Sfoglia per Autore
Heart involvement in Emery-Dreifuss muscular dystrophies: new parameters to detect early atrial fibrosis and vulnerability
2002 Politano, Luisa; Nigro, Ge; Petretta, Vr; Ventriglia, Vm; Santangelo, L; Piluso, Giulio; Panico, F; Nigro, Vincenzo; Comi, Li; Nigro, Gerardo
Clinical, molecular and genetic features of calpainopathy in Slovenia
2002 MEZNARIC PETRUSA, Mmp; Zidar, J; Zupancic, N; Fanin, M; Angelini, C; Piluso, Giulio; Ventriglia, Vm; Politano, Luisa
Identification and analysis of candidate genes for Limb-Girdle Muscular Dystrophies
2002 Nigro, Vincenzo; Piluso, Giulio; Aurino, S; D'Amico, F; Belsito, Angela; Ventriglia, Vm; Politano, Luisa
Multiple heterozygosity for different muscle genes is not rare among individuals with pauci-symptomatic hyperCKemia
2002 Politano, Luisa; Nigro, Vincenzo; Aurino, S; Belsito, Angela; D'Amico, F; Piluso, Giulio; Ventriglia, Vm; Passamano, L; Palladino, A; Esposito, Mg; Paciello, O; Freda, Fulvio
Different phenotypic expression in three related families with limb-girdle muscular dystrophy (LGMD2I) due to mutations in fukutin-related-protein gene
2003 Politano, Luisa; D'Amico, F; Passamano, L; Ventriglia, Vm; Palladino, A; Aurino, S; Piluso, Giulio; Nigro, G; Nigro, Vincenzo
Genetic heterogeneity of FG syndrome: a fourth locus (FGS4) maps to Xp11.4-p11.3 in an Italian family
2003 Piluso, Giulio; Carella, M; D'Avanzo, M; Santinelli, R; Carrano, Em; D'Avanzo, A; D'Adamo, Ap; Gasparini, P; Nigro, Vincenzo
Scanning for mutations of the ryanodine receptor (RYR1) gene by denaturing HPLC: detection of three novel malignant hyperthermia alleles
2003 Tammaro, A; Bracco, A; Cozzolino, S; Esposito, M; DI MARTINO, A; Savoia, G; Zeuli, L; Piluso, Giulio; Aurino, S; Nigro, Vincenzo
Gentamicin administration in Duchenne patients with premature stop codon. Preliminary results
2003 Politano, Luisa; Nigro, Gerardo; Nigro, Vincenzo; Piluso, Giulio; Papparella, S; Paciello, O; Comi, Li
Prevalence of the 550delA mutation in calpainopathy (LGMD 2A) in Croatia
2004 Cankiklain, N; Milic, A; Kovac, B; Trlaja, A; Grgicevic, D; Zurak, N; Fardeau, M; Leturcq, F; Kaplan, Jc; Urtizberea, Ja; Politano, Luisa; Piluso, Giulio; Feingold, J.
Molecular diagnosis in LGMD2A: Mutation analysis or protein testing?
2004 Fanin, M; Fulizio, L; Nascimbeni, Ac; Spinazzi, M; Piluso, Giulio; Ventriglia, Vm; Ruzza, G; Siciliano, G; Trevisan, Cp; Politano, Luisa; Nigro, Vincenzo; Angelini, C.
Non invasive assessment of atrial fibrosis in Emery-Dreifuss muscular dystrophy patients by acoustic densitometry
2005 Politano, Luisa; Petretta, V. R.; Palladino, A.; Ventriglia, V. M.; Sannino, P.; Nigro, G. E.; Piluso, Giulio; Comi, L. I.; Nigro, Vincenzo; Nigro, Gerardo
Le Distrofie dei Cingoli autosomiche recessive: calpainopatie e disferlinopatie
2005 Palladino, A; Piluso, Giulio; Ventriglia, Vm; Sannino, P; Aurino, S; Nigro, Vincenzo; Politano, Luisa
Molecular analysis of sarcoglycan genes in LGMD patients recruited using different methods
2005 Aurino, S.; Saccone, V.; Piluso, Giulio; Esposito, M.; Ventriglia, V. M.; Trimarco, L.; Politano, Luisa; Topaloglu, H.; Minetti, C.; Nigro, Vincenzo
