POLITANO, Luisa

POLITANO, Luisa  

Dipartimento di Medicina Sperimentale  

Risultati 1 - 20 di 316 (tempo di esecuzione: 0.03 secondi).
Titolo Data di pubblicazione Autore(i) File
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.
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 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.
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
Advances in basic and clinical research in laminopathies. 1-gen-2013 Politano, Luisa; Carboni, N; Madej Pilarczyk, A; Marchel, M; Nigro, Gerardo; Fidziaóska, A; Opolski, G; Hausmanowa Petrusewicz, I.
Affinity proteomics within rare diseases: a BIO-NMD study for blood biomarkers of muscular dystrophies 1-gen-2014 Ayoglu, B; Chaouch, A; Lochmüller, H; Politano, Luisa; Bertini, E; Spitali, P; Hiller, M; Niks, E; Gualandi, F; Pontén, F; Bushby, K; Aartsma Rus, A; Schwartz, E; Le Priol, Y; Straub, V; Uhlén, M; Cirak, S; 't Hoen, Pa; Muntoni, F; Ferlini, A; Schwenk, Jm; Nilsson, P; Al Khalili Szigyarto, C.
The alliance between genetic biobanks and patient organisations: the experience of the telethon network of genetic biobanks 1-gen-2016 Baldo, Chiara; Casareto, Lorena; Renieri, Alessandra; Merla, Giuseppe; Garavaglia, Barbara; Goldwurm, Stefano; Pegoraro, Elena; Moggio, Maurizio; Mora, Marina; Politano, Luisa; Sangiorgi, Luca; Mazzotti, Raffaella; Viotti, Valeria; Meloni, Ilaria; Pellico, Maria Teresa; Barzaghi, Chiara; Wang, Chiuhui Mary; Monaco, Lucia; Filocamo, Mirella
Analysis of candidate genes modifier for the conduction system impairment in myotonic dystrophy type 1 (DM1) 1-gen-2005 Vallo, L; Bonifazi, E; Rinaldi, F; Contino, G; Iraci, R; Palladino, A; Sannino, P; Politano, Luisa; Botta, A. AND NOVELLI G.
Analysis of caveolin-3 (CAV-3) gene in patients with limb-girdle muscular dystrophies and/or isolated hyperCKemia 1-gen-2002 Politano, Luisa; Fanin, M; Piluso, Giulio; Belsito, Angela; D'Amico, F; Esposito, Mg; Angelini, C; Nigro, G; Nigro, Vincenzo
The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C-terminal peptide of the ClC-1 channel 1-gen-2018 Altamura, Concetta; Lucchiari, Sabrina; Sahbani, Dalila; Ulzi, Gianna; Comi, Giacomo P.; D'Ambrosio, Paola; Petillo, Roberta; Politano, Luisa; Vercelli, Liliana; Mongini, Tiziana; Dotti, Maria Teresa; Cardani, Rosanna; Meola, Giovanni; Lo Monaco, Mauro; Matthews, Emma; Hanna, Michael G.; Carratù, Maria Rosaria; Conte, Diana; Imbrici, Paola; Desaphy, Jean-François
Anterior capsule phimosis and capsular block syndrome in a patient with Steinert myotonic dystrophy: A case report 1-gen-2009 Rosa, N; Lanza, Michele; De Bernardo, M; Borrelli, M; Politano, Luisa