Sfoglia per Autore
A molecular study of a family with Greek hereditary persistence of fetal hemoglobin and beta-thalassemia
1984 B. Giglioni, C. Casini, R. Mantovani, S. Merli, P. Comi, S. Ottolenghi, G. Saglio, C. Camaschella, U. Mazza
Heterogeneity of delta, beta-thalassemia and hereditary persistence of Hb F in the Mediterranean area
1985 S. Ottolenghi, B. Giglioni, P. Comi, S. Guida, C. Casini, S. Merli, R. Mantovani, F. Terragni, D. Aghib, G. Saglio
A protein factor binding to an octamer motif in the gamma-globin promoter disappears upon induction of differentiation and hemoglobin synthesis in K562 cells
1987 R. Mantovani, N. Malgaretti, B. Giglioni, P. Comi, N. Cappellini, S. Nicolis, S. Ottolenghi
Sardinian G gamma-HPFH: a T----C substitution in a conserved "octamer" sequence in the G gamma-globin promoter
1988 S. Ottolenghi, S. Nicolis, R. Taramelli, N. Malgaretti, R. Mantovani, P. Comi, B. Giglioni, M. Longinotti, F. Dore, L. Oggiano
[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
Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis
1993 A. Prelle, M. Moggio, N. Checcarelli, G. Comi, N. Bresolin, A. Battistel, A. Bordoni, G. Scarlato
Chronic progressive external ophthalmoplegia: A correlative study of quantitative molecular data and histochemical and biochemical profile
1994 A. Fassati, A. Bordoni, P. Amboni, F. Fortunato, G. Fagiolari, N. Bresolin, A. Prelle, G. Comi, G. Scarlato
Ryanodine receptor gene point mutation and malignant hyperthermia susceptibility
1995 I. Moroni, E. Gonano, G. Comi, V. Tegazzin, A. Prelle, A. Bordoni, N. Bresolin, G. Scarlato
PROMM syndrome without trinucleotide repeat expansion
1996 G.P. Comi, M. Carpo, E. Nobile-Orazio, C. Rizzi, R. Del Bo, A. Battistel, G. Scarlato
Proximal myotonic myopathy (PROMM) syndrome without CTG expansion: a new case
1996 G.P. Comi, M. Carpo, E. Nobile-Orazio, C. Rizzi, R. Del Bo, A. Prelle, G. Scarlato
The influence of coenzyme Q(10) on total serum calcium concentration in two patients with Kearns-Sayre Syndrome and hypoparathyroidism
1996 A. Papadimitriou, G. Hadjigeorgiou, R. Divari, N. Papagalanis, G. Comi, N. Bresolin
In Vivo Biolistic Technique in Control and Mdx Dystrophic Mice
1996 C.D. Ausenda, N. Bresolin, A. De Liso, M.G. D'Angelo, M. Moggio, R. Del Bo, A. Gallanti, G.P. Comi, Y. Torrente, A. Bordoni, G. Scarlato
5'azacytidine enhances exogenous gene expression in muscle
1997 M. Dangelo, C. Ausenda, Y. Torrente, S. Corti, M. Perini, M. Colucci, G. Comi, N. Bresolin, G. Scarlato
Intra-Aortic injection of myoblasts in Mdx mice: genetic and technetium-99m cell labeling and biodistribution
1997 N. Bresolin, C.D. Ausenda, R. Casati, Y. Torrente, A. DeLiso, M.G. D’Angelo, R. Benti, M. Moggio, S. Baldessari, G.P. Comi, F. Colombo, P. Gerundini, G. Scarlato
Abnormal expression of cyclin-dependent kinase in an atypical case of desminopathy
1998 M. Sciacco, A. Prelle, G.P. Comi, S. Messina, P. Ciscato, M. Carpo, E. Nobile-Orazio, F. Fortunato, G. Mora, V. Bignotti, G. Fagiolari, G. Scarlato, M. Moggio
An atypical case of desminopathy with abnormal expression of cyclin-dependent kinase
1998 M. Sciacco, A. Prelle, G.P. Comi, S. Messina, P. Ciscato, M. Carpo, E. Nobile-Orazio, F. Fortunato, G. Mora, V. Bignotti, G. Fagiolari, G. Scarlato, M. Moggio
5 ' azacytidine enhances exogenous gene expression in skeletal muscle
1999 M. D'Angelo, C. Ausenda, Y. Torrente, A. Bordoni, S. Corti, R. Del Bo, M. Perini, M. Colucci, G. Comi, N. Bresolin, G. Scarlato
Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochrome c oxidase deficiency
1999 V. Tiranti, M. Jaksch, S. Hofmann, C. Galimberti, K. Hoertnagel, L. Lulli, P. Freisinger, L. Bindoff, K.D. Gerbitz, G. Comi, G. Uziel, M. Zeviani, T. Meiringer
Extracorporeal circulation as a new experimental pathway for myoblast implantation in mdx mice
1999 Y. Torrente, M.G. D'Angelo, R. Del Bo, A. DeLiso, R. Casati, R. Benti, S. Corti, G.P. Comi, P. Gerundini, A. Anichini, G. Scarlato, N. Bresolin
A sporadic, atypical case of desminopathy: morphological and immunological characterization
2000 A. Prelle, M. Sciacco, G.P. Comi, S. Messina, M. Carpo, P. Ciscato, E. Nobile Orazio, F. Fortunato, G. Mora, V. Bignotti, G. Fagiolari, M. Moggio, G. Scarlato
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