Sfoglia per Autore
Bezafibrate-induced myopathy: no evidence for defects in muscle metabolism.
1993-01-01 VITA, G; TOSCANO, A; MILETO, G; PITRONE, F; FERRO, MT; GAGLIARDI, E; BRESOLIN ,N; FORTUNATO, F; .MESSINA,C.
CARDIOVASCULAR AUTONOMIC DYSFUNCTION IN MULTIPLE-SCLEROSIS IS LIKELY RELATED TO BRAIN-STEM LESIONS
1993-01-01 Vita, Giuseppe; Fazio, Mc; Milone, S; Blandino, Alfredo; Salvi, L; Messina, Corrado
Rippling muscle disease: evidence for a muscle bioenergetic deficiency
1993-01-01 Toscano, Antonio; Girlanda, Paolo; Barbiroli, B.; Vita, Giuseppe; Dattola, Roberto; Fazio, M. C.; Fortunato, F.; Bresolin, N.; Messina, Corrado
Extra-muscle involvement in Xp21-linked muscular dystrophy: an electroretinography and evoked potentials study
1994-01-01 Vita, G; Girlanda, Paolo; Buceti, R; Sinicropi, S; Quartarone, Angelo; Macaione, Vincenzo; Ferreri, G; SAAD F., A; DANIELI G., A; Messina, C.
Retinal and central nervous system involvement in Xp21-linked muscular dystrophy: an electroretinography and evoked potentials study
1994-01-01 Vita, G; Girlanda, Paolo; Buceti, R; Sinicropi, S; Quartarone, Angelo; Macaione, Vincenzo; Ferreri, G; Messina, C.
CLINICAL VARIABILITY IN BECKER MUSCULAR-DYSTROPHY - GENETIC, BIOCHEMICAL AND IMMUNOHISTOCHEMICAL CORRELATES
1994-01-01 COMI, GP.; PRELLE, A.; BRESOLIN, N.; MOGGIO, M.; BARDONI, A.; GALLANTI, A.; VITA, G.; TOSCANO, A.; FERRO, MT.; BORDONI, A.; FORTUNATO, F.; CISCATO, P.; FELISARI, G.; TEDESCHI, S.; CASTELLI, E.; GARGHENTINO, R.; TURCONI, A.; FRASCHINI, P.; MARCHI, E.; NEGRETTO, GG.; ADOBBATI, L.; MEOLA, G.; TONIN, P.; PAPADIMITRIOU, A.; SCARLATO, G.
IMMUNOCYTOCHEMISTRY OF MUSCLE CYTOSKELETAL PROTEINS IN ACID MALTASE DEFICIENCY
1994-01-01 VITA, G; MIGLIORATO, A.; TOSCANO, A; BORDONI, A; BRESOLIN, N; FIUMARA, A; MESSINA, C.
EXPRESSION OF CYTOSKELETON PROTEINS IN CENTRAL CORE DISEASE
1994-01-01 Vita, Giuseppe; Migliorato, Alba; Baradello, Alice; Mazzeo, Anna; Rodolico, Carmelo; Falsaperla, R; Messina, Corrado
A POSSIBLE MISSENSE MUTATION DETECTED IN THE DYSTROPHIN GENE BY DOUBLE-STRAND CONFORMATION ANALYSIS (DSCA)
1994-01-01 Saad, Fa; Vita, Giuseppe; Toffolatti, L; Danieli, Ga
CONGENITAL MUSCULAR-DYSTROPHY - CORRELATION OF MUSCLE BIOPSY AND CLINICAL-FEATURES
1994-01-01 PARANO E; FIUMARA A; FALSAPERLA R; G. VITA; TRIFILETTI RR
FETUS-LIKE DYSTROPHIN EXPRESSION AND OTHER CYTOSKELETAL PROTEIN ABNORMALITIES IN CENTRONUCLEAR MYOPATHIES
1994-01-01 Mora, M; Morandi, L; Merlini, L; Vita, Giuseppe; Baradello, Alice; Barresi, R; Diblasi, C; Blasevich, F; Gebbia, M; Daniel, S; Cornelio, F.
MUSCLE PHOSPHOGLYCERATE MUTASE (PGAM) DEFICIENCY IN THE 1ST CAUCASIAN PATIENT - BIOCHEMISTRY, MUSCLE CULTURE AND P-31-MR SPECTROSCOPY
1994-01-01 Vita, Giuseppe; Toscano, A; Bresolin, N; Meola, G; Fortunato, F; Baradello, Alice; Barbiroli, B; Frassineti, C; Zaniol, P; Messina, Corrado
CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY IN PATIENT WITH RHEUMATOID-ARTHRITIS
1995-01-01 Zappia, M; Valentino, P; Bono, F; Vita, Giuseppe; Aguglia, U; Messina, Corrado; Quattrone, A.
