UNOLT, MARTA
UNOLT, MARTA
22q and two: 22q11.2 deletion syndrome and coexisting conditions
2018 Cohen, J. L.; Crowley, T. B.; Mcginn, D. E.; Mcdougall, C.; Unolt, M.; Lambert, M. P.; Emanuel, B. S.; Zackai, E. H.; McDonald-McGinn, D. M.
22q11.2 Deletion Syndrome. Impact of Genetics in the Treatment of Conotruncal Heart Defects
2022 Putotto, C.; Pugnaloni, F.; Unolt, M.; Maiolo, S.; Trezzi, M.; Digilio, M. C.; Cirillo, A.; Limongelli, G.; Marino, B.; Calcagni, G.; Versacci, P.
Aortic arch interruption without ductus arteriosus and no ventricular septal defect
2013 Putotto, C.; Unolt, M.; Marino, D.
Atrioventricular septal defect prognosis for patients with down syndrome
2012 Unolt, M.; Putotto, C.; Marino, D.
Atypical cardiac defects in patients with RASopathies: updated data on CARNET study
2020 Calcagni, G.; Gagliostro, G.; Limongelli, G.; Unolt, M.; De Luca, E.; Digilio, M. C.; Baban, A.; Albanese, S. B.; Ferrero, G. B.; Baldassarre, G.; Agnoletti, G.; Banaudi, E.; Marek, J.; Kaski, J. P.; Tuo, G.; Marasini, M.; Cairello, F.; Madrigali, A.; Pacileo, G.; Russo, M. G.; Milanesi, O.; Formigari, R.; Brighenti, M.; Ragni, L.; Donti, A.; Drago, F.; Dallapiccola, B.; Tartaglia, M.; Marino, B.; Versacci, P.
Cardiac defects and genetic syndromes: old uncertainties and new insights
2021 Calcagni, G.; Pugnaloni, F.; Digilio, M. C.; Unolt, M.; Putotto, C.; Niceta, M.; Baban, A.; Sparascio, F. P.; Drago, F.; De Luca, A.; Tartaglia, M.; Marino, B.; Versacci, P.
Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease
2023 Putotto, Carolina; Unolt, Marta; Lambiase, Caterina; Marchetti, Flaminia; Anaclerio, Silvia; Favoriti, Alessandra; Tancredi, Giancarlo; Mastromoro, Gioia; Pugnaloni, Flaminia; Liberati, Natascia; De Luca, Enrica; Tarani, Luigi; De Canditiis, Daniela; Caputo, Viviana; Bernardini, Laura; Digilio, Maria Cristina; Marino, Bruno; Versacci, Paolo
Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study
2022 Putotto, Carolina; Pulvirenti, Federica; Pugnaloni, Flaminia; Isufi, Ina; Unolt, Marta; Anaclerio, Silvia; Caputo, Viviana; Bernardini, Laura; Messina, Elisa; Moretti, Corrado; Tarani, Luigi; Marino, Bruno; Versacci, Paolo
Coexisting genetic findings in a cohort of patients with laboratory confirmation of 22q11.2 deletion syndrome
2022 Pugnaloni, F.; Putotto, C.; Mastromoro, G.; Pulvirenti, F.; Maiolo, S.; Unolt, M.; Digilio, M. C.; Giovannetti, A.; Caputo, V.; Versacci, P.; Marino, B.
