Stefania Corti - Dissemin

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Papers authored by Stefania Corti

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2001 M. Sironi, S. Corti

ORCID

, F. Locatelli, R. Cagliani, G. P. Comi

ORCID

Erratum: A novel splice site mutation (3157+1G>T) in the dystrophin gene causing total exon skipping and DMD phenotype

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R. D. Bo, Roberto Del Bo, Yvan Torrente, Stefania Corti

ORCID

, Maria Grazia D'Angelo, Giacomo Pietro Comi

ORCID

, Gigliola Fagiolari, Sabrina Salani, Agata Cova, Federica Pisati, Maurizio Moggio, Carlo Ausenda, Guglielmo Scarlato, Nereo Bresolin

In vitro and in vivo tetracycline-controlled myogenic conversion of NIH-3T3 cells: Evidence of programmed cell death after muscle cell transplantation

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This paper was not found in any repository, but could be made available legally by the author.

M. Sironi, S. Corti

ORCID

, F. Locatelli, R. Cagliani, G. P. Comi

ORCID

A novel splice site mutation (3157+1G>T) in the dystrophin gene causing total exon skipping and DMD phenotype

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This paper is made freely available by the publisher.

2000 M. G. D'Angelo, Z. Li, R. Del Bo, S. Corti

ORCID

, M. Mericskay, A. DeLiso, A. Fassati, D. Paulin, Y. Torrente, G. P. Comi

ORCID

, G. Scarlato, N. Bresolin

Transplacental injection of somite-derived cells in mdx mouse embryos for the correction of dystrophin deficiency

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This paper is made freely available by the publisher.

1999 Y. Torrente, M. G. D'Angelo, R. Del Bo, A. DeLiso, R. Casati, R. Benti, S. Corti

ORCID

ORCID

, P. Gerundini, A. Anichini, G. Scarlato, N. Bresolin

Extracorporeal circulation as a new experimental pathway for myoblast implantation in mdx mice

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

1998 E. Spaggiari, Perin, D. Brambilla, L. Cappelletti, S. Strazzer, S. Corti

ORCID

, N. Bresolin

Usher syndrome | La sindrome di Usher

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