LOCALIZATION OF VINCULIN AND TALIN AT PERINEURIAL CELLS OF HUMAN SURAL NERVE
1995-01-01 VITA G; MAZZEO A; RODOLICO C; MIGLIORATO A.; GAGLIARDI M; CICCIARELLO R; MUGLIA U; MESSINA C
CHARCOT-MARIE-TOOTH-DISEASE - MOLECULAR CHARACTERIZATION OF PATIENTS FROM CENTRAL AND SOUTHERN ITALY
1995-01-01 GUZZETTA V; SANTORO L; GASPARORIPPA P; RAGNO M; G. VITA; CARUSO G; ANDRIA G
Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and C
1995-01-01 Toscano, Antonio; Fazio, M. C.; Vita, Giuseppe; Cannavo', Salvatore; Bresolin, N.; Bet, L.; Prelle, A.; Barbiroli, B.; Iotti, S; Zaniol, P.; Magaudda, Adriana; Trimarchi, F.; Messina, Corrado
DUPLICATION OF DYSTROPHIN GENE AND DISSIMILAR CLINICAL PHENOTYPE IN THE SAME FAMILY
1995-01-01 TOSCANO, A.; VITIELLO, L.; COMI, GP.; GALVAGNI, F.; MIORIN, M.; PRELLE, A.; FORTUNATO, F.; BARDONI, A.; MORA, M.; FIUMARA, A.; FALSAPERLA, R.; TOMELLERI, G.; TONIN, P.; DANIELI, GA.; VITA,G.
Molecular basis of muscle phosphoglycerate mutase (PGAM-M) deficiency in the italian kindred.
1996-01-01 Toscano, Antonio; Tsujino, S; Vita, Giuseppe; Shanske, S; Messina, Corrado; Dimauro, S.
Lobulated muscle fibers have a normal cytoskeletal network
1996-01-01 Vita, Giuseppe; Monici, Mc; Toscano, Antonio; Messina, Corrado
Uremic autonomic neuropathy: Recovery following bicarbonate hemodialysis
1996-01-01 Vita, Giuseppe; Savica, Vincenzo; Milone, S; Trusso, A; Bellinghieri, Guido; Messina, Corrado
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Bezafibrate-induced myopathy: no evidence for defects in muscle metabolism. | 1-gen-1993 | VITA, G; TOSCANO, A; MILETO, G; PITRONE, F; FERRO, MT; GAGLIARDI, E; BRESOLIN ,N; FORTUNATO, F; .MESSINA,C. | |
CARDIOVASCULAR AUTONOMIC DYSFUNCTION IN MULTIPLE-SCLEROSIS IS LIKELY RELATED TO BRAIN-STEM LESIONS | 1-gen-1993 | Vita, Giuseppe; Fazio, Mc; Milone, S; Blandino, Alfredo; Salvi, L; Messina, Corrado | |
Rippling muscle disease: evidence for a muscle bioenergetic deficiency | 1-gen-1993 | Toscano, Antonio; Girlanda, Paolo; Barbiroli, B.; Vita, Giuseppe; Dattola, Roberto; Fazio, M. C.; Fortunato, F.; Bresolin, N.; Messina, Corrado | |
Extra-muscle involvement in Xp21-linked muscular dystrophy: an electroretinography and evoked potentials study | 1-gen-1994 | Vita, G; Girlanda, Paolo; Buceti, R; Sinicropi, S; Quartarone, Angelo; Macaione, Vincenzo; Ferreri, G; SAAD F., A; DANIELI G., A; Messina, C. | |
Retinal and central nervous system involvement in Xp21-linked muscular dystrophy: an electroretinography and evoked potentials study | 1-gen-1994 | Vita, G; Girlanda, Paolo; Buceti, R; Sinicropi, S; Quartarone, Angelo; Macaione, Vincenzo; Ferreri, G; Messina, C. | |
CLINICAL VARIABILITY IN BECKER MUSCULAR-DYSTROPHY - GENETIC, BIOCHEMICAL AND IMMUNOHISTOCHEMICAL CORRELATES | 1-gen-1994 | COMI, GP.; PRELLE, A.; BRESOLIN, N.; MOGGIO, M.; BARDONI, A.; GALLANTI, A.; VITA, G.; TOSCANO, A.; FERRO, MT.; BORDONI, A.; FORTUNATO, F.; CISCATO, P.; FELISARI, G.; TEDESCHI, S.; CASTELLI, E.; GARGHENTINO, R.; TURCONI, A.; FRASCHINI, P.; MARCHI, E.; NEGRETTO, GG.; ADOBBATI, L.; MEOLA, G.; TONIN, P.; PAPADIMITRIOU, A.; SCARLATO, G. | |