Molecular and Muscle Pathology in a series of Caveolinopathy patients
2005 Fulizio, L; Nascimbeni, Ac; Fanin, M; Piluso, Giulio; Politano, Luisa; Nigro, Vincenzo; Angelini, C.
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes
2005 Piluso, Giulio; Politano, Luisa; Aurino, S; Fanin, M; Ricci, E; Ventriglia, Vm; Belsito, Angela; Totaro, A; Saccone, V; Topaloglu, H; Nascimbeni, Ac; Fulizio, L; Broccolini, A; CANKI KLAIN, N; Comi, Li; Nigro, Gerardo; Angelini, C; Nigro, Vincenzo
The loss of interaction between TRIM32 and ubiquitination machinery is involved in limb-girdle muscular dystrophy 2H
2005 Saccone, V.; Aurino, S.; Meroni, G.; Dionisi, M.; Politano, Luisa; Piluso, Giulio; Nigro, Vincenzo
P.P.6 02 Cardiac and respiratory involvement in autosomal recessive limb-girdle muscular dystrophies
2006 Palladino, A.; Ventriglia, V. M.; Passamano, L.; Aurino, S.; Russo, R.; D’Amico, F.; Petretta, V. R.; Piluso, G.; Comi, L. I.; Nigro, V.; Nigro, G.; Politano, L.
G.P.4.03 Mutations in the lamin A/C gene: An emergent cause of fatal arrhythmias in congenital muscular dystrophies
2006 Politano, L.; Ventriglia, V. M.; Palladino, A.; Piluso, G.; Passamano, L.; Nigro, V.; Petretta, Vito Rocco; Comi, Lucia Ines; Nigro, G.
T.O. 6 Systemic delta-sarcoglycan gene transfer into cardiomyopathic BIO14.6 hamsters by AAV
2006 Vitiello, Adone Carlo; Auricchio, A.; Faraso, S.; Sorrentino, N.; Di Napoli, D.; Castaldo, S.; Nusco, E.; Aurino, S.; Saccone, V.; Piluso, G.; Nigro, V.
Le Distrofie muscolari dei Cingoli autosomiche recessive in Sud Italia: Aspetti clinici, genetici ed epidemiologici
2008 Passamano, L; Ventriglia, V. M.; Palladino, A; Aurino, S; Petretta, V. R.; Damico, F; Paciello, O; Saccone, V; Piluso, Giulio; Papparella, S; Nigro, Vincenzo; Politano, Luisa
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Heart involvement in Emery-Dreifuss muscular dystrophies: new parameters to detect early atrial fibrosis and vulnerability | 1-gen-2002 | Politano, Luisa; Nigro, Ge; Petretta, Vr; Ventriglia, Vm; Santangelo, L; Piluso, Giulio; Panico, F; Nigro, Vincenzo; Comi, Li; Nigro, Gerardo | |
Clinical, molecular and genetic features of calpainopathy in Slovenia | 1-gen-2002 | MEZNARIC PETRUSA, Mmp; Zidar, J; Zupancic, N; Fanin, M; Angelini, C; Piluso, Giulio; Ventriglia, Vm; Politano, Luisa | |
Identification and analysis of candidate genes for Limb-Girdle Muscular Dystrophies | 1-gen-2002 | Nigro, Vincenzo; Piluso, Giulio; Aurino, S; D'Amico, F; Belsito, Angela; Ventriglia, Vm; Politano, Luisa | |
Multiple heterozygosity for different muscle genes is not rare among individuals with pauci-symptomatic hyperCKemia | 1-gen-2002 | Politano, Luisa; Nigro, Vincenzo; Aurino, S; Belsito, Angela; D'Amico, F; Piluso, Giulio; Ventriglia, Vm; Passamano, L; Palladino, A; Esposito, Mg; Paciello, O; Freda, Fulvio | |
Different phenotypic expression in three related families with limb-girdle muscular dystrophy (LGMD2I) due to mutations in fukutin-related-protein gene | 1-gen-2003 | Politano, Luisa; D'Amico, F; Passamano, L; Ventriglia, Vm; Palladino, A; Aurino, S; Piluso, Giulio; Nigro, G; Nigro, Vincenzo | |
Genetic heterogeneity of FG syndrome: a fourth locus (FGS4) maps to Xp11.4-p11.3 in an Italian family | 1-gen-2003 | Piluso, Giulio; Carella, M; D'Avanzo, M; Santinelli, R; Carrano, Em; D'Avanzo, A; D'Adamo, Ap; Gasparini, P; Nigro, Vincenzo | |
Scanning for mutations of the ryanodine receptor (RYR1) gene by denaturing HPLC: detection of three novel malignant hyperthermia alleles | 1-gen-2003 | Tammaro, A; Bracco, A; Cozzolino, S; Esposito, M; DI MARTINO, A; Savoia, G; Zeuli, L; Piluso, Giulio; Aurino, S; Nigro, Vincenzo | |
