONNIS MARZANO, Francesco
Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients
2010-01-01 Hoornaert, Kp; Vereecke, I; Dewinter, C; Rosenberg, T; Beemer, Fa; Leroy, Jg; Bendix, L; Björck, E; Bonduelle, M; Boute, O; Cormier Daire, V; De Die Smulders, C; Dieux Coeslier, A; Dollfus, H; Elting, M; Green, A; Guerci, Vi; Hennekam, Rc; Hilhorts Hofstee, Y; Holder, M; Hoyng, C; Jones, Kj; Josifova, D; Kaitila, I; Kjaergaard, S; Kroes, Yh; Lagerstedt, K; Lees, M; Lemerrer, M; Magnani, Cinzia; Marcelis, C; Martorell, L; Mathieu, M; Mcentagart, M; Mendicino, A; Morton, J; Orazio, G; Paquis, V; Reish, O; Simola, Ko; Smithson, Sf; Temple, Ki; Van Aken, E; Van Bever, Y; van den Ende, J; Van Hagen, Jm; Zelante, L; Zordania, R; De Paepe, A; Leroy, Bp; De Buyzere, M; Coucke, Pj; Mortier, G. R.
Confirmed association between monoamine oxidase A molecular polymorphisms and Sudden Infant Death Syndrome.
2011-01-01 Filonzi, L.; Magnani, Cinzia; NONNIS MARZANO, Francesco
SMC1A Codon 496 Mutations Affect the Cellular Response to Genotoxic Treatments
2011-01-01 Linda, Mannini; Stefania, Menga; Alessandra, Tonelli; Silvia, Zanotti; Maria Teresa, Bassi; Magnani, Cinzia; Antonio, Musio
Value of autopsy in renal malformations: Comparison of clinical diagnosis and post-mortem examination.
2011-01-01 Giordano, Giovanna; Fellegara, Giovanni; Brigati, Francesca; Gramellini, Dandolo; Magnani, Cinzia
The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteria.
2011-01-01 Marangi, G; Ricciardi, S; Orteschi, D; Lattante, S; Murdolo, M; Dallapiccola, B; Biscione, C; Lecce, R; Chiurazzi, P; Romano, C; Greco, D; Pettinato, R; Sorge, G; Pantaleoni, C; Alfei, E; Toldo, I; Magnani, Cinzia; Bonanni, P; Martinez, F; Serra, G; Battaglia, D; Lettori, D; Vasco, G; Baroncini, A; Daolio, C; Zollino, M.
Mandibular distraction in neonates: indications, technique, results
2012-01-01 Sesenna, Enrico; Alice S., Magri; Magnani, Cinzia; Bruno C., Brevi; Marilena L., Anghinoni
Serotonin transporter role in identifying similarities between SIDS and Idiopathic ALTE
2012-01-01 Filonzi, L.; Magnani, Cinzia; Nosetti, L.; Nespoli, L.; Borghi, C.; Vaghi, Marina; NONNIS MARZANO, Francesco
Clinical and Polygraphic Improvement of Breathing Abnormalities After Valproate in a Case of Pitt-Hopkins Syndrome.
2012-01-01 Maini, Ilenia; Cantalupo, Gaetano; Turco, Ec; DE PAOLIS, Fernando; Magnani, Cinzia; Parrino, Liborio; Terzano, Mg; Pisani, Francesco
Argomenti di pediatria.
2013-01-01 Vanelli, Maurizio; Agnetti, Aldo; Bernasconi, Sergio; Bussolati, Ovidio; Caffarelli, Carlo; Carano, Nicola; Ceccarelli, Francesco; DE ANGELIS, Gian Luigi; Magnani, Cinzia; Pizzi, Silvia
Unilateral ectopic parotid gland in CHARGE syndrome.
2013-01-01 Ormitti, Francesca; Ventura, E; Bacciu, Andrea; Crisi, Girolamo; Magnani, Cinzia
Are there any strategies to improve neonatal outcomes associated with epidural analgesia in labor?
2013-01-01 Marta, Armani; Carla, Gaggiano; Sara, Dall'Aglio; Enzo, Romanini; Carmen, Sospiri; Magnani, Cinzia
FAM111A mutations result in hypoparathyroidism and impaired skeletal development
2013-01-01 Unger, Sheila; Górna, Maria W; Le Béchec, Antony; Do Vale Pereira, Sonia; Bedeschi, Maria Francesca; Geiberger, Stefan; Grigelioniene, Giedre; Horemuzova, Eva; Lalatta, Faustina; Lausch, Ekkehart; Magnani, Cinzia; Nampoothiri, Sheela; Nishimura, Gen; Petrella, Duccio; Rojas Ringeling, Francisca; Utsunomiya, Akari; Zabel, Bernhard; Pradervand, Sylvain; Harshman, Keith; Campos Xavier, Belinda; Bonafé, Luisa; Superti Furga, Giulio; Stevenson, Brian; Superti Furga, Andrea
Neonatal forearm compartment syndrome: look for cerebral stroke
2014-01-01 Pavlidis, Elena; Spagnoli, Carlotta; Duca, Maddalena; Ormitti, Francesca; Magnani, Cinzia; Pisani, Francesco
Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 gene
2015-01-01 Negri, Giovanni; Milani, D; Colapietro, P; Forzano, F; Della Monica, M; Rusconi, D; Consonni, L; Caffi, L. G; Finelli, P; Scarano, G; Magnani, Cinzia; Selicorni, A; Spena, S; Larizza, L; Gervasini, C.
