CHIESA, Nicoletta Maria Luigina
CHIESA, Nicoletta Maria Luigina
SCIENZE DELLA SANITA' PUBBLICA E PEDIATRICHE
Analisi del profilo di trascrizione genetica nella sindrome di Noonan.
2010-01-01 Picco G; Cantarella D; Baldassarre G; Marinosci A; Dotta A; Isella C; Crescenzo N; Timeus F; Chiesa N; Merla G; Mazzanti L; Rossi C; Zampino G; Tartaglia M; Silengo M; Medico E; Ferrero GB.
ARRAY-CGH analysis in 92 children with complex syndromic phenotype
2009-01-01 Belligni E; Molinatto C; Biamino E; Chiesa N; Marinosci AL; Vetro A; Girirajan S; Zuffardi O; Eichler E; Ferrero GB; Silengo M
Clinical, biochemical, and molecular spectrum of short/branched-chain acyl-CoA dehydrogenase deficiency: two new cases and review of literature
2019-01-01 Porta, Francesco; Chiesa, Nicoletta; Martinelli, Diego; Spada, Marco
Convergent mutations and kinase fusions lead to oncogenic STAT3 activation in anaplastic large cell lymphoma
2015-01-01 Crescenzo, Ramona; Abate, Francesco; Lasorsa, Elena; Tabbo', Fabrizio; Gaudiano, Marcello; Chiesa, Nicoletta; Di Giacomo, Filomena; Spaccarotella, Elisa; Barbarossa, Luigi; Ercole, Elisabetta; Todaro, Maria; Boi, Michela; Acquaviva, Andrea; Ficarra, Elisa; Novero, Domenico; Rinaldi, Andrea; Tousseyn, Thomas; Rosenwald, Andreas; Kenner, Lukas; Cerroni, Lorenzo; Tzankov, Alexander; Ponzoni, Maurilio; Paulli, Marco; Weisenburger, Dennis; Chan, Wing C.; Iqbal, Javeed; Piris, Miguel A.; Zamo', Alberto; Ciardullo, Carmela; Rossi, Davide; Gaidano, Gianluca; Pileri, Stefano; Tiacci, Enrico; Falini, Brunangelo; Shultz, Leonard D.; Mevellec, Laurence; Vialard, Jorge E.; Piva, Roberto; Bertoni, Francesco; Rabadan, Raul; Inghirami, Giorgio
Eyebrow anomalies as a diagnostic sign of genomic disorders
2010-01-01 Silengo M; Belligni E; Molinatto C; Baldassarre G; Biamino E; Chiesa N; Zuffardi O; Girirajan S; Eichler EE; Ferrero GB
Genotypic and phenotypic spectrum of 44 patients with Noonan syndrome
2009-01-01 Baldassarre G; Rossi C; Chiesa N; Mussa A; Marinosci A; Tartaglia M; Silengo M; Ferrero GB
Incidence of Beckwith-Wiedemann syndrome
2012-01-01 Molinatto C; Mussa A; De Crescenzo N; Chiesa N; Baldassarre G; Selicorni A; Russo S; Riccio A; Silengo M; Ferrero GB.
Molecular and clinical characterization of 37 patients with Noonan syndrome
2009-01-01 Baldassarre G; Rossi C; Tartaglia M; Carta C; Banaudi E; Chiesa N; Silengo MC; Ferrero GB
Molecular dissection of Noonan syndrome by transcriptiome analysis
2009-01-01 Ferrero GB; Cantarella D; Baldassarre G; Isella C; Crescenzo N; Timeus F; Chiesa N; Merla G; Mazzanti L; Rossi C; Zampino G; Tartaglia M; Silengo M; Medico E
Neonatal hepatoblastoma in a newborn with severe phenotype of Beckwith-Wiedemann syndrome.
2011-01-01 Mussa A; Ferrero GB; Ceoloni B; Basso E; Chiesa N; De Crescenzo A; Pepe E; Silengo M; de Sanctis L.
Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome.
2012-01-01 Mussa A; Peruzzi L; Chiesa N; De Crescenzo A; Russo S; Melis D; Tarani L; Baldassarre G; Larizza L; Riccio A; Silengo M; Ferrero GB.
Prevalence of beckwith-wiedemann syndrome in North West of Italy
2013-01-01 Mussa A; Russo S; De Crescenzo A; Chiesa N; Molinatto C; Selicorni A; Richiardi L; Larizza L; Silengo MC; Riccio A; Ferrero GB
SLC25A19 deficiency and bilateral striatal necrosis with polyneuropathy: a new case and review of the literature
2021-01-01 Francesco Porta, Barbara Siri, Nicoletta Chiesa, Federica Ricci, Lulash Nika, Paola Sciortino, Marco Spada.
The KCNQ1OT1 Imprinting Control Region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases.
2012-01-01 Chiesa N; De Crescenzo A; Mishra K; Perone L; Carella M; Palumbo O; Mussa A; Sparago A; Cerrato F; Russo S; Lapi E; Cubellis MV; Kanduri C; Cirillo Silengo M; Riccio A; Ferrero GB.
The overlap between Sotos and Beckwith-Wiedemann syndromes
2010-01-01 Mussa A; Chiesa N; Porta F; Baldassarre G; Silengo MC; Ferrero GB.
