Sfoglia per Autore
The syndrome of carnitine deficiency: morphological and metabolic correlations in two cases
1978 G. Scarlato, G. Pellegrini, C. Cerri, G. Meola, A. Veicsteinas
Erythrocyte spectrofluorometric abnormalities in Duchenne patients and carriers. A new approach to carrier detection
1979 G. Scarlato, G. Meola, V. Silani, L. Manfredi, G. Bottiroli, A. Zanella
Metabolic impairment and membrane abnormality in red cells from Huntington's disease
1980 A. Zanella, C. Izzo, G. Meola, M. Mariani, M.T. Colotti, V. Silani, G. Pellegata, G. Scarlato
Pentazocine-induced neuromuscular syndromes: clinical, immunological and histopathological studies in two cases
1981 C. Mariani, G. Meola, P.L. Meroni, C. Guaita, G. Scarlato
Manifesting carrier of x-linked Duchenne muscular dystrophy
1981 G. Meola, E. Scarpini, V. Silani, G. Scarlato
Morphological studies and quantitative assessment of the effect of chick embryo extract on monolayer cultures of normal human muscle
1982 E. Scarpini, G. Meola, P. Baron, M. Moggio, V. Silani, G. Scarlato
Complex IV change in the mitochondria respiratory chain of chronic external ophtalmoplegia : a review of our cases
1985 N. Bresolin, M. Moggio, L. Bet, G. Meola, A. Bordoni, G. Pellegrini, E. Nobile-Orazio, G. Scarlato
Antigen expression by cultured human Schwann cells
1986 E. Scarpini, G. Meola, E. Nobile-Orazio, P. Baron, S. Beretta, M. Velicogna, G. Zuliani, G. Scarlato
Cytogenetic analysis and muscle differentiation in a girl with severe muscular dystrophy
1986 G. Meola, E. Scarpini, M. Velicogna, G. Scarlato, L. Larizza, A. F. Conti
A comparative analysis of collagen III, IV, laminin and fibronectin in Duchenne muscular dystrophy biopsies and cell cultures
1986 E. Rampoldi, G. Meola, A. M. Conti, M. Velicogna, L. Larizza
Differentiation of human adult and fetal muscle after enzymic dissocation
1987 L. Chianese, E. Scarpini, G. Meola, M. Moggio, M. Velicogna, S. Jann, C. Brigato, R. Azzoni, G. Scarlato
A CASE OF MITOCHONDRIAL MYOPATHY, LACTIC-ACIDOSIS AND COMPLEX-I DEFICIENCY
1990 L. Bet, N. Bresolin, M. Moggio, G. Meola, A. Prelle, A. Schapira, T. Binzoni, A. Chomyn, F. Fortunato, P. Cerretelli, G. Scarlato
[Expression of a defect in the respiratory chain in cultured human cells]
1991 G. Meola, G. Rotondo, M. Velicogna, R. Toppi, V. Sansone, N. Bresolin, G. Comi, A. Bordoni, P. Amati, C. Ausenda
Cytoplasmic restoration and persistence of glucose-6-phosphate dehydrogenase activity in stable hybrid myotubes
1993 V. Sansone, G. Rotondo, G. Bottiroli, J.P. Tremblay, G. Meola
Muscle glucose-6-phosphate dehydrogenase deficiency: restoration of enzymatic activity in hybrid myotubes
1993 G. Meola, J.P. Tremblay, V. Sansone, G. Rotondo, S. Radice, N. Bresolin, J. Huard, G. Scarlato
Stable hybrid myotubes: a new model for studying re-expression of enzymatic activities in vitro
1993 G. Meola, V. Sansone, G. Rotondo, S. Radice, G. Bottiroli, G. Scarlato
Enzymatic activity and morphological differentiation in de novo innervated human muscle cultures
1994 G. Meola, V. Sansone, S. Radice, G. Rotondo, J.P. Tremblay
Neural regulation of acid maltase in an unusual adult onset deficiency
1994 G. Meola, V. Sansone, G. Rotondo, S. Radice, M. Sterlicchio, M. Mauri, N. Bresolin, M. Moggio
Mutation in the S4 segment of the adult skeletal sodium channel gene in an Italian paramyotonia congenita (PC) family
1994 V. Sansone, G. Rotondo, L.J. Ptacek, G. Meola
A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies
1996 G. Meola, V. Sansone, S. Radice, S. Skradski, L. Ptacek
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