POLITANO, Luisa
POLITANO, Luisa
Dipartimento di Medicina Sperimentale
"I have got something positive out of this situation": psychological benefits of caregiving in relatives of young people with muscular dystrophy.
2013 Magliano, Lorenza; Patalano, M; Sagliocchi, A; Scutifero, M; Zaccaro, A; D'Angelo, Mg; Civati, F; Brighina, E; Vita, G; Vita, Gl; Messina, S; Sframeli, M; Pane, M; Lombardo, Me; Scalise, R; D'Amico, A; Colia, G; Catteruccia, M; Balottin, U; Berardinelli, A; Motta, Mc; Angelini, C; Gaiani, A; Semplicini, C; Bello, L; Battini, R; Astrea, G; Ricci, G; Politano, Luisa
1) Comparison between SPECT myocardical scintigraphy with 201Tl and 99mTc-MIBI in patients affected by Duchenne's dystrophy
1994 Mansi, Luigi; Rambaldi, Pier Francesco; Politano, Luisa; Di Gregorio, F; De Rimini, Ml; Limongelli, Fm; Petretta, Vr; Raia, P; Tesauro, P.
1) Study of myocardial perfusion with Tl-201 in patients affected by Duchenne's/Becker's muscolar dystrophy
1994 Mansi, ; Politano, Luisa; Rambaldi, Pier Francesco; De Rimini, Ml; Di Gregorio, F; Pollio, Gg; Comi, Li; Nigro, G; P. Tesauro, P.
238th ENMC International Workshop: Updating management recommendations of cardiac dystrophinopathyHoofddorp, The Netherlands, 30 November - 2 December 2018.
2019 Bourke, Jp; Guglieri, M; Duboc, D; Aartsma-Rus, A; Bandali, A; Bennett, N; Cools, B; Cripe, L; de Groot, I; Dittrich, S; Florian, A; Furlong, P; Goemans, N; Hor, K; van Leperen, F; Macgowan, G; Mcnally, E; Pegoraro, E; Politano, L; Sediva, M; Stara, V; Timmermans, J; Vroom, E; Wahbi, K.
24 month longitudinal data in ambulant boys with D uchenne muscular dystrophy.
2013 Mazzone, Es; Pane, M; Sormani, Mp; Scalise, R; Berardinelli, A; Messina, S; Torrente, Y; D'Amico, A; Doglio, L; Viggiano, E; D'Ambrosio, P; Cavallaro, F; Frosini, S; Bello, L; Bonfiglio, S; De Sanctis, R; Rolle, E; Bianco, F; Magri, F; Rossi, F; Vasco, G; Vita, G; Motta, Mc; Donati, Ma; Sacchini, M; Mongini, T; Pini, A; Battini, R; Pegoraro, E; Previtali, S; Napolitano, S; Bruno, C; Politano, Luisa; Comi, Gp; Bertini, E; Mercuri, E.
42nd ENMC Sponsored International Workshop: X-linked Cardiomyopathies
1997 Nigro, G; Politano, Luisa; Muntoni, F.
6 Min walk test 12 month changes in DMD: correlation with the genotype
2013 Pane, M; Mazzone, E; Sormani, Mp; Scalise, R; Berardinelli, A; Messina, S; Torrente, Y; D'Amico, A; Doglio, L; Viggiano, E; D'Ambrosio, P; Cavallaro, P; Frosini, S; Bello, L; De Sanctis, R; Fanelli, L; Rolle, E; Bianco, F; Magri, F; Vita, Gl; Motta, Mc; Donati, Ma; Mongini, T; Pini, A; Battini, R; Pegoraro, E; Previtali, Sc; Napolitano, S; Bruno, C; Politano, Luisa; Comi, Gp; Bertini, E; Mercuri, E.
6 minute walk test in Duchenne MD patients with different mutations: 12 month changes
2014 Pane, M; Mazzone, Es; Sormani, Mp; Messina, S; Vita, Gl; Fanelli, L; Berardinelli, A; Torrente, Y; D'Amico, A; Lanzillotta, V; Viggiano, E; D'Ambrosio, P; Cavallaro, F; Frosini, S; Bello, L; Bonfiglio, S; Scalise, R; De Sanctis, R; Rolle, E; Bianco, F; Van der Haawue, M; Magri, F; Palermo, C; Rossi, F; Donati, Ma; Alfonsi, C; Sacchini, M; Arnoldi, Mt; Baranello, G; Mongini, T; Pini, A; Battini, R; Pegoraro, E; Previtali, Sc; Napolitano, S; Bruno, C; Politano, Luisa; Comi, Gp; Bertini, E; Morandi, L; Gualandi, F; Ferlini, A; Goemans, N; Mercuri, E.
