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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
Miopatie infiammatorie 1-gen-1987 Politano, Luisa
Premesse di Genetica Medica 1-gen-1987 Politano, Luisa
Miocardiopatie e miopatie infiammatorie. 1-gen-1987 Limongelli, Fm; Politano, Luisa
The incidence and evolution of cardiomyopathy in Duchenne muscular dystrophy 1-gen-1990 Nigro, G; Comi, Li; Politano, Luisa; Bain, Rj
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
Skeletal muscle cytochrome c in X-linked muscle dystrophies 1-gen-1991 Nigro, G; Comi, Li; Politano, Luisa; Limongelli, Fm
The cardiomyopathy of Duchenne/Becker consultands 1-gen-1992 Comi, Li; Nigro, G; Politano, Luisa; Petretta, Vr
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
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
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
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
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.
Dilated cardiomyopathy of muscular dystrophy: a multifaceted approach to management 1-gen-1995 Nigro, G; Comi, Li; Politano, Luisa; Nigro, Vincenzo
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.
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.
Mostrati risultati da 1 a 20 di 316
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