Sfoglia per Autore
[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
Miocardiopatie e miopatie infiammatorie.
1987 Limongelli, Fm; Politano, Luisa
Premesse di Genetica Medica
1987 Politano, Luisa
Miopatie infiammatorie
1987 Politano, Luisa
The incidence and evolution of cardiomyopathy in Duchenne muscular dystrophy
1990 Nigro, G; Comi, Li; Politano, Luisa; Bain, Rj
Skeletal muscle cytochrome c in X-linked muscle dystrophies
1991 Nigro, G; Comi, Li; Politano, Luisa; Limongelli, Fm
Une forme méconnue de myopathie. III. Definition et caractères cliniques
1991 Rideau, Y; Delaubier, A; Foucault, P; Goulet, G; Guillou, C; Renardel, A; Bonneau, D; Colbert, A; Bianchi, C; Politano, Luisa; Vallat, Jm
Detection of a nonsense mutation in the dystrophin gene by multiple SSCP
1992 Nigro, Vincenzo; Politano, Luisa; Nigro, G; Romano, Sc; Molinari, Anna Maria; Puca, Ga
The cardiomyopathy of Duchenne/Becker consultands
1992 Comi, Li; Nigro, G; Politano, Luisa; Petretta, Vr
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.
Mutation of dystrophin gene and cardiomyopathy
1994 Nigro, G; Politano, Luisa; Nigro, Vincenzo; Petretta, Vr; Comi, Li
Novel small mutations along the DMD/BMD gene associated with different phenotypes
1994 Nigro, Vincenzo; Nigro, G; Esposito, Mg; Comi, Li; Molinari, Anna Maria; Puca, Ga; Politano, Luisa
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
INVOLVEMENT OF FREE-RADICALS IN DUCHENNES AND BECKERS DISEASES
1995 Cenicola, Ml; Nigro, G; Tufano, Ma; Politano, Luisa; Comi, Li; Passamano, L; Catalanotti, Piergiorgio; Depaolis, P; Mangrella, M; Rossi, F.
Dilated cardiomyopathy of muscular dystrophy: a multifaceted approach to management
1995 Nigro, G; Comi, Li; Politano, Luisa; Nigro, Vincenzo
Evaluation of the cardiomyopathy in Becker muscular dystrophy
1995 Nigro, G; Comi, Li; Politano, Luisa; Limongelli, Fm; Nigro, Vincenzo; DE RIMINI, Ml; Giugliano, Ma; Petretta, Vr; Passamano, L; Restucci, B.
SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin function
1995 Nigro, Vincenzo; Bruni, P; Ciccodicola, A; Politano, Luisa; Nigro, G; Piluso, Giulio; Cappa, V; Covone, Ae; Romeo, G; D'Urso, M.
Structural basis of cardiomyopathy in Duchenne/Becker carriers. Endomyocardial biopsy evaluation
1995 Nigro, G; DI SOMMA, S; Comi, Li; Politano, Luisa; Papparella, S; Restucci, B; Petretta, V; Giugliano, Mam; Carotenuto, A; Limongelli, Fm; DE DIVITIIS, O.
Correction précoce des inégalités musculaires dans la myopathie: Analyse internationale.
1996 Rideau, Y; Duport, G; Delaubier, A; Guillou, C; Bach, J; Bianchi, C; Forst, R; Forst, J; Nigro, G; Politano, Luisa; Riccio, V.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
[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 | |
Miocardiopatie e miopatie infiammatorie. | 1-gen-1987 | Limongelli, Fm; Politano, Luisa | |
Premesse di Genetica Medica | 1-gen-1987 | Politano, Luisa | |
Miopatie infiammatorie | 1-gen-1987 | Politano, Luisa | |
The incidence and evolution of cardiomyopathy in Duchenne muscular dystrophy | 1-gen-1990 | Nigro, G; Comi, Li; Politano, Luisa; Bain, Rj | |
Skeletal muscle cytochrome c in X-linked muscle dystrophies | 1-gen-1991 | Nigro, G; Comi, Li; Politano, Luisa; Limongelli, Fm | |
Une forme méconnue de myopathie. III. Definition et caractères cliniques | 1-gen-1991 | Rideau, Y; Delaubier, A; Foucault, P; Goulet, G; Guillou, C; Renardel, A; Bonneau, D; Colbert, A; Bianchi, C; Politano, Luisa; Vallat, Jm | |
Detection of a nonsense mutation in the dystrophin gene by multiple SSCP | 1-gen-1992 | Nigro, Vincenzo; Politano, Luisa; Nigro, G; Romano, Sc; Molinari, Anna Maria; Puca, Ga | |
The cardiomyopathy of Duchenne/Becker consultands | 1-gen-1992 | Comi, Li; Nigro, G; Politano, Luisa; Petretta, Vr | |
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. | |
Mutation of dystrophin gene and cardiomyopathy | 1-gen-1994 | Nigro, G; Politano, Luisa; Nigro, Vincenzo; Petretta, Vr; Comi, Li | |
Novel small mutations along the DMD/BMD gene associated with different phenotypes | 1-gen-1994 | Nigro, Vincenzo; Nigro, G; Esposito, Mg; Comi, Li; Molinari, Anna Maria; Puca, Ga; Politano, Luisa | |
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 | |
INVOLVEMENT OF FREE-RADICALS IN DUCHENNES AND BECKERS DISEASES | 1-gen-1995 | Cenicola, Ml; Nigro, G; Tufano, Ma; Politano, Luisa; Comi, Li; Passamano, L; Catalanotti, Piergiorgio; Depaolis, P; Mangrella, M; Rossi, F. | |
Dilated cardiomyopathy of muscular dystrophy: a multifaceted approach to management | 1-gen-1995 | Nigro, G; Comi, Li; Politano, Luisa; Nigro, Vincenzo | |
Evaluation of the cardiomyopathy in Becker muscular dystrophy | 1-gen-1995 | Nigro, G; Comi, Li; Politano, Luisa; Limongelli, Fm; Nigro, Vincenzo; DE RIMINI, Ml; Giugliano, Ma; Petretta, Vr; Passamano, L; Restucci, B. | |
SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin function | 1-gen-1995 | Nigro, Vincenzo; Bruni, P; Ciccodicola, A; Politano, Luisa; Nigro, G; Piluso, Giulio; Cappa, V; Covone, Ae; Romeo, G; D'Urso, M. | |
Structural basis of cardiomyopathy in Duchenne/Becker carriers. Endomyocardial biopsy evaluation | 1-gen-1995 | Nigro, G; DI SOMMA, S; Comi, Li; Politano, Luisa; Papparella, S; Restucci, B; Petretta, V; Giugliano, Mam; Carotenuto, A; Limongelli, Fm; DE DIVITIIS, O. | |
Correction précoce des inégalités musculaires dans la myopathie: Analyse internationale. | 1-gen-1996 | Rideau, Y; Duport, G; Delaubier, A; Guillou, C; Bach, J; Bianchi, C; Forst, R; Forst, J; Nigro, G; Politano, Luisa; Riccio, V. |
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