Transcriptional hallmarks of noonan syndrome and noonan-like syndrome with loose anagen hair
2012-01-01 Ferrero GB; Picco G; Baldassarre G; Flex E; Isella C; Cantarella D; Corà D; Chiesa N; Crescenzio N; Timeus F; Merla G; Mazzanti L; Zampino G; Rossi C; Silengo M; Tartaglia M; Medico E.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Analisi del profilo di trascrizione genetica nella sindrome di Noonan. | 2010 | Picco G; Cantarella D; Baldassarre G; Marinosci A; Dotta A; Isella C; Crescenzo N; Timeus F; Chiesa N; Merla G; Mazzanti L; Rossi C; Zampino G; Tartaglia M; Silengo M; Medico E; Ferrero GB. | |
| ARRAY-CGH analysis in 92 children with complex syndromic phenotype | 2009 | Belligni E; Molinatto C; Biamino E; Chiesa N; Marinosci AL; Vetro A; Girirajan S; Zuffardi O; Eichler E; Ferrero GB; Silengo M | |
| Clinical, biochemical, and molecular spectrum of short/branched-chain acyl-CoA dehydrogenase deficiency: two new cases and review of literature | 2019 | Porta, Francesco; Chiesa, Nicoletta; Martinelli, Diego; Spada, Marco | |
| Convergent mutations and kinase fusions lead to oncogenic STAT3 activation in anaplastic large cell lymphoma | 2015 | Crescenzo, Ramona; Abate, Francesco; Lasorsa, Elena; Tabbo', Fabrizio; Gaudiano, Marcello; Chiesa, Nicoletta; Di Giacomo, Filomena; Spaccarotella, Elisa; Barbarossa, Luigi; Ercole, Elisabetta; Todaro, Maria; Boi, Michela; Acquaviva, Andrea; Ficarra, Elisa; Novero, Domenico; Rinaldi, Andrea; Tousseyn, Thomas; Rosenwald, Andreas; Kenner, Lukas; Cerroni, Lorenzo; Tzankov, Alexander; Ponzoni, Maurilio; Paulli, Marco; Weisenburger, Dennis; Chan, Wing C.; Iqbal, Javeed; Piris, Miguel A.; Zamo', Alberto; Ciardullo, Carmela; Rossi, Davide; Gaidano, Gianluca; Pileri, Stefano; Tiacci, Enrico; Falini, Brunangelo; Shultz, Leonard D.; Mevellec, Laurence; Vialard, Jorge E.; Piva, Roberto; Bertoni, Francesco; Rabadan, Raul; Inghirami, Giorgio | |
| Eyebrow anomalies as a diagnostic sign of genomic disorders | 2010 | Silengo M; Belligni E; Molinatto C; Baldassarre G; Biamino E; Chiesa N; Zuffardi O; Girirajan S; Eichler EE; Ferrero GB | |
| Genotypic and phenotypic spectrum of 44 patients with Noonan syndrome | 2009 | Baldassarre G; Rossi C; Chiesa N; Mussa A; Marinosci A; Tartaglia M; Silengo M; Ferrero GB | |
| Incidence of Beckwith-Wiedemann syndrome | 2012 | Molinatto C; Mussa A; De Crescenzo N; Chiesa N; Baldassarre G; Selicorni A; Russo S; Riccio A; Silengo M; Ferrero GB. | |
| Molecular and clinical characterization of 37 patients with Noonan syndrome | 2009 | Baldassarre G; Rossi C; Tartaglia M; Carta C; Banaudi E; Chiesa N; Silengo MC; Ferrero GB | |
| Molecular dissection of Noonan syndrome by transcriptiome analysis | 2009 | Ferrero GB; Cantarella D; Baldassarre G; Isella C; Crescenzo N; Timeus F; Chiesa N; Merla G; Mazzanti L; Rossi C; Zampino G; Tartaglia M; Silengo M; Medico E | |
| Neonatal hepatoblastoma in a newborn with severe phenotype of Beckwith-Wiedemann syndrome. | 2011 | Mussa A; Ferrero GB; Ceoloni B; Basso E; Chiesa N; De Crescenzo A; Pepe E; Silengo M; de Sanctis L. | |
| Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome. | 2012 | Mussa A; Peruzzi L; Chiesa N; De Crescenzo A; Russo S; Melis D; Tarani L; Baldassarre G; Larizza L; Riccio A; Silengo M; Ferrero GB. | |
| Prevalence of beckwith-wiedemann syndrome in North West of Italy | 2013 | Mussa A; Russo S; De Crescenzo A; Chiesa N; Molinatto C; Selicorni A; Richiardi L; Larizza L; Silengo MC; Riccio A; Ferrero GB | |
| SLC25A19 deficiency and bilateral striatal necrosis with polyneuropathy: a new case and review of the literature | 2021 | Francesco Porta, Barbara Siri, Nicoletta Chiesa, Federica Ricci, Lulash Nika, Paola Sciortino, Marco Spada. | |
| The KCNQ1OT1 Imprinting Control Region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases. | 2012 | Chiesa N; De Crescenzo A; Mishra K; Perone L; Carella M; Palumbo O; Mussa A; Sparago A; Cerrato F; Russo S; Lapi E; Cubellis MV; Kanduri C; Cirillo Silengo M; Riccio A; Ferrero GB. | |
| The overlap between Sotos and Beckwith-Wiedemann syndromes | 2010 | Mussa A; Chiesa N; Porta F; Baldassarre G; Silengo MC; Ferrero GB. | |
| Transcriptional hallmarks of noonan syndrome and noonan-like syndrome with loose anagen hair | 2012 | Ferrero GB; Picco G; Baldassarre G; Flex E; Isella C; Cantarella D; Corà D; Chiesa N; Crescenzio N; Timeus F; Merla G; Mazzanti L; Zampino G; Rossi C; Silengo M; Tartaglia M; Medico E. |