Universal newborn hearing screening: The experience of the University Hospital of Parma
2015-01-01 Magnani, Cinzia; Bacchi, Giovanna; Borghini, Anna Maria; Del Monte, Daniela; Fava, Giovanni; Occasio, Anna Maria; Sarti, Annarita; Vincenti, Vincenzo
Recessive bullous dermolysis of the newborn in preterm siblings with a missense mutation in type VII collagen
2015-01-01 Boccaletti, Valeria; Zambruno, Giovanna; Castiglia, Daniele; Magnani, Cinzia; Tognetti, Elena; Fabrizi, Giuseppe; Cortelazzi, Chiara; Pagliarello, Calogero; DI NUZZO, Sergio
Insights into genotype-phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein-Taybi syndrome patients
2015-01-01 Spena, S; Milani, D; Rusconi, D; Negri, Giovanni; Colapietro, P; Elcioglu, N; Bedeschi, F; Pilotta, A; Spaccini, L; Ficcadenti, A; Magnani, Cinzia; Scarano, G; Selicorni, A; Larizza, L; Gervasini, C.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Assistential-diagnostic guidelines: Apparent life-threatening events (ALTE) [Linee guida diagnostico-assistenziale: ALTE (Apparent Life-Threatening Events)] | 1-gen-2009 | Piumelli, R; Di Pietro, P; Longhi, L; Donzelli, G; Cutrera, R; Nespoli, L; Magnani, Cinzia; Nassi, N; Becherucci, P; Chiappini, E; Lapi, F; Vannacci, A; Mari, F; Nosetti, L; Rimini, A; Salvatore, S; Paglietti, Mg; Palmieri, A; Pomo, R; Vitale, A; Dalla Casa, P; DE ANGELIS, Gian Luigi; Macchiarini, A; NONNIS MARZANO, Francesco; Pisani, Francesco; Podestà, A. | |
| Craniosynostosis, hydrocephalus, Chiari I malformation and radioulnar synostosis: Probably a new syndrome | 1-gen-2009 | Valeria, Capra; Patrizia De, Marco; Elisa, Merello; Ave Maria, Baffico; Maurizia, Baldi; Maria Teresa, Divizia; Stefania, Gimelli; Delphine, Mallet; Alessandro, Raso; Samantha, Mascelli; Paolo, Toma`; Andrea, Rossi; Marco, Pavanello; Armando, Cama; Magnani, Cinzia | |
| Evidence that polymorphic deletion of theGlutathione S-Transferase Gene, GSTM1,is associated with Esophageal Atresia. | 1-gen-2010 | Filonzi, Laura; Magnani, Cinzia; DE ANGELIS, Gian Luigi; Dallaglio, S.; NONNIS MARZANO, Francesco | |
| Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients | 1-gen-2010 | Hoornaert, Kp; Vereecke, I; Dewinter, C; Rosenberg, T; Beemer, Fa; Leroy, Jg; Bendix, L; Björck, E; Bonduelle, M; Boute, O; Cormier Daire, V; De Die Smulders, C; Dieux Coeslier, A; Dollfus, H; Elting, M; Green, A; Guerci, Vi; Hennekam, Rc; Hilhorts Hofstee, Y; Holder, M; Hoyng, C; Jones, Kj; Josifova, D; Kaitila, I; Kjaergaard, S; Kroes, Yh; Lagerstedt, K; Lees, M; Lemerrer, M; Magnani, Cinzia; Marcelis, C; Martorell, L; Mathieu, M; Mcentagart, M; Mendicino, A; Morton, J; Orazio, G; Paquis, V; Reish, O; Simola, Ko; Smithson, Sf; Temple, Ki; Van Aken, E; Van Bever, Y; van den Ende, J; Van Hagen, Jm; Zelante, L; Zordania, R; De Paepe, A; Leroy, Bp; De Buyzere, M; Coucke, Pj; Mortier, G. R. | |
| Confirmed association between monoamine oxidase A molecular polymorphisms and Sudden Infant Death Syndrome. | 1-gen-2011 | Filonzi, L.; Magnani, Cinzia; NONNIS MARZANO, Francesco | |
| SMC1A Codon 496 Mutations Affect the Cellular Response to Genotoxic Treatments | 1-gen-2011 | Linda, Mannini; Stefania, Menga; Alessandra, Tonelli; Silvia, Zanotti; Maria Teresa, Bassi; Magnani, Cinzia; Antonio, Musio | |
| Value of autopsy in renal malformations: Comparison of clinical diagnosis and post-mortem examination. | 1-gen-2011 | Giordano, Giovanna; Fellegara, Giovanni; Brigati, Francesca; Gramellini, Dandolo; Magnani, Cinzia | |