IMMUNOCYTOCHEMISTRY OF MUSCLE CYTOSKELETAL PROTEINS IN ACID MALTASE DEFICIENCY | 1-gen-1994 | VITA, G; MIGLIORATO, A.; TOSCANO, A; BORDONI, A; BRESOLIN, N; FIUMARA, A; MESSINA, C. | |
EXPRESSION OF CYTOSKELETON PROTEINS IN CENTRAL CORE DISEASE | 1-gen-1994 | Vita, Giuseppe; Migliorato, Alba; Baradello, Alice; Mazzeo, Anna; Rodolico, Carmelo; Falsaperla, R; Messina, Corrado | |
A POSSIBLE MISSENSE MUTATION DETECTED IN THE DYSTROPHIN GENE BY DOUBLE-STRAND CONFORMATION ANALYSIS (DSCA) | 1-gen-1994 | Saad, Fa; Vita, Giuseppe; Toffolatti, L; Danieli, Ga | |
CONGENITAL MUSCULAR-DYSTROPHY - CORRELATION OF MUSCLE BIOPSY AND CLINICAL-FEATURES | 1-gen-1994 | PARANO E; FIUMARA A; FALSAPERLA R; G. VITA; TRIFILETTI RR | |
FETUS-LIKE DYSTROPHIN EXPRESSION AND OTHER CYTOSKELETAL PROTEIN ABNORMALITIES IN CENTRONUCLEAR MYOPATHIES | 1-gen-1994 | Mora, M; Morandi, L; Merlini, L; Vita, Giuseppe; Baradello, Alice; Barresi, R; Diblasi, C; Blasevich, F; Gebbia, M; Daniel, S; Cornelio, F. | |
MUSCLE PHOSPHOGLYCERATE MUTASE (PGAM) DEFICIENCY IN THE 1ST CAUCASIAN PATIENT - BIOCHEMISTRY, MUSCLE CULTURE AND P-31-MR SPECTROSCOPY | 1-gen-1994 | Vita, Giuseppe; Toscano, A; Bresolin, N; Meola, G; Fortunato, F; Baradello, Alice; Barbiroli, B; Frassineti, C; Zaniol, P; Messina, Corrado | |
CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY IN PATIENT WITH RHEUMATOID-ARTHRITIS | 1-gen-1995 | Zappia, M; Valentino, P; Bono, F; Vita, Giuseppe; Aguglia, U; Messina, Corrado; Quattrone, A. | |
LOCALIZATION OF VINCULIN AND TALIN AT PERINEURIAL CELLS OF HUMAN SURAL NERVE | 1-gen-1995 | VITA G; MAZZEO A; RODOLICO C; MIGLIORATO A.; GAGLIARDI M; CICCIARELLO R; MUGLIA U; MESSINA C | |
CHARCOT-MARIE-TOOTH-DISEASE - MOLECULAR CHARACTERIZATION OF PATIENTS FROM CENTRAL AND SOUTHERN ITALY | 1-gen-1995 | GUZZETTA V; SANTORO L; GASPARORIPPA P; RAGNO M; G. VITA; CARUSO G; ANDRIA G | |
Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and C | 1-gen-1995 | Toscano, Antonio; Fazio, M. C.; Vita, Giuseppe; Cannavo', Salvatore; Bresolin, N.; Bet, L.; Prelle, A.; Barbiroli, B.; Iotti, S; Zaniol, P.; Magaudda, Adriana; Trimarchi, F.; Messina, Corrado | |
DUPLICATION OF DYSTROPHIN GENE AND DISSIMILAR CLINICAL PHENOTYPE IN THE SAME FAMILY | 1-gen-1995 | TOSCANO, A.; VITIELLO, L.; COMI, GP.; GALVAGNI, F.; MIORIN, M.; PRELLE, A.; FORTUNATO, F.; BARDONI, A.; MORA, M.; FIUMARA, A.; FALSAPERLA, R.; TOMELLERI, G.; TONIN, P.; DANIELI, GA.; VITA,G. | |
Molecular basis of muscle phosphoglycerate mutase (PGAM-M) deficiency in the italian kindred. | 1-gen-1996 | Toscano, Antonio; Tsujino, S; Vita, Giuseppe; Shanske, S; Messina, Corrado; Dimauro, S. | |
Lobulated muscle fibers have a normal cytoskeletal network | 1-gen-1996 | Vita, Giuseppe; Monici, Mc; Toscano, Antonio; Messina, Corrado | |
Uremic autonomic neuropathy: Recovery following bicarbonate hemodialysis | 1-gen-1996 | Vita, Giuseppe; Savica, Vincenzo; Milone, S; Trusso, A; Bellinghieri, Guido; Messina, Corrado |
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