: Single Nucleotide Polymorphisms analysis of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients
2008 Rinaldi, F; Botta, A; Vallo, L; Contino, G; Morgante, A; Iraci, R; Cavalli, C; Silvestri, G; Ventriglia, Vm; Politano, Luisa; Novelli, G.
[Serum isoenzymes in the diagnosis of some physiopathological conditions in the uterus]
1978 Politano, Luisa; Sola, V; Limoncelli, F; Cobellis, G; Panariello, S; Izzo, Alfredo
A novel homozygous beta-sarcoglycan gene mutation: case description.
2012 Ricci, G; Simoncini, C; Volpi, L; Logerfo, A; Servadio, A; Dell’Osso, G; Politano, Luisa; Nigro, Vincenzo; Siciliano, G.
A novel mutation in CPT2 gene in two unrelated patients from Campania region
2012 Taglia, A; Picillo, E; Viggiano, E; Baratta, S; Cecio, Mr; D’Ambrosio, P; Rimoldi, M; Passamano, L; Palladino, A; Taroni, F; Politano, Luisa
A preliminary randomized study of growth hormone administration in Becker and Duchenne muscular dystrophies
2003 Cittadini, A; Comi, Li; Longobardi, S; Petretta, Vr; Casaburi, C; Passamano, L; Merola, B; DURANTE MANGONI, Emanuele; Sacca, L; Politano, Luisa
A rare co-occurrence of phosphorylase kinase deficiency (GSD type IXd) and alpha-glycosidase deficiency (GSD Type II) in a 53-year-old man presenting with an atypical glycogen storage disease phenotype
2024 Picillo, E.; Onore, M. E.; Passamano, L.; Nigro, V.; Politano, L.
A report of two deflazacort treatment protocols in Duchenne muscular dystrophy
2003 Biggar, Wd; Nigro, G; Politano, Luisa; Harris, V; Passamano, L; Vaisar, J; Alman, B; Palladino, A; DE LUCA, F.
A report on 528 intragenic deletions detected in DMD and BMD patients by an Italian collaborative study
1994 Mioni, F.; Danieli, G. A.; Cao, A.; Cau, M.; COLONNA R, S.; Covone, A. E.; Leonardis, P. DE; DE LEO, R.; Esposito, M. G.; Felicetti, L.; Ferlini, A.; Nigro, Vincenzo; Politano, Luisa
A Unique Myopathy Syndrome in a Patient Disclosing Clinical, Laboratory, and Genetic Findings of Late-Onset Pompe Disease, Together with a Lack of Dysferlin on Muscle Biopsy
2015 Sampaolo, Simone; Lombardi, Luca; Pascarella, Angelo; Picillo, Esther; Farina, Olimpia; Esposito, Teresa; Politano, Luisa; DI IORIO, Giuseppe
ACE inhibition to slow progression of myocardial fibrosis in muscular dystrophies
2018 Russo, Vincenzo; Papa, Andrea Antonio; Williams, Emmanuel Ato; Rago, Anna; Palladino, Alberto; Politano, Luisa; Nigro, Gerardo
Acta Myologica (myopathies, cardiomyopathies and neuromyopathies)
2012 Nigro, G; Politano, Luisa
Adults with spinal muscular atrophy: a large-scale natural history study shows gender effect on disease
2022 Maggi, Lorenzo; Bello, Luca; Bonanno, Silvia; Govoni, Alessandra; Caponnetto, Claudia; Passamano, Luigia; Grandis, Marina; Trojsi, Francesca; Cerri, Federica; Gardani, Alice; Ferraro, Manfredi; Gadaleta, Giulio; Zangaro, Vittoria; Caumo, Luca; Maioli, Mariantonietta; Tanel, Raffaella; Saccani, Elena; Meneri, Megi; Vacchiano, Veria; Ricci, Giulia; Sorarù, Gianni; D'Errico, Eustachio; Bortolani, Sara; Pavesi, Giovanni; Gellera, Cinzia; Zanin, Riccardo; Corti, Stefania; Silvestrini, Mauro; Politano, Luisa; Schenone, Angelo; Previtali, Stefano Carlo; Berardinelli, Angela; Turri, Mara; Verriello, Lorenzo; Coccia, Michela; Mantegazza, Renato; Liguori, Rocco; Filosto, Massimiliano; Marrosu, Gianni; Tiziano, Francesco Danilo; Siciliano, Gabriele; Simone, Isabella Laura; Mongini, Tiziana; Comi, Giacomo; Pegoraro, Elena