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
2020 Zhao, Y.; Diacou, A.; Johnston, H. R.; Musfee, F. I.; McDonald-McGinn, D. M.; Mcginn, D.; Crowley, T. B.; Repetto, G. M.; Swillen, A.; Breckpot, J.; Vermeesch, J. R.; Kates, W. R.; Digilio, M. C.; Unolt, M.; Marino, B.; Pontillo, M.; Armando, M.; DI FABIO, Fabio; Vicari, S.; van den Bree, M.; Moss, H.; Owen, M. J.; Murphy, K. C.; Murphy, C. M.; Murphy, D.; Schoch, K.; Shashi, V.; Tassone, F.; Simon, T. J.; Shprintzen, R. J.; Campbell, L.; Philip, N.; Heine-Suner, D.; Garcia-Minaur, S.; Fernandez, L.; Antonarakis, S. E.; Biondi, M.; Boot, E.; Breetvelt, E.; Busa, T.; Butcher, N.; Buzzanca, A.; Carmel, M.; Cleynen, I.; Cutler, D.; Dallapiccola, B.; de la Fuente Sanches, M. A.; Epstein, M. P.; Evers, R.; Fernandez, L.; Fritsch, R.; Algas, F. G.; Guo, T.; Gur, R.; Hestand, M. S.; Heung, T.; Hooper, S.; Jin, A.; Kushan-Wells, L.; Laorden-Nieto, A. T.; Lattanzi, G.; Marshall, C.; Mccabe, K.; Michaelovsky, E.; Ornstein, C.; Silversides, C.; Tran, O.; van Duin, E. D. A.; Vergaelen, E.; Warren, S. T.; Weinberger, R.; Weizman, A.; Zhang, Z.; Zwick, M.; Bearden, C. E.; Vingerhoets, C.; van Amelsvoort, T.; Eliez, S.; Schneider, M.; Vorstman, J. A. S.; Gothelf, D.; Zackai, E.; Agopian, A. J.; Gur, R. E.; Bassett, A. S.; Emanuel, B. S.; Goldmuntz, E.; Mitchell, L. E.; Wang, T.; Morrow, B. E.
Congenital heart defects in molecularly confirmed KBG syndrome patients
2021 Digilio, M. C.; Calcagni, G.; Gnazzo, M.; Versacci, P.; Dentici, M. L.; Capolino, R.; Sinibaldi, L.; Baban, A.; Putotto, C.; Alfieri, P.; Unolt, M.; Lepri, F. R.; Alesi, V.; Genovese, S.; Novelli, A.; Marino, B.; Dallapiccola, B.
Congenital heart disease and genetic syndromes: new insights into molecular mechanisms
2017 Calcagni, Giulio; Unolt, Marta; Digilio, Maria Cristina; Baban, Anwar; Versacci, Paolo; Tartaglia, Marco; Baldini, Antonio; Marino, Bruno
Congenital heart disease, genetic syndromes, and major noncardiac malformations
2012 Unolt, M.; Putotto, C.; Marino, D.
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers
2018 Unolt, Marta; Versacci, Paolo; Anaclerio, Silvia; Lambiase, Caterina; Calcagni, Giulio; Trezzi, Matteo; Carotti, Adriano; Crowley, Terrence Blaine; Zackai, Elaine H.; Goldmuntz, Elizabeth; Gaynor, James William; Digilio, Maria Cristina; Mcdonald-Mcginn, Donna M.; Marino, Bruno
Congenital heart diseases in women
2013 Putotto, C; Unolt, M; Caiaro, A; MARINO TAUSSIG DE BODONIA, Bruno; Massaccesi, V; Digilio, Mc
Crossed pulmonary arteries. an underestimated cardiovascular variant with a strong association with genetic syndromes{\textemdash}A report of 74 cases with systematic review of the literature
2022 Mastromoro, Gioia; Calcagni, Giulio; Vignaroli, Walter; Anaclerio, Silvia; Pugnaloni, Flaminia; Rinelli, Gabriele; Secinaro, Aurelio; Bordonaro, Veronica; Putotto, Carolina; Unolt, Marta; Cristina Digilio, Maria; Marino, Bruno; Versacci, Paolo
Double outlet right ventricle versus aortic dextroposition: morphologically distinct defects
2013 Restivo, A; Unolt, M; Putotto, C; MARINO TAUSSIG DE BODONIA, Bruno
Double-orifice left atrioventricular valve in patients with atrioventricular septal defect with and without down syndrome
2013 Unolt, M.; Putotto, C.; Marino, D.
Double-outlet left ventricle with l-malposition of the great arteries and subpulmonary ventricular septal defect