Gentamicin administration in Duchenne patients with premature stop codon. Preliminary results | 1-gen-2003 | Politano, Luisa; Nigro, Gerardo; Nigro, Vincenzo; Piluso, Giulio; Papparella, S; Paciello, O; Comi, Li | |
Prevalence of the 550delA mutation in calpainopathy (LGMD 2A) in Croatia | 1-gen-2004 | Cankiklain, N; Milic, A; Kovac, B; Trlaja, A; Grgicevic, D; Zurak, N; Fardeau, M; Leturcq, F; Kaplan, Jc; Urtizberea, Ja; Politano, Luisa; Piluso, Giulio; Feingold, J. | |
Molecular diagnosis in LGMD2A: Mutation analysis or protein testing? | 1-gen-2004 | Fanin, M; Fulizio, L; Nascimbeni, Ac; Spinazzi, M; Piluso, Giulio; Ventriglia, Vm; Ruzza, G; Siciliano, G; Trevisan, Cp; Politano, Luisa; Nigro, Vincenzo; Angelini, C. | |
Non invasive assessment of atrial fibrosis in Emery-Dreifuss muscular dystrophy patients by acoustic densitometry | 1-gen-2005 | Politano, Luisa; Petretta, V. R.; Palladino, A.; Ventriglia, V. M.; Sannino, P.; Nigro, G. E.; Piluso, Giulio; Comi, L. I.; Nigro, Vincenzo; Nigro, Gerardo | |
Le Distrofie dei Cingoli autosomiche recessive: calpainopatie e disferlinopatie | 1-gen-2005 | Palladino, A; Piluso, Giulio; Ventriglia, Vm; Sannino, P; Aurino, S; Nigro, Vincenzo; Politano, Luisa | |
Molecular analysis of sarcoglycan genes in LGMD patients recruited using different methods | 1-gen-2005 | Aurino, S.; Saccone, V.; Piluso, Giulio; Esposito, M.; Ventriglia, V. M.; Trimarco, L.; Politano, Luisa; Topaloglu, H.; Minetti, C.; Nigro, Vincenzo | |
Molecular and Muscle Pathology in a series of Caveolinopathy patients | 1-gen-2005 | Fulizio, L; Nascimbeni, Ac; Fanin, M; Piluso, Giulio; Politano, Luisa; Nigro, Vincenzo; Angelini, C. | |
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes | 1-gen-2005 | Piluso, Giulio; Politano, Luisa; Aurino, S; Fanin, M; Ricci, E; Ventriglia, Vm; Belsito, Angela; Totaro, A; Saccone, V; Topaloglu, H; Nascimbeni, Ac; Fulizio, L; Broccolini, A; CANKI KLAIN, N; Comi, Li; Nigro, Gerardo; Angelini, C; Nigro, Vincenzo | |
The loss of interaction between TRIM32 and ubiquitination machinery is involved in limb-girdle muscular dystrophy 2H | 1-gen-2005 | Saccone, V.; Aurino, S.; Meroni, G.; Dionisi, M.; Politano, Luisa; Piluso, Giulio; Nigro, Vincenzo | |
P.P.6 02 Cardiac and respiratory involvement in autosomal recessive limb-girdle muscular dystrophies | 1-gen-2006 | Palladino, A.; Ventriglia, V. M.; Passamano, L.; Aurino, S.; Russo, R.; D’Amico, F.; Petretta, V. R.; Piluso, G.; Comi, L. I.; Nigro, V.; Nigro, G.; Politano, L. | |
G.P.4.03 Mutations in the lamin A/C gene: An emergent cause of fatal arrhythmias in congenital muscular dystrophies | 1-gen-2006 | Politano, L.; Ventriglia, V. M.; Palladino, A.; Piluso, G.; Passamano, L.; Nigro, V.; Petretta, Vito Rocco; Comi, Lucia Ines; Nigro, G. | |
T.O. 6 Systemic delta-sarcoglycan gene transfer into cardiomyopathic BIO14.6 hamsters by AAV | 1-gen-2006 | Vitiello, Adone Carlo; Auricchio, A.; Faraso, S.; Sorrentino, N.; Di Napoli, D.; Castaldo, S.; Nusco, E.; Aurino, S.; Saccone, V.; Piluso, G.; Nigro, V. | |
Le Distrofie muscolari dei Cingoli autosomiche recessive in Sud Italia: Aspetti clinici, genetici ed epidemiologici | 1-gen-2008 | Passamano, L; Ventriglia, V. M.; Palladino, A; Aurino, S; Petretta, V. R.; Damico, F; Paciello, O; Saccone, V; Piluso, Giulio; Papparella, S; Nigro, Vincenzo; Politano, Luisa |
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