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| "I have got something positive out of this situation": psychological benefits of caregiving in relatives of young people with muscular dystrophy. | 1-gen-2013 | Magliano, Lorenza; Patalano, M; Sagliocchi, A; Scutifero, M; Zaccaro, A; D'Angelo, Mg; Civati, F; Brighina, E; Vita, G; Vita, Gl; Messina, S; Sframeli, M; Pane, M; Lombardo, Me; Scalise, R; D'Amico, A; Colia, G; Catteruccia, M; Balottin, U; Berardinelli, A; Motta, Mc; Angelini, C; Gaiani, A; Semplicini, C; Bello, L; Battini, R; Astrea, G; Ricci, G; Politano, Luisa | |
| 1) Comparison between SPECT myocardical scintigraphy with 201Tl and 99mTc-MIBI in patients affected by Duchenne's dystrophy | 1-gen-1994 | Mansi, Luigi; Rambaldi, Pier Francesco; Politano, Luisa; Di Gregorio, F; De Rimini, Ml; Limongelli, Fm; Petretta, Vr; Raia, P; Tesauro, P. | |
| 1) Study of myocardial perfusion with Tl-201 in patients affected by Duchenne's/Becker's muscolar dystrophy | 1-gen-1994 | Mansi, ; Politano, Luisa; Rambaldi, Pier Francesco; De Rimini, Ml; Di Gregorio, F; Pollio, Gg; Comi, Li; Nigro, G; P. Tesauro, P. | |
| 238th ENMC International Workshop: Updating management recommendations of cardiac dystrophinopathyHoofddorp, The Netherlands, 30 November - 2 December 2018. | 1-gen-2019 | Bourke, Jp; Guglieri, M; Duboc, D; Aartsma-Rus, A; Bandali, A; Bennett, N; Cools, B; Cripe, L; de Groot, I; Dittrich, S; Florian, A; Furlong, P; Goemans, N; Hor, K; van Leperen, F; Macgowan, G; Mcnally, E; Pegoraro, E; Politano, L; Sediva, M; Stara, V; Timmermans, J; Vroom, E; Wahbi, K. | |
| 24 month longitudinal data in ambulant boys with D uchenne muscular dystrophy. | 1-gen-2013 | Mazzone, Es; Pane, M; Sormani, Mp; Scalise, R; Berardinelli, A; Messina, S; Torrente, Y; D'Amico, A; Doglio, L; Viggiano, E; D'Ambrosio, P; Cavallaro, F; Frosini, S; Bello, L; Bonfiglio, S; De Sanctis, R; Rolle, E; Bianco, F; Magri, F; Rossi, F; Vasco, G; Vita, G; Motta, Mc; Donati, Ma; Sacchini, M; Mongini, T; Pini, A; Battini, R; Pegoraro, E; Previtali, S; Napolitano, S; Bruno, C; Politano, Luisa; Comi, Gp; Bertini, E; Mercuri, E. | |
| 42nd ENMC Sponsored International Workshop: X-linked Cardiomyopathies | 1-gen-1997 | Nigro, G; Politano, Luisa; Muntoni, F. | |
| 6 Min walk test 12 month changes in DMD: correlation with the genotype | 1-gen-2013 | Pane, M; Mazzone, E; Sormani, Mp; Scalise, R; Berardinelli, A; Messina, S; Torrente, Y; D'Amico, A; Doglio, L; Viggiano, E; D'Ambrosio, P; Cavallaro, P; Frosini, S; Bello, L; De Sanctis, R; Fanelli, L; Rolle, E; Bianco, F; Magri, F; Vita, Gl; Motta, Mc; Donati, Ma; Mongini, T; Pini, A; Battini, R; Pegoraro, E; Previtali, Sc; Napolitano, S; Bruno, C; Politano, Luisa; Comi, Gp; Bertini, E; Mercuri, E. | |
| 6 minute walk test in Duchenne MD patients with different mutations: 12 month changes | 1-gen-2014 | Pane, M; Mazzone, Es; Sormani, Mp; Messina, S; Vita, Gl; Fanelli, L; Berardinelli, A; Torrente, Y; D'Amico, A; Lanzillotta, V; Viggiano, E; D'Ambrosio, P; Cavallaro, F; Frosini, S; Bello, L; Bonfiglio, S; Scalise, R; De Sanctis, R; Rolle, E; Bianco, F; Van der Haawue, M; Magri, F; Palermo, C; Rossi, F; Donati, Ma; Alfonsi, C; Sacchini, M; Arnoldi, Mt; Baranello, G; Mongini, T; Pini, A; Battini, R; Pegoraro, E; Previtali, Sc; Napolitano, S; Bruno, C; Politano, Luisa; Comi, Gp; Bertini, E; Morandi, L; Gualandi, F; Ferlini, A; Goemans, N; Mercuri, E. | |