2013 Putotto, C.; Unolt, M.; Marino, D.
Factors that negatively affect the prognosis of pediatric community-acquired pneumonia in district hospital in Tanzania
2017 Caggiano, Serena; Ullmann, Nicola; de Vitis, Elisa; Trivelli, Marzia; Mariani, Chiara; Podagrosi, Maria; Ursitti, Fabiana; Bertolaso, Chiara; Putotto, Carolina; Unolt, Marta; Pietravalle, Andrea; Pansa, Paola; Mphayokulela, Kajoro; Lemmo, Maria Incoronata; Mkwambe, Michael; Kazaura, Joseph; Duse, Marzia; Nieddu, Francesco; Azzari, Chiara; Cutrera, Renato
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 22q and two: 22q11.2 deletion syndrome and coexisting conditions | 2018 | Cohen, J. L.; Crowley, T. B.; Mcginn, D. E.; Mcdougall, C.; Unolt, M.; Lambert, M. P.; Emanuel, B. S.; Zackai, E. H.; McDonald-McGinn, D. M. | |
| 22q11.2 Deletion Syndrome. Impact of Genetics in the Treatment of Conotruncal Heart Defects | 2022 | Putotto, C.; Pugnaloni, F.; Unolt, M.; Maiolo, S.; Trezzi, M.; Digilio, M. C.; Cirillo, A.; Limongelli, G.; Marino, B.; Calcagni, G.; Versacci, P. | |
| Aortic arch interruption without ductus arteriosus and no ventricular septal defect | 2013 | Putotto, C.; Unolt, M.; Marino, D. | |
| Atrioventricular septal defect prognosis for patients with down syndrome | 2012 | Unolt, M.; Putotto, C.; Marino, D. | |
| Atypical cardiac defects in patients with RASopathies: updated data on CARNET study | 2020 | Calcagni, G.; Gagliostro, G.; Limongelli, G.; Unolt, M.; De Luca, E.; Digilio, M. C.; Baban, A.; Albanese, S. B.; Ferrero, G. B.; Baldassarre, G.; Agnoletti, G.; Banaudi, E.; Marek, J.; Kaski, J. P.; Tuo, G.; Marasini, M.; Cairello, F.; Madrigali, A.; Pacileo, G.; Russo, M. G.; Milanesi, O.; Formigari, R.; Brighenti, M.; Ragni, L.; Donti, A.; Drago, F.; Dallapiccola, B.; Tartaglia, M.; Marino, B.; Versacci, P. | |
| Cardiac defects and genetic syndromes: old uncertainties and new insights | 2021 | Calcagni, G.; Pugnaloni, F.; Digilio, M. C.; Unolt, M.; Putotto, C.; Niceta, M.; Baban, A.; Sparascio, F. P.; Drago, F.; De Luca, A.; Tartaglia, M.; Marino, B.; Versacci, P. | |
| Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease | 2023 | Putotto, Carolina; Unolt, Marta; Lambiase, Caterina; Marchetti, Flaminia; Anaclerio, Silvia; Favoriti, Alessandra; Tancredi, Giancarlo; Mastromoro, Gioia; Pugnaloni, Flaminia; Liberati, Natascia; De Luca, Enrica; Tarani, Luigi; De Canditiis, Daniela; Caputo, Viviana; Bernardini, Laura; Digilio, Maria Cristina; Marino, Bruno; Versacci, Paolo | |
| Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study | 2022 | Putotto, Carolina; Pulvirenti, Federica; Pugnaloni, Flaminia; Isufi, Ina; Unolt, Marta; Anaclerio, Silvia; Caputo, Viviana; Bernardini, Laura; Messina, Elisa; Moretti, Corrado; Tarani, Luigi; Marino, Bruno; Versacci, Paolo | |
| Coexisting genetic findings in a cohort of patients with laboratory confirmation of 22q11.2 deletion syndrome | 2022 | Pugnaloni, F.; Putotto, C.; Mastromoro, G.; Pulvirenti, F.; Maiolo, S.; Unolt, M.; Digilio, M. C.; Giovannetti, A.; Caputo, V.; Versacci, P.; Marino, B. | |
| Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects | 2020 | Zhao, Y.; Diacou, A.; Johnston, H. R.; Musfee, F. I.; McDonald-McGinn, D. M.; Mcginn, D.; Crowley, T. B.; Repetto, G. M.; Swillen, A.; Breckpot, J.; Vermeesch, J. R.; Kates, W. R.; Digilio, M. C.; Unolt, M.; Marino, B.; Pontillo, M.; Armando, M.; DI FABIO, Fabio; Vicari, S.; van den Bree, M.; Moss, H.; Owen, M. J.; Murphy, K. C.; Murphy, C. M.; Murphy, D.; Schoch, K.; Shashi, V.; Tassone, F.; Simon, T. J.; Shprintzen, R. J.; Campbell, L.; Philip, N.; Heine-Suner, D.; Garcia-Minaur, S.; Fernandez, L.; Antonarakis, S. E.; Biondi, M.; Boot, E.; Breetvelt, E.; Busa, T.; Butcher, N.; Buzzanca, A.; Carmel, M.; Cleynen, I.; Cutler, D.; Dallapiccola, B.; de la Fuente Sanches, M. A.; Epstein, M. P.; Evers, R.; Fernandez, L.; Fritsch, R.; Algas, F. G.; Guo, T.; Gur, R.; Hestand, M. S.; Heung, T.; Hooper, S.; Jin, A.; Kushan-Wells, L.; Laorden-Nieto, A. T.; Lattanzi, G.; Marshall, C.; Mccabe, K.; Michaelovsky, E.; Ornstein, C.; Silversides, C.; Tran, O.; van Duin, E. D. A.; Vergaelen, E.; Warren, S. T.; Weinberger, R.; Weizman, A.; Zhang, Z.; Zwick, M.; Bearden, C. E.; Vingerhoets, C.; van Amelsvoort, T.; Eliez, S.; Schneider, M.; Vorstman, J. A. S.; Gothelf, D.; Zackai, E.; Agopian, A. J.; Gur, R. E.; Bassett, A. S.; Emanuel, B. S.; Goldmuntz, E.; Mitchell, L. E.; Wang, T.; Morrow, B. E. | |
| Congenital heart defects in molecularly confirmed KBG syndrome patients | 2021 | Digilio, M. C.; Calcagni, G.; Gnazzo, M.; Versacci, P.; Dentici, M. L.; Capolino, R.; Sinibaldi, L.; Baban, A.; Putotto, C.; Alfieri, P.; Unolt, M.; Lepri, F. R.; Alesi, V.; Genovese, S.; Novelli, A.; Marino, B.; Dallapiccola, B. | |
| Congenital heart disease and genetic syndromes: new insights into molecular mechanisms | 2017 | Calcagni, Giulio; Unolt, Marta; Digilio, Maria Cristina; Baban, Anwar; Versacci, Paolo; Tartaglia, Marco; Baldini, Antonio; Marino, Bruno | |
| Congenital heart disease, genetic syndromes, and major noncardiac malformations | 2012 | Unolt, M.; Putotto, C.; Marino, D. | |
| Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers | 2018 | Unolt, Marta; Versacci, Paolo; Anaclerio, Silvia; Lambiase, Caterina; Calcagni, Giulio; Trezzi, Matteo; Carotti, Adriano; Crowley, Terrence Blaine; Zackai, Elaine H.; Goldmuntz, Elizabeth; Gaynor, James William; Digilio, Maria Cristina; Mcdonald-Mcginn, Donna M.; Marino, Bruno | |
| Congenital heart diseases in women | 2013 | Putotto, C; Unolt, M; Caiaro, A; MARINO TAUSSIG DE BODONIA, Bruno; Massaccesi, V; Digilio, Mc | |
| Crossed pulmonary arteries. an underestimated cardiovascular variant with a strong association with genetic syndromes{\textemdash}A report of 74 cases with systematic review of the literature | 2022 | Mastromoro, Gioia; Calcagni, Giulio; Vignaroli, Walter; Anaclerio, Silvia; Pugnaloni, Flaminia; Rinelli, Gabriele; Secinaro, Aurelio; Bordonaro, Veronica; Putotto, Carolina; Unolt, Marta; Cristina Digilio, Maria; Marino, Bruno; Versacci, Paolo | |
| Double outlet right ventricle versus aortic dextroposition: morphologically distinct defects | 2013 | Restivo, A; Unolt, M; Putotto, C; MARINO TAUSSIG DE BODONIA, Bruno | |
| Double-orifice left atrioventricular valve in patients with atrioventricular septal defect with and without down syndrome | 2013 | Unolt, M.; Putotto, C.; Marino, D. | |
| Double-outlet left ventricle with l-malposition of the great arteries and subpulmonary ventricular septal defect | 2013 | Putotto, C.; Unolt, M.; Marino, D. | |
| Factors that negatively affect the prognosis of pediatric community-acquired pneumonia in district hospital in Tanzania | 2017 | Caggiano, Serena; Ullmann, Nicola; de Vitis, Elisa; Trivelli, Marzia; Mariani, Chiara; Podagrosi, Maria; Ursitti, Fabiana; Bertolaso, Chiara; Putotto, Carolina; Unolt, Marta; Pietravalle, Andrea; Pansa, Paola; Mphayokulela, Kajoro; Lemmo, Maria Incoronata; Mkwambe, Michael; Kazaura, Joseph; Duse, Marzia; Nieddu, Francesco; Azzari, Chiara; Cutrera, Renato |