| The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteria. | 1-gen-2011 | Marangi, G; Ricciardi, S; Orteschi, D; Lattante, S; Murdolo, M; Dallapiccola, B; Biscione, C; Lecce, R; Chiurazzi, P; Romano, C; Greco, D; Pettinato, R; Sorge, G; Pantaleoni, C; Alfei, E; Toldo, I; Magnani, Cinzia; Bonanni, P; Martinez, F; Serra, G; Battaglia, D; Lettori, D; Vasco, G; Baroncini, A; Daolio, C; Zollino, M. | |
| Mandibular distraction in neonates: indications, technique, results | 1-gen-2012 | Sesenna, Enrico; Alice S., Magri; Magnani, Cinzia; Bruno C., Brevi; Marilena L., Anghinoni | |
| Serotonin transporter role in identifying similarities between SIDS and Idiopathic ALTE | 1-gen-2012 | Filonzi, L.; Magnani, Cinzia; Nosetti, L.; Nespoli, L.; Borghi, C.; Vaghi, Marina; NONNIS MARZANO, Francesco | |
| Clinical and Polygraphic Improvement of Breathing Abnormalities After Valproate in a Case of Pitt-Hopkins Syndrome. | 1-gen-2012 | Maini, Ilenia; Cantalupo, Gaetano; Turco, Ec; DE PAOLIS, Fernando; Magnani, Cinzia; Parrino, Liborio; Terzano, Mg; Pisani, Francesco | |
| Argomenti di pediatria. | 1-gen-2013 | Vanelli, Maurizio; Agnetti, Aldo; Bernasconi, Sergio; Bussolati, Ovidio; Caffarelli, Carlo; Carano, Nicola; Ceccarelli, Francesco; DE ANGELIS, Gian Luigi; Magnani, Cinzia; Pizzi, Silvia | |
| Unilateral ectopic parotid gland in CHARGE syndrome. | 1-gen-2013 | Ormitti, Francesca; Ventura, E; Bacciu, Andrea; Crisi, Girolamo; Magnani, Cinzia | |
| Are there any strategies to improve neonatal outcomes associated with epidural analgesia in labor? | 1-gen-2013 | Marta, Armani; Carla, Gaggiano; Sara, Dall'Aglio; Enzo, Romanini; Carmen, Sospiri; Magnani, Cinzia | |
| FAM111A mutations result in hypoparathyroidism and impaired skeletal development | 1-gen-2013 | Unger, Sheila; Górna, Maria W; Le Béchec, Antony; Do Vale Pereira, Sonia; Bedeschi, Maria Francesca; Geiberger, Stefan; Grigelioniene, Giedre; Horemuzova, Eva; Lalatta, Faustina; Lausch, Ekkehart; Magnani, Cinzia; Nampoothiri, Sheela; Nishimura, Gen; Petrella, Duccio; Rojas Ringeling, Francisca; Utsunomiya, Akari; Zabel, Bernhard; Pradervand, Sylvain; Harshman, Keith; Campos Xavier, Belinda; Bonafé, Luisa; Superti Furga, Giulio; Stevenson, Brian; Superti Furga, Andrea | |
| Neonatal forearm compartment syndrome: look for cerebral stroke | 1-gen-2014 | Pavlidis, Elena; Spagnoli, Carlotta; Duca, Maddalena; Ormitti, Francesca; Magnani, Cinzia; Pisani, Francesco | |
| Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 gene | 1-gen-2015 | Negri, Giovanni; Milani, D; Colapietro, P; Forzano, F; Della Monica, M; Rusconi, D; Consonni, L; Caffi, L. G; Finelli, P; Scarano, G; Magnani, Cinzia; Selicorni, A; Spena, S; Larizza, L; Gervasini, C. | |
| Universal newborn hearing screening: The experience of the University Hospital of Parma | 1-gen-2015 | Magnani, Cinzia; Bacchi, Giovanna; Borghini, Anna Maria; Del Monte, Daniela; Fava, Giovanni; Occasio, Anna Maria; Sarti, Annarita; Vincenti, Vincenzo | |
| Recessive bullous dermolysis of the newborn in preterm siblings with a missense mutation in type VII collagen | 1-gen-2015 | Boccaletti, Valeria; Zambruno, Giovanna; Castiglia, Daniele; Magnani, Cinzia; Tognetti, Elena; Fabrizi, Giuseppe; Cortelazzi, Chiara; Pagliarello, Calogero; DI NUZZO, Sergio | |
| Insights into genotype-phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein-Taybi syndrome patients | 1-gen-2015 | Spena, S; Milani, D; Rusconi, D; Negri, Giovanni; Colapietro, P; Elcioglu, N; Bedeschi, F; Pilotta, A; Spaccini, L; Ficcadenti, A; Magnani, Cinzia; Scarano, G; Selicorni, A; Larizza, L; Gervasini, C. |
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