| : Single Nucleotide Polymorphisms analysis of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients | 1-gen-2008 | Rinaldi, F; Botta, A; Vallo, L; Contino, G; Morgante, A; Iraci, R; Cavalli, C; Silvestri, G; Ventriglia, Vm; Politano, Luisa; Novelli, G. | |
| [Serum isoenzymes in the diagnosis of some physiopathological conditions in the uterus] | 1-gen-1978 | Politano, Luisa; Sola, V; Limoncelli, F; Cobellis, G; Panariello, S; Izzo, Alfredo | |
| A novel homozygous beta-sarcoglycan gene mutation: case description. | 1-gen-2012 | Ricci, G; Simoncini, C; Volpi, L; Logerfo, A; Servadio, A; Dell’Osso, G; Politano, Luisa; Nigro, Vincenzo; Siciliano, G. | |
| A novel mutation in CPT2 gene in two unrelated patients from Campania region | 1-gen-2012 | Taglia, A; Picillo, E; Viggiano, E; Baratta, S; Cecio, Mr; D’Ambrosio, P; Rimoldi, M; Passamano, L; Palladino, A; Taroni, F; Politano, Luisa | |
| A preliminary randomized study of growth hormone administration in Becker and Duchenne muscular dystrophies | 1-gen-2003 | Cittadini, A; Comi, Li; Longobardi, S; Petretta, Vr; Casaburi, C; Passamano, L; Merola, B; DURANTE MANGONI, Emanuele; Sacca, L; Politano, Luisa | |
| A rare co-occurrence of phosphorylase kinase deficiency (GSD type IXd) and alpha-glycosidase deficiency (GSD Type II) in a 53-year-old man presenting with an atypical glycogen storage disease phenotype | 1-gen-2024 | Picillo, E.; Onore, M. E.; Passamano, L.; Nigro, V.; Politano, L. | |
| A report of two deflazacort treatment protocols in Duchenne muscular dystrophy | 1-gen-2003 | Biggar, Wd; Nigro, G; Politano, Luisa; Harris, V; Passamano, L; Vaisar, J; Alman, B; Palladino, A; DE LUCA, F. | |
| A report on 528 intragenic deletions detected in DMD and BMD patients by an Italian collaborative study | 1-gen-1994 | Mioni, F.; Danieli, G. A.; Cao, A.; Cau, M.; COLONNA R, S.; Covone, A. E.; Leonardis, P. DE; DE LEO, R.; Esposito, M. G.; Felicetti, L.; Ferlini, A.; Nigro, Vincenzo; Politano, Luisa | |
| A Unique Myopathy Syndrome in a Patient Disclosing Clinical, Laboratory, and Genetic Findings of Late-Onset Pompe Disease, Together with a Lack of Dysferlin on Muscle Biopsy | 1-gen-2015 | Sampaolo, Simone; Lombardi, Luca; Pascarella, Angelo; Picillo, Esther; Farina, Olimpia; Esposito, Teresa; Politano, Luisa; DI IORIO, Giuseppe | |
| ACE inhibition to slow progression of myocardial fibrosis in muscular dystrophies | 1-gen-2018 | Russo, Vincenzo; Papa, Andrea Antonio; Williams, Emmanuel Ato; Rago, Anna; Palladino, Alberto; Politano, Luisa; Nigro, Gerardo | |
| Acta Myologica (myopathies, cardiomyopathies and neuromyopathies) | 1-gen-2012 | Nigro, G; Politano, Luisa | |
| Adults with spinal muscular atrophy: a large-scale natural history study shows gender effect on disease | 1-gen-2022 | Maggi, Lorenzo; Bello, Luca; Bonanno, Silvia; Govoni, Alessandra; Caponnetto, Claudia; Passamano, Luigia; Grandis, Marina; Trojsi, Francesca; Cerri, Federica; Gardani, Alice; Ferraro, Manfredi; Gadaleta, Giulio; Zangaro, Vittoria; Caumo, Luca; Maioli, Mariantonietta; Tanel, Raffaella; Saccani, Elena; Meneri, Megi; Vacchiano, Veria; Ricci, Giulia; Sorarù, Gianni; D'Errico, Eustachio; Bortolani, Sara; Pavesi, Giovanni; Gellera, Cinzia; Zanin, Riccardo; Corti, Stefania; Silvestrini, Mauro; Politano, Luisa; Schenone, Angelo; Previtali, Stefano Carlo; Berardinelli, Angela; Turri, Mara; Verriello, Lorenzo; Coccia, Michela; Mantegazza, Renato; Liguori, Rocco; Filosto, Massimiliano; Marrosu, Gianni; Tiziano, Francesco Danilo; Siciliano, Gabriele; Simone, Isabella Laura; Mongini, Tiziana; Comi, Giacomo; Pegoraro, Elena |